Choose a cancer type (or all), switch between products, technologies, targets, trials, pairings, ideas, companies, and institutions, then sort and filter. Every row links to its page. The rank is a disclosed documentation-and-evidence score, not a measure of clinical benefit.
Small-molecule CYP17A1 inhibitor · Abiraterone is a pill that shuts down testosterone production everywhere, including inside the tumour. Discovered at the Institute of Cancer Research, now generic and used from the first metastatic diagnosis.
Small-molecule covalent BTK inhibitor (second generation) · Acalabrutinib is a cleaner BTK blocker with fewer heart and bleeding problems than ibrutinib. In February 2026 it became half of the first all-oral, fixed-duration CLL regimen.
Small-molecule inhibitor (KRAS G12C) · Adagrasib was the second KRAS G12C inhibitor, with a long half-life and brain penetration, and is approved in lung and colorectal cancer.
Bispecific antibody (EGFR×MET) · A two-armed antibody that blocks EGFR and its escape partner MET, now first-line for EGFR-mutant lung cancer with lazertinib.
Monoclonal antibody (anti-PD-L1) · A PD-L1 blocker used in lung, liver, and bladder cancer. In 2026 it became the first drug approved based on a blood test showing leftover cancer after bladder surgery.
Small-molecule hypomethylating agent (cytotoxic) · A gentle chemotherapy that switches silenced genes back on. With venetoclax it became the standard for older people with AML who cannot take intensive treatment.
Small-molecule HIF-2α inhibitor · Belzutifan is the first HIF-2α inhibitor, born from Nobel-winning biology, and is now approved after kidney cancer surgery with pembrolizumab.
Monoclonal antibody (anti-VEGF) · The first drug to starve tumours of blood vessels. Approved in 2004 for bowel cancer, it remains a standard partner for chemotherapy in many cancers and is the add-on that makes late-line pills work better.
Bispecific T-cell engager (CD19×CD3) · Blinatumomab was the first T-cell engager (2014), and is now given to children and adults with leukaemia even when in remission, because it improves survival.
Proteasome inhibitor · Bortezomib was the first proteasome inhibitor: it jams the cell's protein-recycling machine, which antibody-factory plasma cells cannot tolerate.
Small-molecule multi-kinase inhibitor (MET, VEGFR2, AXL, RET) · A pill that blocks both blood-vessel growth and the MET escape pathway, used in kidney, liver, thyroid and, since 2025, neuroendocrine cancers.
Oral SERD · Camizestrant is an oral oestrogen-receptor degrader approved in September 2026 for a new kind of decision: switching treatment when a blood test shows resistance developing, before the cancer visibly grows.
Monoclonal antibody (anti-PD-1) · One of China's most widely used PD-1 blockers, approved there for oesophageal, liver, lung, and other cancers; not approved in the US.
Small-molecule AKT inhibitor · Capivasertib (Truqap) is the first AKT inhibitor, for breast cancer with PI3K-pathway mutations and, since 2026, for prostate cancer with PTEN loss.
Cytotoxic regimen · CAPOX combines oral capecitabine with oxaliplatin as a pill-based alternative to FOLFOX. Three months of it after surgery is enough for many stage III colon cancers.
Cytotoxic chemotherapy (platinum) · Carboplatin is a platinum chemotherapy that crosslinks DNA; it is part of the standard pre-surgery regimen for triple-negative breast cancer.
Monoclonal antibody (anti-PD-1) · A PD-1 blocker that is the standard for advanced skin squamous cell carcinoma, and in 2025 became the first adjuvant immunotherapy for it.
Monoclonal antibody (anti-EGFR) · An antibody that blocks the EGFR growth receptor. It works in bowel cancers with a normal RAS gene, especially left-sided ones, and is a key partner in the BRAF combination.
CAR-T (BCMA) · Ciltacabtagene autoleucel is a one-time BCMA CAR-T for myeloma that, in CARTITUDE-4, cut the risk of death by about 45% compared with standard regimens.
Cytotoxic chemotherapy (platinum) · Cisplatin is the original platinum chemotherapy, discovered by accident in 1965; it cures testicular cancer and makes radiation work better in cervical and head and neck cancer.
Alkylating agent (oxazaphosphorine prodrug) · One of the most widely used chemotherapy drugs: part of CHOP for lymphoma, AC for breast cancer, VAC for childhood sarcomas, and used to prepare patients for CAR-T and transplant.
Small-molecule kinase inhibitors (BRAF + MEK) · Dabrafenib plus trametinib is the BRAF-plus-MEK pill combination, approved for BRAF V600E lung cancer and, since 2022, for any solid tumour with that mutation.
Actinomycin antibiotic (transcription inhibitor) · The first antibiotic used as an anticancer drug (1954) and still the core of chemotherapy for Wilms tumour, rhabdomyosarcoma and gestational trophoblastic disease.
Monoclonal antibody (anti-CD38) · The CD38 antibody that turned triplets into quadruplets: adding it to standard induction roughly halves the risk of myeloma progressing.
Small-molecule pan-RAS(ON) inhibitor · The first drug that blocks all active RAS variants, approved by the FDA in August 2026 for metastatic pancreatic cancer, where KRAS drives 90% of tumours.
Small-molecule kinase inhibitor (BCR::ABL1, SRC) · Dasatinib is a second-generation BCR::ABL1 pill that, combined with the immunotherapy blinatumomab, can put Ph-positive ALL into deep remission with no chemotherapy at all.
ADC · Datopotamab deruxtecan (Datroway) is the second TROP2 ADC and shares Enhertu's payload. In 2026 it became a first-line option for triple-negative breast cancer patients who cannot receive immunotherapy.
Monoclonal antibody (anti-GD2, chimeric) · The antibody that raised cure rates in high-risk childhood neuroblastoma by about 20 points when given after transplant with immune boosters and retinoid.
Cytotoxic chemotherapy (taxane) · The first chemotherapy to extend life in prostate cancer (2004), now part of triplet therapy at first metastatic diagnosis.
Monoclonal antibody (anti-PD-1) · Dostarlimab is a PD-1 blocker famous for making rectal cancer disappear without surgery in every patient with a mismatch-repair-deficient tumour.
Cytotoxic chemotherapy (anthracycline) · The red chemotherapy drug from a soil bacterium that is still the backbone of treatment for sarcoma, lymphoma and breast cancer, limited by cumulative heart damage.
Monoclonal antibody (anti-PD-L1) · A PD-L1 blocker that became standard after chemoradiation for stage III lung cancer, and now in bladder, biliary, and gastric cancers.
Small-molecule kinase inhibitor (BRAF) · Encorafenib is a BRAF inhibitor that, with cetuximab and chemotherapy, became first-line standard for BRAF-mutant colorectal cancer in 2026.
Small-molecule AR antagonist · The most widely used androgen-receptor blocker, approved across every stage of advanced prostate cancer, including rising PSA after surgery.
Bispecific T-cell engager (CD20×CD3) · Epcoritamab is an under-the-skin injection that pulls T cells onto lymphoma cells; it is approved for relapsed large B-cell and follicular lymphoma, and moving toward first line.
Topoisomerase II inhibitor (podophyllotoxin derivative) · Etoposide is a chemotherapy from the mayapple plant, essential to curing testicular cancer (BEP), treating small-cell lung cancer, lymphomas, childhood sarcomas and leukaemias, and used in transplant conditioning.
Small-molecule mTOR inhibitor · An mTOR-blocking pill that doubled progression-free time with exemestane in 2012 and is now paired with the oral SERD giredestrant.
Fluoropyrimidine antimetabolite · The 1957 chemotherapy that remains the backbone of treatment for bowel, stomach, pancreatic, anal, head and neck and breast cancers, and as a cream for skin precancers.
Cytotoxic regimen · FOLFOX is the workhorse chemotherapy combination for bowel cancer, used after surgery to cure and in advanced disease as the backbone that targeted drugs are added to.
Bispecific T-cell engager (CD20×CD3, 2:1) · Glofitamab is a fixed-duration bispecific for large B-cell lymphoma, with OS benefit when combined with chemotherapy.
Small-molecule covalent BTK inhibitor (first generation) · The pill that ended chemotherapy for most CLL. It blocks the survival signal B cells depend on, and it was the first drug to beat chemoimmunotherapy in nearly every CLL setting.
Cytotoxic chemotherapy (alkylating agent) · Ifosfamide is an alkylating chemotherapy partnered with doxorubicin in sarcoma and with etoposide in Ewing sarcoma, given with a bladder-protecting drug.
Small-molecule kinase inhibitor (BCR-ABL, KIT, PDGFRA) · The drug that started the targeted therapy era in 2001, turning chronic myeloid leukaemia into a manageable condition with near-normal life expectancy.
Monoclonal antibody (anti-CTLA-4) · Ipilimumab was the first checkpoint inhibitor (2011), and proved the immune system could be unleashed against cancer.
Topoisomerase I inhibitor (camptothecin prodrug) · Irinotecan is a topoisomerase-blocking chemotherapy central to bowel and pancreatic cancer regimens (FOLFIRI, FOLFIRINOX, NALIRIFOX) and to salvage therapy in childhood sarcomas; it carries the same warhead as the deruxtecan ADC payloads.
Immunomodulatory drug (cereblon E3 ligase modulator) · A thalidomide descendant that switches on the cell's protein-disposal system against two myeloma survival factors, and is the backbone of myeloma maintenance and many lymphoma regimens.
Small-molecule multi-kinase inhibitor (VEGFR, FGFR, PDGFR, RET, KIT) · An oral anti-angiogenic pill that matched sorafenib in liver cancer with higher response rates, and partners with pembrolizumab in kidney and endometrial cancer.
Small-molecule aromatase inhibitor · Daily pills that stop the body making oestrogen after menopause, the backbone of hormone therapy for most breast cancers.
TIL cell therapy · Lifileucel was the first approved TIL therapy: the patient's own tumour-fighting immune cells are expanded to billions and given back.
CAR-T (CD19, defined CD4:CD8) · Lisocabtagene maraleucel is the only CAR-T approved for chronic lymphocytic leukaemia, for patients whose disease has outrun both BTK and BCL-2 inhibitors.
Small-molecule kinase inhibitor (ALK/ROS1) · An ALK inhibitor with the longest disease control ever recorded for a targeted lung cancer pill: 60% progression-free at five years.
Cytotoxic (transcription inhibitor) · A marine-derived chemotherapy that jams cancer's gene-reading machinery, approved for relapsed small-cell lung cancer and, since 2025, as first-line maintenance with atezolizumab.
Radioligand therapy (beta) · Lutetium-177 dotatate was the first modern radioligand therapy (2018), for neuroendocrine tumours, and is now used in first line.
Alkylating agent (nitrogen mustard) · The myeloma chemotherapy that is also the standard high-dose conditioning before autologous transplant, and, delivered directly into the liver's blood supply or the eye, treats uveal melanoma metastases and retinoblastoma.
Antifolate (DHFR inhibitor) · The 1948 antifolate that produced the first chemotherapy remissions in childhood leukaemia and the first cure of a solid tumour; still essential in ALL, lymphoma, osteosarcoma and CNS lymphoma.
Small-molecule PARP inhibitor · Niraparib is a PARP inhibitor approved as maintenance for ovarian cancer regardless of BRCA status, and in prostate cancer with abiraterone.
Monoclonal antibody (anti-PD-1) · Nivolumab was the second PD-1 blocker and is often combined with ipilimumab. Long-term data show about half of advanced melanoma patients alive at 10 years on the combination.
Prophylactic vaccine (virus-like particles) · A vaccine against nine HPV types that prevents about 90% of cervical cancers, and now works with a single dose.
Monoclonal antibody (anti-CD20, glycoengineered type II) · Obinutuzumab is a supercharged CD20 antibody that, paired with venetoclax for one year, gives many CLL patients years off all treatment.
Small-molecule PARP inhibitor · Olaparib was the first PARP inhibitor, and turned an inherited BRCA mutation from a risk factor into a drug target, including after surgery in breast cancer.
Device (tumour treating fields) · Optune is a wearable device delivering electric fields that disrupt cell division. It is approved for glioblastoma and, in 2026, pancreatic cancer.
Small-molecule kinase inhibitor (EGFR) · Osimertinib (Tagrisso) is the standard pill for EGFR-mutant lung cancer, now also given after surgery and with chemotherapy or after chemoradiation.
Cytotoxic chemotherapy (taxane) · A microtubule poison discovered in the Pacific yew tree, among the most used chemotherapies in breast, lung, and ovarian cancer.
Small-molecule CDK4/6 inhibitor · Palbociclib was the first CDK4/6 inhibitor (2015), and in 2026 became the first approved as maintenance in HER2-positive, hormone-positive breast cancer.
Monoclonal antibody (anti-PD-1) · The most widely used cancer immunotherapy, approved in more than 40 settings, including before and after surgery for triple-negative breast cancer.
Monoclonal antibody (anti-HER2, dimerisation domain) · A second HER2 antibody that binds a different spot from trastuzumab, blocking HER2 from pairing with HER3; together they extended survival by 16 months in CLEOPATRA.
Small-molecule non-covalent (reversible) BTK inhibitor · A BTK blocker that works after the older ones stop, because it grips a different part of the enzyme. Fully approved for CLL in December 2025.
Small-molecule kinase inhibitor (pan-BCR::ABL1 incl. T315I) · Ponatinib is the only BCR::ABL1 inhibitor that covers the T315I resistance mutation. In 2024 it became the preferred pill for newly diagnosed Ph-positive ALL.
Monoclonal antibody (anti-VEGFR2) · An antibody that blocks the VEGF receptor, approved in liver cancer only for patients with a high AFP blood level, the first biomarker-selected HCC drug.
Fixed-dose bispecific combination (anti-LAG-3 + anti-PD-1) · Opdualag combines relatlimab, the first drug targeting the LAG-3 immune brake, with nivolumab for melanoma.
Small-molecule menin inhibitor · Revumenib (Revuforj) is the first menin inhibitor (2024), for acute leukaemias with KMT2A rearrangements or NPM1 mutations.
Small-molecule CDK4/6 inhibitor · Ribociclib is the CDK4/6 inhibitor with the most consistent survival benefit, approved for a broad population of early breast cancer patients since 2024.
Monoclonal antibody (anti-CD20, chimeric) · Rituximab was the first antibody ever approved for cancer (1997). It made chemoimmunotherapy the CLL standard for a decade, and biosimilars keep it cheap and everywhere.
ADC · The first TROP2-targeted ADC. It delivers a strong chemotherapy directly to breast and bladder cancer cells and is now a first-line option in triple-negative breast cancer.
Small-molecule kinase inhibitor (RET) · Selpercatinib is a selective RET inhibitor approved for any tumour with a RET fusion, with a further label update in July 2026.
Small-molecule BCL-2 inhibitor (second generation) · Sonrotoclax is a more potent, shorter-acting successor to venetoclax. It was approved for mantle cell lymphoma in May 2026 and is in late-stage trials with zanubrutinib for CLL.
Small-molecule multi-kinase inhibitor (VEGFR, PDGFR, KIT) · Sunitinib is an anti-angiogenic pill approved for pancreatic neuroendocrine tumours, kidney cancer and GIST.
Bispecific T-cell engager (BCMA×CD3) · Teclistamab was the first off-the-shelf bispecific for multiple myeloma, and is now approved after just one prior line of therapy.
Oral alkylating chemotherapy · The only chemotherapy proven to extend life in glioblastoma, given during and after radiation. It works best when the tumour has switched off a repair gene called MGMT.
CAR-T (CD19) · Tisagenlecleucel was the first CAR-T therapy ever approved (2017), for children and young adults whose leukaemia had come back after everything else.
Monoclonal antibody (anti-PD-1) · A Chinese-developed PD-1 blocker, engineered to avoid a side-channel that may blunt other PD-1 drugs, now approved in the US and EU for oesophageal and stomach cancer.
Monoclonal antibody (anti-HER2) · The first targeted antibody for a solid tumour (1998), which turned HER2-positive breast cancer from the worst subtype into one of the most treatable.
ADC · Trastuzumab deruxtecan (Enhertu) is the most successful ADC ever. It redefined HER2 by working in tumours with only tiny amounts of the protein, and in 2026 moved into early-stage breast cancer.
ADC · Trastuzumab emtansine (Kadcyla, T-DM1) was the first ADC for a solid tumour (2013). It is still standard after surgery for HER2+ breast cancer patients whose tumour did not fully respond to pre-surgery treatment.
Small-molecule BCL-2 inhibitor · A pill that removes the survival shield from leukaemia cells, enabling chemotherapy-free, time-limited treatment for CLL.
PROTAC oestrogen receptor degrader · Vepdegestrant is the first PROTAC ever approved (2026): a pill that tags the oestrogen receptor for destruction, for breast cancers with ESR1 mutations.
Vinca alkaloid (microtubule inhibitor) · A plant-derived chemotherapy from the Madagascar periwinkle that has been in almost every childhood leukaemia and lymphoma regimen since the 1960s.
Oncolytic virus (HSV-1) · Vusolimogene oderparepvec is an engineered herpes virus injected into melanoma tumours, approved in August 2026 with nivolumab after immunotherapy failure.
Biparatopic bispecific antibody (HER2) · Zanidatamab (Ziihera) is an antibody that grabs HER2 at two different spots, approved for HER2+ bile duct cancer.
Small-molecule covalent BTK inhibitor (second generation) · Zanubrutinib is the only BTK blocker to beat ibrutinib on both efficacy and safety in a head-to-head trial. It is now the most prescribed BTK inhibitor in CLL.
Small-molecule menin inhibitor · Ziftomenib is the second menin inhibitor for leukaemia, approved in November 2025 as a once-daily pill for relapsed NPM1-mutated AML.
AI digital pathology prognostic/predictive test · The first AI tool cleared by the FDA to predict both prognosis and treatment benefit from a routine biopsy slide, in prostate cancer.
Live bacterial immunotherapy (intravesical) · A weakened tuberculosis vaccine put directly into the bladder. Since 1976 it has been the most effective treatment for early bladder cancer, and it remains in chronic short supply.
Cytotoxic (antifolate) · Pemetrexed is the chemotherapy that, with a platinum drug, became the first approved treatment for mesothelioma in 2004, and is still the backbone today.
Cytotoxic regimen · Platinum plus etoposide has been the chemotherapy backbone of small-cell lung cancer for over 40 years, and is now given with immunotherapy.
Small-molecule kinase inhibitor (KIT/PDGFRA switch-control) · A fourth-line GIST drug that locks KIT in an off state regardless of which resistance mutation the tumour has acquired.
Blood-based colorectal cancer screening test · The first FDA-approved blood test for colorectal cancer screening (2024), now optionally reporting other cancers too.
Small-molecule SERM · The original targeted cancer drug (1977): a pill that blocks oestrogen's effect on breast cancer and halves recurrence, still essential for premenopausal women.
Small-molecule kinase inhibitor (BRAF V600) · Vemurafenib was the first BRAF inhibitor (2011); it shrank melanomas in weeks and proved that a single mutation could be drugged in a solid tumour.
Monoclonal antibody (anti-Claudin 18.2) · Zolbetuximab is the first drug against Claudin 18.2, a protein exposed on stomach cancer cells. Added to chemotherapy it extends survival by two to three months; nausea is the price.
Small-molecule allosteric ABL1 inhibitor (STAMP) · Asciminib is a BCR::ABL1 blocker that binds a different pocket from every other TKI, approved for all newly diagnosed chronic myeloid leukaemia in 2024 and now being tested in Ph-positive ALL.
Monoclonal antibody (anti-PD-L1) · Avelumab is a PD-L1 blocker given as maintenance after chemotherapy for advanced bladder cancer, which lengthened survival by about seven months.
ADC · Polatuzumab vedotin is an ADC against CD79b that, swapped into the classic R-CHOP regimen, became the first improvement on frontline lymphoma therapy in twenty years.
Cytotoxic (topoisomerase-I inhibitor) · Topotecan is the long-standing second-line chemotherapy for relapsed small-cell lung cancer, and now the comparator that new drugs must beat.
Cytotoxic regimen · The intensive chemotherapy that has induced remission in fit AML patients since 1973: seven days of one drug, three of another. Still the backbone that targeted drugs are added to.
ADC · Inotuzumab ozogamicin is an antibody carrying a DNA-cutting toxin to CD22 on leukaemia cells. It gets far more relapsed ALL patients into remission than chemotherapy and bridges them to transplant.
Small-molecule pan-TRK inhibitor (first generation) · The first drug approved for a gene fusion regardless of where the cancer started; it works in about 75% of NTRK-fusion cancers, from infant fibrosarcoma to salivary and thyroid cancers.
Small-molecule multi-kinase inhibitor (VEGFR, PDGFR, RAF) · The first drug ever to extend life in advanced liver cancer (2007), now mostly a comparator arm that newer combinations are measured against.
Glycopeptide antibiotic (DNA-cleaving) · Bleomycin is the 'B' in BEP for testicular cancer and ABVD for Hodgkin lymphoma; its unique danger is scarring of the lungs, so lung function is monitored and it is often dropped when safe.
Small-molecule TRK/ROS1/ALK TKI (CNS-penetrant) · Entrectinib (Rozlytrek) is a pill for NTRK-fusion cancers and ROS1 lung cancer that reaches brain metastases.
Small-molecule kinase inhibitor (FLT3, type I) · A single pill that beats salvage chemotherapy for relapsed FLT3-mutated AML, and the backbone of the triplets now being tested in frontline disease.
Bispecific T-cell engager (CD20×CD3) · Mosunetuzumab is a fixed-duration CD20 bispecific approved for follicular lymphoma and studied with polatuzumab in large B-cell lymphoma.
Targeted alpha therapy (bone-seeking) · Radium-223 was the first alpha-emitting drug ever approved (2013). It homes to bone like calcium and treats prostate cancer that has spread only to bone.
Small-molecule JAK1/JAK2 inhibitor · Ruxolitinib was the first JAK inhibitor: it shrinks the spleen and relieves symptoms in myelofibrosis and controls blood counts in polycythaemia vera, without eliminating the disease clone.
Monoclonal antibody (anti-CD19, Fc-enhanced) · A CD19 antibody given with lenalidomide for lymphoma patients who cannot have a transplant; in 2026 it showed the first frontline gain over R-CHOP in high-risk disease.
Oncolytic virus (HSV-1) · Talimogene laherparepvec (T-VEC, Imlygic) was the first approved oncolytic virus (2015), injected into melanoma skin lesions.
Bispecific antibody (HER2×HER3) · Zenocutuzumab is the first drug for cancers driven by NRG1 gene fusions, working by blocking HER3 from receiving its growth signal.
Small-molecule kinase inhibitor (VEGFR) · Axitinib is a selective VEGF-receptor pill, now given mainly with pembrolizumab or avelumab as first-line kidney cancer treatment.
Oral hypomethylating agent · Oral decitabine-cedazuridine is a pill version of the hypomethylating chemotherapy that, since May 2026, lets older AML patients take their whole venetoclax regimen at home.
ADC · Gemtuzumab ozogamicin (Mylotarg) was the very first ADC: approved in 2000, withdrawn in 2010 for toxicity, and re-approved in 2017 at a lower fractionated dose. Its history is cautionary and instructive.
Erythroid maturation agent (activin receptor IIB ligand trap, Fc fusion) · An injection that helps the marrow finish making red cells, reducing or removing the need for transfusions in lower-risk MDS and beta-thalassaemia.
IL-15 superagonist (intravesical, with BCG) · Nogapendekin alfa inbakicept is an engineered version of the immune-boosting protein IL-15, given with BCG into the bladder, approved in 2024 for early bladder cancer that BCG alone no longer controls.
Radiopharmaceutical (beta/gamma emitter, natural uptake) · The original targeted radiotherapy: thyroid cells soak up iodine, so radioactive iodine destroys leftover thyroid tissue and metastases while sparing everything else.
Anti-PD-1 monoclonal antibody (IgG4) · Retifanlimab is a PD-1 antibody approved for Merkel cell carcinoma and, with chemotherapy, as the first immunotherapy standard for advanced anal cancer.
Peptide hormone analogue (SSTR2 agonist) · Monthly injections of a synthetic hormone that both quiets tumour hormone symptoms and slows tumour growth, the first treatment for most neuroendocrine tumours.
Small-molecule smoothened (hedgehog) inhibitor · Vismodegib was the first hedgehog-pathway drug, for basal cell carcinomas too advanced for surgery; it shrinks most tumours but muscle cramps, taste loss and hair loss make long-term use hard.
Small-molecule RAF/MEK clamp + FAK inhibitor · Avutometinib plus defactinib is the first treatment approved specifically for low-grade serous ovarian cancer, a slow-growing type driven by the RAS pathway.
Alkylating agent (nitrogen mustard-purine hybrid) · An East German chemotherapy rediscovered in the 2000s that became the backbone partner for rituximab in follicular, mantle cell and Waldenström lymphomas.
Bispecific T-cell engager (BCMA×CD3) · Elranatamab is Pfizer's BCMA bispecific, given under the skin every week then every two weeks, for myeloma after four prior lines.
Cytotoxic regimen · FLOT is the four-drug chemotherapy given before and after surgery for stomach cancer in the West; since 2025 immunotherapy is added to it.
Cytotoxic regimen · FOLFIRI is the other backbone bowel-cancer chemotherapy, swapping oxaliplatin for irinotecan. Used first or second line and, since 2026, with the BRAF combination.
Oral SERD · Imlunestrant is Lilly's oral oestrogen-receptor degrader, approved in 2025 for ESR1-mutant breast cancer and shown to work with abemaciclib regardless of mutation.
Small-molecule PI3Kα inhibitor and degrader · Inavolisib is a PI3K drug that also destroys the mutant protein, approved in 2024 with palbociclib and fulvestrant for PIK3CA-mutant breast cancer.
Small-molecule kinase inhibitor (EGFR) · A third-generation EGFR pill used together with amivantamab as the first regimen to beat osimertinib in EGFR-mutant lung cancer.
Monoclonal antibody (anti-GD2, humanised) · Naxitamab is a humanised anti-GD2 antibody from Memorial Sloan Kettering, given as an outpatient with GM-CSF for relapsed neuroblastoma in bone or marrow.
Small-molecule gamma-secretase inhibitor · Nirogacestat is the first approved medicine for desmoid tumours, locally invasive growths that do not spread but can be crippling; it works by blocking Notch signalling.
Monoclonal antibody (anti-EGFR) · Panitumumab is a fully human EGFR antibody, the preferred first-line partner for chemotherapy in left-sided, RAS-normal bowel cancer after the PARADIGM trial.
Small-molecule kinase inhibitor (FLT3-ITD, type II) · Quizartinib is a more selective FLT3 blocker that, added to chemotherapy, roughly doubled median survival in the highest-risk FLT3 subtype.
Small-molecule type II RAF inhibitor · Tovorafenib is a pill for the most common childhood brain tumour, low-grade glioma driven by BRAF changes, approved in 2024.
Monoclonal antibody (anti-CTLA-4) · Tremelimumab is AstraZeneca's CTLA-4 antibody, given as a single priming dose with durvalumab and chemotherapy in lung and liver cancer.
Cytotoxic chemotherapy (oral nucleoside) · An oral chemotherapy pill for bowel cancer that has stopped responding to everything else; with bevacizumab it extends life by about three months.
Small-molecule kinase inhibitor (PDGFRA D842V / KIT) · Avapritinib is the first drug for GIST driven by the PDGFRA D842V mutation, which resists every other kinase inhibitor; it is also approved for systemic mastocytosis.
Small-molecule ALK/ROS1/MET TKI (first generation) · Crizotinib was the first ALK inhibitor, approved four years after ALK fusions were found in lung cancer; it was also the first drug for ROS1 lung cancer and for ALK-positive lymphoma and inflammatory myofibroblastic tumour in children.
Small-molecule ornithine decarboxylase inhibitor · Eflornithine (DFMO) is an old sleeping-sickness drug repurposed as the first oral maintenance therapy for high-risk neuroblastoma, approved in December 2023 to reduce relapse after immunotherapy.
Injectable SERD · Fulvestrant is a monthly injection that destroys the oestrogen receptor; it is the standard partner for many targeted drugs after hormone therapy stops working.
Nucleoside analogue (deoxycytidine) · A versatile chemotherapy used in pancreatic, bladder, lung, ovarian, breast and biliary cancers, in nasopharyngeal cancer, and as a bladder instillation.
Small-molecule multikinase inhibitor (FLT3) · The first drug to improve survival in FLT3-mutated AML, added to standard chemotherapy: median survival went from about two years to more than six.
Alkylating antibiotic (bioreductive) · The chemotherapy given with radiation to cure anal cancer without surgery, used as a bladder instillation after tumour resection, and since 2020-25 in gel form for upper-tract and recurrent bladder cancers.
CAR-T (CD19, fast off-rate) · A CD19 CAR-T built to grip and release quickly, which cut severe side effects and gave adults with relapsed ALL a real chance at durable remission.
Small-molecule PARP inhibitor · A PARP inhibitor for BRCA-mutated ovarian and prostate cancer whose original maker went bankrupt; still available, with a narrowed label.
Bispecific T-cell engager (GPRC5D×CD3) · Talquetamab is the first drug against GPRC5D, a second myeloma target used after BCMA therapies stop working; taste and skin side effects are its signature.
ADC · Hengrui's HER2 ADC, approved in China for lung cancer and showing Enhertu-scale results in breast cancer, part of a wave of Chinese ADCs heading for global trials.
Small-molecule kinase inhibitor (ALK) · Alectinib is a well-tolerated ALK pill, standard first line for years and, since 2024, the first targeted therapy given after surgery for ALK-positive lung cancer.
Monoclonal antibody (anti-VEGF) · A blood-vessel-blocking antibody that shrinks glioblastoma on scans and reduces swelling, but has never been shown to help patients live longer.
Small-molecule kinase inhibitor (MEK1/2) · Binimetinib is the MEK inhibitor partnered with encorafenib; blocking the next step in the same relay stops the tumour rerouting around the BRAF block.
Bispecific antibody (PD-1×CTLA-4) · A Chinese two-armed antibody that blocks PD-1 and CTLA-4 together, approved in China for cervical cancer and extending survival even in PD-L1-negative tumours.
Small-molecule imipridone (ClpP agonist / DRD2 antagonist) · Dordaviprone is the first drug ever approved for a lethal childhood and young-adult brain tumour, diffuse midline glioma with the H3 K27M mutation (August 2025).
Cytotoxic regimen · FOLFIRINOX is a four-drug chemotherapy combination that, in 2011, became the first treatment to meaningfully extend life in metastatic pancreatic cancer; it is now the standard before and after surgery.
Small-molecule kinase inhibitor (VEGFR1-3) · A Chinese-discovered pill that blocks the blood-vessel receptors, approved in 2023 for bowel cancer after all standard treatments.
Small-molecule irreversible kinase inhibitor (FGFR1-4) · Futibatinib is a covalent FGFR inhibitor for FGFR2-fusion bile duct cancer, with the highest response rate of the first-generation drugs.
Small-molecule pan-PI3K/mTOR inhibitor · An intravenous drug that blocks the whole PI3K/mTOR pathway, approved in July 2026 for hormone-positive breast cancer.
Telomerase inhibitor (oligonucleotide) · Imetelstat is the first telomerase-blocking drug approved for any cancer; it frees many lower-risk MDS patients from transfusions after growth factors have failed.
Personalised mRNA neoantigen vaccine · A custom mRNA vaccine encoding up to 34 of a patient's own tumour mutations. In August 2026 it became the first personalised cancer vaccine to win a phase 3 trial.
Bispecific antibody (PD-1×VEGF) · A Chinese bispecific that beat Keytruda head-to-head on progression-free survival in lung cancer, the first drug ever to do so.
Bispecific ADC · Izalontamab brengitecan is the first bispecific ADC to succeed in a phase 3 trial, hitting two growth receptors at once in triple-negative breast cancer.
Adrenolytic agent (DDD derivative) · A relative of the insecticide DDT that is the only drug specific to adrenal cortex cancer; it needs blood-level monitoring and permanent steroid replacement.
Small-molecule JAK1/JAK2/ACVR1 inhibitor · Momelotinib is the JAK inhibitor designed for anaemic myelofibrosis patients: it can improve haemoglobin while shrinking the spleen.
Small-molecule BCR-ABL1 TKI (second generation) · Nilotinib is a second-generation CML pill that produces deeper responses faster than imatinib, at the cost of cardiovascular and metabolic side effects.
Gene-expression prognostic/predictive assay · A 21-gene test that tells most women with early hormone-positive breast cancer whether they can safely skip chemotherapy.
Oral cereblon E3 ligase modulator (IMiD) · The third-generation thalidomide analogue for myeloma that has failed lenalidomide, and since 2020 the first new drug for Kaposi sarcoma in two decades.
Small-molecule kinase inhibitor (ROS1 / NTRK) · A ROS1 and NTRK pill that also works after other ROS1 drugs fail, with dizziness as its signature side effect.
ADC · Sacituzumab tirumotecan is a third TROP2 ADC from China, licensed to Merck for a very large global programme. It is approved in China; in the US it has a priority voucher but not yet approval.
Tumour-informed ctDNA MRD test · The most widely used blood test for detecting leftover cancer after surgery, personalised to each patient's tumour mutations.
Intravenous mTOR inhibitor (rapamycin analogue) · A weekly infusion that was the first drug to extend survival in poor-risk kidney cancer (2007), and in 2024 the first targeted drug to improve outcomes in childhood rhabdomyosarcoma.
Small-molecule kinase inhibitor (VEGFR) · Tivozanib is a highly selective VEGF-receptor pill for kidney cancer after two or more prior treatments, notable for its tolerability and for a trial that closed the door on immunotherapy rechallenge.
Small-molecule PI3Kα inhibitor · Alpelisib was the first PI3K drug for PIK3CA-mutant breast cancer (2019). It is effective, but high blood sugar and rash limited its use, and newer drugs are displacing it.
AI digital pathology risk test · An FDA-cleared AI test (May 2026) that reads breast cancer slides to estimate recurrence risk in early hormone-positive disease.
Autologous CD19 CAR-T (CD28 costimulatory domain) · Brexucabtagene autoleucel is the CAR-T therapy for mantle cell lymphoma and adult acute lymphoblastic leukaemia, giving long remissions after BTK inhibitors fail.
Intravesical drug-eluting device · TAR-200 is a small pretzel-shaped device placed in the bladder that releases gemcitabine for three weeks at a time. It was approved in 2025 for early bladder cancer that no longer responds to BCG.
Bispecific T-cell engager (BCMA×CD3) · Linvoseltamab is Regeneron's BCMA bispecific, approved in July 2025 with the highest complete-response rate of the class in its pivotal study.
Bispecific T-cell engager (CD20×CD3) · Odronextamab is Regeneron's CD20 bispecific, approved in Europe for lymphoma and in the US for follicular lymphoma after earlier FDA rejections over confirmatory-trial enrolment.
Third-generation platinum (DACH-platinum) · The platinum drug that works in bowel cancer where cisplatin does not, the 'OX' in FOLFOX and CAPOX; its cost is nerve damage in hands and feet.
Cytotoxic (liposomal anthracycline) · Doxorubicin wrapped in a fatty bubble so it reaches tumours with less heart damage; a workhorse of relapsed ovarian cancer.
Anti-PD-1 monoclonal antibody (IgG1, Fc-engineered null) · Penpulimab is a Chinese PD-1 antibody approved in the US in 2025 for nasopharyngeal carcinoma, the second after toripalimab.
Hormonal therapy (progestin) · Progesterone-like hormones that can reverse early endometrial cancer in women who want to keep their uterus, and control advanced hormone-sensitive disease.
Monoclonal antibody (anti-PD-1) · Serplulimab is a Chinese PD-1 antibody with the largest survival gain of any first-line small-cell lung cancer immunotherapy trial, approved in China, Europe, and the UK but not yet the US.
Small-molecule kinase inhibitor (HER2) · Sevabertinib is an oral HER2 inhibitor for lung cancers with HER2 mutations, approved in November 2025 as an alternative to Enhertu and zongertinib.
Small-molecule chemoprotectant · An old antidote proven in two paediatric trials to halve permanent hearing loss from cisplatin, and approved in 2022 as the first drug to prevent a chemotherapy side effect in children.
Small-molecule kinase inhibitor (CSF1R) · Vimseltinib is a pill approved in February 2025 for tenosynovial giant cell tumour, a benign but destructive joint tumour, offering an alternative to repeated surgery.
Semi-synthetic vinca alkaloid · Vinorelbine is a vinca chemotherapy for lung and breast cancer, available orally, and is now part of maintenance therapy that improved survival in childhood rhabdomyosarcoma.
Small-molecule kinase inhibitor (HER2) · Zongertinib was the first oral HER2 inhibitor for lung cancer with HER2 mutations, approved in 2025 and moved to first line in 2026.
ImmTAC (PRAME TCR × CD3 bispecific) · Tebentafusp's successor: a soluble T-cell receptor that recognises a fragment of PRAME, a protein present in most melanomas and many other cancers, and drags T cells onto the tumour.
Small-molecule AR antagonist · Darolutamide is an AR blocker that barely enters the brain, so it causes fewer falls and cognitive side effects; it is approved with and without chemotherapy.
Small-molecule kinase inhibitor (pan-FGFR) · The first targeted pill for bladder cancer, for the roughly 20% of tumours with FGFR3 alterations, used after immunotherapy.
Small-molecule JAK2/FLT3 inhibitor · A second JAK inhibitor for myelofibrosis that works after ruxolitinib fails; it carries a boxed warning for a rare brain toxicity (Wernicke encephalopathy) so thiamine is checked.
PET radiotracer (somatostatin receptor ligand) · The PET scan for neuroendocrine tumours that finds far more disease than older scans and confirms eligibility for lutetium radioligand therapy (the theranostic pair).
Monoclonal antibody (anti-CD38) · Isatuximab is Sanofi's CD38 antibody, approved in frontline transplant-ineligible myeloma (IMROZ) and, from July 2026, as an under-the-skin injection.
Small-molecule reversible HER2/EGFR kinase inhibitor · Lapatinib was the first HER2-blocking pill (2007) and is now mostly a comparator arm and a late-line option, displaced by tucatinib and ADCs.
GnRH agonist depot · Leuprolide is the injectable that shuts off testosterone production, the foundation of hormone therapy for prostate cancer since the 1980s; it is also used for ovarian suppression in premenopausal breast cancer.
Fc-engineered monoclonal antibody (anti-HER2) · A trastuzumab look-alike with an engineered tail that binds immune cells more tightly; approved in 2020 but rarely used after ADCs arrived.
Non-replicating adenoviral gene therapy (intravesical) · Nadofaragene firadenovec is the first gene therapy for bladder cancer: a virus that makes bladder cells produce interferon for weeks, given once every three months.
Cytotoxic regimen · NALIRIFOX is a version of FOLFIRINOX using a liposome-wrapped irinotecan, approved in 2024 as a first-line option for metastatic pancreatic cancer.
Small-molecule irreversible pan-HER kinase inhibitor · A pill taken for a year after trastuzumab to further reduce recurrence in HER2-positive, hormone-positive breast cancer, limited by severe diarrhoea.
Small-molecule kinase inhibitor (VEGFR/PDGFR/KIT) · Pazopanib is the only multi-kinase inhibitor approved for soft-tissue sarcoma (excluding fat-derived tumours), used after chemotherapy fails.
ADC (anti-CD123 antibody, IGN payload) · Pivekimab sunirine is an antibody-drug conjugate against CD123, approved in 2026 for blastic plasmacytoid dendritic cell neoplasm as the second targeted drug for this rare cancer.
Small-molecule kinase inhibitor (RET) · Pralsetinib is the second selective RET pill for lung cancer, less used than selpercatinib after a change of owner and label.
Small-molecule irreversible pan-HER kinase inhibitor · Pyrotinib is China's HER2 pill, widely used there with capecitabine and as a comparator for the new Chinese HER2 ADCs.
Small-molecule glucocorticoid receptor antagonist · A first-in-class drug that blocks cortisol signalling in tumour cells, approved in 2026 for platinum-resistant ovarian cancer with chemotherapy.
Small-molecule XPO1 (nuclear export) inhibitor · Selinexor is a first-in-class pill that traps tumour-suppressor proteins inside the nucleus; approved in myeloma, it failed its endometrial cancer test in 2026.
Biosimilar monoclonal antibody (anti-HER2) · Near-identical copies of Herceptin, approved since 2017, that cut the price of HER2 treatment and widened access worldwide.
Small-molecule kinase inhibitor (RET, VEGFR, EGFR) · Vandetanib was the first drug approved for medullary thyroid cancer (2011), now largely replaced by RET-selective selpercatinib.
Recombinant interleukin-2 (cytokine) · High-dose interleukin-2 was the first immunotherapy to cure a small fraction of patients with metastatic melanoma and kidney cancer, at the cost of ICU-level toxicity; today it mainly supports TIL therapy.
Small-molecule kinase inhibitors (MET) · Capmatinib and tepotinib are two pills for the roughly 3% of lung cancers with a MET exon 14 skipping mutation.
Proteasome inhibitor (irreversible) · Carfilzomib is a second-generation proteasome inhibitor with less nerve damage but more heart and blood-pressure effects.
Liposomal cytotoxic formulation · The two old chemotherapy drugs packed together into tiny fat bubbles at a fixed ratio, which doubled five-year survival in older adults with high-risk AML.
Small-molecule EGFR TKI (first generation, reversible) · Erlotinib was one of the first EGFR pills for lung cancer; it was approved before anyone knew EGFR mutations predicted who would respond, then redefined by them.
Comprehensive genomic profiling test · The FDA-approved tissue (324 genes) and blood genomic tests that serve as companion diagnostics for dozens of drugs.
Cytotoxic regimen · Gemcitabine plus nab-paclitaxel is the gentler of the two standard chemotherapy backbones for pancreatic cancer, and the base on which most new drugs are being tested.
Defucosylated anti-CCR4 monoclonal antibody · Mogamulizumab is an antibody that clears cancerous T cells from the blood in mycosis fungoides and Sézary syndrome, the leukaemic form of skin lymphoma.
Small-molecule IDH1 inhibitor · Olutasidenib is a second IDH1 inhibitor for relapsed AML, with a higher response rate in its pivotal cohort than ivosidenib had in its own.
Recombinant cytotoxin (IL-3 fused to diphtheria toxin) · Tagraxofusp is a fusion of the growth factor IL-3 with a bacterial toxin that homes to CD123 on a rare, aggressive blood cancer.
Cytotoxic (DNA minor-groove binder) · A chemotherapy derived from a sea squirt, used with liposomal doxorubicin in relapsed ovarian cancer in Europe and for sarcomas.
Small-molecule kinase inhibitor (ROS1) · A ROS1 inhibitor approved in July 2026 that works after other ROS1 drugs fail and avoids their brain side effects.
Personalised mRNA neoantigen vaccine · BioNTech's personalised vaccine, notable for a small pancreatic cancer study where vaccine responders stayed cancer-free for years.
Small-molecule BCR-ABL1/SRC TKI · Bosutinib is a CML pill with less cardiovascular and pleural toxicity than its rivals; its main side effect is diarrhoea.
Photoimmunotherapy conjugate (anti-EGFR antibody–IR700 dye) · Cetuximab sarotalocan is an EGFR antibody carrying a light-activated dye: after infusion, a red laser is shone on the tumour and the cells burst. It has been approved in Japan since 2020.
Anti-PD-L1 monoclonal antibody (IgG1, ADCC-competent) · Cosibelimab is a PD-L1 antibody approved in December 2024 for advanced cutaneous squamous cell carcinoma, offering a third immunotherapy choice.
Small-molecule steroidal aromatase inactivator · Exemestane is a steroidal aromatase inhibitor, the partner of everolimus and the agent tested with ovarian suppression in young women.
Small-molecule EGFR TKI (first generation, reversible) · The lung-cancer pill whose dramatic responses in a few patients led to the discovery of EGFR mutations in 2004.
GnRH agonist · Monthly or 3-monthly injections that switch off the ovaries, letting premenopausal women use aromatase inhibitors and lowering recurrence in higher-risk cases.
Bispecific antibody (EGFR × LGR5) · A two-armed antibody that blocks EGFR while gripping LGR5, a marker of cancer stem cells, so it hits the cells that regrow tumours.
Long-acting mono-pegylated interferon alfa · Ropeginterferon alfa-2b is a long-acting interferon for polycythaemia vera that, unlike hydroxyurea, can shrink the mutant clone over years.
Small-molecule smoothened inhibitor · Sonidegib (Odomzo) is the second hedgehog inhibitor for locally advanced basal cell carcinoma, similar in effect and side effects to vismodegib.
Vinca alkaloid (microtubule inhibitor) · Vinblastine is the vinca alkaloid in ABVD, the standard Hodgkin lymphoma regimen, and was formerly in the cisplatin combinations that first cured testicular cancer.
Oral ROCK2 inhibitor · Belumosudil is a pill for chronic graft-versus-host disease, the long-term immune complication of donor stem-cell transplants used to cure blood cancers.
Small-molecule BTK degrader (CDAC) · Instead of blocking BTK, this pill destroys it, so it works even when the enzyme has mutated to escape every inhibitor.
Purine nucleoside analogue · A one-week infusion that puts most people with hairy cell leukaemia into remission for years; also used in multiple sclerosis in tablet form.
Small-molecule IDH2 inhibitor · Enasidenib is the IDH2 counterpart of ivosidenib, approved in the US for relapsed disease but never approved in Europe after it failed to extend survival in a confirmatory trial.
Synthetic halichondrin B analogue (microtubule dynamics inhibitor) · A sea-sponge-derived chemotherapy that extended survival in heavily pretreated breast cancer and in liposarcoma, where almost nothing else had.
Oral SERD · Giredestrant is Roche's oral SERD: it failed to beat an aromatase inhibitor in first-line metastatic disease but succeeded after surgery and after CDK4/6 failure.
Oral ribonucleotide reductase inhibitor (cytoreductive) · Hydroxyurea is a cheap, decades-old pill that lowers high blood counts in polycythaemia vera and essential thrombocythaemia and is also the main drug for sickle cell disease.
Small-molecule PI3Kδ inhibitor · Idelalisib was the first PI3K inhibitor for blood cancers; it is effective in CLL with rituximab but so toxic (colitis, hepatitis, pneumonitis, infections) that the class has largely been abandoned.
Small-molecule CSF1R/KIT/FLT3 inhibitor · Pexidartinib is the first drug for tenosynovial giant cell tumour, a benign but destructive joint tumour; it is effective but has liver toxicity that requires a restricted programme.
Hepcidin mimetic peptide · Rusfertide is the first drug to control polycythaemia vera's excess red cells by restricting iron, sparing patients repeated blood removal.
Radioligand therapy (beta) · 177Lu-PSMA-I&T is a second PSMA radioligand, chemically different from Pluvicto, that has passed two phase 3 trials on progression but has not yet shown a survival benefit.
Enzyme therapy · An enzyme that starves leukaemia cells of an amino acid they cannot make; a mainstay of childhood ALL therapy for 50 years, with new versions solving allergy and supply problems.
Oral first-generation non-steroidal antiandrogen · The old antiandrogen pill used to block the testosterone flare from GnRH agonists and in combined androgen blockade; superseded by enzalutamide-class drugs.
Oncolytic adenovirus (intravesical) · Cretostimogene is a virus engineered to multiply only in bladder cancer cells with a broken RB pathway, instilled into the bladder. It cleared carcinoma in situ in 75% of BCG-unresponsive patients.
PET radiotracer (synthetic amino acid) · Fluciclovine F-18 was the first PET tracer approved for finding recurrent prostate cancer after treatment (2016), and has been largely superseded since 2020 by PSMA PET.
Liposomal muramyl tripeptide (macrophage activator) · An immune-activating drug approved in Europe for osteosarcoma after a trial suggested it improved survival; the FDA never approved it, and it remains one of oncology's transatlantic disagreements.
Class I HDAC inhibitor (cyclic peptide) · Romidepsin is an epigenetic drug for T-cell lymphomas of the skin and lymph nodes; its US lymph-node indication was withdrawn when a confirmatory trial failed.
Radiopharmaceutical lymphatic mapping agent · The purpose-built tracer for sentinel lymph node mapping in breast cancer, melanoma and oral cancer, replacing off-label sulfur colloid.
Oral cereblon modulator (first IMiD) · Thalidomide is the drug behind the 1960s birth-defect tragedy, rehabilitated as the first immunomodulatory myeloma drug and the parent of lenalidomide and pomalidomide.
Radioligand therapy (beta) · A second lutetium radioligand for neuroendocrine tumours that beat the standard pill everolimus in a head-to-head trial and is awaiting an FDA decision.
Inorganic arsenical (differentiation agent) · An ancient poison turned cure: with retinoic acid it cures more than 95% of acute promyelocytic leukaemia without conventional chemotherapy.
Pan-HDAC inhibitor (hydroxamate) · Belinostat is an HDAC inhibitor for relapsed peripheral T-cell lymphoma; about a quarter of patients respond, and it can be used in patients with low platelets.
PD-1 antibody + oral VEGFR2 inhibitor · A Chinese immunotherapy-plus-anti-angiogenic pill combination that clearly beat sorafenib in liver cancer, yet remains unapproved in the US after three manufacturing-related rejections.
GnRH antagonist depot · An injectable hormone blocker for prostate cancer that lowers testosterone within days without the initial surge caused by agonists.
Theranostic pair (peptide radioligand) · A FAP-targeted theranostic pair: one version images almost any solid tumour, the other treats it with radiation.
PET radiotracer (oestrogen receptor ligand) · A PET scan that shows which breast cancer deposits still have oestrogen receptors, helping decide whether hormone therapy will work when biopsy is impractical.
Small-molecule smoothened (hedgehog) inhibitor · Glasdegib is a hedgehog-pathway pill that, with low-dose chemotherapy, extends survival in older AML patients who cannot have intensive treatment; it has largely been displaced by venetoclax combinations.
Oral proteasome inhibitor (boronate) · Ixazomib (Ninlaro) is the first oral proteasome inhibitor for multiple myeloma, enabling an all-oral triplet with lenalidomide and dexamethasone.
Folate receptor-targeted near-infrared fluorescent imaging agent · An injected dye that makes ovarian and lung cancer deposits glow during surgery so surgeons can find lesions they would otherwise miss.
Protease-activated fluorescent imaging agent · A cavity-imaging dye used during breast lumpectomy to spot leftover tumour before the operation ends, reducing second surgeries.
Antifolate (DHFR inhibitor) · Pralatrexate was the first drug approved specifically for relapsed peripheral T-cell lymphoma; about a third of patients respond.
ADC · Rinatabart sesutecan is a next-generation folate-receptor ADC with a topoisomerase payload that responds in both ovarian and endometrial cancer regardless of receptor level.
Small-molecule EGFR exon 20 insertion TKI (irreversible) · An oral drug for EGFR exon 20 insertion lung cancer that succeeded where mobocertinib failed; approved in China (2023) and the US (2025).
Alkylating conditioning agent (busulfan analogue) · A conditioning chemotherapy given before donor stem-cell transplant in AML and MDS; it was long used in Europe and reached the US in 2025.
Oral retinoid (differentiation agent) · The vitamin-A derivative that made acute promyelocytic leukaemia the first cancer cured by differentiation therapy rather than by killing cells.
Small-molecule ALK/EGFR TKI (second generation) · Brigatinib is an ALK pill with strong brain activity, approved first after crizotinib and then first line after beating it in ALTA-1L.
Small-molecule ALK TKI (second generation) · Ceritinib is a second-generation ALK pill for lung cancer, effective after crizotinib but with gastrointestinal toxicity that limited uptake.
Small-molecule pan-ErbB TKI (second generation, irreversible) · A second-generation EGFR pill that beat gefitinib on survival in EGFR-mutant lung cancer but was quickly overshadowed by osimertinib.
Anti-SLAMF7 monoclonal antibody · An immune-stimulating antibody for myeloma that works only in combination, adding benefit to lenalidomide or pomalidomide.
Monoclonal antibody (anti-LAG-3) · Fianlimab is Regeneron's LAG-3 blocker. Promising early data with cemiplimab did not hold up against pembrolizumab in a first-line phase 3 in 2026.
Small-molecule ROS1 TKI (next generation, CNS-penetrant) · A ROS1 lung-cancer pill approved in 2025 that works in the brain and after crizotinib, with fewer dizziness-type side effects than repotrectinib.
Small-molecule multi-kinase inhibitor (FGFR1-3, VEGFR, Aurora, JAK) · A next-generation FGFR inhibitor designed to work after pemigatinib or futibatinib stop working, now in a global phase 3.
Bispecific T-cell engager (STEAP1×CD3, XmAb 2+1) · Xaluritamig is Amgen's T-cell engager for prostate cancer, now in two phase 3 trials, aiming to do for prostate cancer what tarlatamab did for small-cell lung cancer.
Small-molecule RAS(ON) G12D-selective inhibitor · The first drug aimed specifically at KRAS G12D, the single most common mutation in pancreatic cancer. Early combination data in 2026 showed half of previously treated patients responding.
Fluorescence-guided surgery agent (protoporphyrin IX precursor) · A drink taken before brain surgery that makes high-grade glioma glow under blue light, letting surgeons remove more tumour safely.
Small-molecule EZH2 inhibitor · An epigenetic drug that may re-sensitise prostate cancer to hormone therapy, in three phase 3 trials with enzalutamide.
Small-molecule kinase inhibitor (ALK) · A fourth-generation ALK pill that works after lorlatinib and avoids the TRK-related brain side effects; under FDA priority review with a decision due 27 November 2026.
Radioligand therapy (beta, norepinephrine transporter) · High-dose radioactive MIBG delivers radiation from inside neuroblastoma cells that take up noradrenaline; used for relapsed disease and tested in upfront therapy.
Targeted alpha therapy (lead-212) · An alpha-particle version of neuroendocrine radioligand therapy that produced responses in over half of patients who had never had PRRT, with FDA Breakthrough designation.
Autologous cellular immunotherapy (antigen-presenting cell vaccine) · Sipuleucel-T was the first therapeutic cancer vaccine approved (2010): it lengthened survival in metastatic prostate cancer by about four months without shrinking tumours or lowering PSA.
CAR-T (BCMA, D-domain binder) · Anitocabtagene autoleucel is a BCMA CAR-T with a novel small synthetic binder that produced responses in 97% of heavily pretreated patients; an FDA decision is due in December 2026.
ADC · ARX788 is a HER2 ADC with a precisely placed, non-cleavable payload that beat lapatinib-capecitabine in China and showed activity in brain metastases.
Small-molecule CDK4-selective inhibitor · A next-generation pill that blocks only CDK4, not CDK6, to keep the benefit of today's drugs without the low blood counts.
Gene-expression genomic classifier · A 22-gene test on the biopsy or surgical specimen that predicts spread and death, used to decide on surveillance or adding hormone therapy.
Bifunctional antibody (EGFR × TGF-β trap) · Ficerafusp alfa is an EGFR antibody fused to a TGF-beta sponge, designed to remove the immune-suppressing signal that keeps HPV-negative throat cancers cold.
Small-molecule non-covalent BTK inhibitor · Nemtabrutinib is Merck's reversible BTK blocker, active against the C481S escape mutation, being tested against ibrutinib and acalabrutinib in first-line CLL.
Monoclonal antibody (anti-FGFR2b) · Bemarituzumab is an antibody against FGFR2b, a growth receptor overproduced in about a third of stomach cancers. It improved survival early in its phase 3 trial, but the gain faded with longer follow-up.
Off-the-shelf lymph-node-targeted KRAS peptide vaccine · A ready-made vaccine against the seven commonest KRAS mutations, given after pancreatic cancer surgery. Its phase 2 missed the main goal in 2026 but showed signs of activity.
Molecular glue degrader (CELMoD, IKZF1/3) · Golcadomide is a next-generation lenalidomide-like pill that degrades two lymphoma transcription factors far more potently, now in phase 3 with R-CHOP.
TCR-T (NY-ESO-1) · Letetresgene autoleucel is a second engineered T-cell receptor therapy for sarcoma, targeting NY-ESO-1 in synovial sarcoma and myxoid/round cell liposarcoma; a BLA is expected by the end of 2026.
Oral cytotoxic regimen · CAPTEM (capecitabine plus temozolomide) is an all-oral chemotherapy pair that shrinks pancreatic neuroendocrine tumours in about a third of patients.
Autologous dendritic cell vaccine (tumour lysate) · A personalised vaccine made from the patient's own immune cells and tumour. Its 20-year-old phase 3 trial reported longer survival, but the way the result was analysed has divided the field.
CELMoD (cereblon E3 ligase modulator) · Iberdomide is a far more potent successor to lenalidomide, now in phase 3 as post-transplant maintenance and in relapsed disease.
Gene-expression prognostic assay · A 70-gene test that tells whether an early breast cancer is genomically low or high risk, used to decide who can skip chemotherapy.
CELMoD (cereblon E3 ligase modulator) · Mezigdomide is the most potent oral cereblon modulator, producing responses in about 40% of triple-class-refractory myeloma with dexamethasone alone.
Small-molecule RAS(ON) G12C-selective inhibitor · A next-generation KRAS G12C drug that hits the active form of the protein, from the same company as daraxonrasib.
Monoclonal antibody (anti-CD47) · The first 'don't eat me' signal blocker. Gilead paid $4.9B for it; it was stopped in 2024 after trials showed more deaths, not fewer.
Bicycle toxin conjugate (Nectin-4, MMAE) · A tiny peptide instead of an antibody carries the same payload as Padcev to Nectin-4, with far less rash and neuropathy in early data, but its developer stepped back in 2026.
Small-molecule non-covalent KRAS G12D inhibitor · MRTX1133 was the first potent chemical tool against KRAS G12D, and proved the mutation could be drugged even though it lacks the reactive handle G12C has.
Small molecule (IDO1 inhibitor) · An enzyme blocker meant to stop tumours starving T cells of tryptophan. Its 2018 phase 3 failure ended an entire class overnight.
Recombinant type I interferon (cytokine) · Interferon alfa was the first biologic cancer drug (1986). It treated hairy cell leukaemia, CML, melanoma, kidney cancer and Kaposi sarcoma, and has been replaced almost everywhere by better-tolerated agents.
Small-molecule kinase inhibitor (VEGFR/FGFR/PDGFR) · An anti-angiogenic pill that looked promising in mesothelioma in a small trial but failed in the large one.
Small-molecule EZH2 inhibitor · Tazemetostat was the first EZH2 inhibitor, approved for epithelioid sarcoma and follicular lymphoma in 2020 and withdrawn worldwide in 2026 after secondary blood cancers.
Peptide vaccine (EGFRvIII) · A vaccine against a glioblastoma-specific mutant protein that looked promising for years and then failed its phase 3 trial in 2016. It is a landmark failure.
Engineered cytokine (PEGylated IL-2) · Bempegaldesleukin was a re-engineered interleukin-2 meant to be a safer version of a famous old immunotherapy. It added nothing to nivolumab in three phase 3 trials.
Small molecule (claimed PARP inhibitor) · Billed as the first PARP inhibitor for triple-negative breast cancer, it failed its phase 3 in 2011. It turned out not to inhibit PARP at all.
Small molecule (STING agonist, intratumoural) · ADU-S100 was the first STING agonist in the clinic. Injected directly into tumours, it produced almost no responses, alone or with checkpoint blockade.
Anti-CD22 immunotoxin (Pseudomonas exotoxin A fragment) · An immunotoxin for hairy cell leukaemia that produced lasting remissions in relapsed patients but was withdrawn from sale in 2023 for commercial reasons.
ADC · Rovalpituzumab tesirine (Rova-T) was the first drug against DLL3 in small-cell lung cancer. AbbVie bought it for $5.8B and abandoned it after two failed phase 3 trials. The target later worked with a different weapon.
Intravenous pan-class I PI3K inhibitor (α/δ predominant) · Copanlisib is an intravenous PI3K inhibitor for relapsed follicular lymphoma, approved in 2017 and withdrawn in 2023 when its confirmatory trial failed.
Small molecule (p53 reactivator) · Eprenetapopt (APR-246) was a drug meant to refold mutant p53, the most common broken protein in cancer. Its phase 3 in blood cancer failed in 2020.
Small-molecule AR N-terminal domain inhibitor · A drug designed to block the part of the androgen receptor that resistant variants keep; its phase 2 was stopped for futility and development ended.
Oral PI3Kδ / CK1ε inhibitor · A PI3K inhibitor for marginal zone and follicular lymphoma approved in 2021 and withdrawn in 2022 after the UNITY-CLL trial suggested more deaths.
Small-molecule EGFR exon 20 insertion TKI (irreversible) · Mobocertinib was the first oral drug for EGFR exon 20 insertion lung cancer, approved in 2021 and withdrawn in 2023-24 after its confirmatory trial failed.
ADC · A HER2 ADC with a DNA-alkylating payload that beat chemotherapy in a phase 3 trial yet never reached the market, because eye and lung toxicity and a stronger rival arrived first.
Peptide-drug conjugate · A myeloma drug given accelerated approval in 2021 and withdrawn in the US months later when its confirmatory trial suggested it shortened survival.
Pan-HDAC inhibitor · An HDAC inhibitor for relapsed myeloma approved in 2015 and withdrawn in 2021 after its confirmatory trial was never completed.
Withdrawn
evidence + links
2
2015
1
How the rank is computed
For a chosen cancer: standard-of-care mention +40, in its pipeline +25, in its history +10, directly linked +15, linked through one of its drugs +5. Always: evidence tier (approved 10 … concept 0) plus half a point per connection in the graph, capped at 10. With Personalise on: a match to one of your biomarkers +20, approval in your region +10, a standard-of-care setting matching your stage +15. It ranks documentation and evidence, not clinical benefit.