Carboplatin
Carboplatin is a platinum chemotherapy that crosslinks DNA; it is part of the standard pre-surgery regimen for triple-negative breast cancer.
Generic since 2004. In TNBC, adding carboplatin to neoadjuvant chemotherapy raised pathologic complete response (BrighTNess, GeparSixto) and is part of the KEYNOTE-522 backbone.
1.Carboplatin is aquated inside the cell to a reactive platinum species
- Route
- IV infusion
- Schedule
- AUC 5-6 mg/mL·min every 3 weeks (Calvert formula) or AUC 1.5-2 weekly with paclitaxel (KEYNOTE-522 backbone)
- Dose modifications
- Reduce for thrombocytopenia; renal-function-based dosing
- Monitoring
- Blood counts, creatinine, hypersensitivity after multiple cycles
Source: www.fda.gov/drugs/resources-information-approved-drugs/oncology-cancer-hematologic-malignancies-approval-notifications. Doses are for orientation; the current label governs.
- Medicare
- Part B (clinician-administered)
Given by infusion or injection in a clinic or hospital outpatient department, so it is a Part B drug: Medicare pays 80% after the Part B deductible and the patient owes 20% coinsurance, uncapped in Original Medicare unless a Medigap policy applies. HCPCS J9045. Generic; supply shortages in 2023 affected access more than coverage did.
- Commercial insurance
- covered on label
Multi-source generic; covered under the medical benefit without prior authorisation in most plans, as part of standard regimens.
Sources: Medicare.gov: Chemotherapy · Medicare.gov: Prescription drugs (outpatient, Part B). Not medical or financial advice; verify with your plan.
- Notes
- Long-established generic: never subject to a technology appraisal; funded routinely through hospital formularies and NHS England systemic anti-cancer therapy protocols.
- NHS England
- Routinely funded for the appraised indication (or via managed access)
Sources: NICE search: carboplatin. Funding decisions are indication-specific and change monthly; verify with NICE and your treating team.
Approvals
| Region | Year | Indication |
|---|---|---|
| US | 1989 | Ovarian cancer (now broad use) |
| Adverse event |
|---|
| Thrombocytopenia |
| Anaemia |
| Neutropenia |
| Nausea and vomiting |
| Hypersensitivity (after ≥6 cycles) |
| Peripheral neuropathy (with paclitaxel) |
Events listed without rates were not read from a primary source; see the label. Blank cells mean the figure was not sourced, not that it is zero.
| Country | Reimbursement | List price | Assistance |
|---|---|---|---|
| United Statesgeneric | Medicare Part B; generic | not disclosed | — |
| United Kingdomgeneric | NHS standard; generic | not disclosed | — |
List prices are manufacturer or Medicare figures where publicly disclosed; net prices after rebates are usually lower. Reimbursement changes; check the payer.
Trials
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Landmark trials in OnCo
Women with newly diagnosed advanced or recurrent endometrial cancer should receive a PD-1 antibody (dostarlimab or pembrolizumab) with their chemotherapy, and mismatch repair testing is now essential because women with dMMR tumours gain a very large and durable benefit. The gain in mismatch-repair-proficient tumours is real but smaller, and molecular classification (POLE, p53, MMR) is increasingly used to decide who benefits most.
Patients with operable stage II-III lung cancer without EGFR or ALK alterations should have chemo-immunotherapy discussed before surgery rather than only afterwards. Three pre-operative cycles do not compromise the operation and improve cure rates. Whether to continue immunotherapy after surgery, as the perioperative trials do, and whether patients with pCR need any further treatment, remain open questions.
For stage II-III triple-negative breast cancer, chemotherapy plus pembrolizumab before surgery and pembrolizumab alone afterwards is now the standard approach worldwide, and the survival gain is real, not just a surrogate. It does not apply to stage I disease or to hormone-receptor-positive or HER2-positive cancers. The price is a year of immunotherapy with a meaningful chance of a permanent endocrine side effect such as hypothyroidism or adrenal insufficiency.
Most patients with newly diagnosed advanced non-squamous lung cancer that lacks a targetable mutation should receive chemotherapy plus pembrolizumab; those with PD-L1 of 50% or more may reasonably receive pembrolizumab alone. About one in five patients is alive at five years, compared with roughly one in ten with chemotherapy alone. Patients with EGFR or ALK alterations were excluded and should have targeted therapy first.
Latest papers
topQuery for this drug: (TITLE:"Carboplatin" OR ABSTRACT:"Carboplatin") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about Carboplatin, not a curated reading list.
Pages like this
not linked directly; found by shared links- ProductPaclitaxel / nab-paclitaxel
Shares A strategic reserve of essential generic cancer drugs to end recurring shortages, A non-profit manufacturer for generic cancer drugs in chronic shortage, Choose regimens by infusion-chair hours, not just efficacy, where chairs are the constraint, Pooled international procurement of essential adult cancer medicines.
- ProductCisplatin
Shares Antiemetics for chemotherapy-induced nausea and vomiting, INTERLACE, Platinum-sensitive / platinum-resistant, Vulvar cancer.
- InstitutionGOG Foundation
Shares GOG-0218 & ICON7 (bevacizumab), OUTBACK / ANZGOG 0902 / GOG-0274, RUBY / ENGOT-EN6 / GOG-3031, NRG-GY018 / KEYNOTE-868.
- CompanyMerck & Co. (MSD)
Shares KEYNOTE-189: pembrolizumab plus chemotherapy as first treatment for non-squamous lung cancer without a driver mutation, Vulvar cancer, KEYNOTE-522: adding pembrolizumab before and after surgery in early triple-negative breast cancer, Anal cancer (squamous cell carcinoma).
- TermPathologic complete response (pCR)
Shares Sibylle Loibl, German Breast Group (GBG), CROSS, KEYNOTE-522.
- ProductCyclophosphamide
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- TechnologyIMRT / IGRT (modern external beam)
Shares Induction chemotherapy → chemoradiation (locally advanced cervical cancer), OUTBACK / ANZGOG 0902 / GOG-0274, INTERLACE, Institute of Oncology Ljubljana.
- ProductEtoposide
Shares Testicular germ cell tumours, Wilms tumour (nephroblastoma), Retinoblastoma, Neuroendocrine tumours.