OnCo
drugsProductApproved2004🇪🇺🇬🇧🇯🇵🇨🇳🇦🇺

Bevacizumab

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.

Humanised anti-VEGF-A IgG1. Standard with first- and second-line chemotherapy in mCRC (all RAS statuses, right-sided tumours), with trifluridine/tipiracil in refractory disease (SUNLIGHT), and in ovarian, cervical, NSCLC, RCC, HCC (with atezolizumab), and glioblastoma. Biosimilars since 2017 have cut its cost sharply. Hypertension, proteinuria, bleeding, wound-healing delay, and rare GI perforation.

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Bevacizumab Fab bound to VEGF (PDB 1BJ1), backbone trace
RCSB PDB
Mechanism, step by step
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1.Bevacizumab binds VEGF-A in the blood and tumour

Modality
Monoclonal antibody (anti-VEGF)
Mechanism
Neutralises circulating VEGF-A, reducing angiogenesis and normalising tumour vasculature.
Brand / code
Avastin (and biosimilars)
Dosing & schedule
Route
Intravenous
Schedule
5-10 mg/kg every 2 weeks (mCRC); 15 mg/kg every 3 weeks in other tumours
Dose modifications
Hold 28 days around surgery; stop for GI perforation or severe haemorrhage
Monitoring
Blood pressure, urine protein

Source: www.accessdata.fda.gov/drugsatfda_docs/label/2022/125085s340lbl.pdf. 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 J9035 for Avastin; biosimilars (Mvasi, Zirabev, Alymsys, Vegzelma, Avzivi) have their own codes and lower patient coinsurance.

Commercial insurance
step therapy common

Commercial plans almost universally prefer a bevacizumab biosimilar over Avastin; prior authorisation checks indication.

Assistance programmes

20% Part B coinsurance on a high-cost infusion adds up quickly: Medigap Plan G or N, Medicare Advantage maximum out-of-pocket, Medicaid dual eligibility, or a charity fund are the usual buffers.

Sources: Medicare.gov: Chemotherapy · Medicare.gov: Prescription drugs (outpatient, Part B) · FDA: Biosimilars. Not medical or financial advice; verify with your plan.

Not recommendedNICE TA212 · 2010
Appraised for
Metastatic colorectal cancer with oxaliplatin or fluorouracil-based chemotherapy
Notes
NICE has never recommended bevacizumab for colorectal (TA118, TA212), ovarian (TA284, TA285), breast (TA214) or cervical cancer. It was widely funded by the pre-2016 Cancer Drugs Fund and later removed. Biosimilars (from 2020) have cut the price; some indications are funded via local policies. Bevacizumab with atezolizumab for HCC is funded under TA666.
NHS England
Not routinely funded

Sources: NICE TA212. Funding decisions are indication-specific and change monthly; verify with NICE and your treating team.

Regulatory

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  1. Feb 2004ApprovalUS

    First anti-angiogenic approval (AVF2107)

  2. 26 Feb 2004ApprovalUS

    First anti-angiogenic approval (colorectal)

  3. 14 Aug 2014ApprovalUS

    Cervical cancer with chemotherapy (GOG-0240)

  4. Sept 2017ApprovalUS

    First biosimilar (bevacizumab-awwb) approved

  5. 13 Jun 2018ApprovalUS

    First-line ovarian cancer (GOG-0218)

  6. 8 May 2020ApprovalUS

    With olaparib as HRD-positive maintenance (PAOLA-1)

  7. Aug 2023Label changeUS

    With trifluridine/tipiracil in refractory mCRC

Approvals

RegionYearIndication
US2004First-line metastatic colorectal cancer with 5-FU chemotherapy
US2006NSCLC; later ovarian, cervical, RCC, glioblastoma, HCC
US2023Refractory mCRC with trifluridine/tipiracil (SUNLIGHT)
US2004Metastatic colorectal cancer (first)
US2014Platinum-resistant ovarian cancer with chemotherapy; recurrent/metastatic cervical cancer with chemotherapy
US2018First-line stage III-IV ovarian cancer after surgery
US2020First-line maintenance with olaparib in HRD-positive ovarian cancer

Safety

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Toxicity profile
Adverse eventAny gradeGrade 3+
Hypertension
Common; manageable
Proteinuria
GI perforation
Rare, boxed warning
Bleeding
Epistaxis common; serious haemorrhage rare
Impaired wound healing
Boxed warning
Hypertension
GOG-0218 concurrent + maintenance arm
42%
17%
Gastrointestinal perforation
2.6%
Proteinuria ≥ grade 3
1.6%

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.

Trials

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ClinicalTrials.gov · phase 2/3
refreshed 2026-09-09
2390 studies19 recruiting84 Phase 220 Phase 3
Search “Bevacizumab” on ClinicalTrials.gov →
Counts are from a name search and may include unrelated studies; up to 100 studies are summarised.

Recruiting now (live from ClinicalTrials.gov)

Recruiting trials near you · live from ClinicalTrials.gov
Bevacizumab
intervention: Bevacizumab
Open on ClinicalTrials.gov →

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Landmark trials in OnCo

Latest papers

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Literature trend1,558 papers in the last 12 months+10% vs prior 12How this is computed
Latest papers · live from Europe PMC
Open in Europe PMC

Query for this drug: (TITLE:"Bevacizumab" OR ABSTRACT:"Bevacizumab" OR TITLE:"Avastin" OR ABSTRACT:"Avastin" OR TITLE:"and biosimilars" OR ABSTRACT:"and biosimilars") 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 Bevacizumab, not a curated reading list.

Connected

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