OnCo
technologiesTechnologyStandard of care

Anti-angiogenic therapy

Anti-angiogenic therapy cuts off the tumour's blood supply; it is now mostly used to help immunotherapy work better.

Anti-angiogenic drugs include bevacizumab, ramucirumab, and VEGFR TKIs. Alone they extend PFS modestly; with PD-1 blockade they are standard in RCC, HCC (atezolizumab-bevacizumab), and endometrial cancer (lenvatinib-pembrolizumab). PD-1×VEGF bispecifics are the consolidation of this idea.

Schematic · not to scale
Tumour signals VEGF · New vessels blocked

How it works

Blockade of VEGF signalling normalises vasculature and reduces immunosuppressive myeloid cells.

Strengths
  • Broad, combinable
Limitations
  • Hypertension, bleeding, proteinuria
  • Small single-agent benefit
Since
2004

Products

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ApprovedSmall-molecule kinase inhibitor (VEGFR)
Axitinib · Inlyta

Axitinib is a selective VEGF-receptor pill, now given mainly with pembrolizumab or avelumab as first-line kidney cancer treatment.

ApprovedMonoclonal antibody (anti-VEGF)
Bevacizumab · Avastin (and biosimilars)

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.

ApprovedMonoclonal antibody (anti-VEGF)
Bevacizumab (glioblastoma use) · Avastin

A blood-vessel-blocking antibody that shrinks glioblastoma on scans and reduces swelling, but has never been shown to help patients live longer.

ApprovedSmall-molecule multi-kinase inhibitor (MET, VEGFR2, AXL, RET)
Cabozantinib · Cabometyx

A pill that blocks both blood-vessel growth and the MET escape pathway, used in kidney, liver, thyroid and, since 2025, neuroendocrine cancers.

Under reviewPD-1 antibody + oral VEGFR2 inhibitor
Camrelizumab + rivoceranib

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.

ApprovedSmall-molecule kinase inhibitor (VEGFR1-3)
Fruquintinib · Fruzaqla

A Chinese-discovered pill that blocks the blood-vessel receptors, approved in 2023 for bowel cancer after all standard treatments.

ApprovedSmall-molecule multi-kinase inhibitor (VEGFR, FGFR, PDGFR, RET, KIT)
Lenvatinib · Lenvima

An oral anti-angiogenic pill that matched sorafenib in liver cancer with higher response rates, and partners with pembrolizumab in kidney and endometrial cancer.

NegativeSmall-molecule kinase inhibitor (VEGFR/FGFR/PDGFR)
Nintedanib · Ofev (fibrosis); Vargatef (NSCLC, EU)

An anti-angiogenic pill that looked promising in mesothelioma in a small trial but failed in the large one.

ApprovedSmall-molecule kinase inhibitor (VEGFR/PDGFR/KIT)
Pazopanib · Votrient

Pazopanib is the only multi-kinase inhibitor approved for soft-tissue sarcoma (excluding fat-derived tumours), used after chemotherapy fails.

ApprovedMonoclonal antibody (anti-VEGFR2)
Ramucirumab · Cyramza

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.

ApprovedSmall-molecule multi-kinase inhibitor
Regorafenib · Stivarga

A sorafenib successor that became the first second-line drug proven to prolong life in liver cancer (2017).

ApprovedSmall-molecule multi-kinase inhibitor (VEGFR, PDGFR, RAF)
Sorafenib · Nexavar

The first drug ever to extend life in advanced liver cancer (2007), now mostly a comparator arm that newer combinations are measured against.

ApprovedSmall-molecule multi-kinase inhibitor (VEGFR, PDGFR, KIT)
Sunitinib · Sutent

Sunitinib is an anti-angiogenic pill approved for pancreatic neuroendocrine tumours, kidney cancer and GIST.

Not mapped hereOral cereblon modulator (first IMiD)
Thalidomide · Thalomid

Thalidomide is the drug behind the 1960s birth-defect tragedy, rehabilitated as the first immunomodulatory myeloma drug and the parent of lenalidomide and pomalidomide.

ApprovedSmall-molecule kinase inhibitor (VEGFR)
Tivozanib · Fotivda

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.

Key papers

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rctThe Lancet 2025
HARMONi-2: ivonescimab, a PD-1 x VEGF bispecific, beats pembrolizumab head-to-head in PD-L1-positive lung cancer

For the first time a new drug has beaten pembrolizumab, the global first-line standard, in a randomised lung cancer trial, and it did so by combining checkpoint blockade with anti-angiogenesis in one molecule. For patients outside China nothing changes yet: the drug is not approved in the West, the trial was single-country, and survival benefit has not been shown. If confirmed in the global HARMONi-3 and HARMONi-7 trials, PD-1 x VEGF bispecifics could replace PD-1 antibodies as the immunotherapy backbone.

rctNew England Journal of Medicine 2021changed practice
CLEAR: lenvatinib plus pembrolizumab versus sunitinib as first treatment for advanced kidney cancer

Patients with newly diagnosed advanced clear-cell kidney cancer should receive an immunotherapy-based combination; lenvatinib plus pembrolizumab gives the highest response rate and longest PFS of the available options, at the cost of more side effects requiring dose adjustment. Sunitinib alone is no longer an appropriate standard. Choosing among the combinations depends on risk group, symptoms, comorbidity and the value placed on treatment-free survival, which favours nivolumab plus ipilimumab in intermediate and poor risk.

rctNew England Journal of Medicine 2020changed practice
IMbrave150: atezolizumab plus bevacizumab replaces sorafenib as first treatment for advanced liver cancer

Patients with advanced liver cancer and good liver function should be offered atezolizumab plus bevacizumab (or durvalumab plus tremelimumab) rather than sorafenib as first treatment; median survival is now around 19 months and about a quarter of patients respond. Endoscopy to treat varices before starting bevacizumab is essential because of bleeding risk. Patients with poorer liver function (Child-Pugh B) or autoimmune disease or transplants were not studied.

rctNew England Journal of Medicine 2019changed practice
PAOLA-1: olaparib added to bevacizumab maintenance in newly diagnosed ovarian cancer, with benefit confined to HRD-positive tumours

Women with newly diagnosed advanced ovarian cancer should have their tumour tested for BRCA mutations and homologous recombination deficiency, because those who are HRD-positive gain years of additional disease control and better survival from adding olaparib to bevacizumab maintenance. Those who are HRD-negative gain nothing from olaparib in this combination and should not be exposed to its toxicity and cost. HRD testing has become a routine part of ovarian cancer care as a result.

Latest papers

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Literature trend2,564 papers in the last 12 months+16% vs prior 12How this is computed
Latest papers · live from Europe PMC
Open in Europe PMC

Query for this technology: (TITLE:"anti-angiogenic" OR ABSTRACT:"anti-angiogenic" OR TITLE:"antiangiogenic" OR ABSTRACT:"antiangiogenic" OR TITLE:"VEGF inhibitor" OR ABSTRACT:"VEGF inhibitor" OR TITLE:"bevacizumab" OR ABSTRACT:"bevacizumab") 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 Anti-angiogenic therapy, not a curated reading list.

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