Adverse effects of anticancer agents that target the VEGF pathway
Abstract
Antiangiogenesis agents that target the VEGF/VEGF receptor pathway have become an important part of standard therapy in multiple cancer indications. With expanded clinical experience with this class of agents has come the increasing recognition of the diverse adverse effects related to disturbance of VEGF-dependent physiological functions and homeostasis in the cardiovascular and renal systems, as well as wound healing and tissue repair. Although most adverse effects of VEGF inhibitors are modest and manageable, some are associated with serious and life-threatening consequences, particularly in high-risk patients and in certain clinical settings. This Review examines the toxicity profiles of anti-VEGF antibodies and small-molecule inhibitors. The potential mechanisms of the adverse effects, risk factors, and the implications for selection of patients and management are discussed.
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In HARBOR, monthly ranibizumab was linked to more geographic atrophy than PRN (HR, 1.3; 95% CI, 1.0-1.7).
“In the HARBOR trial, eyes that received monthly ranibizumab had a higher incidence of geographic atrophy when compared with PRN treatment (HR, 1.3; 95% CI, 1.0–1.7).29”
From Five-Year Outcomes with Anti–Vascular Endothelial Growth Factor Treatment of Neovascular Age-Related Macular Degeneration (2016) · cites this paper as [29]
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Interstitial Nephritis Secondary to Bevacizumab Treatment in Metastatic Leiomyosarcoma
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Ranibizumab and Bevacizumab for Treatment of Neovascular Age-related Macular Degeneration
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- Authors
- Chen, H. X., & Cleck, J. N.
- Affiliations
- National Institutes of Health (US)
- ORCID
- Chen, Helen X.
- Venue
- Nature Reviews Clinical Oncology
- Published
- 2009-07-07
- Volume
- 6
- Issue
- 8
- Pages
- 465-477
- ISSN
- 1759-4774 (ISSN-L)
- 1759-4782
- OpenAlex
- W1975058097
- Cited by
- 560
- References
- 97
- Citations by year
- 2026: 15 · 2025: 19 · 2024: 36 · 2023: 33 · 2022: 23 · 2021: 33 · 2020: 24 · 2019: 38 · 2018: 34 · 2017: 30 · 2016: 33 · 2015: 26 · 2014: 50 · 2013: 44 · 2012: 50
- FWCI
- 2.96
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Clinical Oncology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Health Sciences › Medicine › Dermatology › Chemotherapy-related skin toxicity
- Health Sciences › Medicine › Oncology › Lymphatic System and Diseases
- Keywords
- VEGF inhibitors, anti-angiogenic therapy, adverse effects, drug toxicity, anti-VEGF antibody, cardiotoxicity, nephrotoxicity, wound healing, tissue repair, risk factors, patient selection, adverse effects management
- MeSH terms
- Bevacizumab, Sorafenib, Sunitinib, Antibodies, Monoclonal, Antineoplastic Agents, Benzenesulfonates, Brain Diseases, Cardiovascular Diseases, Clinical Trials as Topic, Drug Interactions, Forecasting, Gastrointestinal Diseases, Hemorrhage, Humans, Indoles, Kidney Diseases, Neoplasm Proteins, Niacinamide, Phenylurea Compounds, Pyridines, Pyrroles, Risk Factors, Wound Healing, Drug Delivery Systems, Capillary Leak Syndrome, Angiogenesis Inhibitors, Receptors, Vascular Endothelial Growth Factor, Vascular Endothelial Growth Factor A, Protein Kinase Inhibitors, Antibodies, Monoclonal, Humanized
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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