Evidence map›Paper›PMID 41575788›Full record

ArticleKidney3602026

Bevacizumab-Associated Renal Adverse Events Signal Better Prognosis in Ovarian Cancer: A Double-Edged Vascular Endothelial Growth Factor Inhibition.

Cristina Riaza, Marta Álvarez-Nadal, Antonio Casado, Gloria Marquina, Marta Calvo, Antolina Rodríguez-Moreno, Marta Rivero, Ana I Sánchez-Fructuoso, Clara García-Carro

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Article in Kidney360, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Cristina RiazaNephrology Department, San Carlos Clinical University Hospital, IdISSC, Madrid, Spain.ORCID 0009-0004-5154-7898
Marta Álvarez-NadalNephrology Department, San Carlos Clinical University Hospital, IdISSC, Madrid, Spain.ORCID 0000-0002-2247-1845
Antonio CasadoDepartment of Medical Oncology, School of Medicine, San Carlos Clinical University Hospital, EURACAN Referral Centre, UCM, IdissC, Madrid, Spain.ORCID 0000-0002-8200-3306
Gloria MarquinaDepartment of Medical Oncology, School of Medicine, San Carlos Clinical University Hospital, EURACAN Referral Centre, UCM, IdissC, Madrid, Spain.ORCID 0000-0002-8961-9787
Marta CalvoNephrology Department, San Carlos Clinical University Hospital, IdISSC, Madrid, Spain.ORCID 0000-0002-5894-5360
Antolina Rodríguez-MorenoNephrology Department, San Carlos Clinical University Hospital, IdISSC, Madrid, Spain.ORCID 0000-0003-0093-1676
Marta RiveroNephrology Department, San Carlos Clinical University Hospital, IdISSC, Madrid, Spain.
Ana I Sánchez-FructuosoNephrology Department, San Carlos Clinical University Hospital, IdISSC, Madrid, Spain.ORCID 0000-0001-7017-9729
Clara García-CarroNephrology Department, San Carlos Clinical University Hospital, IdISSC, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

key pointsRenal adverse events occurred in 34.7% of patients with bevacizumab-treated ovarian cancer, with hypertension being the most frequent manifestation. Pre-existing hypertension was the only independent risk factor for developing renal adverse events during bevacizumab therapy. The occurrence of renal adverse events was independently associated with improved overall survival, suggesting effective vascular endothelial growth factor pathway inhibition.

backgroundBevacizumab, a monoclonal antibody targeting vascular endothelial growth factor-A, is a cornerstone in ovarian cancer (OC). Bevacizumab is associated with renal adverse events, including hypertension (HTN), proteinuria, and AKI. The incidence, risk factors, and prognostic effect of these renal events remain poorly defined. This study aimed to determine the incidence, risk factors, and association with mortality of renal events in patients with OC treated with bevacizumab.

methodsWe conducted a retrospective single-center study including 147 patients with OC treated with bevacizumab between 2011 and 2023. Renal events were defined as new-onset or worsening HTN (grade ≥2), proteinuria (grade ≥2), and/or AKI, as per Common Terminology Criteria for Adverse Events v5.0 and Kidney Disease Improving Global Outcomes guidelines.

resultsOver a median follow-up of 52 months, 34.7% of patients developed a renal event, most commonly HTN (27.9%), followed by proteinuria (6.8%) and AKI (6.8%). Only a history of HTN was identified as an independent risk factor for renal event ( P = 0.0078). Importantly, patients with renal events had significantly longer survival compared with those who did not ( P = 0.0243). In the multivariate analysis, the occurrence of a renal event emerged as a protective factor against mortality.

conclusionsIn conclusion, renal events occurred in 34.7% of bevacizumab-treated patients. HTN was a risk factor for renal event, but renal events seemed to be a protective factor against mortality. Rather than signaling harm, their presence may reflect effective Vascular endothelial growth factor pathway inhibition and greater antitumor response. Routine monitoring and early nephrological management of HTN, proteinuria, and AKI are essential to optimize treatment continuity and outcomes.

Indexed as

Acute Kidney InjuryAntineoplastic Agents, ImmunologicalBevacizumabHypertensionOvarian NeoplasmsProteinuriaAgedAngiogenesis InhibitorsFemaleHumansIncidenceMiddle AgedPrognosisRetrospective StudiesRisk FactorsVascular Endothelial Growth Factor AAngiogenesis InhibitorsAntineoplastic Agents, ImmunologicalBevacizumabVascular Endothelial Growth Factor AAKIcancerhypertensionproteinuriarenal injuryVEGF

Identifiers

PMID41575788
PMCPMC13229414

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.