BEVACIZUMAB-CONTAINING TREATMENT for RELAPSED or REFRACTORY WILMS TUMOR.

Bevacizumab Wilms tumor relapse review trials

Journal

Expert review of anticancer therapy
ISSN: 1744-8328
Titre abrégé: Expert Rev Anticancer Ther
Pays: England
ID NLM: 101123358

Informations de publication

Date de publication:
17 Jul 2024
Historique:
medline: 17 7 2024
pubmed: 17 7 2024
entrez: 17 7 2024
Statut: aheadofprint

Résumé

Angiogenesis is critical for tumor growth and metastasis. Bevacizumab is an antiangiogenic drug used to treat various adult and childhood solid tumors. Its potential efficacy in Wilms tumor (WT) with poor prognosis is not established. The response to bevacizumab-containing regimens in relapsed or refractory WT was reviewed in available literature. Searches were conducted using Pubmed, Scopus and ClinicalTrials.gov databases. Eight papers were identified, published between 2007 and 2020 including 6 treatment regimens, predominantly vincristine, irinotecan and bevacizumab (VIB) ± temozolomide (VITB). Among 16 evaluable patients, there were two complete responses, 7 partial responses, 5 patients achieved stable disease (SD) and two patients had progressive disease. Objective responses (OR) were observed in 56% of all cases. OR or SD was observed in 89% (8/9) patients who received VIB/VITB. Bevacizumab was generally well tolerated. Related toxicities included hypertension, proteinuria and delayed wound healing. This review suggests potential effectiveness and good tolerability of bevacizumab in the setting of relapsed/refractory WT when used in combination with other drugs. Such combination therapies may serve as a bridging treatment option to other interventions and more personalized treatment options in the future, however focused trials are needed to obtain additional evidence.

Identifiants

pubmed: 39016020
doi: 10.1080/14737140.2024.2381537
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Sarah Al-Jilaihawi (S)

Department of Paediatric Oncology, Bristol Royal Hospital for Children, Bristol, UK.

Filippo Spreafico (F)

Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.

Annelies Mavinkurve-Groothuis (A)

Department of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Jarno Drost (J)

Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Oncode Institute, Utrecht, The Netherlands.

Daniela Perotti (D)

Predictive Medicine: Molecular Bases of Genetic Risk and Genetic Testing Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.

Christa Koenig (C)

Pediatric Hematology/Oncology, Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Switzerland.

Jesper Brok (J)

Department of Pediatric Hematology and Oncology, Rigshospitalet, Copenhagen, Denmark.

Classifications MeSH