Phase II randomised discontinuation trial of brivanib in patients with advanced solid tumours.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
10 2019
Historique:
received: 28 05 2019
revised: 20 07 2019
accepted: 23 07 2019
pubmed: 16 9 2019
medline: 10 6 2020
entrez: 16 9 2019
Statut: ppublish

Résumé

Brivanib is a selective inhibitor of vascular endothelial growth factor and fibroblast growth factor (FGF) signalling. We performed a phase II randomised discontinuation trial of brivanib in 7 tumour types (soft-tissue sarcomas [STS], ovarian cancer, breast cancer, pancreatic cancer, non-small-cell lung cancer [NSCLC], gastric/esophageal cancer and transitional cell carcinoma [TCC]). During a 12-week open-label lead-in period, patients received brivanib 800 mg daily and were evaluated for FGF2 status by immunohistochemistry. Patients with stable disease at week 12 were randomised to brivanib or placebo. A study steering committee evaluated week 12 response to determine if enrolment in a tumour type would continue. The primary objective was progression-free survival (PFS) for brivanib versus placebo in patients with FGF2-positive tumours. A total of 595 patients were treated, and stable disease was observed at the week 12 randomisation point in all tumour types. Closure decisions were made for breast cancer, pancreatic cancer, NSCLC, gastric cancer and TCC. Criteria for expansion were met for STS and ovarian cancer. In 53 randomised patients with STS and FGF2-positive tumours, the median PFS was 2.8 months for brivanib and 1.4 months for placebo (hazard ratio [HR]: 0.58, p = 0.08). For all randomised patients with sarcomas, the median PFS was 2.8 months (95% confidence interval [CI]: 1.4-4.0) for those treated with brivanib compared with 1.4 months (95% CI: 1.3-1.6) for placebo (HR = 0.64, 95% CI: 0.38-1.07; p = 0.09). In the 36 randomised patients with ovarian cancer and FGF2-positive tumours, the median PFS was 4.0 (95% CI: 2.6-4.2) months for brivanib and 2.0 months (95% CI: 1.2-2.7) for placebo (HR: 0.56, 95% CI: 0.26-1.22). For all randomised patients with ovarian cancer, the median PFS in those randomised to brivanib was 4.0 months (95% CI: 2.6-4.2) and was 2.0 months (95% CI: 1.2-2.7) in those randomised to placebo (HR = 0.54, 95% CI: 0.25-1.17; p = 0.11). Brivanib demonstrated activity in STS and ovarian cancer with an acceptable safety profile. FGF2 expression, as defined in the protocol, is not a predictive biomarker of the efficacy of brivanib.

Sections du résumé

BACKGROUND
Brivanib is a selective inhibitor of vascular endothelial growth factor and fibroblast growth factor (FGF) signalling. We performed a phase II randomised discontinuation trial of brivanib in 7 tumour types (soft-tissue sarcomas [STS], ovarian cancer, breast cancer, pancreatic cancer, non-small-cell lung cancer [NSCLC], gastric/esophageal cancer and transitional cell carcinoma [TCC]).
PATIENTS AND METHODS
During a 12-week open-label lead-in period, patients received brivanib 800 mg daily and were evaluated for FGF2 status by immunohistochemistry. Patients with stable disease at week 12 were randomised to brivanib or placebo. A study steering committee evaluated week 12 response to determine if enrolment in a tumour type would continue. The primary objective was progression-free survival (PFS) for brivanib versus placebo in patients with FGF2-positive tumours.
RESULTS
A total of 595 patients were treated, and stable disease was observed at the week 12 randomisation point in all tumour types. Closure decisions were made for breast cancer, pancreatic cancer, NSCLC, gastric cancer and TCC. Criteria for expansion were met for STS and ovarian cancer. In 53 randomised patients with STS and FGF2-positive tumours, the median PFS was 2.8 months for brivanib and 1.4 months for placebo (hazard ratio [HR]: 0.58, p = 0.08). For all randomised patients with sarcomas, the median PFS was 2.8 months (95% confidence interval [CI]: 1.4-4.0) for those treated with brivanib compared with 1.4 months (95% CI: 1.3-1.6) for placebo (HR = 0.64, 95% CI: 0.38-1.07; p = 0.09). In the 36 randomised patients with ovarian cancer and FGF2-positive tumours, the median PFS was 4.0 (95% CI: 2.6-4.2) months for brivanib and 2.0 months (95% CI: 1.2-2.7) for placebo (HR: 0.56, 95% CI: 0.26-1.22). For all randomised patients with ovarian cancer, the median PFS in those randomised to brivanib was 4.0 months (95% CI: 2.6-4.2) and was 2.0 months (95% CI: 1.2-2.7) in those randomised to placebo (HR = 0.54, 95% CI: 0.25-1.17; p = 0.11).
CONCLUSION
Brivanib demonstrated activity in STS and ovarian cancer with an acceptable safety profile. FGF2 expression, as defined in the protocol, is not a predictive biomarker of the efficacy of brivanib.

Identifiants

pubmed: 31522033
pii: S0959-8049(19)30443-5
doi: 10.1016/j.ejca.2019.07.024
pmc: PMC8852771
mid: NIHMS1701814
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Biomarkers, Tumor 0
Triazines 0
brivanib DDU33B674I
Alanine OF5P57N2ZX

Types de publication

Clinical Trial, Phase II Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

132-139

Subventions

Organisme : Cancer Research UK
ID : 11650
Pays : United Kingdom
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

Copyright © 2019 The Author(s). Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Robin L Jones (RL)

Royal Marsden Hospital, Institute of Cancer Research, London, United Kingdom. Electronic address: robin.jones4@nhs.net.

Mark J Ratain (MJ)

University of Chicago, Chicago, IL, USA.

Peter J O'Dwyer (PJ)

University of Pennsylvania, Philadelphia, PA, USA.

Lillian L Siu (LL)

Princess Margaret Cancer Centre, Toronto, ON, USA.

Jacek Jassem (J)

Medical University of Gdansk, Gdansk, Poland.

Jacques Medioni (J)

Hôpital Européen Georges Pompidou, Paris, France; Paris-Descartes University, Paris, France.

Maja DeJonge (M)

Erasmus University Medical Center, Rotterdam, the Netherlands.

Charles Rudin (C)

Johns Hopkins University, Baltimore, MD, USA.

Michael Sawyer (M)

Cross Cancer Institute, Edmonton, AB, USA.

David Khayat (D)

Petrie-Salpetriere Hospital, Paris, France.

Ahmad Awada (A)

Institut Jules Bordet, Brussels, Belgium.

Judith M P G M de Vos-Geelen (JMPGM)

Department of Internal Medicine, Division of Medical Oncology, GROW - School for Oncology and Developmental Biology, Maastricht UMC+, Maastricht, the Netherlands.

T R Jeffry Evans (TRJ)

Beatson West of Scotland Cancer Centre, University of Glasgow, Glasgow, United Kingdom.

Jennifer Obel (J)

North Shore University Health System, Evanston, IL, USA.

Bruce Brockstein (B)

North Shore University Health System, Evanston, IL, USA.

Jacques DeGreve (J)

University Hospital Brussels, Brussels, Belgium.

Jean-Francois Baurain (JF)

Centre du Cancer, Cu Saint-Luc/UCL, Brussels, Belgium.

Robert Maki (R)

Monter Cancer Center, Lake Success, NY, USA.

David D'Adamo (D)

Eisai Inc, Woodcliff Lake, NJ Previously Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

Mark Dickson (M)

Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

Samir Undevia (S)

University of Chicago, Chicago, IL, USA.

David Geary (D)

University of Chicago, Chicago, IL, USA.

Linda Janisch (L)

University of Chicago, Chicago, IL, USA.

Philippe L Bedard (PL)

Princess Margaret Cancer Centre, Toronto, ON, USA.

Albiruni R Abdul Razak (AR)

Princess Margaret Cancer Centre, Toronto, ON, USA.

Rebecca Kristeleit (R)

Royal Marsden Hospital, Institute of Cancer Research, London, United Kingdom.

Joanna Vitfell-Rasmussen (J)

Royal Marsden Hospital, Institute of Cancer Research, London, United Kingdom.

Ian Walters (I)

Intensity Therapeutics Inc, Westport, CT Previously BMS, USA.

Stan B Kaye (SB)

Royal Marsden Hospital, Institute of Cancer Research, London, United Kingdom.

Gary Schwartz (G)

Columbia University, New York, NY, USA.

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Classifications MeSH