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Binimetinib in combination with nivolumab or nivolumab and ipilimumab in patients with previously treated microsatellite-stable metastatic colorectal cancer with RAS mutations in an open-label phase 1b/2 study.
Elez, Elena; Cubillo, Antonio; Alfonso, Pilar Garcia; Middleton, Mark R; Chau, Ian; Alkuzweny, Baha; Alcasid, Ann; Zhang, Xiaosong; Van Cutsem, Eric.
Afiliação
  • Elez E; Medical Oncology Department, Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology, Universitat Autònoma de Barcelona, Barcelona, Spain. meelez@vhio.net.
  • Cubillo A; Centro Integral, Oncológico Clara Campal, HM CIOCC, Madrid, Spain.
  • Alfonso PG; Facultad HM Hospitales de Ciencias de La Salud UCJC, 28050, Madrid, Spain.
  • Middleton MR; Medical Oncology Service, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Universidad Complutense, Madrid, Spain.
  • Chau I; Department of Oncology, NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.
  • Alkuzweny B; Gastrointestinal Unit, Royal Marsden Hospital, London & Surrey, UK.
  • Alcasid A; Formerly Pfizer, Inc, San Diego, CA, USA.
  • Zhang X; Pfizer Inc, Collegeville, PA, USA.
  • Van Cutsem E; Pfizer, Inc, New York, NY, USA.
BMC Cancer ; 24(1): 446, 2024 Apr 11.
Article em En | MEDLINE | ID: mdl-38600471
ABSTRACT

BACKGROUND:

In patients with previously treated RAS-mutated microsatellite-stable (MSS) metastatic colorectal cancer (mCRC), a multicenter open-label phase 1b/2 trial was conducted to define the safety and efficacy of the MEK1/MEK2 inhibitor binimetinib in combination with the immune checkpoint inhibitor (ICI) nivolumab (anti-PD-1) or nivolumab and another ICI, ipilimumab (anti-CTLA4).

METHODS:

In phase 1b, participants were randomly assigned to Arm 1A (binimetinib 45 mg twice daily [BID] plus nivolumab 480 mg once every 4 weeks [Q4W]) or Arm 1B (binimetinib 45 mg BID plus nivolumab 480 mg Q4W and ipilimumab 1 mg/kg once every 8 weeks [Q8W]) to determine the maximum tolerable dose (MTD) and recommended phase 2 dose (RP2D) of binimetinib. The MTD/RP2D was defined as the highest dosage combination that did not cause medically unacceptable dose-limiting toxicities in more than 35% of treated participants in Cycle 1. During phase 2, participants were randomly assigned to Arm 2A (binimetinib MTD/RP2D plus nivolumab) or Arm 2B (binimetinib MTD/RP2D plus nivolumab and ipilimumab) to assess the safety and clinical activity of these combinations.

RESULTS:

In phase 1b, 21 participants were randomized to Arm 1A or Arm 1B; during phase 2, 54 participants were randomized to Arm 2A or Arm 2B. The binimetinib MTD/RP2D was determined to be 45 mg BID. In phase 2, no participants receiving binimetinib plus nivolumab achieved a response. Of the 27 participants receiving binimetinib, nivolumab, and ipilimumab, the overall response rate was 7.4% (90% CI 1.3, 21.5). Out of 75 participants overall, 74 (98.7%) reported treatment-related adverse events (AEs), of whom 17 (22.7%) reported treatment-related serious AEs.

CONCLUSIONS:

The RP2D binimetinib regimen had a safety profile similar to previous binimetinib studies or nivolumab and ipilimumab combination studies. There was a lack of clinical benefit with either drug combination. Therefore, these data do not support further development of binimetinib in combination with nivolumab or nivolumab and ipilimumab in RAS-mutated MSS mCRC. TRIAL REGISTRATION NCT03271047 (09/01/2017).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzimidazóis / Neoplasias Colorretais / Nivolumabe Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzimidazóis / Neoplasias Colorretais / Nivolumabe Idioma: En Ano de publicação: 2024 Tipo de documento: Article