Ramucirumab in Combination with Pembrolizumab in Treatment-Naïve Advanced Gastric or GEJ Adenocarcinoma: Safety and Antitumor Activity from the Phase 1a/b JVDF Trial.

gastric/gastroesophageal junction adenocarcinoma pembrolizumab phase 1b ramucirumab

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
15 Oct 2020
Historique:
received: 28 08 2020
revised: 05 10 2020
accepted: 13 10 2020
entrez: 20 10 2020
pubmed: 21 10 2020
medline: 21 10 2020
Statut: epublish

Résumé

Ramucirumab (anti-VEGFR2) plus pembrolizumab (anti-PD1) demonstrated promising antitumor activity and tolerability among patients with previously treated advanced cancers, supporting growing evidence that combination therapies modulating the tumor microenvironment may expand the spectrum of patients who respond to checkpoint inhibitors. Here we present the results of this combination in first-line patients with metastatic G/GEJ cancer. Twenty-eight patients (≥18 years) with no prior systemic chemotherapy in the advanced/metastatic setting received ramucirumab (8 mg/kg days 1 and 8) plus pembrolizumab (200 mg day 1) every 3 weeks as part of JVDF phase 1a/b study. The primary endpoint was safety. Secondary endpoints included progression-free survival (PFS), objective response rate (ORR), and overall survival (OS). Tumors were PD-L1-positive (combined positive score ≥ 1) in 19 and -negative in 6 patients. Eighteen patients experienced grade 3 treatment-related adverse events, most commonly hypertension (14%) and elevated alanine/aspartate aminotransferase (11% each), with no grade 4 or 5 reported. The ORR was 25% (PD-L1-positive, 32%; PD-L1-negative, 17%) with duration of response not reached. PFS was 5.6 months (PD-L1-positive, 8.6 months; PD-L1-negative, 4.3 months), and OS 14.6 months (PD-L1-positive, 17.3 months; PD-L1-negative, 11.3 months). Acknowledging study design limitations, ramucirumab plus pembrolizumab had encouraging durable clinical activity with no unexpected toxicities in treatment-naïve biomarker-unselected metastatic G/GEJ cancer, and improved outcomes in patients with PD-L1-positive tumors.

Identifiants

pubmed: 33076423
pii: cancers12102985
doi: 10.3390/cancers12102985
pmc: PMC7602637
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : Eli Lilly and Company
ID : N/A

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Auteurs

Ian Chau (I)

Gastrointestinal Units, Royal Marsden Hospital, London SM2 5PT, UK.

Nicolas Penel (N)

General Oncology Department, Medical Oncology Department, Oscar Lambret Cancer Center, 59020 Lille, France.

Andres O Soriano (AO)

Sarah Cannon Research Institute/Florida Cancer Specialists, Englewood, FL 34223, USA.

Hendrik-Tobias Arkenau (HT)

Sarah Cannon Research Institute United Kingdom and University College London, London W1G 6AD, UK.

Jennifer Cultrera (J)

Sarah Cannon Research Institute/Florida Cancer Specialists Leesburg South, Leesburg, FL 34748, USA.

Rafael Santana-Davila (R)

Department of Medicine, University of Washington Medicine, Seattle Cancer Care Alliance, Seattle, WA 98109, USA.

Emiliano Calvo (E)

Early Phase Clinical Drug Development Program, START Madrid-CIOCC, Centro Integral Oncológico Clara Campal, 28050 Madrid, Spain.

Christophe Le Tourneau (C)

Department of Drug Development and Innovation, Institut Curie, 75005 Paris, France.

Lars Zender (L)

Department of Internal Medicine VIII, University Hospital Tübingen, 72076 Tübingen, Germany.

Johanna C Bendell (JC)

Sarah Cannon Research Institute/Tennessee Oncology, Nashville, TN 37203, USA.

Gu Mi (G)

Eli Lilly and Company, Indianapolis, IN 46285, USA.

Ling Gao (L)

Eli Lilly and Company, Indianapolis, IN 46285, USA.

Samuel Clark McNeely (SC)

Eli Lilly and Company, Indianapolis, IN 46285, USA.

Joana M Oliveira (JM)

Eli Lilly and Company, New York, NY 10016, USA.

David Ferry (D)

Eli Lilly and Company, New York, NY 10016, USA.

Roy S Herbst (RS)

Yale Cancer Center, New Haven, CT 06520, USA.

Charles S Fuchs (CS)

Yale Cancer Center, New Haven, CT 06520, USA.
Smilow Cancer Hospital, New Haven, CT 06473, USA.

Classifications MeSH