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Biomarker analyses of second-line ramucirumab in patients with advanced gastric cancer from RAINBOW, a global, randomized, double-blind, phase 3 study

Authors
Van Cutsem, E.Muro, K.Cunningham, D.Bodoky, G.Sobrero, A.Cascinu, S.Ajani, J.Oh, S. C.Al-Batran, S. E.Wainberg, Z. A.Wijayawardana, S. R.Melemed, S.Ferry, D.Hozak, R. R.Ohtsu, A.
Issue Date
3월-2020
Publisher
ELSEVIER SCI LTD
Keywords
Ramucirumab; Gastric cancer; Gastroesophageal junction cancer; Biomarker; Predictive; Prognostic
Citation
EUROPEAN JOURNAL OF CANCER, v.127, pp.150 - 157
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN JOURNAL OF CANCER
Volume
127
Start Page
150
End Page
157
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/57530
DOI
10.1016/j.ejca.2019.10.026
ISSN
0959-8049
Abstract
Background: The RAINBOW trial showed that second-line ramucirumab with paclitaxel prolongs overall survival (OS) and progression-free survival (PFS) compared with placebo plus paclitaxel for treatment of advanced gastric/gastroesophageal junction cancer. Plasma samples were collected from patients during the trial and tested to identify predictive and prognostic biomarkers. Patients and methods: Circulating factors in plasma samples from mutually exclusive subsets of RAINBOW patients were assayed using: Intertek assays (24 markers, 380 samples, 57% of patients) and Lilly-developed assay (LDA) platform (5 markers, 257 samples, 39% of patients). Time-trend plots were generated for each marker from the Intertek assays. Baseline patient data were dichotomized into low- and high-marker subgroups. Markers were analyzed for predictive effects using interaction models and for prognostic effects using main-effects models. Results: The Intertek and LDA populations were representative of the full trial population. Plasma levels of VEGF-D and PlGF increased from baseline levels during treatment, then declined after treatment discontinued. Angiopoietin-2 exhibited a decrease during treatment, then increased after treatment discontinuation. No clear time trend was evident with the other markers. Analyses of baseline biomarker expression and its relationship with efficacy variables found no biomarker was predictive for efficacy outcomes, including VEGF-D. However, CRP, HGF, ICAM-3, IL-8, SAA, and VCAM-1 were identified as potential prognostic markers with low baseline levels corresponding to longer OS and PFS. Conclusions: Pharmacodynamic and prognostic relationships were found from the exploratory biomarker analyses in RAINBOW; however, no predictive markers for ramucirumab in gastric cancer were identified in this trial. (C) 2019 The Author(s). Published by Elsevier Ltd.
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