Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/18421
Title: Rilotumumab plus epirubicin, cisplatin, and capecitabine as first-line therapy in advanced MET-positive gastric or gastro-oesophageal junction cancer (RILOMET-1): a randomised, double-blind, placebo-controlled, phase 3 trial.
Authors: Catenacci, Daniel V T;Tebbutt, Niall C;Davidenko, Irina;Murad, André M;Al-Batran, Salah-Eddin;Ilson, David H;Tjulandin, Sergei;Gotovkin, Evengy;Karaszewska, Boguslawa;Bondarenko, Igor;Tejani, Mohamedtaki A;Udrea, Anghel A;Tehfe, Mustapha;De Vita, Ferdinando;Turkington, Cheryl;Tang, Rui;Ang, Agnes;Zhang, Yilong;Hoang, Tien;Sidhu, Roger;Cunningham, David
Affiliation: University of Chicago, Chicago, IL, USA
Austin Health, Heidelberg, Victoria, Australia
State Budgetary Healthcare Institution, Clinical Oncology Dispensary #1, Krasnodar Region Ministry of Healthcare, Krasnodar, Russia
Hospital das Clínicas da Universidade Federal de Minas Gerais, Horizonte, Brazil
Institute of Clinical Cancer Research, Krankenhaus Nordwest, University Cancer Center, Frankfurt, German
Memorial Sloan Kettering Cancer Center, New York, NY, USA
Russian Cancer Research Center, Moscow, Russia
Regional Budgetary Institution of Public Health Ivanovo Regional Oncology Dispensary, Ivanovo, Russia
Przychodnia Lekarska Komed Oddzial Jednego Dnia, Konin, Poland
Dnipropetrovsk Medical Academy, City Multifield Clinical Hospital 4, Dnipropetrovsk, Ukraine
University of Rochester Medical Center, James P Wilmot Cancer Center, Rochester, NY, USA
SC Medisprof SRL, Cluj-Napoca, Romania
Centre Hospitalier de L'Universite de Montreal Notre-Dame, Montreal, QC, Canada
Second University of Naples School of Medicine, Naples, Italy
Amgen, Cambridge, UK
Amgen, Thousand Oaks, CA, USA
Royal Marsden Hospital, London and Surrey, UK
Issue Date: Nov-2017
EDate: 2017-09-25
Citation: The Lancet. Oncology 2017; 18(11): 1467-1482
Abstract: Rilotumumab is a fully human monoclonal antibody that selectively targets the ligand of the MET receptor, hepatocyte growth factor (HGF). We aimed to assess the efficacy, safety, and pharmacokinetics of rilotumumab combined with epirubicin, cisplatin, and capecitabine, and to assess potential biomarkers, in patients with advanced MET-positive gastric or gastro-oesophageal junction adenocarcinoma. This multicentre, randomised, double-blind, placebo-controlled, phase 3 study was done at 152 centres in 27 countries. We recruited adults (aged ≥18 years) with unresectable locally advanced or metastatic gastric or gastro-oesophageal junction adenocarcinoma, an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, MET-positive tumours (≥25% of tumour cells with membrane staining of ≥1+ staining intensity), and evaluable disease, who had not received previous systemic therapy. Eligible patients were randomly assigned (1:1) via a computerised voice response system to receive rilotumumab 15 mg/kg intravenously or placebo in combination with pen-label chemotherapy (epirubicin 50 mg/m2 intravenously; cisplatin 60 mg/m2 intravenously; capecitabine 625 mg/m2 orally twice daily) in 21-day cycles for up to ten cycles. After completion of chemotherapy, patients continued to receive rilotumumab or placebo monotherapy until disease progression, intolerability, withdrawal of consent, or study termination. Randomisation was stratified by disease extent and ECOG performance status. Both patients and physicians were masked to study treatment assignment. The primary endpoint was overall survival, analysed by intention to treat. We report the final analysis. This study is registered with ClinicalTrials.gov, number NCT01697072. Between Nov 7, 2012, and Nov 21, 2014, 609 patients were randomly assigned to rilotumumab plus epirubicin, cisplatin, and capecitabine (rilotumumab group; n=304) or placebo plus epirubicin, cisplatin, and capecitabine (placebo group; n=305). Study treatment was stopped early after an independent data monitoring committee found a higher number of deaths in the rilotumumab group than in the placebo group; all patients in the rilotumumab group subsequently discontinued all study treatment. Median follow-up was 7·7 months (IQR 3·6-12·0) for patients in the rilotumumab group and 9·4 months (5·3-13·1) for patients in the placebo group. Median overall survival was 8·8 months (95% CI 7·7-10·2) in the rilotumumab group compared with 10·7 months (9·6-12·4) in the placebo group (stratified hazard ratio 1·34, 95% CI 1·10-1·63; p=0·003). The most common grade 3 or worse adverse events in the rilotumumab and placebo groups were neutropenia (86 [29%] of 298 patients vs 97 [32%] of 299 patients), anaemia (37 [12%] vs 43 [14%]), and fatigue (30 [10%] vs 35 [12%]). The frequency of serious adverse events was similar in the rilotumumab and placebo groups (142 [48%] vs 149 [50%]). More deaths due to adverse events occurred in the rilotumumab group than the placebo group (42 [14%] vs 31 [10%]). In the rilotumumab group, 33 (11%) of 298 patients had fatal adverse events due to disease progression, and nine (3%) had fatal events not due to disease progression. In the placebo group, 23 (8%) of 299 patients had fatal adverse events due to disease progression, and eight (3%) had fatal events not due to disease progression. Ligand-blocking inhibition of the MET pathway with rilotumumab is not effective in improving clinical outcomes in patients with MET-positive gastric or gastro-oesophageal adenocarcinoma. Amgen.
URI: http://ahro.austin.org.au/austinjspui/handle/1/18421
DOI: 10.1016/S1470-2045(17)30566-1
PubMed URL: 28958504
Type: Clinical Trial, Phase III
Journal Article
Multicenter Study
Randomized Controlled Trial
Appears in Collections:Journal articles

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