Journal Article

Ramucirumab plus paclitaxel as switch maintenance versus continuation of first-line oxaliplatin-based chemotherapy in patients with advanced HER2-negative gastric or gastro-oesophageal junction cancer (ARMANI): a randomised, open-label, multicentre, phase 3 trial

De Vita, Ferdinando, Airò, Giulia, Sciortino, Carolina, Fassan, Matteo, Niger, Monica, Strippoli, Antonia, Spallanzani, Andrea, Chini, Claudio, Lonardi, Sara, Giommoni, Elisa, Raimondi, Alessandra, Prisciandaro, Michele, Miceli, Rosalba, Fornaro, Lorenzo, Nappo, Floriana, Latiano, Tiziana, Randon, Giovanni, Giuliani, Francesco, Cardellino, Giovanni Gerardo, Di Bartolomeo, Maria, Bethaz, Valerie, Di Donato, Samantha, Tamberi, Stefano, Pietrantonio, Filippo, Morano, Federica, Pircher, Chiara Carlotta, Brunetti, Oronzo, Marchesi, Silvia, Palermo, Federica, Garattini, Silvio Ken, Ceccon, Carlotta, Bittoni, Alessandro

2024

Overview

Paclitaxel plus ramucirumab is recommended as a second-line treatment regimen in patients with advanced HER2-negative gastric or gastro-oesophageal junction cancer. We aimed to assess whether switch maintenance or early second-line therapy with paclitaxel plus ramucirumab improved outcomes compared with continuation of oxaliplatin and fluoropyrimidine doublet chemotherapy as a first-line strategy. ARMANI was a multicentre, open-label, randomised, phase 3 trial done in 31 hospitals in Italy. We enrolled patients aged 18 years or older with an Eastern Cooperative Oncology Group performance status of 0 or 1 and locally advanced unresectable or metastatic HER2-negative gastric or gastro-oesophageal junction cancer, who had disease control after 3 months of FOLFOX (leucovorin, fluorouracil, and oxaliplatin) or CAPOX (capecitabine and oxaliplatin). Patients were randomly assigned (1:1) to either paclitaxel 80 mg/m2 on days 1, 8, and 15 plus ramucirumab at 8 mg/kg on days 1 and 15 every 28 days intravenously (switch maintenance group) or continuation of oxaliplatin-based doublet chemotherapy (FOLFOX or CAPOX) for an additional 12 weeks, followed by fluoropyrimidine monotherapy maintenance (control group). Randomisation was stratified by previous gastrectomy (no vs yes), peritoneal carcinomatosis (yes vs no), and primary tumour location (gastro-oesophageal junction vs gastric). Treatment group allocation was done using a web-based system with a minimisation algorithm implementing a random component. The primary endpoint was progression-free survival, analysed on an intention-to-treat basis. The safety population included patients who received at least one dose of the study treatment. This study is registered with ClinicalTrials.gov, NCT02934464, and is complete. Between Jan 1, 2017, and Oct 2, 2023, 280 patients were randomly assigned to receive paclitaxel plus ramucirumab (switch maintenance group; n=144) or to continue FOLFOX or CAPOX (control group; n=136). All patients were White. 180 (64%) of 280 patients were male and 100 (36%) were female. At a median follow-up of 43·7 months (IQR 24·0–57·9), 253 (90%) of 280 patients had a progression-free survival event: 131 (91%) of 144 patients in the switch maintenance group and 122 (90%) of 136 patients in the control group. Median progression-free survival was 6·6 months (95% CI 5·9–7·8) in the switch maintenance group and 3·5 months (2·8–4·2) in the control group (HR 0·61, 95% CI 0·48–0·79; p=0·0002). The assumption of proportional hazards was violated; in an analysis of 24-month restricted mean survival time, restricted mean progression-free survival was 8·8 months (95% CI 7·7–9·9) in the switch maintenance group and 6·1 months (5·0–7·2) in the control group (p=0·0010). The most frequent grade 3–4 treatment-related adverse events were neutropenia (37 [26%] patients in the switch maintenance group vs 13 [10%] patients in the control group), peripheral neuropathy (eight [6%] vs nine [7%]) and arterial hypertension (nine [6%] vs none). Serious adverse events occurred in 28 (20%) of 141 patients in the experimental group and 15 (11%) of 135 patients in the control group; these events were treatment-related in two (1%) patients in the switch maintenance group (pulmonary embolism) and two (1%) patients in the control group (mucositis and anaemia). No treatment-related deaths occurred. Paclitaxel and ramucirumab switch maintenance could be a potential treatment strategy in patients with advanced HER2-negative gastric or gastro-oesophageal junction cancer who are not eligible for immunotherapy or targeted agents. Partly funded by Eli Lilly.

• Publisher: Elsevier Ltd,Elsevier Limited
• Subject: 5-Fluorouracil / Abdomen / Adult / Adverse events / Aged / Antibodies, Monoclonal, Humanized - administration & dosage / Antibodies, Monoclonal, Humanized - adverse effects / Anticoagulants / Antineoplastic Combined Chemotherapy Protocols - administration & dosage / Antineoplastic Combined Chemotherapy Protocols - adverse effects / Antineoplastic Combined Chemotherapy Protocols - therapeutic use / Cancer / Cancer therapies / Chemotherapy / Clinical trials / Consent / Disease control / Embolism / Erb-b2 Receptor Tyrosine Kinases - metabolism / ErbB-2 protein / Esophageal Neoplasms - drug therapy / Esophageal Neoplasms - mortality / Esophageal Neoplasms - pathology / Esophagogastric Junction - drug effects / Esophagogastric Junction - pathology / Esophagus / Female / Fluorouracil - administration & dosage / Gastrectomy / Gastric cancer / Hematology, Oncology, and Palliative Medicine / Humans / Immunotherapy / Induction therapy / Italy / Maintenance Chemotherapy / Male / Metastases / Metastasis / Middle Aged / Monoclonal antibodies / Mucositis / Neutropenia / Oxaliplatin / Oxaliplatin - administration & dosage / Paclitaxel / Paclitaxel - administration & dosage / Paclitaxel - adverse effects / Patients / Peripheral neuropathy / Population studies / Progression-Free Survival / Ramucirumab / Stomach Neoplasms - drug therapy / Stomach Neoplasms - mortality / Stomach Neoplasms - pathology / Survival / Targeted cancer therapy / Tumors