Atezolizumab Plus Carboplatin and Etoposide in Patients with Untreated Extensive-Stage Small-Cell Lung Cancer: Interim Results of the MAURIS Phase IIIb Trial

医学 阿替唑单抗 卡铂 依托泊苷 临时的 中期分析 不利影响 肿瘤科 肺癌 内科学 临床试验 临床研究阶段 外科 化疗 癌症 免疫疗法 顺铂 彭布罗利珠单抗 考古 历史
作者
Emilio Bria,Floriana Morgillo,Marina Chiara Garassino,Fortunato Ciardiello,Andrea Ardizzoni,Alessio Stefani,Francesco Verderame,Alessandro Morabito,Antonio Chella,Giuseppe Tonini,Marina Gilli,Ester Del Signore,Rossana Berardi,Manlio Mencoboni,Alessandra Bearz,Angelo Delmonte,M.R. Migliorino,Cesare Gridelli,Antonio Pazzola,Manuela Iero
出处
期刊:Oncologist [Wiley]
卷期号:29 (5): e690-e698 被引量:4
标识
DOI:10.1093/oncolo/oyad342
摘要

Abstract Background MAURIS is an Italian multicenter, open-label, phase IIIb ongoing trial, aiming at evaluating the safety and effectiveness of atezolizumab + carboplatin/etoposide in patients with newly diagnosed, extensive-stage small-cell lung cancer (ES-SCLC). The primary objective is the safety evaluation. Materials and Methods Patients received atezolizumab + carboplatin/etoposide Q3W for 4-6 cycles in the induction phase, followed by atezolizumab maintenance Q3W. We presented the interim analysis on safety (referring to the induction phase) and clinical effectiveness, in all patients (N = 154) and in subgroups that received ≤3 (N = 23), 4 (N = 43), and 5-6 cycles (N = 89) of induction. Results At a median follow-up of 10.5 months, 139 patients (90.3%) discontinued treatment. Serious adverse events occurred in 29.9% of patients overall, and the rate was lower in patients with 5-6 cycles (19.1%) than in those with 4 (34.9%) or ≤3 (63.6%) cycles. Immune-mediated adverse events were reported in 14.9%, 15.7%, 11.6%, and 18.2% of patients, overall and by subgroup, respectively. The median overall survival and progression-free survival were 10.7 and 5.5 months, respectively. Overall, 111 patients (71.6%) had a tumor response. Conclusions Interim results provide further evidences about safety and efficacy profile of atezolizumab + carboplatin/etoposide treatment in a ES-SCLC patient population closer to that observed in clinical practice. Clinical Trial Registration Eudract No. 2019-001146-17, NCT04028050.

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