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

  • 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
  • , Marta Rita Migliorino
  • , Cesare Gridelli
  • , Antonio Pazzola
  • , Manuela Iero
  • Filippo De Marinis
  • University of Campania Luigi Vanvitelli
  • The University of Chicago
  • Alma Mater Studiorum University of Bologna
  • Ospedale V. Cervello
  • IRCCS Istituto nazionale tumori Fondazione Giovanni Pascale - Napoli
  • University of Pisa
  • Universita Campus Bio-Medico di Roma
  • IRCCS Istituto Europeo di Oncologia - Milano
  • Marche Polytechnic University
  • Azienda Ospedaliera Villa Scassi
  • IRCCS Centro di Riferimento Oncologico - Aviano PN
  • IRCCS Istituto scientifico romagnolo per lo studio e la cura dei tumori - Meldola (FC)
  • San Camillo Hospital
  • Azienda Ospedaliera S.G. Moscati
  • University Hospital of Sassari
  • F. Hoffmann-La Roche AG

Research output: Contribution to journalArticle

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.This analysis is based on interim data from the MAURIS study, an Italian multicenter, phase IIIb ongoing trial to evaluate treatment with atezolizumab plus carboplatin/etoposide in patients with newly diagnosed extensive-stage small-cell lung cancer.
Original languageEnglish
Pages (from-to)N/A-N/A
JournalTHE ONCOLOGIST
DOIs
Publication statusPublished - 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • atezolizumab
  • chemotherapy
  • extensive-stage small cell lung cancer
  • induction

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