Atezolizumab for First-Line Treatment of PD-L1-Selected Patients with NSCLC. Academic Article uri icon

Overview

abstract

  • BACKGROUND: The efficacy and safety of the anti-programmed death ligand 1 (PD-L1) monoclonal antibody atezolizumab, as compared with those of platinum-based chemotherapy, as first-line treatment for patients with metastatic non-small-cell lung cancer (NSCLC) with PD-L1 expression are not known. METHODS: We conducted a randomized, open-label, phase 3 trial involving patients with metastatic nonsquamous or squamous NSCLC who had not previously received chemotherapy and who had PD-L1 expression on at least 1% of tumor cells or at least 1% of tumor-infiltrating immune cells as assessed by the SP142 immunohistochemical assay. Patients were assigned in a 1:1 ratio to receive atezolizumab or chemotherapy. Overall survival (primary end point) was tested hierarchically according to PD-L1 expression status among patients in the intention-to-treat population whose tumors were wild-type with respect to EGFR mutations or ALK translocations. Within the population with EGFR and ALK wild-type tumors, overall survival and progression-free survival were also prospectively assessed in subgroups defined according to findings on two PD-L1 assays as well as by blood-based tumor mutational burden. RESULTS: Overall, 572 patients were enrolled. In the subgroup of patients with EGFR and ALK wild-type tumors who had the highest expression of PD-L1 (205 patients), the median overall survival was longer by 7.1 months in the atezolizumab group than in the chemotherapy group (20.2 months vs. 13.1 months; hazard ratio for death, 0.59; P = 0.01). Among all the patients who could be evaluated for safety, adverse events occurred in 90.2% of the patients in the atezolizumab group and in 94.7% of those in the chemotherapy group; grade 3 or 4 adverse events occurred in 30.1% and 52.5% of the patients in the respective groups. Overall and progression-free survival favored atezolizumab in the subgroups with a high blood-based tumor mutational burden. CONCLUSIONS: Atezolizumab treatment resulted in significantly longer overall survival than platinum-based chemotherapy among patients with NSCLC with high PD-L1 expression, regardless of histologic type. (Funded by F. Hoffmann-La Roche/Genentech; IMpower110 ClinicalTrials.gov number, NCT02409342.).

authors

  • Herbst, Roy S
  • Giaccone, Giuseppe
  • de Marinis, Filippo
  • Reinmuth, Niels
  • Vergnenegre, Alain
  • Barrios, Carlos H
  • Morise, Masahiro
  • Felip, Enriqueta
  • Andric, Zoran
  • Geater, Sarayut
  • Özgüroğlu, Mustafa
  • Zou, Wei
  • Sandler, Alan
  • Enquist, Ida
  • Komatsubara, Kimberly
  • Deng, Yu
  • Kuriki, Hiroshi
  • Wen, Xiaohui
  • McCleland, Mark
  • Mocci, Simonetta
  • Jassem, Jacek
  • Spigel, David R

publication date

  • October 1, 2020

Research

keywords

  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • B7-H1 Antigen
  • Carcinoma, Non-Small-Cell Lung
  • Lung Neoplasms

Identity

Scopus Document Identifier

  • 85092392792

Digital Object Identifier (DOI)

  • 10.1056/NEJMoa1917346

PubMed ID

  • 32997907

Additional Document Info

volume

  • 383

issue

  • 14