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ORIGINAL RESEARCH article

Front. Oncol.
Sec. Thoracic Oncology
Volume 14 - 2024 | doi: 10.3389/fonc.2024.1442909

Real-world treatment patterns, biomarker testing and clinical outcomes of metastatic non-small cell lung cancer patients in the immunotherapy era

Provisionally accepted
Lior Apter Lior Apter 1Sarah Sharman Moser Sarah Sharman Moser 2*Ashwini Arunachalam Ashwini Arunachalam 3Sivan Gazit Sivan Gazit 2Moshe Hoshen Moshe Hoshen 2Gabriel Chodick Gabriel Chodick 4Nava Siegelmann-Danieli Nava Siegelmann-Danieli 1
  • 1 Maccabi Health Care Services, Tel Aviv, Israel
  • 2 Kahan-Sagol-Maccabi Research and Innovation Institute, Tel-Aviv, Israel
  • 3 Merck (United States), Kenilworth, New Jersey, United States
  • 4 Tel Aviv University, Tel Aviv, Tel Aviv, Israel

The final, formatted version of the article will be published soon.

    Background: Treatment for first-line (1L) metastatic non-small cell cancer (mNSCLC) changed with the introduction of immunotherapy. We describe treatment utilization and clinical outcomes in a real-world mNSCLC cohort in a 2.7-million-member state-mandated health provider.Methods: Newly diagnosed mNSCLC patients initiating systemic anti-cancer treatment Jan 2017-Dec 2020 were identified from the National Cancer Registry. Real-world Time on Treatment (rwToT) was defined as the length of time between first and last administration date of treatment.Real-world Overall Survival (rwOS) was estimated using Kaplan Meier analysis. Outcomes were assessed at a minimum of 6 months' follow-up (cutoff: 30 th June 2021).Results: Among 843 patients, 85% had adenocarcinoma (NSQ) and 15% squamous cell carcinoma (SQ) histology: of these 43% and 26% were female, median age was 67 and 69 years, and 55% and 48% with 0-1 ECOG performance status respectively (missing:27% and 30% respectively). Median follow-up for the entire cohort was 27.1 months (95% CI: 24.7-29.6). NSQ patients with no known EGFR/ALK/ROS1 aberrations received PD-1 inhibitor monotherapy (PDM) (N=147), or combination (PDC) (N=194), or platinum-based chemotherapy (PBC, N=133). Median rwToT was 4.5 (95% CI: 3.5-7.6), 5.2 (95% CI: 4.6-7.6) and 2.3 (95% CI: 2.1-3.0) months respectively; for the subgroup of patients with ECOG PS 0-1, rwToT was 9.4 (95% CI: 5.0-20.8), 7.1 (95% CI: 5.0-10.1) and 2.9 (95% CI: 2.2-4.1) months respectively. Median rwOS from 1L was 12.5 (95% CI: 9.9-17.9), 14.8 (95% CI: 10.5-19.4) and 9.1 (95% CI: 7.1-11.5) months; for the subgroup of patients with ECOG PS 0-1, median rwOS was 25.1 (95% CI: 14.9-not reached [NR]), 17.6 (95% CI: 14.3-NR) and 11.3 (95% CI: 9.2-21.3) months respectively. For ECOG PS 0-1 and PDL1 >=50% patients, median rwOS was 25.1 months (95% CI: 13.9-NR) and NR for PDM and PDC respectively. For ECOG PS 0-1 and PDL1 <50% patients, median rwOS was 14.3 (95% CI: 10.1-NR) and 11.2 (95% CI: 9.1-21.3) months for PDC and PBC respectively.Our real-world data supports the benefit of single agent PD-1 inhibitor monotherapy for patients with PD-L1 high expression or PD-1 inhibitor combination for all patients diagnosed with mNSCLC with no known EGFR/ALK/ROS1 aberrations, initiating 1L treatment.

    Keywords: Non-small cell lung cancer, tyrosine kinase inhibitors, Survival, EGFR mutation, PD-1

    Received: 03 Jun 2024; Accepted: 01 Oct 2024.

    Copyright: © 2024 Apter, Sharman Moser, Arunachalam, Gazit, Hoshen, Chodick and Siegelmann-Danieli. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Sarah Sharman Moser, Kahan-Sagol-Maccabi Research and Innovation Institute, Tel-Aviv, Israel

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