Clinical impact of first-line platinum plus two-day etoposide combined with immunotherapy in extensive-stage small cell lung cancer: Retrospective monocentric study—E-twoposide.
Abstract
e20161 Background: Standard first line treatment for extensive-stage small cell lung cancer typically includes carboplatin, etoposide over 3 days, and immunotherapy. In our center, a modified regimen using a two-day schedule for chemotherapy was implemented with the goal of simplifying treatment delivery while maintaining efficacy. This retrospective study imed to evlauate the clinical outcomes and safety of this approach. Methods: We included all patients with ES-SCLC treated between january 2021 and december 2024 with the following regim : carboplatin (AUC 5) on day 1, etoposide 150mg/m2 on days 1 and 2, combined with immunotherapy (eithe durvalumab or atezolizumab). Primary endpoints were progression free survival and overall survival. Secondary endpoints included treatement related toxicities. Results: A total of 87 patients were included. The median PFS was 4.8 months and the median OS was 11.3months. Grade 3 and 4 adverse events occured in 61% of patients principally haematologic disorders. Unexpected toxicities or treatment-related deaths were not observed. Conclusions: A modified two-day chemotherapy regimen combined with immunotherapy appears to offer comparable efficacy and acceptable safety to the standard approach. This modified regimen allowed the release of 268 chemotherapy treatment slots in our center and, pending prospective evaluation, may represent a feasible alternative to the standard schedule.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (6)
Youssef Oulkhouir
Angers University Hospital, Angers, France
Severine LY
University Hospital Angers, Angers, France
Amelie Ifrah
Angers University Hospital, Angers, France
José Hureaux
Angers University Hospital, Angers, France
Thierry Urban
Angers University Hospital, Angers, France
Gérard Zalcman
Arnaud Scherpereel, MD, PhD, CHU Lille, Univ. Lille, Inserm, U1366-UMR9020—CRCLille—Cancer Research Center of Lille, OncoThAI, ONCOLille, Lille, France; Aaron S. Mansfield, MD, Mayo Clinic, Rochester, MN; Francesco Grossi, MD, Medical Oncology Division, Department of Medicine and Technological Innovation, University of Insubria, Varese, Italy; Sanjay Popat, PhD, FRCP, The Royal Marsden Hospital, London, United Kingdom; Paul Baas, MD, PhD, The Netherlands Cancer Institute and Leiden University Medical Center, Amsterdam, the Netherlands; Anna K. Nowak, PhD, MBBS, University of Western Australia, Perth, WA, Australia; Anne S. Tsao, MD, MBA, University of Texas MD Anderson Cancer Center, Houston, TX; Nobukazu Fujimoto, MD, PhD, Okayama Rosai Hospital, Okayama, Japan; Solange Peters, MD, PhD, Lausanne University Hospital, Lausanne, Switzerland; Yolanda Bautista Aragon, MD, Centro Médico Nacional Siglo XXI, Mexico City, Mexico; Toby Talbot, MD, The Sunrise Centre, Royal Cornwall Hospitals NHS Trust, Truro, Unite...