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Poster Display

66P - Real-world data of first-line chemo-immunotherapy for patients with extensive stage SCLC: A multicentre experience from Switzerland and the UK

Date

08 Dec 2022

Session

Poster Display

Presenters

Laura Moliner Jimenez

Citation

Annals of Oncology (2022) 16 (suppl_1): 100102-100102. 10.1016/iotech/iotech100102

Authors

L. Moliner Jimenez1, N.M. Zellweger2, S.M. Schmidt3, C. Waibel4, P.R. Froesch5, P. Häuptle6, V. Blum7, L. Holer8, M. Frueh3, S. Bhagani9, H.J. Gray10, S. Cox11, T. Khalid12, D.C. Scott13, S.D. Robinson14, L. Hennah15, C. Handforth16, L.A. Mauti17, R. Califano18, S.I. Rothschild2

Author affiliations

  • 1 The Christie NHS Foundation Trust, Manchester/GB
  • 2 Universitätsspital Basel, 4031 - Basel/CH
  • 3 Kantonsspital St. Gallen, St. Gallen/CH
  • 4 Kantonsspital Baden, Baden/CH
  • 5 EOC - Ospedale Regionale di Locarno - Istituto Oncologico Svizzera Italiana (IOSI), Locarno/CH
  • 6 Kantonsspital Liestal Medizinische Universitätsklinik, Liestal/CH
  • 7 Luzerner Kantonsspital, Luzern/CH
  • 8 SAKK - Swiss Group for Clinical Cancer Research, Bern/CH
  • 9 Leicester Royal Infirmary - University Hospitals of Leicester NHS Trust, Leicester/GB
  • 10 BWSCC - Beatson West of Scotland Cancer Centre - NHS Greater Glasgow and Clyde, Glasgow/GB
  • 11 Velindre Cancer Centre - Velindre NHS University Trust - NHS Wales, Cardiff/GB
  • 12 Dorset Cancer Centre, University Hospitals Dorset NHS Foundation Trust, Poole/GB
  • 13 University Hospital Southampton- NHS Foundation Trust, Southampton/GB
  • 14 The Royal Marsden Hospital, London/GB
  • 15 Chelsea and Westminster Hospital - NHS Trust, London/GB
  • 16 Huddersfield Royal Infirmary - Calderdale and Huddersfield NHS Foundation Trust, Huddersfield/GB
  • 17 KSW - Kantonsspital Winterthur, Winterthur/CH
  • 18 The Christie NHS Foundation Trust and Division of Cancer Sciences, University of Manchester, Manchester/GB

Resources

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Abstract 66P

Background

The addition of immunotherapy (either atezolizumab or durvalumab) to platinum-etoposide for patients with extensive stage SCLC (ES-SCLC) has been recently established as standard first-line treatment based on IMPOWER133 and CASPIAN trials. Yet, the efficacy and safety in a real-world setting remains unclear.

Methods

We retrospectively evaluated patients with ES-SCLC treated with either atezolizumab or durvalumab plus platinum-etoposide between October 2018 and October 2021 in ten centres in the UK and ten centres in Switzerland. Responses were assessed using RECIST v1.1 criteria. Median PFS and OS were analyzed by the Kaplan-Meier method.

Results

A total of 436 patients were included. Median age was 67 years, 228 (52.3%) were males, 209 patients (47.9%) were current and 203 (46.6%) former smokers. 63 patients (14.4%) had an ECOG performance status (PS) ≥2. 385 patients (88.3%) were initially diagnosed with ES-SCLC. Liver and brain metastases were diagnosed in 170 (39.0%) and 87 (20.0%) of patients, respectively. At the time of analysis, 284 patients (65.1%) had died. Most of the patients received atezolizumab (n=427, 97.9%) in combination with chemotherapy, 2.1% received durvalumab. Most patients (n=422, 96.8%) were treated with carboplatin/etoposide. Overall response rate was 71.8% (95%CI 67.3-76.0%) with a median duration of response of 3.5 months (95%CI 3.3-4.0). Median PFS and OS were 5.5 (95%CI 5.3-5.7) and 9.3 months (95%CI 8.4-10.4), respectively. Immune related adverse events (AEs) were seen in 21.8% of patients. 5 patients (1.1%) developed a grade 5 AE. 174 patients (39.9%) received a subsequent systemic therapy. Among patients with brain metastases at diagnosis, mPFS and mOS were 4.8 months (95%CI 4.4-5.5) and 8.6 (95%CI 6.9-10.8), respectively.

Conclusions

Data from our large series show shorter OS than what reported in the trials. Known poor prognostic factors (mainly ECOG PS ≥2 and brain metastases) were more common in our cohort of patients at baseline and may have determined a shorter OS. This is the largest real-world evidence dataset evaluating patients with ES-SCLC treated with first-line chemo-immunotherapy, and could help to optimise clinical management of these patients.

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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