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ePoster Display

1655P - Real-world outcome of patients with relapsed or refractory small cell lung cancer treated with checkpoint inhibitors in Tertiary Care Centers across Germany

Date

16 Sep 2021

Session

ePoster Display

Topics

Tumour Site

Small Cell Lung Cancer

Presenters

Jan Stratmann

Citation

Annals of Oncology (2021) 32 (suppl_5): S1164-S1174. 10.1016/annonc/annonc680

Authors

J.A. Stratmann1, R. Timalsina1, A. Atmaca2, V. Rosery3, N. Frost4, J. Alt5, C.F. Waller6, N. Reinmuth7, G. Rohde8, M. Wermke9, A. Becker von Rose10, M. Moeller11, M. Sebastian1

Author affiliations

  • 1 Department Of Hematology And Oncology, Johan Goethe University Clinic Frankfurt am Main, 60596 - Frankfurt am Main/DE
  • 2 Klinik Für Onkologieund Hämtologie, Nordwest-Krankenhaus, 60488 - Frankfurt am Main/DE
  • 3 Department Of Internal Medicine, University Clinic Essen, 45147 - Essen/DE
  • 4 Department Of Infectious Diseases And Pneumonology, Universitätsklinik Charité, Campus Virchow Klinikum, 13353 - Berlin/DE
  • 5 Iii. Med. Klinik U. Poliklinik, Universitätsmedizin Mainz, 55131 - Mainz/DE
  • 6 Internal Medicine I, Oncology And Stem Cell Transplantation, University Clinic Freiburg, 79106 - Freiburg/DE
  • 7 Thoracic Oncology Department, Asklepios Lung Clinic, 82131 - Munich-Gauting/DE
  • 8 Department Of Respiratory Medicine, University Hospital, Frankfurt, 60596 - Frankfurt/DE
  • 9 University Hospital Carl-gustav-carus, Universitätsklinikum Dresden, 01307 - Dresden/DE
  • 10 Department Of Internal Medicine Iii, Klinikum rechts der Isar, Technical University Munich, 81675 - München/DE
  • 11 Department Of Internal Medicine Ii, Martha-Maria Hospital Halle-Dölau, 06120 - Halle/DE

Resources

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Abstract 1655P

Background

Checkpoint Inhibitors (CPI) have achieved modest clinical activity as salvage therapy in relapsed small cell lung cancer in prospective clinical trials. Data regarding the real-world efficacy and safety of CPI in relapsed / refractory SCLC is widely lacking.

Methods

We present real-world data collected from 10 tertiary care hospitals across Germany of patients with R/R SCLC who were treated with single agent or combination checkpoint-inhibitors focusing on subgroups that were underrepresented in prospective clinical trials, in particular patients with poor performance status and brain metastases.

Results

112 patients who were treated with CPI between 01/2017 and 04/2020 were included (male, 63%; ECOG 0-1, 70%). 52.3% received nivolumab monotherapy, 40.5% nivolumab + ipilimumab (other 7.2%). Median follow up was 21 months (95% CI, 9.3-33.5 months). Patients were heavily pretreated with a median line of 2 prior therapies (range, 1-8). Overall disease control rate (DCR) was 31.5% and differed numerically between single (25.9%) and combination CPI treatment (40.0%)(p=0.12). The median duration of response was 21.5 months (95% CI, 14.8-28.3 months) and was significantly higher for combination CPI (NE) vs single agent CPI (9.1m; 95% CI, 6.7-11.6m)(HR, 0.59; 95% CI, 0.36-0-94). Median real-world PFS and OS for all patients were 2.2 (95% CI, 1.8-2.7 months) and 5.8 months (95% CI, 1.7-9.8 months) and did not differ between single or combination CPI (HR, 1.02; 95% CI, 0.64-1.63). Overall 12- and 18-month survival was 33.9% and 23.2%, respectively. Treatment beyond progression was documented in 30.4%. Adverse events (AE) were documented in 81%, 2 patients were permanently discontinued due to AEs.

Conclusions

A noteworthy proportion of patients with heavily pretreated R/R SCLC derives long-term clinical benefit from checkpoint inhibitor therapy with long duration of responses. DOR was significantly different between single and combination CPI, but did not translate into longer OS.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

J.A. Stratmann: Financial Interests, Personal, Advisory Board: BMS; Financial Interests, Personal, Advisory Board: Amgen; Financial Interests, Personal, Advisory Board: Novartis; Financial Interests, Personal, Funding: AstraZeneca; Financial Interests, Personal, Advisory Board: Roche. A. Atmaca: Financial Interests, Personal, Advisory Board: BMS. N. Frost: Financial Interests, Personal, Advisory Board: AbbVie; Financial Interests, Personal, Advisory Board: Boehringer Ingelheim; Financial Interests, Personal, Advisory Board: BMS; Financial Interests, Personal, Advisory Board: Pfizer; Financial Interests, Personal, Advisory Board: Takeda; Financial Interests, Personal, Advisory Board: MSD; Financial Interests, Personal, Advisory Board: Roche; Financial Interests, Personal, Advisory Board: AstraZeneca; Financial Interests, Personal, Advisory Board: Amgen; Financial Interests, Personal, Advisory Board: Sanofi; Financial Interests, Personal, Advisory Board: Novartis; Financial Interests, Personal, Advisory Board: BelGene. J. Alt: Financial Interests, Personal, Advisory Board: BMS. C.F. Waller: Financial Interests, Personal, Advisory Board: BMS; Financial Interests, Personal, Advisory Board: AstraZeneca; Financial Interests, Personal, Advisory Board: Boehringer Ingelheim; Financial Interests, Personal, Advisory Board: Chugai; Financial Interests, Personal, Advisory Board: Pfizer; Financial Interests, Personal, Advisory Board: Roche; Financial Interests, Personal, Advisory Board: Takeda; Financial Interests, Personal, Advisory Role: Mylan; Financial Interests, Personal, Advisory Role: Alvotech; Financial Interests, Personal, Other: Ipsen; Financial Interests, Personal, Other: Lilly. M. Wermke: Financial Interests, Personal, Advisory Board: Roche; Financial Interests, Personal, Advisory Board: AstraZeneca; Financial Interests, Personal, Advisory Board: Boehringer Ingelheim; Financial Interests, Personal, Advisory Board: Kite; Financial Interests, Personal, Advisory Board: Novartis; Financial Interests, Personal, Advisory Board: Merck; Financial Interests, Personal, Advisory Board: BMS; Financial Interests, Personal, Advisory Board: Heidelberg Pharma; Financial Interests, Personal, Advisory Board: Glenmark. M. Sebastian: Financial Interests, Personal, Research Grant: AstraZeneca; Financial Interests, Personal, Advisory Board: Pfizer; Financial Interests, Personal, Advisory Board: BMS; Financial Interests, Personal, Advisory Board: MSD; Financial Interests, Personal, Advisory Board: Boehringer Ingelheim; Financial Interests, Personal, Advisory Board: CureVac; Financial Interests, Personal, Advisory Board: BioNTech; Financial Interests, Personal, Advisory Board: Amgen; Financial Interests, Personal, Advisory Board: Janssen-Cilag; Financial Interests, Personal, Advisory Board: Novartis; Financial Interests, Personal, Advisory Board: Takeda; Financial Interests, Personal, Advisory Board: Sanofi; Financial Interests, Personal, Advisory Board: Roche; Financial Interests, Personal, Advisory Board: Merck. All other authors have declared no conflicts of interest.

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