Evidence mapPaperPMID 42473071Full record

ArticleCancer medicine2026

The Favorable Short-Term Efficacy of Preexisting COPD for Extensive-Stage Small-Cell Lung Cancer Receiving Immunotherapy.

Ya Chen, Hongyu Liu, Junqiang Zhang

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Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Ya ChenDivision of Life Science and Medicine, Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, China.
Hongyu LiuDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Soochow University, Suzhou, China.
Junqiang ZhangDivision of Life Science and Medicine, Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, China.ORCID https://orcid.org/0000-0002-9124-9957

Funding

Anhui Province Health and Scientific Research Project AHWJ2024BAd30029Research Project of the Anhui Provincial Department of Education 2025AHGXZK40669
6 · The paper itself

Abstract

backgroundPreexisting chronic obstructive pulmonary disease (COPD) is associated with favorable clinical efficacy in NSCLC patients undergoing immune checkpoint inhibitors (ICIs). But the impact of COPD comorbidities on SCLC patients that are receiving immunotherapy remains unclear.

methodsPatients with extensive-stage SCLC (ES-SCLC) received carboplatin combined with etoposide (carboplatin-etoposide, EC group) or durvalumab plus carboplatin-etoposide (EC + PD-L1 group) treatment as first line therapy were collected. In EC + PD-L1 group, survival of patients with preexisting COPD and patients without preexisting COPD were further compared.

resultsA total of 120 ES-SCLC patients who met the eligibility criteria were included in this study. The median overall survival (OS) and the progression-free survival (PFS) were significantly longer in the EC + PD-L1 group than in the EC group, with a HR of 0.37 (95% CI, 0.16-0.88; p = 0.001) and 0.42 (95% CI, 0.23-0.77; p < 0.001), respectively. We further stratified groups by COPD status in EC + PD-L1 group and EC group. In EC + PD-L1 group, PFS was significantly prolonged in COPD group compared with the non-COPD group, with a HR of 0.57 (95% CI, 0.35-0.96; p = 0.018). The COPD group demonstrated a numerically higher objective response rate than the non-COPD group, though the difference was not statistically significant (p = 0.292). No OS benefit was found between the groups.

conclusionPreexisting COPD status may be associated with favorable clinical efficacy in ES-SCLC patients undergoing ICIs.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsImmune Checkpoint InhibitorsImmunotherapyLung NeoplasmsPulmonary Disease, Chronic ObstructiveSmall Cell Lung CarcinomaAgedAged, 80 and overAntibodies, MonoclonalCarboplatinEtoposideFemaleHumansMaleMiddle AgedNeoplasm StagingAntibodies, MonoclonalCarboplatindurvalumabEtoposideImmune Checkpoint Inhibitors

Identifiers

PMID42473071
PMCPMC13382078

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.