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Heterogeneity in advanced pulmonary sarcomatoid carcinoma and its efficacy to immune checkpoint inhibitors

  • Mengqing Xie
  • , Tianqing Chu
  • , Xiaorong Dong
  • , Huijuan Wang
  • , Qian Chu
  • , Xiuyu Cai
  • , Jialei Wang
  • , Yu Yao
  • , Lin Wu
  • , Feng Ye
  • , Bo Zhu
  • , Caicun Zhou
  • , Chunxia Su
  • Tongji University
  • Shanghai Jiao Tong University
  • Huazhong University of Science and Technology
  • Henan Cancer Hospital
  • Sun Yat-Sen University Cancer Center
  • Fudan University
  • The First Affiliated Hospital of Xi’an Jiaotong University
  • Central South University
  • The First Affiliated Hospital of Xiamen University
  • Army Medical University

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Background: Immune checkpoint inhibitors (ICIs) have improved the prognosis of patients with non-small cell lung cancer but rarely been explored in pulmonary sarcomatoid carcinoma (PSC). This multicenter study aimed to evaluate the effectiveness of ICIs for PSC and its underlying mechanism. Methods: Advanced PSC who received ICIs between August 2018 and May 2022 from 11 centers in China were included. Clinical characteristics and treatment information were collected. Whole-exome sequencing (WES) and whole transcriptome sequencing were conducted on pre-treatment samples to explore the mechanism. Results: 113 patients with PSC were enrolled, the median PFS for patients receiving ICIs therapy was 8.77 months (95 % confidence interval, 4.21 to 13.32). Combining ICIs with anti-angiogenic agents significantly increased PFS (p = 0.04). Liver metastasis and combination therapy with anti-angiogenic agents were independent risk factors for PFS (Hazard Ratio [HR] = 3.652, p = 0.019 and HR = 0.435, p = 0.017, respectively). WES showed that PSC presented with a TMB of 6.3 mutations per million base pairs. High expression of TNFα signaling and glycolysis related gene showed a better prognosis. Conclusions: ICIs showed promising benefits for advanced PSC, and the addition of anti-angiogenic therapy might be a more effective treatment strategy for this disease.

Original languageEnglish
Article number114260
JournalEuropean Journal of Cancer
Volume209
DOIs
StatePublished - Sep 2024
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Anti-angiogenic therapy
  • Immunotherapy
  • NSCLC
  • Rare tumor
  • Tumor microenvironment

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