Women patients with small-cell lung cancer using immunotherapy in a real-world cohort achieved long-term survival.

Yuling He, Lingdong Kong, Xumeng Ji, Minglei Zhuo, Tongtong An, Bo Jia, Yujia Chi, Jingjing Wang, Jun Zhao, Jianjie Li, Xue Yang, Hanxiao Chen, Xiaoyu Zhai, Yidi Tai, Lu Ding, Ziping Wang, Yuyan Wang
Author Information
  1. Yuling He: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  2. Lingdong Kong: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  3. Xumeng Ji: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  4. Minglei Zhuo: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China. ORCID
  5. Tongtong An: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  6. Bo Jia: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  7. Yujia Chi: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  8. Jingjing Wang: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  9. Jun Zhao: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China. ORCID
  10. Jianjie Li: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  11. Xue Yang: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China. ORCID
  12. Hanxiao Chen: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China. ORCID
  13. Xiaoyu Zhai: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  14. Yidi Tai: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  15. Lu Ding: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
  16. Ziping Wang: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China. ORCID
  17. Yuyan Wang: Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department I of Thoracic Oncology, Peking University Cancer Hospital & Institute, Beijing, China. ORCID

Abstract

BACKGROUND: Usage of immune checkpoint inhibitors (ICIs) has prolonged the overall survival (OS) of patients with extensive-stage small-cell lung cancer (ES-SCLC). In clinical trials, males accounted for a large proportion, leading to the uncertainty of its efficacy in female patients. We therefore conducted this study to explore the efficacy and safety of using ICIs in female patients with ES-SCLC.
METHODS: We retrospectively enrolled female SCLC patients and subdivided them into two groups. Group A (n = 40) was defined as ES-SCLC patients who received first-line standard chemotherapy with or without ICIs. Group B (n = 47) included relapsed SCLC patients who were administered with second-line therapies. Kaplan-Meier methodology was used to calculate survival analysis. Chi-squared tests were used to analyze the incidence of adverse events (AEs).
RESULTS: Median progression-free survival (PFS) and median OS favored the ICI-contained cohorts (Group A PFS: 8.3 vs. 6.1 months; OS: not reached vs. 11.3 months; Group B PFS: 15.1 vs. 3.3 months; OS: 35.3 vs. 8.3 months), especially in those patients who received second-line immunotherapies. Patients who received immunotherapy had a slightly higher incidence rate of grade ≥3 AEs (Group A: 71.4% vs. 46.2%; Group B: 44.5% vs. 13.2%). Those who developed grade ≥3 AEs in first-line ICIs cohort had a more favorable survival (PFS: 8.3 vs. 3.2 months; OS: not reached vs. 5.1 months).
CONCLUSIONS: Our study suggested that female ES-SCLC patients treated with immunotherapy tended to achieve a relatively longer survival. The incidence of AEs (grade ≥3) was higher in women patients receiving ICIs, which requires monitoring more closely.

Keywords

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Grants

  1. JC202309/Peking University Cancer Hospital

MeSH Term

Humans
Female
Small Cell Lung Carcinoma
Lung Neoplasms
Immunotherapy
Middle Aged
Retrospective Studies
Aged
Immune Checkpoint Inhibitors
Adult
Survival Rate

Chemicals

Immune Checkpoint Inhibitors

Word Cloud

Created with Highcharts 10.0.0patientsvssurvivalGroupICIsfemale3ES-SCLCAEsimmunotherapylungcancerreceivedincidencePFS:8OS:3 monthsgrade≥3OSsmall-cellefficacystudyusingSCLCfirst-lineBsecond-lineusedadverseevents1 monthsreachedhigher2%cohortBACKGROUND:Usageimmunecheckpointinhibitorsprolongedoverallextensive-stageclinicaltrialsmalesaccountedlargeproportionleadinguncertaintythereforeconductedexploresafetyMETHODS:retrospectivelyenrolledsubdividedtwogroupsn = 40definedstandardchemotherapywithoutn = 47includedrelapsedadministeredtherapiesKaplan-MeiermethodologycalculateanalysisChi-squaredtestsanalyzeRESULTS:Medianprogression-freePFSmedianfavoredICI-containedcohorts61115135especiallyimmunotherapiesPatientsslightlyrateA:714%46B:445%13developedfavorable2 months5CONCLUSIONS:suggestedtreatedtendedachieverelativelylongerwomenreceivingrequiresmonitoringcloselyWomenreal-worldachievedlong-termsmall‐cellbenefit

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