免疫检查点抑制剂联合铂基双药化疗治疗东部合作肿瘤大分期小细胞肺癌患者的疗效:一项单机构回顾性研究

IF 3.1 2区 医学 Q2 ONCOLOGY
Cancer Medicine Pub Date : 2025-09-10 DOI:10.1002/cam4.71136
Kosuke Sakai, Shigeru Ishii, Shin Yokosuka, Tomoyuki Takahashi, Yuichiro Kawano, Hiroaki Nishimura, Yoshiki Kuwabara, Maiko Sasaki-Toda, Yumiko Ogawa-Kobayashi, Satoshi Kikuchi, Yusuke Hirata, Hiroyuki Kyoyama, Gaku Moriyama, Nobuyuki Koyama, Kazutsugu Uematsu
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引用次数: 0

摘要

背景小细胞肺癌(SCLC)的预后仍然很差,尤其是广泛期SCLC患者。IMpower133和CASPIAN试验揭示了免疫检查点抑制剂(ICIs)对具有良好表现状态(PS)的大分期SCLC患者的疗效。本研究的目的是探讨ICIs对不良PS患者的疗效。患者和方法入选2019年9月- 2022年12月在埼玉医科大学(Kawagoe, Japan)埼玉医学中心就诊的大分期SCLC患者,随访至2024年2月。客观缓解率(ORR)和总生存期(OS)比较了接受含铂双重化疗联合ICI (atezolizumab或durvalumab; ICI组)和单独接受含铂双重化疗(非ICI组)的患者。结果按东部肿瘤合作小组绩效状态(ECOG-PS)进行分层(即0-1和2-3)。结果共74例患者纳入研究(中位生存期:327天)。在ECOG-PS 0-1的患者中,ICI组(n = 17)和非ICI组(n = 23)的ORR分别为76.5%和56.5%;OS分别为406天和379天。在ECOG-PS 2-3患者中,ICI组(n = 15)和非ICI组(n = 16)的ORR分别为93.3%和56.3%;OS分别为446天和169天。这一证据表明,ICI的加入显著改善了OS (p = 0.00661)和提高了ORR。结论在广泛期SCLC和ECOG-PS 2-3患者中,在铂双药化疗基础上加用atezolizumab或durvalumab可改善ORR,改善预后。这些发现表明,在理想的临床试验人群之外,化学免疫治疗可能是一种可行的治疗选择,解决了未满足的临床需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy of Immune Checkpoint Inhibitors in Combination With Platinum-Based Doublet Chemotherapy for Extensive-Stage Small-Cell Lung Cancer Patients With Eastern Cooperative Oncology Group-Performance Status 2–3: A Single-Institution Retrospective Study

Efficacy of Immune Checkpoint Inhibitors in Combination With Platinum-Based Doublet Chemotherapy for Extensive-Stage Small-Cell Lung Cancer Patients With Eastern Cooperative Oncology Group-Performance Status 2–3: A Single-Institution Retrospective Study

Background

The prognosis of small-cell lung cancer (SCLC) remains poor, particularly in patients with extensive-stage SCLC. The IMpower133 and CASPIAN trials revealed the efficacy of immune checkpoint inhibitors (ICIs) in extensive-stage SCLC patients with good performance status (PS). The aim of this study was to investigate the efficacy of ICIs in patients with poor PS.

Patients and Methods

Patients with extensive-stage SCLC who visited Saitama Medical Center, Saitama Medical University (Kawagoe, Japan) (September 2019–December 2022) were enrolled and followed up until February 2024. Objective response rate (ORR) and overall survival (OS) were compared between patients who received platinum-based doublet chemotherapy with an ICI (atezolizumab or durvalumab; ICI group) and those treated with platinum-based doublet chemotherapy alone (non-ICI group). Results were stratified by the Eastern Cooperative Oncology Group performance status (ECOG-PS) (i.e., 0–1 and 2–3).

Results

A total of 74 patients were included in the study (median OS: 327 days). In patients with ECOG-PS 0–1, ORR was 76.5% and 56.5% in the ICI group (n = 17) and non-ICI group (n = 23), respectively; OS was 406 and 379 days, respectively. In patients with ECOG-PS 2–3, ORR was 93.3% and 56.3% in the ICI group (n = 15) and non-ICI group (n = 16), respectively; OS was 446 days and 169 days, respectively. This evidence indicates that the addition of an ICI significantly improved OS (p = 0.00661) and enhanced ORR.

Conclusion

In patients with extensive-stage SCLC and ECOG-PS 2–3, the addition of atezolizumab or durvalumab to platinum-doublet chemotherapies improved the ORR, resulting in a better prognosis. These findings suggest that chemoimmunotherapy may be a feasible treatment option beyond the ideal clinical trial populations, addressing an unmet clinical need.

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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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