Atezolizumab联合化疗治疗非小细胞肺癌的临床疗效

Cancer diagnosis & prognosis Pub Date : 2025-01-03 eCollection Date: 2025-01-01 DOI:10.21873/cdp.10418
Takeshi Numata, Ryota Nakamura, Toshihiro Shiozawa, Hiroko Watanabe, Shinichiro Okauchi, Gen Ogara, Tomohiro Tamura, Norihiro Kikuchi, Kunihiko Miyazaki, Shigen Hayashi, Takaaki Yamashita, Koichi Kurishima, Masaharu Inagaki, Hiroaki Satoh, Takayuki Kaburagi, Takeo Endo, Nobuyuki Hizawa
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引用次数: 0

摘要

背景/目的:Atezolizumab是抗PD-L1抗体之一,靶向癌细胞和抗原提呈细胞上表达的PD-L1。这种免疫检查点抑制剂现在通常与化疗联合使用。本研究的目的是确认atezolizumab联合化疗的治疗结果,并确定预后因素,特别关注在现实世界的临床实践中转移部位的影响。患者和方法:回顾性分析2018年5月至2024年8月我院11家医院非小细胞肺癌患者接受阿特唑单抗联合化疗的临床资料。结果:141例患者的中位无进展生存期为8.0个月,中位总生存期为19.0个月。多变量分析显示,“无肝转移”、“无肾上腺转移”、“一线atezolizumab联合化疗”和“良好的表现状态”与无进展生存期和总生存期相关。27.7%的患者出现免疫相关不良事件,9.9%的患者出现3级或以上不良事件,2.1%的患者出现5级不良事件。结论:atezolizumab联合化疗治疗非小细胞肺癌患者的疗效和免疫相关不良事件与以往的临床试验相当。为了确保合适的患者得到最有效的治疗,确定详细的预后因素是很重要的,包括临床信息,如受影响的转移器官。人们热切期待在这一领域继续进行研究和进一步积累知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outcomes of Combined Atezolizumab Plus Chemotherapy in Non-small Cell Lung Cancer Patients in Clinical Practice.

Background/aim: Atezolizumab, one of the anti-PD-L1 antibodies, targets PD-L1 expressed on cancer cells and antigen-presenting cells. This immune checkpoint inhibitor is now commonly used in combination with chemotherapy. The objectives of this study were to confirm the treatment outcomes of combined atezolizumab plus chemotherapy, and to identify prognostic factors, with a particular focus on the impact of the site of metastasis in real-world clinical practice.

Patients and methods: A retrospective review of clinical information on non-small cell lung cancer patients who received combined atezolizumab plus chemotherapy from May 2018 to August 2024 at our 11 hospitals was conducted.

Results: The 141 patients evaluated had a median progression-free survival of 8.0 months and a median overall survival of 19.0 months. Multivariate analyses showed that 'absence of liver metastases', 'absence of adrenal metastases', 'first-line combined atezolizumab plus chemotherapy', and 'good performance status' were associated with progression-free survival and overall survival. Immune-related adverse events were observed in 27.7% of patients, with grade 3 or higher in 9.9% of patients, and grade 5 in 2.1% of patients.

Conclusion: Efficacy and immune-related adverse events associated with the combination of atezolizumab and chemotherapy in non-small cell lung cancer patients were comparable to previous clinical trials. To ensure that appropriate patients receive the most effective treatment, it is important to identify detailed prognostic factors, including clinical information, such as the affected metastatic organs. Continued research and further accumulation of knowledge in this area are eagerly anticipated.

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