Multicenter Retrospective Analysis of Pulmonary Sarcomatoid Carcinoma Clinically Diagnosed Using Small Biopsy Specimens.

Cancer diagnosis & prognosis Pub Date : 2025-05-03 eCollection Date: 2025-05-01 DOI:10.21873/cdp.10448
Minehiko Inomata, Takeshi Tsuda, Tomomi Ichikawa, Masahiro Matsumoto, Isami Mizushima, Kenji Azechi, Naoki Takata, Nozomu Murayama, Zenta Seto, Kotaro Tokui, Yasuaki Masaki, Seisuke Okazawa, Shingo Imanishi, Toshiro Miwa, Ryuji Hayashi, Hirokazu Taniguchi
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Abstract

Background/aim: Pulmonary sarcomatoid carcinoma is a rare disease known for its aggressiveness, with numerous studies evaluating the efficacy of various therapeutic approaches. However, pulmonary sarcomatoid carcinoma is histologically defined according to WHO classification based on surgical specimens, whereas in clinical practice, most cases of advanced lung cancer are diagnosed based on small biopsy specimens. This retrospective study aimed to present the clinical course of patients diagnosed with pulmonary sarcomatoid carcinoma based on small biopsy specimens.

Patients and methods: Data of patients who were diagnosed with pulmonary sarcomatoid carcinoma based on small biopsy specimens and treated with platinum-doublet chemotherapy and/or an immune checkpoint inhibitor-containing regimen between 2005 and 2022 were analyzed.

Results: Data from 12 patients were analyzed, including five patients treated with platinum-doublet chemotherapy and 11 patients treated with an immune checkpoint inhibitor-containing regimen. The median progression-free survival among the five patients treated with platinum-doublet chemotherapy was 1.5 months [95% confidence interval (CI)=0.7-4.1]. Of these, four patients subsequently received immune checkpoint inhibitor-containing therapy. The median overall survival from the initiation of platinum-doublet chemotherapy in these five patients was 14.7 months (95%CI=1.2-16.2). In contrast, 11 patients treated with immune checkpoint inhibitor therapy showed a median progression-free survival and overall survival of 8.9 months [95%CI=0.3-not estimated (NE)] and 10.8 months (95%CI=1.0-NE), respectively.

Conclusion: Pulmonary sarcomatoid carcinoma diagnosed based on small biopsy specimens is refractory to platinum-doublet chemotherapy, and immune checkpoint inhibitor therapy may improve the prognosis.

肺肉瘤样癌临床小活检标本多中心回顾性分析。
背景/目的:肺肉瘤样癌是一种罕见的疾病,以其侵袭性而闻名,许多研究评估了各种治疗方法的疗效。然而,肺肉瘤样癌的组织学定义是根据WHO基于手术标本的分类,而在临床实践中,大多数晚期肺癌病例是基于小活检标本诊断的。本回顾性研究旨在介绍基于小活检标本诊断为肺肉瘤样癌患者的临床病程。患者和方法:分析2005年至2022年间,基于小活检标本诊断为肺肉瘤样癌并接受铂双药化疗和/或含免疫检查点抑制剂方案治疗的患者的数据。结果:分析了12例患者的数据,包括5例接受铂双药化疗的患者和11例接受含免疫检查点抑制剂方案治疗的患者。接受铂双药化疗的5例患者的中位无进展生存期为1.5个月[95%置信区间(CI)=0.7-4.1]。其中,4名患者随后接受了含免疫检查点抑制剂的治疗。这5例患者从铂双药化疗开始的中位总生存期为14.7个月(95%CI=1.2-16.2)。相比之下,接受免疫检查点抑制剂治疗的11例患者的中位无进展生存期和总生存期分别为8.9个月和10.8个月[95%CI=0.3-not estimated (NE)]和10.8个月(95%CI=1.0-NE)。结论:基于小活检标本诊断的肺肉瘤样癌对铂双药化疗难治,免疫检查点抑制剂治疗可改善预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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