Inomata Minehiko, Tsuda Takeshi, Ichikawa Tomomi, Matsumoto Masahiro, Mizushima Isami, Azechi Kenji, Takata Naoki, Murayama Nozomu, Seto Zenta, Tokui Kotaro, Masaki Yasuaki, Okazawa Seisuke, Imanishi Shingo, Miwa Toshiro, Hayashi Ryuji, Taniguchi Hirokazu
First Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.
Department of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
Cancer Diagn Progn. 2025 May 3;5(3):363-369. doi: 10.21873/cdp.10448. eCollection 2025 May-Jun.
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.
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.
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.
Pulmonary sarcomatoid carcinoma diagnosed based on small biopsy specimens is refractory to platinum-doublet chemotherapy, and immune checkpoint inhibitor therapy may improve the prognosis.
背景/目的:肺肉瘤样癌是一种以侵袭性著称的罕见疾病,有众多研究评估了各种治疗方法的疗效。然而,肺肉瘤样癌在组织学上是根据世界卫生组织基于手术标本的分类来定义的,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。这项回顾性研究旨在呈现基于小活检标本诊断为肺肉瘤样癌的患者的临床病程。
分析了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类双药化疗和/或含免疫检查点抑制剂方案治疗的患者数据。
分析了12例患者的数据,其中5例接受铂类双药化疗,11例接受含免疫检查点抑制剂方案治疗。接受铂类双药化疗的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例患者随后接受了含免疫检查点抑制剂的治疗。这5例患者从开始铂类双药化疗起的中位总生存期为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[95%CI = 0.3 - 未估计(NE)]和10.8个月(95%CI = 1.0 - NE)。
基于小活检标本诊断的肺肉瘤样癌对铂类双药化疗耐药,免疫检查点抑制剂治疗可能改善预后。