[Clinicopathological Characteristics and Prognosis Analysis of 
39 Patients with Pulmonary Sarcomatoid Carcinoma].

Q4 Medicine
Cen Chen, Zhanliang Ren, Yujie Dong, Ying Wang, Yuan Gao, Hongxia Li, Tongmei Zhang
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引用次数: 0

Abstract

Background: Pulmonary sarcomatoid carcinoma (PSC) is a rare subtype of non-small cell lung cancer (NSCLC), which is featured by low incidence, high malignancy rate, robust aggressive behavior and inferior prognosis. To date, there is no standardized treatment. The aim of this study is to better understand and accumulate more clinical experience of the disease by summarizing the clinicopathological features, diagnosis methods, therapeutic regimen and prognostic factors of PSC.

Methods: A total of 39 patients with PSC who diagnosed and received treatment in Beijing Chest Hospital from December 2013 to December 2023 were retrospectively recruited, and information including demographic characteristics, clinicopathological features, tumor-node-metastasis (TNM) stage, diagnosis method and therapeutic regimen were carefully collected. Meanwhile, follow-up was conducted. Kaplan-Meier method was used to analyze the prognostic factors of the disease.

Results: The PSC patients in this study ranged in age from 45 to 76 years old, including 35 males and 4 females. There were no specific clinical manifestations of PSC at initial diagnosis. Among the 39 patients, 20 underwent surgical resection and 19 received palliative chemoradiation or symptomatic supportive treatment. The 1-year and 5-year survival rates were 61.90% and 35.20% respectively. Univariate analysis indicated that family history of carcinoma, primary tumor site, TNM stage, lymph node metastasis, distant metastasis, whether or not received surgical resection, surgical method, treatment regimens, tumor tissue programmed cell death ligand 1 (PD-L1) expression ≥1% and mesenchymal-epithelial transition factor (MET) pathway abnormalities were correlated with the overall survival (OS) of patients (P<0.05). In the subsequent multivariate analysis, lymph node metastasis emerged as the only independent prognosticator in predicting inferior OS (P=0.037).

Conclusions: PSC is rarely seen in clinical practice and commonly occurs in elder men with smoking history. Tumor tissue PD-L1 expression ≥1% and MET abnormalities may predict inferior prognosis of PSC and lymph node metastasis was determined as the independent prognosticator of PSC. Surgical resection along with adjuvant medical treatment is the cornerstone for early and locally advanced patients, and the clinical utility of molecular targeting therapy and immunotherapy in PSC needs to be further investigated.

[39例肺肉瘤样癌患者的临床病理特征和预后分析]
背景:肺肉瘤样癌(PSC)是非小细胞肺癌(NSCLC)的一种罕见亚型,具有发病率低、恶性率高、侵袭性强、预后差等特点。迄今为止,尚无标准化的治疗方法。本研究旨在通过总结PSC的临床病理特征、诊断方法、治疗方案和预后因素,更好地了解该病并积累更多临床经验:方法:回顾性招募2013年12月至2023年12月在北京胸科医院确诊并接受治疗的39例PSC患者,仔细收集其人口学特征、临床病理学特征、肿瘤结节转移(TNM)分期、诊断方法和治疗方案等信息。同时进行了随访。采用 Kaplan-Meier 法分析疾病的预后因素:研究中的 PSC 患者年龄在 45 岁至 76 岁之间,其中男性 35 人,女性 4 人。初诊时无特殊临床表现。在39名患者中,20人接受了手术切除,19人接受了姑息化疗或对症支持治疗。1年和5年生存率分别为61.90%和35.20%。单变量分析表明,癌家族史、原发肿瘤部位、TNM分期、淋巴结转移、远处转移、是否接受手术切除、手术方法、治疗方案、肿瘤组织细胞程序性死亡配体1(PD-L1)表达≥1%以及间质-上皮转化因子(MET)通路异常与患者的总生存率(OS)相关(结论:PSC在临床上很少见,但在肿瘤学中却被认为是一种 "不可逆 "的疾病:PSC在临床上很少见,常见于有吸烟史的老年男性。肿瘤组织PD-L1表达≥1%和MET异常可预测PSC的不良预后,淋巴结转移被确定为PSC的独立预后指标。手术切除和辅助药物治疗是早期和局部晚期患者的基石,而分子靶向治疗和免疫治疗在PSC中的临床应用还有待进一步研究。
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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来源期刊
中国肺癌杂志
中国肺癌杂志 Medicine-Pulmonary and Respiratory Medicine
CiteScore
1.40
自引率
0.00%
发文量
5131
审稿时长
14 weeks
期刊介绍: Chinese Journal of Lung Cancer(CJLC, pISSN 1009-3419, eISSN 1999-6187), a monthly Open Access journal, is hosted by Chinese Anti-Cancer Association, Chinese Antituberculosis Association, Tianjin Medical University General Hospital. CJLC was indexed in DOAJ, EMBASE/SCOPUS, Chemical Abstract(CA), CSA-Biological Science, HINARI, EBSCO-CINAHL,CABI Abstract, Global Health, CNKI, etc. Editor-in-Chief: Professor Qinghua ZHOU.
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