• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

67 例肺肉瘤样癌的临床病理和预后特征:18 年单中心经验。

Clinicopathological and Prognostic Features of 67 Cases with Pulmonary Sarcomatoid Carcinoma: An 18-Year Single-Centre Experience.

机构信息

Department of Medical Oncology, Istanbul University Institute of Oncology, Istanbul, Turkey.

Department of Thoracic Surgery, Istanbul University Istanbul Faculty of Medicine, Istanbul, Turkey.

出版信息

Oncol Res Treat. 2021;44(11):590-601. doi: 10.1159/000519454. Epub 2021 Sep 23.

DOI:10.1159/000519454
PMID:34555834
Abstract

INTRODUCTION

Pulmonary sarcomatoid carcinoma (PSC) is a very rare subtype of non-small-cell lung cancer (NSCLC). It is frequently diagnosed in the advanced stage and is resistant to conventional chemotherapeutics. Due to the unique nature and rarity, we evaluated the epidemiological, clinicopathological, and survival data of PSC patients treated at our centre.

PATIENTS AND METHODS

We retrospectively collected demographic and clinical data of 67 PSC patients from a single tertiary referral hospital, between the 2000 and 2018. Univariate and multivariate analyses were performed to determine the risk factors affecting survival.

RESULTS

The median age was 61 years, and the percentage of male was 74.6%. Most of the patients had a smoking history (76.9%). The most common PSC subtype was pleomorphic carcinoma (46.3%). The median overall survival (OS) was 55.4 months, and the 5-year OS rate was 47.5%. Advanced stage, T4 tumour, and positive lymph node involvement were associated with poor OS (p < 0.05). The patients with negative epithelial markers had poorer prognosis (p = 0.027) and had more frequently stage IV disease (p = 0.016). Surgical treatment and stage IV disease were determined to be independent prognostic factors.

CONCLUSION

PSC is an extremely rare and aggressive variant of NSCLC. Positive epithelial markers may have favourable prognostic significance in PSC. Resection of the tumour with a negative surgical margin is crucial for better survival. The prognosis of the disease is very poor in the metastatic stage.

摘要

简介

肺肉瘤样癌(PSC)是一种非常罕见的非小细胞肺癌(NSCLC)亚型。它通常在晚期被诊断,并且对常规化疗药物具有耐药性。由于其独特的性质和罕见性,我们评估了在我们中心治疗的 PSC 患者的流行病学、临床病理和生存数据。

患者和方法

我们回顾性地收集了 2000 年至 2018 年间一家三级转诊医院的 67 名 PSC 患者的人口统计学和临床数据。进行单因素和多因素分析以确定影响生存的危险因素。

结果

中位年龄为 61 岁,男性比例为 74.6%。大多数患者有吸烟史(76.9%)。最常见的 PSC 亚型是多形性癌(46.3%)。中位总生存期(OS)为 55.4 个月,5 年 OS 率为 47.5%。晚期、T4 肿瘤和阳性淋巴结受累与较差的 OS 相关(p < 0.05)。上皮标志物阴性的患者预后较差(p = 0.027),且更常处于 IV 期疾病(p = 0.016)。手术治疗和 IV 期疾病被确定为独立的预后因素。

结论

PSC 是一种非常罕见且侵袭性的 NSCLC 变体。上皮标志物阳性可能对 PSC 具有有利的预后意义。切除有阴性手术切缘的肿瘤对于更好的生存至关重要。在转移阶段,疾病的预后非常差。

相似文献

1
Clinicopathological and Prognostic Features of 67 Cases with Pulmonary Sarcomatoid Carcinoma: An 18-Year Single-Centre Experience.67 例肺肉瘤样癌的临床病理和预后特征:18 年单中心经验。
Oncol Res Treat. 2021;44(11):590-601. doi: 10.1159/000519454. Epub 2021 Sep 23.
2
[Clinicopathological Characteristics and Prognosis Analysis of 
39 Patients with Pulmonary Sarcomatoid Carcinoma].39例肺肉瘤样癌的临床病理特征及预后分析
Zhongguo Fei Ai Za Zhi. 2024 Jul 20;27(7):514-522. doi: 10.3779/j.issn.1009-3419.2024.101.18.
3
Pulmonary sarcomatoid carcinoma: an analysis of a rare cancer from the Surveillance, Epidemiology, and End Results database.肺肉瘤样癌:来自监测、流行病学和最终结果数据库的罕见癌症分析。
Eur J Cardiothorac Surg. 2018 Apr 1;53(4):828-834. doi: 10.1093/ejcts/ezx417.
4
Pulmonary sarcomatoid carcinoma: a clinicopathologic study and prognostic analysis of 51 cases.肺肉瘤样癌:51 例临床病理研究和预后分析。
World J Surg Oncol. 2013 Oct 2;11:252. doi: 10.1186/1477-7819-11-252.
5
Characteristics and Prognostic Analysis of 55 Patients With Pulmonary Sarcomatoid Carcinoma.55例肺肉瘤样癌患者的特征及预后分析
Front Oncol. 2022 May 3;12:833486. doi: 10.3389/fonc.2022.833486. eCollection 2022.
6
Sarcomatoid carcinoma of the lung: a rare histological subtype of non-small cell lung cancer with a poor prognosis even at earlier tumour stages.肺肉瘤样癌:非小细胞肺癌中一种罕见的组织学亚型,即使在肿瘤早期预后也较差。
Interact Cardiovasc Thorac Surg. 2017 Mar 1;24(3):407-413. doi: 10.1093/icvts/ivw392.
7
Preoperative CT findings and prognosis of pulmonary sarcomatoid carcinoma: comparison with conventional NSCLC of similar tumor size.术前 CT 表现与肺肉瘤样癌预后的相关性研究:与肿瘤大小相似的传统 NSCLC 比较。
BMC Med Imaging. 2023 Aug 14;23(1):105. doi: 10.1186/s12880-023-01065-8.
8
Pulmonary Sarcomatoid Carcinoma: An Analysis of the National Cancer Data Base.肺肉瘤样癌:国家癌症数据库分析
Clin Lung Cancer. 2017 May;18(3):286-292. doi: 10.1016/j.cllc.2016.11.016. Epub 2016 Dec 7.
9
Sarcomatoid Carcinoma of the Lung: The Mayo Clinic Experience in 127 Patients.肺肉瘤样癌:梅奥诊所 127 例患者的经验。
Clin Lung Cancer. 2018 May;19(3):e323-e333. doi: 10.1016/j.cllc.2017.12.008. Epub 2017 Dec 21.
10
Pathologic Findings and Long-Term Results After Surgical Treatment for Pulmonary Sarcomatoid Tumors: A Multicenter Analysis.肺肉瘤样肿瘤手术治疗后的病理结果及长期疗效:一项多中心分析
Ann Thorac Surg. 2017 Apr;103(4):1142-1150. doi: 10.1016/j.athoracsur.2016.08.114. Epub 2016 Dec 24.

引用本文的文献

1
Pulmonary pleomorphic carcinoma associated with cystic airspace and recurrent spontaneous pneumothorax: A case report.伴有囊状气腔和复发性自发性气胸的肺多形性癌:一例报告
Oncol Lett. 2025 May 2;30(1):321. doi: 10.3892/ol.2025.15067. eCollection 2025 Jul.
2
Case report: Pulmonary sarcomatoid carcinoma demonstrating rapid growth on follow-up CT.病例报告:肺肉瘤样癌在随访CT上显示快速生长。
Front Oncol. 2024 Jul 8;14:1393203. doi: 10.3389/fonc.2024.1393203. eCollection 2024.
3
Biological characteristics and clinical treatment of pulmonary sarcomatoid carcinoma: a narrative review.
肺肉瘤样癌的生物学特性及临床治疗:一项叙述性综述
Transl Lung Cancer Res. 2024 Mar 29;13(3):635-653. doi: 10.21037/tlcr-24-127. Epub 2024 Mar 27.
4
Survival analysis and nomogram for pulmonary sarcomatoid carcinoma: an SEER analysis and external validation.肺肉瘤样癌的生存分析和列线图:SEER 分析和外部验证。
BMJ Open. 2023 Oct 17;13(10):e072260. doi: 10.1136/bmjopen-2023-072260.
5
Integrated Clinical, Molecular and Immunological Characterization of Pulmonary Sarcomatoid Carcinomas Reveals an Immune Escape Mechanism That May Influence Therapeutic Strategies.对肺肉瘤样癌进行临床、分子和免疫综合特征分析揭示了一种可能影响治疗策略的免疫逃逸机制。
Int J Mol Sci. 2023 Jun 23;24(13):10558. doi: 10.3390/ijms241310558.
6
Multimodality Treatment of Pulmonary Sarcomatoid Carcinoma: A Review of Current State of Art.肺肉瘤样癌的多模态治疗:当前技术水平综述
J Oncol. 2022 Mar 25;2022:8541157. doi: 10.1155/2022/8541157. eCollection 2022.