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手术切除的肺肉瘤样癌:2010 年全国回顾性研究。

Surgically resected sarcomatoid carcinoma of the lung: a nationwide retrospective study in 2010.

机构信息

Division of Thoracic Surgery, Keio University School of Medicine, 35, Shinanomachi, Shinjuku-Ku, Tokyo, 160-8582, Japan.

Department of General Thoracic Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

出版信息

BMC Cancer. 2024 Aug 2;24(1):938. doi: 10.1186/s12885-024-12728-2.

Abstract

BACKGROUND

Sarcomatoid carcinoma of the lung is a rare histological type of non-small cell lung cancer with a poor prognosis. We aimed to investigate the clinicopathological characteristics and prognostic factors of surgically resected sarcomatoid carcinoma of the lung.

METHODS

We retrospectively reviewed 14999 patients who underwent surgical resection for non-small cell lung cancer accumulated by the Japanese Joint Committee of Lung Cancer Registry in 2010. Clinicopathological characteristics and survival were compared between the sarcomatoid carcinoma and other non-small cell cancer groups. The prognostic factors in the sarcomatoid carcinoma group were identified using a multivariate Cox proportional hazard model.

RESULTS

Patients with sarcomatoid carcinoma comprised 1.4% of all patients. The sarcomatoid carcinoma group demonstrated a more aggressive pathology with presentation at more advanced stages, requiring more frequent extensive surgical resections. The sarcomatoid carcinoma group had remarkably poorer overall and recurrence-free survival than the other non-small cell lung cancer group. Adjuvant chemotherapy was associated with improved survival for pathological stage II-III sarcomatoid carcinoma cases rather than for pathological stage I disease. In the multivariate analysis, larger tumor size, lymphatic permeation, and no adjuvant chemotherapy were associated with the sarcomatoid carcinoma group's overall and recurrence-free survival.

CONCLUSIONS

Surgically resected sarcomatoid carcinoma of the lung has a higher aggressive and metastatic potential and a worse prognosis than other non-small cell lung cancers. Adjuvant chemotherapy, which was associated with enhanced survival in patients with pathological stage II-III of the disease, could be considered for treating patients with pathological stage II-III sarcomatoid carcinoma of the lung.

摘要

背景

肺肉瘤样癌是一种罕见的非小细胞肺癌组织学类型,预后较差。我们旨在研究手术切除的肺肉瘤样癌的临床病理特征和预后因素。

方法

我们回顾性分析了 2010 年日本肺癌登记处累积的 14999 例接受非小细胞肺癌手术切除的患者。比较肉瘤样癌与其他非小细胞癌组的临床病理特征和生存情况。采用多变量 Cox 比例风险模型确定肉瘤样癌组的预后因素。

结果

肉瘤样癌患者占所有患者的 1.4%。肉瘤样癌组具有更具侵袭性的病理表现,处于更晚期,需要更频繁的广泛手术切除。肉瘤样癌组的总生存率和无复发生存率明显低于其他非小细胞肺癌组。辅助化疗与病理分期 II-III 期肉瘤样癌患者的生存改善相关,而与病理分期 I 期疾病无关。在多变量分析中,肿瘤较大、淋巴管浸润和无辅助化疗与肉瘤样癌组的总生存率和无复发生存率相关。

结论

手术切除的肺肉瘤样癌具有更高的侵袭性和转移性潜力,预后较其他非小细胞肺癌差。辅助化疗与疾病病理分期 II-III 期患者的生存改善相关,可考虑对病理分期 II-III 期肺肉瘤样癌患者进行辅助化疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a62/11295483/e3b363057653/12885_2024_12728_Fig1_HTML.jpg

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