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酪氨酸激酶抑制剂治疗后肺腺癌转化为小细胞肺癌患者的预后

Patients outcomes in lung adenocarcinoma transforming to small-cell lung cancer after tyrosine kinase inhibitor therapy.

作者信息

Wang Shuai, Wang Yongsen, Wu Xuan, Yang Li, Zhang Xiaoju

机构信息

Department of Respiratory and Critical Care Medicine, Zhengzhou University People's Hospital, Henan Provincial People's Hospital, No. 7, Weiwu Road, Zhengzhou, 450000, China.

Department of Molecular Pathology, Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, China.

出版信息

World J Surg Oncol. 2025 Feb 1;23(1):34. doi: 10.1186/s12957-025-03687-4.

Abstract

BACKGROUND

Non-small cell lung cancer (NSCLC) transforming to small cell lung cancer (SCLC) is one of the mechanisms of resistance to tyrosine kinase inhibitors (TKIs). Cases of NSCLC transforming into SCLC have been discovered. However, we lack concentrated data on the characteristics of this population and the transformed SCLC to aid our insight of the biology and clinical value of NSCLC transforming with positive.

METHODS

We systematically reviewed the published literatures and summarized the pathological and clinical characteristics, and the prognosis, of published cases.

RESULTS

140 patients with lung adenocarcinoma (LUAD) were included in this study, with a median age of 56.8 years. The median time from the first diagnosis of LUAD transforming to SCLC (ttSCLC) was 20.0 months. The median overall survival (mOS) after the diagnosis of SCLC was 11.0 months (95% CI, 7.41 to 14.59 months). In the univariate analysis, ever smoking (either former or current) was a promising predictor of a shorter ttSCLC (HR, 1.73; 95% CI, 1.14 to 2.62; P = 0.010). TKIs therapy administered as a second line and beyond treatment was related to a significant delay in SCLC onset compared to first-line therapy (HR, 0.62; 95% CI, 0.40 to 0.96; P = 0.031). The median progression-free survival (mPFS) on first-line platinum plus etoposide after the conversion to SCLC was 3.0 months. Female appeared to be related to worse outcomes after transformation of SCLC.

CONCLUSION

Transformed SCLC exhibited poor response to primary SCLC classic chemotherapy and immunotherapy. It carries a worse prognosis. Exploring novel therapeutic strategies for transformed SCLC is imperative.

摘要

背景

非小细胞肺癌(NSCLC)转化为小细胞肺癌(SCLC)是对酪氨酸激酶抑制剂(TKIs)耐药的机制之一。已发现NSCLC转化为SCLC的病例。然而,我们缺乏关于该人群特征及转化后的SCLC的集中数据,以帮助我们了解NSCLC正向转化的生物学特性和临床价值。

方法

我们系统回顾了已发表的文献,并总结了已发表病例的病理和临床特征以及预后情况。

结果

本研究纳入了140例肺腺癌(LUAD)患者,中位年龄为56.8岁。从首次诊断LUAD转化为SCLC(ttSCLC)的中位时间为20.0个月。SCLC诊断后的中位总生存期(mOS)为11.0个月(95%CI,7.41至14.59个月)。在单因素分析中,曾经吸烟(既往或当前吸烟)是ttSCLC较短的一个有前景的预测因素(HR,1.73;95%CI,1.14至2.62;P = 0.010)。与一线治疗相比,二线及以上治疗使用TKIs与SCLC发病显著延迟相关(HR,0.62;95%CI,0.40至0.96;P = 0.031)。转化为SCLC后一线铂类加依托泊苷治疗的中位无进展生存期(mPFS)为3.0个月。女性在SCLC转化后似乎与较差的预后相关。

结论

转化后的SCLC对原发性SCLC经典化疗和免疫治疗反应较差。其预后更差。探索针对转化后SCLC的新型治疗策略势在必行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a3/11787757/b3afc0e2a48c/12957_2025_3687_Fig1_HTML.jpg

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