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安罗替尼治疗广泛期小细胞肺癌患者肿瘤空洞的预后价值。

Prognostic value of tumor cavitation in extensive-stage small-cell lung cancer patients treated with anlotinib.

机构信息

Department of Pulmonary Medicine, Shanghai Chest Hospital, Shanghai Jiaotong University, Huaihai West Road No. 241, Shanghai, China.

出版信息

J Cancer Res Clin Oncol. 2020 Feb;146(2):401-406. doi: 10.1007/s00432-019-03064-1. Epub 2019 Nov 6.

Abstract

PURPOSE

Anlotinib is a novel multi-target tyrosine kinase inhibitor (TKI) for tumor angiogenesis and tumor cell proliferation. The efficacy of anlotinib as a third-line or beyond therapy for SCLC was confirmed in the ALTER1202 trial. For lung cancer patients treated with antiangiogenesis agents, the phenomenon of cavitation is commonly seen in the lung target lesions. The impact of tumor cavitation on survival in lung cancer patients treated with vascular-targeted therapy remains controversial. Our retrospective study was to investigate the prognostic value of tumor cavitation in extensive-stage SCLC patients treated with anlotinib.

METHODS

A total of 73 extensive-stage SCLC patients confirmed by histopathology from January 2018 to January 2019 were retrospectively analyzed. All patients received anlotinib therapy at Shanghai Chest Hospital. We defined tumor cavitation of the lung target lesions as that part of solid component was changed to air-filled area according to chest CT. Progression-free survival (PFS) was calculated from the beginning of anlotinib therapy to the disease progression or the last follow-up visit.

RESULTS

Eleven (15.0%) patients had tumor cavitation during anlotinib therapy. The ORR of the 73 patients was 15.1%. Multivariate logistic regression analysis showed that tumor cavitation during anlotinib therapy was not associated with gender (P = 0.630), age (P = 0.190), smoking status (P = 0.165), anatomy type (P = 0.641), and the line of anlotinib therapy (P = 0.302). The median PFS of all patients was 2.6 months (95%CI 2.1-3.2). According to the univariate analysis, the median PFS in patients with and without tumor cavitation was 5.0 months and 2.2 months, respectively, and the difference was statistically significant (P = 0.041). According to the multivariate analysis, tumor cavitation was an independent factor for PFS after adjusting gender, age, smoking status, anatomy type, the line of anlotinib therapy, tumor cavitation, and response to anlotinib (adjusted HR 0.316, 95%CI 0.142-0.702; P = 0.005).

CONCLUSIONS

In 73 extensive-stage SCLC patients treated with anlotinib, no demographic/clinical characteristic was related to tumor cavitation, and tumor cavitation was an independent factor in predicting better PFS.

摘要

目的

安罗替尼是一种新型的多靶点酪氨酸激酶抑制剂(TKI),可用于肿瘤血管生成和肿瘤细胞增殖。ALTER1202 试验证实,安罗替尼作为三线或三线以上治疗小细胞肺癌(SCLC)的疗效。对于接受抗血管生成药物治疗的肺癌患者,肺部靶病灶中常见空洞现象。肿瘤空洞对接受血管靶向治疗的肺癌患者生存的影响仍存在争议。我们的回顾性研究旨在探讨安罗替尼治疗广泛期 SCLC 患者中肿瘤空洞的预后价值。

方法

回顾性分析 2018 年 1 月至 2019 年 1 月间经组织病理学证实的 73 例广泛期 SCLC 患者。所有患者均在上海胸科医院接受安罗替尼治疗。我们将肺部靶病灶的肿瘤空洞定义为根据胸部 CT,实性成分的一部分转变为充气区域。无进展生存期(PFS)从安罗替尼治疗开始到疾病进展或最后一次随访进行计算。

结果

73 例患者中,11 例(15.0%)患者在安罗替尼治疗期间出现肿瘤空洞。73 例患者的客观缓解率(ORR)为 15.1%。多因素 logistic 回归分析显示,安罗替尼治疗期间的肿瘤空洞与性别(P=0.630)、年龄(P=0.190)、吸烟状态(P=0.165)、解剖类型(P=0.641)和安罗替尼治疗线数(P=0.302)无关。所有患者的中位 PFS 为 2.6 个月(95%CI 2.1-3.2)。根据单因素分析,有肿瘤空洞和无肿瘤空洞的患者中位 PFS 分别为 5.0 个月和 2.2 个月,差异有统计学意义(P=0.041)。根据多因素分析,在调整性别、年龄、吸烟状态、解剖类型、安罗替尼治疗线数、肿瘤空洞和安罗替尼治疗反应后,肿瘤空洞是 PFS 的独立因素(调整 HR 0.316,95%CI 0.142-0.702;P=0.005)。

结论

在 73 例接受安罗替尼治疗的广泛期 SCLC 患者中,无人口统计学/临床特征与肿瘤空洞有关,肿瘤空洞是预测更好 PFS 的独立因素。

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