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安罗替尼作为三线或三线以上治疗难治性小细胞肺癌的真实世界疗效和安全性。

Real-world efficacy and safety of anlotinib as third- or further-line treatment in refractory small cell lung cancer.

机构信息

Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Science, Jinan, 250117, Shandong Province, China.

Department of Respiratory Disease, Zhejiang Provincial People's Hospital, Hangzhou, 310000, Zhejiang Province, China.

出版信息

J Cancer Res Clin Oncol. 2022 Oct;148(10):2661-2671. doi: 10.1007/s00432-021-03848-4. Epub 2021 Nov 8.

Abstract

PURPOSE

As a novel antiangiogenic multi-target tyrosine kinase inhibitor recently approved in China, anlotinib has exhibited promising anticancer efficacy and acceptable safety profile in the salvage treatment of small cell lung cancer (SCLC) in clinical trials. Here we retrospectively investigated the efficacy and safety of anlotinib as third- or further-line treatment in patients with refractory SCLC.

PATIENTS AND METHODS

A total of 40 patients with refractory SCLC treated with anlotinib monotherapy were included in this study. The clinicopathological data, treatment information, survival data and safety data were retrospectively collected. Survival curves were constructed using the Kaplan-Meier method. Univariate analysis was performed by log-rank testing.

RESULTS

Altogether, 40 patients of extensive-stage SCLC or progressive limited-stage SCLC received anlotinib monotherapy as third- or further-line treatment from July 2018 to June 2020. Four patients achieved partial response (PR), 14 patients achieved stable disease (SD), no complete response (CR) was recorded, and 22 patients experienced progressive disease (PD). The disease control rate (DCR) was 45.0%. The median progression-free survival (PFS) was 3.0 months (95% CI 2.241-3.759), and the median overall survival (OS) was 7.8 months (95% CI 3.190-12.410). The common adverse effects (AEs) included hypertension, fatigue, anorexia, cough, rash and nausea. Grade 3 treatment-related AEs occurred in 3 (7.5%) patients. One patient interrupted anlotinib treatment due to repeated grade 1 epistaxis. Univariate analysis revealed that patients without liver metastases, previously treated with radiotherapy or with Eastern Cooperative Oncology Group (ECOG) scores of 0 or 1 had longer OS with anlotinib treatment. Cox regression analysis demonstrated that patients without liver metastases and patients with ECOG score ≤ 1 had longer PFS, while patients without liver metastases had longer OS.

CONCLUSION

Anlotinib is beneficial to refractory SCLC as third- or further-line treatment, especially in patients without liver metastasis and with better physical status. Related adverse effects are tolerable and manageable.

摘要

目的

安罗替尼是一种新型抗血管生成多靶点酪氨酸激酶抑制剂,在中国已被批准用于小细胞肺癌(SCLC)的三线或后线治疗。本研究回顾性分析安罗替尼在治疗难治性 SCLC 患者中的疗效和安全性。

方法

共纳入 40 例接受安罗替尼单药治疗的难治性 SCLC 患者。回顾性收集患者的临床病理资料、治疗信息、生存数据和安全性数据。采用 Kaplan-Meier 法绘制生存曲线,采用对数秩检验进行单因素分析。

结果

40 例广泛期或进展期局限期 SCLC 患者自 2018 年 7 月至 2020 年 6 月接受安罗替尼三线或后线治疗。其中 4 例患者达部分缓解(PR),14 例患者达疾病稳定(SD),无完全缓解(CR),22 例患者疾病进展(PD)。疾病控制率(DCR)为 45.0%。中位无进展生存期(PFS)为 3.0 个月(95%CI 2.241-3.759),中位总生存期(OS)为 7.8 个月(95%CI 3.190-12.410)。常见不良反应(AE)包括高血压、乏力、厌食、咳嗽、皮疹和恶心。3 例(7.5%)患者发生 3 级治疗相关 AE。1 例患者因 1 级反复鼻出血而中断安罗替尼治疗。单因素分析显示,无肝转移、既往接受过放疗或 ECOG 评分 0 或 1 的患者,接受安罗替尼治疗的 OS 更长。Cox 回归分析显示,无肝转移和 ECOG 评分≤1 的患者 PFS 更长,而无肝转移的患者 OS 更长。

结论

安罗替尼对难治性 SCLC 三线或后线治疗有益,尤其是对无肝转移且体能状况较好的患者。相关不良反应可耐受且可管理。

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