A phase II study of anlotinib plus whole brain radiation therapy for patients with NSCLC with multiple brain metastases

被引:0
|
作者
Gu, Dayong [1 ,2 ,3 ]
Yu, Hongliang [1 ,2 ,3 ]
Ding, Naixin [1 ,2 ,3 ]
Xu, Jianhua [1 ,2 ,3 ]
Qian, Pudong [1 ,2 ,3 ]
Zhu, Jun [1 ,2 ,3 ]
Jiang, Ming [2 ,3 ,4 ]
Tao, Hua [1 ,2 ,3 ]
Zhu, Xiangzhi [1 ,2 ,3 ]
机构
[1] Nanjing Med Univ, Affiliated Canc Hosp, Dept Radiat Oncol, 42 Baiziting Rd, Nanjing 210007, Jiangsu, Peoples R China
[2] Jiangsu Canc Hosp, 42 Baiziting Rd, Nanjing 210007, Peoples R China
[3] Jiangsu Inst Canc Res, 42 Baiziting Rd, Nanjing 210007, Peoples R China
[4] Nanjing Med Univ, Affiliated Canc Hosp, Dept Thorac Surg, Nanjing, Peoples R China
关键词
Whole-brain radiotherapy; anlotinib; non-small cell lung cancer; brain metastasis; intracranial progression-free survival; CELL LUNG-CANCER; RADIOTHERAPY; NORMALIZATION; MULTICENTER; DIAGNOSIS; SURVIVAL; TRIAL;
D O I
10.1080/07853890.2024.2401618
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Whole brain radiotherapy (WBRT) is the mainstay of treatment for patients with non-small cell lung cancer (NSCLC) with multiple brain metastases (BMs); however, the BRAIN study showed that the efficacy of WBRT is unsatisfactory. This prospective phase II study aimed to evaluate the efficacy and safety of WBRT combined with anlotinib, a novel anti-angiogenic multi-target tyrosine kinase inhibitor (TKI), in patients with multiple BMs (>3) from advanced NSCLC. Methods: Patients with advanced NSCLC with multiple BMs who had received two or more lines of treatment were eligible for enrolment into this study. All patients were treated with anlotinib (8-12 mg, QD, on days 1-14 of a 21-day cycle) combined with WBRT (DT 30 Gy/12 F), followed by maintenance therapy with anlotinib until disease progression or treatment intolerance. The primary endpoint of this study was the intracranial progression-free survival (iPFS). The secondary endpoints were intracranial objective response rate (iORR), intracranial disease control rate (iDCR), overall survival (OS) and treatment safety. Results: Between May 2019 and January 2021, 28 patients were enrolled, all of whom were evaluable for efficacy and safety. The median age was 57.7 years, and 46.4% were male. Twenty-five patients had adenocarcinoma (89.3%), six had EGFR mutations (21.4%) and two had ALK mutations (7.1%). The median iPFS was 11.1 months (95% confidence interval (CI): 5.4-16.8 months) and the median OS was 13.4 months (95% CI: 5.2-21.6 months). The iORR was 71.4% (six complete responses + 14 partial responses). The most frequently observed adverse events (AEs) were hypertension (71.4%), fatigue (64.3%), anorexia (46.4%), and foot and hand skin reactions (25.0%). No patients developed >= grade 4 AEs. No intracranial haemorrhages occurred during treatment. Dose adjustment due to AEs occurred in 17.9% of patients. Conclusions: Anlotinib combined with WBRT is effective and well-tolerated in patients with NSCLC with multiple BMs.
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