Efficacy and safety of the VEGFR2 inhibitor Apatinib for metastatic soft tissue sarcoma: Chinese cohort data from NCT03121846

被引:14
作者
Liu, Xinyue [1 ,2 ,8 ]
Xu, Jin [3 ]
Li, Feng [1 ,2 ,8 ]
Liao, Zhichao [1 ,2 ]
Ren, Zhiwu [1 ,2 ]
Zhu, Lei [2 ,4 ]
Shi, Yehui [2 ,5 ]
Zhao, Gang [2 ,6 ]
Bai, Xu [2 ,7 ]
Zhao, Jun [1 ,2 ]
Xing, Ruwei [1 ,2 ]
Teng, Sheng [1 ,2 ]
Yang, Yun [1 ,2 ]
Yang, Jilong [1 ,2 ,8 ]
机构
[1] Tianjin Med Univ Canc Inst & Hosp, Dept Bone & Soft Tissue Tumor, Huanhuxi Rd, Tianjin 300060, Peoples R China
[2] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Tianjin 300060, Peoples R China
[3] Tianjin Hosp, Dept Anesthesiol, Tianjin 300000, Peoples R China
[4] Tianjin Med Univ Canc Inst & Hosp, Mol Imaging, Tianjin 300060, Peoples R China
[5] Tianjin Med Univ Canc Inst & Hosp, Pharmacol Res Ctr, Tianjin 300060, Peoples R China
[6] Tianjin Med Univ Canc Inst & Hosp, Pathol, Tianjin 300060, Peoples R China
[7] Tianjin Med Univ Canc Inst & Hosp, Radiat Oncol, Tianjin 300060, Peoples R China
[8] Key Lab Mol Canc Epidemiol, Tianjin 300060, Peoples R China
关键词
Soft tissue sarcoma; Apatinib; Efficacy; Progression-free survival; Toxicity; PHASE-II; DOUBLE-BLIND; PAZOPANIB; CHEMOTHERAPY; ANGIOGENESIS; EXPRESSION; THERAPIES; TRIAL; BONE;
D O I
10.1016/j.biopha.2019.109587
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: There is no standard treatment for stage IV soft tissue sarcoma (STS) after the failure of Adriamycin-based chemotherapy. This phase II study (NCT03121846) assessed the efficacy and safety of apatinib (YN968D1), a new tyrosine kinase inhibitor that targets VEGFR-2, for patients with stage IV STS after chemotherapy failure. Methods: Forty-two subjects with stage IV STSs who had failed chemotherapy and who received Apatinib were recruited between September 2015 and February 2018. The primary endpoint was progression-free survival (PFS), and the secondary endpoints were the PFS rate (PFR), objective response rate (ORR), and disease control rate (DCR) at week 12. Treatment-related adverse effects (AEs) were evaluated. Results: Forty-two subjects were evaluated for AEs and 38 subjects were evaluated for efficacy. At 12 weeks, the PFR, ORR, and DCR were 70%, 26.32% (10/38), and 86.84% (33/38), respectively. Regarding overall responses, the ORR and DCR were 23.68% (9/38) and 57.89% (22/38), respectively. The median PFS was 7.87 months, and the median overall survival (OS) was 17.55 months. The most common AEs included hypertension (n = 18, 42.86%), hand-foot-skin reaction (n = 15, 35.71%), apositia (n = 13, 30.95%), and proteinuria (n = 11, 26.19%). No subjects had grade 4 AEs and 11 subjects (26.19%) experienced grade 3 AEs, mainly hypertension, hand-foot-skin reaction, proteinuria, apositia, fatigue, pain, and dysgeusia. Notably, the subjects who experienced hypertension, hand-foot-skin reaction, or proteinuria had significantly longer OS than those without these AEs (P = 0.0003). Conclusion: With the largest Chinese STS cohort to date, we report that apatinib show good efficacy in advanced STS subjects with significant higher ORR and some adverse events may predict prognosis.
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页数:8
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