Application of apatinib after multifaceted therapies for metastatic breast cancer.
Application of apatinib after multifaceted therapies for metastatic breast cancer.
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阿帕替尼在转移性乳腺癌多方面治疗后的应用
DOI:
10.21037/tcr-19-2588
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发表时间:
2020-08
影响因子:
0.9
通讯作者:
Cheng J
中科院分区:
文献类型:
--
作者:
Wang J;Chen Y;Chen R;Wu L;Cheng J
Apatinib is a small molecule tyrosine kinase inhibitor (TKI) that is taken orally and has high specificity for vascular endothelial growth factor receptor 2 (VEGFR-2). This study explored the efficacy and toxicity of apatinib in patients with metastatic breast cancer (MBC) who failed to respond to multifaceted therapy. A total of 61 patients with MBC who were unresponsive to previous multifaceted chemotherapy were included in this study. The treatment regimens were either a combination of apatinib and chemotherapy or apatinib administered singly with a dose range of 250 mg every second day to 500 mg per day. Progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and toxicity were used as outcome measures. Of the 61 patients, partial response (PR) was observed in 14 patients (23.0%), stable disease (SD) was observed in 30 patients (49.2%), and progressive disease (PD) was observed in 17 patients (27.8%). The DCR was 44/61 (72.1%), and the ORR was 14/61 (23.0%). Of the 44 patients who achieved PR or SD, the median PFS was 4 months and 15 days. Patients with intracranial metastases were found to benefit from apatinib. Furthermore, 11 patients underwent next generation sequencing (NGS) and 5 of these had a P53 mutation. Of those 5 cases, the ORR and DCR were 0% and 20.0%, respectively. Of the 6 cases with wild-type P53, the ORR was 50.0%, and the DCR was 100.0%. Multivariate regression analysis found that hypertension was an independent prognostic factor of better DCR. Apatinib showed good efficacy and manageable toxicity in patients with MBC that had not responded to multifaceted therapy.
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影响因子:
8.4
作者:
Eisenhauer, E. A.;Therasse, P.;Verweij, J.
通讯作者:
Verweij, J.
影响因子:
9.2
作者:
ter Veer, Emil;Mohammad, Nadia Haj;van Valkenhoef, Gert;Ngai, Lok Lam;Mali, Rosa M. A.;van Oijen, Martijn G. H.;van Laarhoven, Hanneke W. M.
通讯作者:
van Laarhoven, Hanneke W. M.
影响因子:
6.2
作者:
Ferrero, Jean-Marc;Hardy-Bessard, Anne-Claire;Largillier, Remy
通讯作者:
Largillier, Remy
影响因子:
5.8
作者:
Tong, Xiu-zhen;Wang, Fang;Fu, Li-wu
通讯作者:
Fu, Li-wu
影响因子:
11.2
作者:
Mi YJ;Liang YJ;Huang HB;Zhao HY;Wu CP;Wang F;Tao LY;Zhang CZ;Dai CL;Tiwari AK;Ma XX;To KK;Ambudkar SV;Chen ZS;Fu LW
通讯作者:
Fu LW