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Comparison of apatinib and capecitabine (Xeloda) with capecitabine (Xeloda) in advanced triple-negative breast cancer as third-line therapy

机译:阿帕替尼和卡培他滨(希罗达)与卡培他滨(希罗达)在晚期三阴性乳腺癌中作为三线治疗的比较

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摘要

The treatment of advanced triple-negative breast cancer, which failed in first-line or second-line therapy, is a significant challenge. We conducted this retrospective study to explore the efficacy and safety of apatinib and capecitabine as the third-line treatment for advanced triple-negative breast cancer.This retrospective study involved 44 advanced triple-negative breast cancer patients who failed in first-line or second-line therapy in Tangshan People's Hospital from January 2016 to February 2017. Twenty-two patients received apatinib and capecitabine, while 22 patients were treated with capecitabine monotherapy as third-line therapy. The progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and adverse events were compared between 2 groups.The apatinib and capecitabine group exhibited a higher PFS than capecitabine group (P = .001). Meanwhile, ORR and DCR in apatinib and capecitabine group were better than in capecitabine group (P = .042; .016). The 2 groups showed no significant difference in adverse events except degree I-II bleeding (P = .021). Both the apatinib and capecitabine and the capecitabine regimens revealed good tolerability.The apatinib and capecitabine regimen can achieve a better efficacy and similar serious adverse events compared with capecitabine regimen as the third-line treatment for advanced triple-negative breast cancer.
机译:一线或二线治疗失败的晚期三阴性乳腺癌的治疗是一项重大挑战。我们进行了这项回顾性研究,以探讨阿帕替尼和卡培他滨作为晚期三重阴性乳腺癌三线治疗的有效性和安全性。这项回顾性研究涉及44例在一线或二线治疗失败的晚期三阴性乳腺癌患者。于2016年1月至2017年2月在唐山市人民医院接受线治疗。22例患者接受了阿帕替尼和卡培他滨治疗,而22例患者接受了卡培他滨单药治疗作为三线治疗。比较两组的无进展生存期(PFS),客观缓解率(ORR),疾病控制率(DCR)和不良事件。阿帕替尼和卡培他滨组的PFS高于卡培他滨组(P = 0.001) 。同时,阿帕替尼和卡培他滨组的ORR和DCR优于卡培他滨组(P = .042; .016)。除I-II度出血外,两组的不良反应均无显着性差异(P = .021)。阿帕替尼和卡培他滨方案以及卡培他滨方案均显示出良好的耐受性。与卡培他滨方案作为晚期三重阴性乳腺癌的三线治疗方案相比,阿帕替尼和卡培他滨方案可获得更好的疗效和相似的严重不良事件。

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