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转移性乳腺癌患者在接受卡培他滨为基础的联合化疗缓解后,使用卡培他滨单药维持治疗。

Single-agent capecitabine maintenance therapy after response to capecitabine-based combination chemotherapy in patients with metastatic breast cancer.

机构信息

Department of Breast Cancer, Affiliated Hospital of Academy of Military Medical Sciences, Beijing, China.

出版信息

Anticancer Drugs. 2012 Aug;23(7):718-23. doi: 10.1097/CAD.0b013e328351802e.

DOI:10.1097/CAD.0b013e328351802e
PMID:22739713
Abstract

We performed an analysis of the efficacy of capecitabine monotherapy as maintenance treatment for metastatic breast cancer (MBC) after response to capecitabine-based chemotherapy [capecitabine plus docetaxel (XT) or vinorelbine (XN)] as a first-line or a second-line treatment. Sixty-four Chinese patients with histologically confirmed MBC received capecitabine maintenance therapy after disease stabilization or maximal response to capecitabine-based combination chemotherapy. Single-agent capecitabine was administered at a dose of 1000 mg/m(2) twice daily for 14 days, followed by a 7-day rest period, every 3 weeks. The median time to progression, the primary endpoint of the study, was 4.4 months (95% confidence interval, 3.4-5.4 months). Fifty-nine patients were evaluable for response. Capecitabine maintenance therapy produced an objective response rate of 5.1% (95% confidence interval, 3.9-6.3%). The incidence of grade 3/4 leukopenia (3.1%) and neutropenia (4.7%) was significantly lower (P<0.001) with capecitabine monotherapy than with combination chemotherapy (46.9 and 54.7%, respectively). Conversely, the incidence of grade 3 hand-foot syndrome was higher with capecitabine maintenance therapy than with combination therapy (14.1 vs. 0%, respectively; P=0.003). Capecitabine monotherapy is an effective maintenance treatment after response to capecitabine-based combination chemotherapy in MBC with a favorable safety profile.

摘要

我们分析了卡培他滨单药作为转移性乳腺癌(MBC)一线或二线治疗后对卡培他滨为基础的化疗[卡培他滨联合多西紫杉醇(XT)或长春瑞滨(XN)]有反应的维持治疗的疗效。64 例组织学证实的 MBC 患者在卡培他滨联合化疗达到疾病稳定或最大缓解后接受卡培他滨维持治疗。单药卡培他滨的剂量为 1000 mg/m(2),每日 2 次,连用 14 天,然后休息 7 天,每 3 周一次。研究的主要终点是无进展生存期(PFS),中位数为 4.4 个月(95%置信区间,3.4-5.4 个月)。59 例患者可评估疗效。卡培他滨维持治疗的客观缓解率为 5.1%(95%置信区间,3.9-6.3%)。卡培他滨单药治疗的 3/4 级白细胞减少(3.1%)和中性粒细胞减少(4.7%)的发生率明显低于联合化疗(分别为 46.9%和 54.7%;P<0.001)。相反,卡培他滨维持治疗的 3 级手足综合征的发生率高于联合治疗(分别为 14.1%和 0%;P=0.003)。卡培他滨单药治疗在转移性乳腺癌一线或二线治疗后对卡培他滨为基础的化疗有反应,是一种有效的维持治疗方法,具有良好的安全性。

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