Liang Xu, Di Lijun, Song Guohong, Yan Ying, Wang Chaoying, Jiang Hanfang, Li Huiping
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Breast Oncology, Peking University Cancer Hospital & Institute, Beijing 100142, China.
Chin J Cancer Res. 2014 Oct;26(5):550-7. doi: 10.3978/j.issn.1000-9604.2014.10.02.
To investigate the efficacy and safety of capecitabine maintenance therapy (MT) after initial capecitabine plus docetaxel (XT) chemotherapy in patients with metastatic triple-negative breast cancer (mTNBC).
Fifty-five mTNBC patients treated with XT chemotherapy between May 2007 and June 2013 were retrospectively analyzed. When initial disease control was achieved by the combination chemotherapy, capecitabine was continued for 32 patients (MT), while 23 patients remained without any treatment (non-MT). We compared progression-free survival (PFS) and safety of both groups.
The median PFS of 55 patients was 8.1 months, overall median PFS time of 32 patients in the capecitabine MT group and 23 in the non-MT group was 10.1 vs. 6.7 months (P=0.032), respectively. When compared PFS time of maintenance treatment, single-agent capecitabine prolonged PFS by 7.1 months, for non-MT patients, the PFS without any treatment was 3.1 months, and this between-group difference was statistically significant (P=0.003). Adverse events, including of hematologic toxicity, gastrointestinal toxicities, hand-foot syndrome and abnormal liver function were not significantly different between two groups.
After initial disease control was achieved with the XT combination chemotherapy, capecitabine MT can significantly prolong PFS time with a favorable safety profile in mTNBC patients.
探讨卡培他滨维持治疗(MT)在转移性三阴性乳腺癌(mTNBC)患者初始接受卡培他滨联合多西他赛(XT)化疗后的疗效及安全性。
回顾性分析2007年5月至2013年6月间接受XT化疗的55例mTNBC患者。当联合化疗实现初始疾病控制后,32例患者继续使用卡培他滨(MT组),而23例患者未接受任何治疗(非MT组)。我们比较了两组的无进展生存期(PFS)和安全性。
55例患者的中位PFS为8.1个月,卡培他滨MT组32例患者和非MT组23例患者的总体中位PFS时间分别为10.1个月和6.7个月(P = 0.032)。比较维持治疗的PFS时间时,单药卡培他滨使PFS延长7.1个月,对于非MT患者,未接受任何治疗的PFS为3.1个月,组间差异具有统计学意义(P = 0.003)。两组间不良事件,包括血液学毒性、胃肠道毒性、手足综合征和肝功能异常,无显著差异。
在XT联合化疗实现初始疾病控制后,卡培他滨MT可显著延长mTNBC患者的PFS时间,且安全性良好。