Prognostic Factors Influencing Progression-Free Survival in HER2-Positive Metastatic Breast Cancer Patients Who Were Treated With A Combination of Lapatinib and Capecitabine

被引:5
作者
Dogan, Izzet [1 ]
Paksoy, Nail [1 ]
Ak, Naziye [1 ]
Vatansever, Sezai [1 ]
Saip, Pinar [1 ]
Aydiner, Adnan [1 ]
机构
[1] Istanbul Univ, Dept Med Oncol, Inst Oncol, Istanbul, Turkiye
关键词
Breast cancer; metastasis; HER2; neu receptor; lapatinib; capecitabine; BRAIN METASTASES; PLUS CAPECITABINE; OUTCOMES;
D O I
10.4274/ejbh.galenos.2023.2022-12-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The aim was to assess the prognostic variables in human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer patients receiving lapatinib plus capecitabine. Materials and Methods: Retrospective data on HER2-positive metastatic breast cancer patients who received lapatinib and capecitabine were analyzed. Survival outcome was obtained with Cox regression analysis and the Kaplan-Meier method.Results: The study included 102 patients. Forty-four (43.1%) patients had de novo metastatic disease. The most frequent metastatic sites were, in order, bone (61.8%), brain (57.8%), liver (35.3%), and lung (34.3%). All of the patients had previously received chemotherapy based on trastuzumab. With combined lapatinib and capecitabine, complete response was observed in 7.8%, partial response in 30.4%, and stable disease in 24.5%. Progression -free survival was 8 (95% confidence interval, 5.1-10.8) months. In multivariable analysis, endocrine therapy (p = 0.02), de novo metastatic disease (p = 0.02), and age (p = 0.02) were prognostic factors for progression-free survival. However, the number of chemotherapy cycles with trastuzumab, palliative radiotherapy, history of breast surgery, and the number of metastatic sites were not significant in this respect.Conclusion: These results have demonstrated the effectiveness of lapatinib plus capecitabine in metastatic HER2-positive breast cancer patients. Furthermore, unfavorable prognostic factors for progression-free survival were shown to be hormone-negative tumor, de novo metastatic disease, and young age.
引用
收藏
页码:128 / 133
页数:6
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