Efficacy of lapatinib combined with capecitabine in patients with HER2-positive metastatic breast cancer in a real-world study

被引:10
|
作者
Gui, Xinyu [1 ]
Li, Huiping [1 ]
Yan, Ying [1 ]
Zhang, Ruyan [1 ]
机构
[1] Peking Univ Canc Hosp & Inst, Key Lab Carcinogenesis & Translat Res, Minist Educ Beijing, Dept Breast Oncol, 52 Fucheng Rd, Beijing 100142, Peoples R China
关键词
human epidermal growth factor receptor-2-positive; metastatic breast cancer; lapatinib; capecitabine; progression-free survival; BRAIN METASTASES; PLUS CAPECITABINE; TRASTUZUMAB; COMBINATION;
D O I
10.3892/ol.2020.12241
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of the present study was to determine the efficacy and safety of lapatinib-based treatment for patients with human epidermal growth factor receptor-2-positive (HER2(+)) metastatic breast cancer (MBC). The aim of the present real-world study was to investigate the medical records and follow-up information of 92 patients with HER2(+) MBC who received a lapatinib-based regimen at the recurrent/metastatic stage, 78 of whom had been pretreated with trastuzumab. The results demonstrated that the median progression-free survival (PFS) was 5.8 months and the overall survival (OS) was 21.5 months, with an objective response rate (ORR) of 21.7%, disease control rate (DCR) of 87.0% and clinical benefit rate (CBR) of 47.8%. In the patients receiving a lapatinib-based regimen as first-, second- and third/later-line treatment, the median PFS was 10.4, 5.2 and 5.1 months (P=0.048), the median OS was 32.9, 29.1 and 13.0 months (P<0.001), the ORR was 38.9, 23.3 and 13.60%, and the DCR was 100, 83.3 and 84.1%, respectively. In the trastuzumab-resistant (n=71) and trastuzumab-sensitive (n=21) patients, the median PFS was 5.2 and 9.1 months (P=0.032), and the median OS was 21.4 and 44.3 months (P=0.003), respectively. In the patients who received lapatinib plus chemotherapy (n=68), the median PFS with lapatinib plus capecitabine (n=38) was 8.1 months, as compared with the 5.1 months with lapatinib plus other chemotherapy agents (n=30; P=0.005). The median PFS of 14 patients with brain metastases was 8.4 months, with an ORR of 35.7% and a DCR of 85.7%. Multivariate analysis revealed that the line of lapatinib-based treatment and its combination with capecitabine or a different agent were independent prognostic factors for the median PFS in patients with HER2(+) MBC. A limited number of adverse events were observed with the combination of lapatinib and capecitabine. Therefore, the findings of the present study suggested that lapatinib-based treatment is effective in patients with HER2(+) MBC (even in trastuzumab-pretreated patients), and the combination of lapatinib with capecitabine may be recommended due to its good efficacy, convenience and tolerability.
引用
收藏
页数:9
相关论文
共 50 条
  • [21] A multicenter, retrospective, real-world study of inetetamab combined with pyrotinib and vinorelbine as treatment for HER2-positive metastatic breast cancer
    Jin, N.
    Yin, Y.
    Li, W.
    Huang, X.
    [J]. ANNALS OF ONCOLOGY, 2023, 34 : S1492 - S1492
  • [22] Efficacy and safety of inetetamab-containing regimens in patients with HER2-positive metastatic breast cancer: a real-world retrospective study in China
    Liu, Xiaoyu
    Zhang, Peng
    Li, Chao
    Song, Xiang
    Liu, Zhaoyun
    Shao, Wenna
    Li, Sumei
    Wang, Xinzhao
    Yu, Zhiyong
    [J]. FRONTIERS IN ONCOLOGY, 2023, 13
  • [23] Clinical recommendations for the use of lapatinib ditosylate plus capecitabine for patients with advanced or metastatic HER2-positive breast cancer
    Snyder, Raymond D.
    Boyle, Frances M.
    Chan, Arlene
    Craft, Paul S.
    De Boer, Richard
    Mainwaring, Paul N.
    McCarthy, Nicole J.
    Wilcken, Nicholas R.
    [J]. ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2009, 5 (01) : 4 - 16
  • [24] Lapatinib can restore capecitabine sensitivity in HER2-positive breast cancer
    Cha, Y.
    Kim, H. P.
    Han, S. W.
    Oh, D. Y.
    Kim, J. H.
    Im, S. A.
    Bang, Y. J.
    Kim, T. Y.
    [J]. CANCER RESEARCH, 2009, 69 (02) : 249S - 250S
  • [25] Real-world study of trastuzumab and pertuzumab combined with chemotherapy in neoadjuvant treatment for patients with HER2-positive breast cancer
    Ma, Xiangmin
    Zhang, Xiangmei
    Zhou, Xinping
    Ren, Xiaofei
    Ma, Xindi
    Zhang, Weifang
    Yang, Ruiling
    Song, Tao
    Liu, Yunjiang
    [J]. MEDICINE, 2022, 101 (40) : E30892
  • [26] LAPATINIB AND CAPECITABINE IN THE TREATMENT OF HER2-POSITIVE BREAST CANCER WITH BRAIN METASTASES
    Dubianski, R.
    Brewczynska, E.
    Lemanska, I.
    Szombara, E.
    Nowecki, Z. I.
    [J]. ANNALS OF ONCOLOGY, 2014, 25
  • [27] Correlation of efficacy between EGFR gene copy number and lapatinib/capecitabine therapy in HER2-positive metastatic breast cancer
    Fabi, A.
    Di Benedetto, A.
    Merola, R.
    Metro, G.
    Mottolese, M.
    Papaldo, P.
    Ferretti, G.
    Vici, P.
    Sperduti, I.
    Cognetti, F.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
  • [28] The efficacy and safety of epirubicin and cyclophosphamide combined with pyrotinib in neoadjuvant treatment for HER2-positive breast cancer: A real-world study
    Li, Fu
    Liang, Yimin
    Luo, Ming
    Shen, Jiayue
    Zhou, Taosheng
    Liang, Yajing
    Tang, Xiaoqi
    Yuan, Huiming
    Zeng, Jian
    [J]. FRONTIERS IN ONCOLOGY, 2023, 13
  • [29] Efficacy and safety of trastuzumab emtansine in older patients with HER2-positive advanced breast cancer: a real-world study
    Cil, Ibrahim
    Kucukarda, Ahmet
    Atci, Muhammed Mustafa
    Secmeler, Saban
    Paksoy, Nail
    Ferhatoglu, Ferhat
    Ak, Naziye
    Ayhan, Murat
    Ozyukseler, Deniz Tataroglu
    Onder, Arif Hakan
    Avci, Okan
    Oyman, Abdilkerim
    Okten, Ilker Nihat
    Gulturk, Ilkay
    Akagunduz, Baran
    Basoglu, Tugba
    Cakir, Emre
    Hacibekiroglu, Ilhan
    Ozcelik, Melike
    Aydiner, Adnan
    [J]. TUMORI JOURNAL, 2022, 108 (01): : 19 - 25
  • [30] Efficacy and safety of the combination of lapatinib plus capecitabine for HER2-positive advanced breast cancer.
    Aravantino-Fatorou, E.
    Christodoulou, C.
    Nikolakopoulou, A.
    Galani, E.
    Klouvas, G.
    Acholos, V.
    Karapanagiotidis, G.
    Batziou, E.
    Tsakalos, G.
    Skarlos, D.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)