Comparison of the efficacy and survival analysis of neoadjuvant chemotherapy for Her-2-positive breast cancer

被引:5
作者
Li, Si [1 ]
Wei, Wei [1 ]
Jiang, Yi [1 ]
Li, Qiuyun [1 ]
Huang, Qinghua [1 ]
Yang, Huawei [1 ]
Liu, Jianlun [1 ,2 ]
机构
[1] Guangxi Med Univ, Affiliated Tumor Hosp, Dept Breast Surg, 71 Hedi Rd, Nanning 530021, Guangxi, Peoples R China
[2] Guangxi Med Univ, Longdong Hosp, Dept Gen Surg, Nanning, Guangxi, Peoples R China
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2018年 / 12卷
关键词
Her-2-positive breast cancer; neoadjuvant chemotherapy; trastuzumab; efficacy; survival analysis; toxic side effects; PHASE-II; PREOPERATIVE CHEMOTHERAPY; ADJUVANT TRASTUZUMAB; CAPECITABINE; MULTICENTER; PACLITAXEL; AMPLIFICATION; EXPRESSION; DOCETAXEL; ANTIBODY;
D O I
10.2147/DDDT.S171534
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Purpose: The objective of this research was to compare the short- and long-term efficacy of the following four neoadjuvant chemotherapy (NAC) regimens: docetaxel/carboplatin/trastuzumab (TCH), docetaxel/epirubicin/cyclophosphamide (TEC), Xeloda/epirubicin/cyclophosphamide followed by Xeloda/docetaxel (XEC-XT), and 5-fluorouracil/epirubicin/cyclophosphamide followed by docetaxel (FEC-T) in human epidermal growth factor receptor-2-positive (Her-2-positive) breast cancer. Patients and methods: According to treatment preferences, 139 patients with Her-2-positive breast cancer were divided into the following four groups: 39 patients in the TCH group, 35 patients in the TEC group, 33 patients in the XEC-XT group, and 32 patients in the FEC-T group. The primary end points were disease-free survival (DFS) and 5-year overall survival (5-year OS). The secondary end points were the efficacy and toxicity of NAC. Results: The TCH, TEC, XEC-XT, and FEC-T groups demonstrated overall response rates of 87.1%, 74.3%, 75.8%, and 62.5% (P=0.031), respectively, and pathological complete response rates of 25.6%, 18.2%, 20.0%, and 18.2% (P=0.041), respectively. The DFS rates for the TCH, TEC, XEC-XT, and FEC-T groups were 84.6%, 62.9%, 65.7%, and 46.9% (P=0.01), respectively. The 5-year OS rates for the TCH, TEC, XEC-XT, and FEC-T groups were 87.2%, 69.7%, 71.4%, and 59.4% (P=0.069), respectively. The mean survival time was 59.3 months (TCH group), 53.5 months (TEiC group), 55.3 months (XEiC-XT group), and 52.4 months (FEC-T group). The difference in survival among the four groups was statistically significant (P=0.04). Conclusion: In four NAC regimens for the treatment of Her-2-positive breast cancer, the TCH group exhibited better DFS and 5-year OS. The TCH regimen significantly enhanced the pathological complete remission rate of NAC with similar side effects compared to the TEC, XEC-XT, and FEC-T regimens. In terms of long-term efficacy, the XEC-XT treatment was superior to the FEC-T and TEC treatment, and there was no significant difference between the FEC-T and TEC groups.
引用
收藏
页码:3085 / 3093
页数:9
相关论文
共 35 条
  • [1] Chemotherapy (CT) and hormonotherapy (HT) as neoadjuvant treatment in luminal breast cancer patients: results from the GEICAM/2006-03, a multicenter, randomized, phase-II study
    Alba, E.
    Calvo, L.
    Albanell, J.
    De la Haba, J. R.
    Arcusa Lanza, A.
    Chacon, J. I.
    Sanchez-Rovira, P.
    Plazaola, A.
    Lopez Garcia-Asenjo, J. A.
    Bermejo, B.
    Carrasco, E.
    Lluch, A.
    [J]. ANNALS OF ONCOLOGY, 2012, 23 (12) : 3069 - 3074
  • [2] Allred DC, 1998, MODERN PATHOL, V11, P155
  • [3] ALMASRI NM, 2005, BREAST CANCER RES, V7, P1
  • [4] Baselga J, 1998, CANCER RES, V58, P2825
  • [5] Blum JL, 2001, CANCER, V92, P1759, DOI 10.1002/1097-0142(20011001)92:7<1759::AID-CNCR1691>3.0.CO
  • [6] 2-A
  • [7] Multicenter phase II study of capecitabine in paclitaxel-refractory metastatic breast cancer
    Blum, JL
    Jones, SE
    Buzdar, AU
    LoRusso, PM
    Kuter, I
    Vogel, C
    Osterwalder, B
    Burger, HU
    Brown, CS
    Griffin, T
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (02) : 485 - 493
  • [8] The triple negative paradox: Primary tumor chemosensitivity of breast cancer subtypes
    Carey, Lisa A.
    Dees, E. Claire
    Sawyer, Lynda
    Gatti, Lisa
    Moore, Dominic T.
    Collichio, Frances
    Ollila, David W.
    Sartor, Carolyn I.
    Graham, Mark L.
    Perou, Charles M.
    [J]. CLINICAL CANCER RESEARCH, 2007, 13 (08) : 2329 - 2334
  • [9] Grading dermatologic adverse events of cancer treatments: The Common Terminology Criteria for Adverse Events Version 4.0
    Chen, Alice P.
    Setser, Ann
    Anadkat, Milan J.
    Cotliar, Jonathan
    Olsen, Elise A.
    Garden, Benjamin C.
    Lacouture, Mario E.
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2012, 67 (05) : 1025 - 1039
  • [10] New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1)
    Eisenhauer, E. A.
    Therasse, P.
    Bogaerts, J.
    Schwartz, L. H.
    Sargent, D.
    Ford, R.
    Dancey, J.
    Arbuck, S.
    Gwyther, S.
    Mooney, M.
    Rubinstein, L.
    Shankar, L.
    Dodd, L.
    Kaplan, R.
    Lacombe, D.
    Verweij, J.
    [J]. EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) : 228 - 247