Maintenance chemotherapy after 6 cycles of platinum-doublet regimen in anthracycline-and taxane-pretreated metastatic breast cancer

被引:2
作者
Joung, Eun Kyo [1 ]
Yang, Ji Hyun [2 ]
Oh, Sooeun [3 ,4 ]
Park, Se Jun [5 ]
Lee, Jieun [4 ,5 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Internal Med, Seoul, South Korea
[2] Catholic Univ Korea, Coll Med, Dept Internal Med, Div Med Oncol,Uijeongbu St Marys Hosp, Uijongbu, South Korea
[3] Catholic Univ Korea, Dept Hosp Pathol, Coll Med, Seoul, South Korea
[4] Catholic Univ Korea, Canc Res Inst, Seoul, South Korea
[5] Catholic Univ Korea, Coll Med, Dept Internal Med, Div Med Oncol,Seoul St Marys Hosp, 222 Banpo Daero, Seoul 06591, South Korea
关键词
Breast neoplasms; Cisplatin; Maintenance chemotherapy; PLUS CISPLATIN; PHASE-II; GEMCITABINE; CAPECITABINE; MULTICENTER; PACLITAXEL; THERAPY; TRIAL;
D O I
10.3904/kjim.2019.129
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: Sequential monotherapy is recommended for anthracycline-and taxane-resistant metastatic breast cancer (MBC), but combination chemotherapy is considered in patients with visceral crisis. Cisplatin-doublet chemotherapy is a combination regimen for MBC, but prolonged treatment is challenging because of toxicity. We analyzed the role of single-agent maintenance chemotherapy after cisplatin-doublet chemotherapy for MBC. Methods: From January 2011 to December 2017, 96 anthracycline-and taxane-resistant MBC patients were retrospectively reviewed, and 49 patients with a sustained clinical benefit during the initial 6 cycles of cisplatin-doublet chemotherapy were enrolled for study. Patients were treated with gemcitabine-cisplatin (gemcitabine, 1,250 mg/m(2), intravenously [IV], days 1 to 8; cisplatin 60 mg/m(2), IV, day 1) or capecitabine-cisplatin (capecitabine 2,500 mg/m(2), orally, days 1 to 14; cisplatin 60 mg/m(2), IV, day 1) during the induction period. After 6 cycles, 16 patients were switched to single-maintenance treatment (gemcitabine or capecitabine) and the doublet regimen was continued in 24 patients. Survival outcomes (progression-free survival [PFS] and overall survival [OS]) were analyzed. Results: Among the 49 patients who showed a clinical benefit during cisplatin-doublet therapy, 24 were maintained on the doublet regimen, 16 were switched to single-maintenance treatment, and chemotherapy was suspended until disease progression in nine patients. The single-maintenance chemotherapy group showed superior survival than the chemotherapy holiday and doublet regimen groups (median PFS 15.43 months vs. 8.37 and 10.67 months, respectively, p = 0.008; median OS 43.67 months vs. 22.17 and 22.33 months, respectively, p = 0.014). Conclusions: Patients showing a clinical benefit during 6 cisplatin-doublet chemotherapy cycles may have a sustained survival benefit from single-maintenance chemotherapy.
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页码:182 / +
页数:15
相关论文
共 17 条
[1]   4th ESO-ESMO International Consensus Guidelines for Advanced Breast Cancer (ABC 4) [J].
Cardoso, F. ;
Senkus, E. ;
Costa, A. ;
Papadopoulos, E. ;
Aapro, M. ;
Andre, F. ;
Harbeck, N. ;
Aguilar Lopez, B. ;
Barrios, C. H. ;
Bergh, J. ;
Biganzoli, L. ;
Boers-Doers, C. B. ;
Cardoso, M. J. ;
Carey, L. A. ;
Cortes, J. ;
Curigliano, G. ;
Dieras, V. ;
El Saghir, N. S. ;
Eniu, A. ;
Fallowfield, L. ;
Francis, P. A. ;
Gelmon, K. ;
Johnston, S. R. D. ;
Kaufmann, B. ;
Koppikar, S. ;
Krop, I. E. ;
Mayer, M. ;
Nakigudde, G. ;
Offersen, B. V. ;
Ohno, S. ;
Pagani, O. ;
Paluch-Shimon, S. ;
Penault-Llorca, F. ;
Prat, A. ;
Rugo, H. S. ;
Sledge, G. W. ;
Spence, D. ;
Thomssen, C. ;
Vorobiof, D. A. ;
Xu, B. ;
Norton, L. ;
Winer, E. P. .
ANNALS OF ONCOLOGY, 2018, 29 (08) :1634-1657
[2]   Maintenance Chemotherapy for Advanced Non-Small-Cell Lung Cancer: New Life for an Old Idea [J].
Gerber, David E. ;
Schiller, Joan H. .
JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (08) :1009-1020
[3]  
Gnant, 2017, LANCET, V389, P1134
[4]   Cisplatin plus gemcitabine versus paclitaxel plus gemcitabine as first-line therapy for metastatic triple-negative breast cancer (CBCSG006): a randomised, open-label, multicentre, phase 3 trial [J].
Hu, Xi-Chun ;
Zhang, Jian ;
Xu, Bing-He ;
Cai, Li ;
Ragaz, Joseph ;
Wang, Zhong-Hua ;
Wang, Bi-Yun ;
Teng, Yue-E ;
Tong, Zhong-Sheng ;
Pan, Yue-Yin ;
Yin, Yong-Mei ;
Wu, Chang-Ping ;
Jiang, Ze-Fei ;
Wang, Xiao-Jia ;
Lou, Gu-Yin ;
Liu, Dong-Geng ;
Feng, Ji-Feng ;
Luo, Jian-Feng ;
Sun, Kang ;
Gu, Ya-Jia ;
Wu, Jiong ;
Shao, Zhi-Min .
LANCET ONCOLOGY, 2015, 16 (04) :436-446
[5]  
Kim Jung Hwan, 2008, Cancer Res Treat, V40, P101, DOI 10.4143/crt.2008.40.3.101
[6]  
Kohail H, 2012, Hematol Oncol Stem Cell Ther, V5, P42, DOI 10.5144/1658-3876.2012.42
[7]   Capecitabine and cisplatin (XP) combination systemic chemotherapy in heavily pre-treated HER2 negative metastatic breast cancer [J].
Lee, Jieun ;
Kim, Hyun Ho ;
Ro, Sang Mi ;
Yang, Ji Hyun .
PLOS ONE, 2017, 12 (02)
[8]   A phase II study of capecitabine plus cisplatin in metastatic triple-negative breast cancer patients pretreated with anthracyclines and taxanes [J].
Li, Qiao ;
Li, Qing ;
Zhang, Pin ;
Yuan, Peng ;
Wang, Jiayu ;
Ma, Fei ;
Luo, Yang ;
Fan, Ying ;
Cai, Ruigang ;
Xu, Binghe .
CANCER BIOLOGY & THERAPY, 2015, 16 (12) :1746-1753
[9]   HER2-positive breast cancer [J].
Loibl, Sibylle ;
Gianni, Luca .
LANCET, 2017, 389 (10087) :2415-2429
[10]  
Martin M, 2001, Clin Breast Cancer, V2, P190, DOI 10.3816/CBC.2001.n.022