Anthracycline rechallenge using pegylated liposomal doxorubicin in patients with metastatic breast cancer: a pooled analysis using individual data from four prospective trials

被引:24
作者
Al-Batran, S-E [1 ,2 ]
Guentner, M. [3 ]
Pauligk, C. [1 ,2 ]
Scholz, M. [3 ]
Chen, R. [4 ]
Beiss, B. [4 ]
Stopatschinskaja, S. [4 ]
Lerbs, W. [1 ,2 ]
Harbeck, N. [5 ]
Jaeger, E. [1 ,2 ]
机构
[1] Klin Onkol & Hamatol, D-60488 Frankfurt, Germany
[2] Krankenhaus NW Frankfurt, D-60488 Frankfurt, Germany
[3] Trium Anal Online GmbH, Munich, Germany
[4] Merck, Kenilworth, NJ USA
[5] Univ Cologne, Breast Ctr, Cologne, Germany
关键词
pegylated liposomal doxorubicin; metastatic breast cancer; anthracycline; rechallenge; MULTICENTER PHASE-II; 1ST-LINE TREATMENT; PREDICTIVE FACTORS; LINE CHEMOTHERAPY; CLINICAL BENEFIT; CAPECITABINE; DOCETAXEL; CARDIOTOXICITY; GEMCITABINE; COMBINATION;
D O I
10.1038/sj.bjc.6605961
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUND: The aim of this study was to determine the activity of anthracycline rechallenge using pegylated liposomal doxorubicin (PLD) in patients with metastatic breast cancer (MBC) previously treated with conventional anthracyclines. METHODS: Pooled individual data from four prospective trials were used, and the primary end point of the pooled analysis was clinical benefit rate (CBR). The studies comprised 935 patients, of whom 274 had received PLD in the metastatic setting after prior exposure to conventional anthracyclines (rechallenge population). RESULTS: The majority of patients were heavily pretreated. Previous anthracycline therapy was administered in the adjuvant (14%) or metastatic setting (46%), or both (40%). The overall CBR from rechallenge with PLD was 37.2% (95% CI, 32.4-42.0). In univariate analyses, the CBR was significantly higher in patients with less exposure to prior chemotherapy, in taxane-naive patients, and in patients with a favourable Eastern Cooperative Group performance status of 0 vs 1 vs 2 (53.3 vs 35.5 vs 18.2%; P<0.001). In multivariate analyses, performance status proved to be the only independent predictor of the CBR achieved with PLD rechallenge (P=0.038). There was no statistically significant difference in CBR regarding the setting, cumulative dose of and/or resistance to prior anthracyclines, or time since prior anthracycline administration. CONCLUSION: Anthracycline rechallenge using PLD is effective in patients with MBC who have a favourable performance status, regardless of setting, resistance, cumulative dose or time since prior conventional anthracycline therapy. British Journal of Cancer (2010) 103, 1518-1523. doi:10.1038/sj.bjc.6605961 www.bjcancer.com Published online 26 October 2010 (C) 2010 Cancer Research UK
引用
收藏
页码:1518 / 1523
页数:6
相关论文
共 41 条
[1]
Sample size tables for exact single-stage phase II designs [J].
A'Hern, RP .
STATISTICS IN MEDICINE, 2001, 20 (06) :859-866
[2]
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[3]
The clinical benefit of pegylated liposomal doxorubicin in patients with metastatic breast cancer previously treated with conventional anthracyclines: a multicentre phase II trial [J].
Al-Batran, S. -E. ;
Bischoff, J. ;
von Minckwitz, G. ;
Atmaca, A. ;
Kleeberg, U. ;
Meuthen, I. ;
Morack, G. ;
Lerbs, W. ;
Hecker, D. ;
Sehouli, J. ;
Knuth, A. ;
Jager, E. .
BRITISH JOURNAL OF CANCER, 2006, 94 (11) :1615-1620
[4]
Reduced incidence of severe palmar-plantar erythrodysesthesia and mucositis in a prospective multicenter phase II trial with pegylated liposomal doxorubicin at 40 mg/m2 every 4 weeks in previously treated patients with metastatic breast cancer [J].
Al-Batran, SE ;
Meerpohl, HG ;
von Minckwitz, G ;
Atmaca, A ;
Kleeberg, U ;
Harbeck, N ;
Lerbs, W ;
Hecker, D ;
Sehouli, J ;
Knuth, A ;
Jager, E .
ONCOLOGY, 2006, 70 (02) :141-146
[5]
Third consensus on medical treatment of metastatic breast cancer [J].
Beslija, S. ;
Bonneterre, J. ;
Burstein, H. J. ;
Cocquyt, V. ;
Gnant, M. ;
Heinemann, V. ;
Jassem, J. ;
Koestler, W. J. ;
Krainer, M. ;
Menard, S. ;
Petit, T. ;
Petruzelka, L. ;
Possinger, K. ;
Schmid, P. ;
Stadtmauer, E. ;
Stockler, M. ;
Van Belle, S. ;
Vogel, C. ;
Wilcken, N. ;
Wiltschke, C. ;
Zielinski, C. C. ;
Zwierzina, H. .
ANNALS OF ONCOLOGY, 2009, 20 (11) :1771-1785
[6]
Phase II trial of capecitabine and weekly paclitaxel as first-line therapy for metastatic breast cancer [J].
Blum, Joanne L. ;
Dees, E. Claire ;
Chacko, Aparna ;
Doane, Lisa ;
Ethirajan, Sukumar ;
Hopkins, Judith ;
McMahon, Richard ;
Merten, Suzan ;
Negron, Angel ;
Neubauer, Marcus ;
Ilegbodu, Des ;
Boehm, Kristi A. ;
Asmar, Lina ;
O'Shaughnessy, Joyce A. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (27) :4384-4390
[7]
Locally recurrent or metastatic breast cancer: ESMO Clinical Recommendations for diagnosis, treatment and follow-up [J].
Cardoso, F. ;
Castiglione, M. .
ANNALS OF ONCOLOGY, 2009, 20 :15-18
[8]
International Guidelines for Management of Metastatic Breast Cancer: Combination vs Sequential Single-Agent Chemotherapy [J].
Cardoso, Fatima ;
Bedard, Philippe L. ;
Winer, Eric P. ;
Pagani, Olivia ;
Senkus-Konefka, Elzbieta ;
Fallowfield, Lesley J. ;
Kyriakides, Stella ;
Costa, Alberto ;
Cufer, Tanja ;
Albain, Kathy S. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2009, 101 (17) :1174-1181
[9]
Gemcitabine and capecitabine in previously anthracycline-treated metastatic breast cancer: a multicenter phase II study (SOLTI 0301 trial) [J].
Ciruelos, E. M. ;
Cortes, J. ;
Cortes-Funes, H. ;
Mayordomo, J. I. ;
Bermejo, B. ;
Ojeda, B. ;
Garcia, E. ;
Rodriguez, C. A. ;
Munoz, M. ;
Gomez, P. ;
Manso, L. ;
Andres, R. ;
Lluch, A. ;
Saura, C. ;
Mendiola, C. ;
Baselga, J. .
ANNALS OF ONCOLOGY, 2010, 21 (07) :1442-1447
[10]
Estimates of the cancer incidence and mortality in Europe in 2006 [J].
Ferlay, J. ;
Autier, P. ;
Boniol, M. ;
Heanue, M. ;
Colombet, M. ;
Boyle, P. .
ANNALS OF ONCOLOGY, 2007, 18 (03) :581-592