Efficacy of biological agents in metastatic triple-negative breast cancer

被引:56
作者
Bramati, Annalisa [1 ]
Girelli, Serena [1 ]
Torri, Valter [2 ]
Farina, Gabriella [1 ]
Galfrascoli, Elena [1 ]
Piva, Sheila [1 ]
Moretti, Anna [1 ]
Dazzani, Maria Chiara [1 ]
Sburlati, Paola [1 ]
La Verde, Nicla Maria [1 ]
机构
[1] Fatebenefratelli Oftalm, Dept Oncol, I-20121 Milan, Italy
[2] IRCCS Ist Ric Farmacol Mario, Lab Methodol Biomed Res, Dept Oncol, I-20156 Milan, Italy
关键词
Biological agents (BA); Metastatic triple-negative; breast cancer (mTNBC); Bevacizumab; GROWTH-FACTOR RECEPTOR; 1ST-LINE TREATMENT; PHASE-III; PROGESTERONE-RECEPTOR; ESTROGEN-RECEPTOR; DOUBLE-BLIND; COMBINATION; BEVACIZUMAB; PLACEBO; EXPRESSION;
D O I
10.1016/j.ctrv.2014.01.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Metastatic triple-negative breast cancer (mTNBC) represents 15% of invasive breast cancers. Prognosis is poor, and there is no specific target therapy but biological agents combined with chemotherapy may be effective. To assess the role of biological agents in metastatic triple-negative breast cancer we performed a systematic review of phase III randomized controlled trials published from January 2006 to February 2013 and presentations at ESMO, ASCO, and SABCS congresses in 2010-2012. We consulted PubMed and ClinicalTrials.gov. Only studies comparing biological agents and chemotherapy versus chemotherapy alone were considered. Relevant statistical variables were log of the hazard ratio and relative variance for progression-free survival (PFS) and overall survival (OS). Of 353 PubMed publications and 229 studies registered on ClinicalTrials.gov, 10 trials were selected and 5293 patients were analyzed: 1546 had mTNBC. Biological agents considered were bevacizumab, sunitinib, sorafenib, lapatinib, iniparib and cetuximab. In addition, a meta analysis of the four studies containing bevacizumab was performed and it showed a PFS improvement with a relative risk reduction of 35% (95% CI: 25-43%). No effect on OS was observed. No PFS and OS benefit was detected with the other agents. No improvement of OS was detected in patients treated with biological agents plus chemotherapy, while a significant PFS improvement was observed only for bevacizumab and cetuximab. The overall impact of these agents on patient survival was not as great as expected, probably because the molecular basis of this illness needs to be better understood so that treatment can be more appropriately tailored. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:605 / 613
页数:9
相关论文
共 43 条
[1]
Abrams TJ, 2003, MOL CANCER THER, V2, P1011
[2]
[Anonymous], J CLIN ONCOL
[3]
Baselga J, 2013, J CLIN ONCOL
[4]
Sorafenib in Combination With Capecitabine: An Oral Regimen for Patients With HER2-Negative Locally Advanced or Metastatic Breast Cancer [J].
Baselga, Jose ;
Martins Segalla, Jose Getulio ;
Roche, Henri ;
del Giglio, Auro ;
Pinczowski, Helio ;
Ciruelos, Eva M. ;
Cabral Filho, Sebastiao ;
Gomez, Patricia ;
Van Eyll, Brigitte ;
Bermejo, Begona ;
Llombart, Antonio ;
Garicochea, Bernardo ;
Climent Duran, Miguel Angel ;
Gehm Hoff, Paulo Marcelo ;
Espie, Marc ;
Junior Gemeinder de Moraes, Andre Augusto ;
Ribeiro, Ronaldo Albuquerque ;
Mathias, Clarissa ;
Gil Gil, Miguel ;
Ojeda, Belen ;
Morales, Josefa ;
Ro, Sunhee Kwon ;
Li, Shell ;
Costa, Frederico .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (13) :1484-1491
[5]
Phase II Genomics Study of Ixabepilone as Neoadjuvant Treatment for Breast Cancer [J].
Baselga, Jose ;
Zambetti, Milvia ;
Llombart-Cussac, Antoni ;
Manikhas, Georgy ;
Kubista, Ernst ;
Steger, Guenther G. ;
Makhson, Anatoly ;
Tjulandin, Sergei ;
Ludwig, Heinz ;
Verrill, Mark ;
Ciruelos, Eva ;
Egyhazi, Suzanne ;
Xu, Li-An ;
Zerba, Kim E. ;
Lee, Hyerim ;
Clark, Edwin ;
Galbraith, Susan .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (04) :526-534
[6]
Descriptive analysis of estrogen receptor (ER)negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype - A population-based study from the California Cancer Registry [J].
Bauer, Katrina R. ;
Brown, Monica ;
Cress, Rosemary D. ;
Parise, Carol A. ;
Caggiano, Vincent .
CANCER, 2007, 109 (09) :1721-1728
[7]
First-Line Treatment of Advanced Breast Cancer With Sunitinib in Combination With Docetaxel Versus Docetaxel Alone: Results of a Prospective, Randomized Phase III Study [J].
Bergh, Jonas ;
Bondarenko, Igor M. ;
Lichinitser, Mikhail R. ;
Liljegren, Annelie ;
Greil, Richard ;
Voytko, Nataliya L. ;
Makhson, Anatoly N. ;
Cortes, Javier ;
Lortholary, Alain ;
Bischoff, Joachim ;
Chan, Arlene ;
Delaloge, Suzette ;
Huang, Xin ;
Kern, Kenneth A. ;
Giorgetti, Carla .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (09) :921-929
[8]
Effect of adding gefitinib to neoadjuvant chemotherapy in estrogen receptor negative early breast cancer in a randomized phase II trial [J].
Bernsdorf, Mogens ;
Ingvar, Christian ;
Jorgensen, Leif ;
Tuxen, Malgorzata K. ;
Jakobsen, Erik H. ;
Saetersdal, Anna ;
Kimper-Karl, Marie Louise ;
Kroman, Niels ;
Balslev, Eva ;
Ejlertsen, Bent .
BREAST CANCER RESEARCH AND TREATMENT, 2011, 126 (02) :463-470
[9]
Molecular classification and molecular forecasting of breast cancer: Ready for clinical application? [J].
Brenton, JD ;
Carey, LA ;
Ahmed, AA ;
Caldas, C .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (29) :7350-7360
[10]
Detecting an Overall Survival Benefit that Is Derived From Progression-Free Survival [J].
Broglio, Kristine R. ;
Berry, Donald A. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2009, 101 (23) :1642-1649