Gene expression profiling of breast cancer patients treated with docetaxel, doxorubicin, and cyclophosphamide within the GEPARTRIO trial:: HER-2, but not topoisomerase II alpha and microtubule-associated protein tau, is highly predictive of tumor response

被引:56
作者
Rody, A. [1 ]
Karn, T. [1 ]
Gaetje, R. [1 ]
Ahr, A. [1 ]
Solbach, C. [1 ]
Kourtis, K. [1 ]
Munnes, M. [2 ]
Loibl, S. [1 ]
Kissler, S. [1 ]
Ruckhaeberle, E. [1 ]
Holtrich, U. [1 ]
von Minckwitz, G. [1 ,3 ]
Kaufmann, M. [1 ]
机构
[1] Univ Frankfurt, Dept Obstet & Gynecol, D-60590 Frankfurt, Germany
[2] Bayer HealthCare, Diagnost Res, Leverkusen, Germany
[3] German Breast Grp, Neu Isenburg, Germany
关键词
neoadjuvant chemotherapy; breast cancer; gene expression; predictive factors;
D O I
10.1016/j.breast.2006.06.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gene expression analysis in breast cancer patients undergoing neoadjuvant chemotherapy is an interesting tool. for identification of gene signatures and new markers to predict tumor response. However, the detection of predictive markers strongly depends on the drugs used in the specific therapeutic setting. There is growing evidence that topoisomerase II-alpha (TOPO II alpha) is a marker for anthracycline-, and microtubule-associated protein tau (MAPT) for taxane sensitivity. HER-2 has been described as a marker of both anthracycline and taxane sensitivity. We performed gene expression profiling of 50 patients within the GEPARTRIO study, an anthracycline and taxane neoadjuvant chemotherapy trial. Here we investigate the predictive value of TOPO II alpha, MAPT and HER-2 mRNA expression for pathological complete response (pCR) in this setting. Interestingly, HER-2 gene expression was strongly predictive of pCR (P = 0.017) as well as overall response (P = 0.037) and clinical complete response (cCR, P = 0.050). In contrast, for both TOPO II alpha and MAPT no correlation with pCR was observed in our sample group. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:86 / 93
页数:8
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