The use of trastuzumab in the treatment of hormone refractory prostate cancer; phase II trial

被引:128
作者
Ziada, A
Barqawi, A
Glode, LM
Varella-Garcia, M
Crighton, F
Majeski, S
Rosenblum, M
Kane, M
Chen, L
Crawford, ED
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Med, Div Med Oncol, Denver, CO 80262 USA
[2] Anschutz Canc Pavil, Aurora, CO USA
[3] Denver VA Med Ctr, Denver, CO USA
关键词
prostate; cancer; trastuzumab; HER-2; receptor;
D O I
10.1002/pros.20065
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PURPOSE. To investigate the efficacy and toxicity of the antibody to the HER-2/neu receptor (trastuzumab, Herceptin(R)) in the treatment of advanced hormone-refractory prostate cancer (HRPC). MATERIALS AND METHODS. Eighteen patients with HRPC were recruited for this phase 11 trial in which they received trastuzumab for 12 weeks or until disease progression or unacceptable toxicity was documented. HER-2 receptor overexpression was evaluated using immunohistochemistry (IHC) and dual-color fluorescence in-situ hybridization (FISH) assays. RESULTS. Trastuzumab as a single agent demonstrated little efficacy in treating HRPC. Two patients demonstrated stable disease based on a decrease in PSA level to less than 50% of baseline. No patient demonstrated a regression of radiographic bony or soft tissue metastatic disease. The medication was well tolerated in 16 patients (89%), and 2 patients (11%) had to be hospitalized for cardiac complications. CONCLUSIONS. Trastuzumab (Herceptin(R)) as a single agent demonstrated poor efficacy in treating HRPC. Based on promising results in treating breast cancer with regimens using Herceptin(R) and cytotoxic agents, a similar combination approach might demonstrate better efficacy in treating HRPC. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:332 / 337
页数:6
相关论文
共 26 条
[1]  
Agus DB, 1999, CANCER RES, V59, P4761
[2]  
Bubendorf L, 1999, CANCER RES, V59, P803
[3]   Docetaxel (Taxotere) plus trastuzumab (Herceptin) in breast cancer [J].
Burris, HA .
SEMINARS IN ONCOLOGY, 2001, 28 (01) :38-44
[4]   Multinational study of the efficacy and safety of humanized anti-HER2 monoclonal antibody in women who have HER2-overexpressing metastatic breast cancer that has progressed after chemotherapy for metastatic disease [J].
Cobleigh, MA ;
Vogel, CL ;
Tripathy, D ;
Robert, NJ ;
Scholl, S ;
Fehrenbacher, L ;
Wolter, JM ;
Paton, V ;
Shak, S ;
Lieberman, G ;
Slamon, DJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) :2639-2648
[5]   TYROSINE KINASE RECEPTOR WITH EXTENSIVE HOMOLOGY TO EGF RECEPTOR SHARES CHROMOSOMAL LOCATION WITH NEU ONCOGENE [J].
COUSSENS, L ;
YANGFENG, TL ;
LIAO, YC ;
CHEN, E ;
GRAY, A ;
MCGRATH, J ;
SEEBURG, PH ;
LIBERMANN, TA ;
SCHLESSINGER, J ;
FRANCKE, U ;
LEVINSON, A ;
ULLRICH, A .
SCIENCE, 1985, 230 (4730) :1132-1139
[6]   DOWN-MODULATION OF AN ONCOGENE PROTEIN PRODUCT AND REVERSION OF THE TRANSFORMED PHENOTYPE BY MONOCLONAL-ANTIBODIES [J].
DREBIN, JA ;
LINK, VC ;
STERN, DF ;
WEINBERG, RA ;
GREENE, MI .
CELL, 1985, 41 (03) :695-706
[7]  
DREBIN JA, 1988, ONCOGENE, V2, P387
[8]   Phase II study of weekly docetaxel and trastuzumab for patients with HER-2-overexpressing metastatic breast cancer [J].
Esteva, FJ ;
Valero, V ;
Booser, D ;
Guerra, LT ;
Murray, JL ;
Pusztai, L ;
Cristofanilli, M ;
Arun, B ;
Esmaeli, B ;
Fritsche, HA ;
Sneige, N ;
Smith, TL ;
Hortobagyi, GN .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (07) :1800-1808
[9]   MONOCLONAL-ANTIBODIES DIRECTED TO THE ERBB-2 RECEPTOR INHIBIT IN-VIVO TUMOR-CELL GROWTH [J].
HARWERTH, IM ;
WELS, W ;
SCHLEGEL, J ;
MULLER, M ;
HYNES, NE .
BRITISH JOURNAL OF CANCER, 1993, 68 (06) :1140-1145
[10]   P185HER2 MONOCLONAL-ANTIBODY HAS ANTIPROLIFERATIVE EFFECTS INVITRO AND SENSITIZES HUMAN-BREAST TUMOR-CELLS TO TUMOR NECROSIS FACTOR [J].
HUDZIAK, RM ;
LEWIS, GD ;
WINGET, M ;
FENDLY, BM ;
SHEPARD, HM ;
ULLRICH, A .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (03) :1165-1172