Docetaxel and exisulind in hormone-refractory prostate cancer

被引:12
作者
Ryan, CW [1 ]
Stadler, WM [1 ]
Vogelzang, NJ [1 ]
机构
[1] Univ Chicago, Dept Med, Hematol Oncol Sect, Chicago, IL 60637 USA
关键词
D O I
10.1053/sonc.2001.26903
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Single-agent docetaxel has been shown to produce a significant decrease in prostate-specific antigen (PSA) levels among patients with hormone-refractory prostate cancer (HRPC). A recent study also showed that exisulind, a sulfone metabolite of the nonsteroidal anti-inflammatory drug sulindac, lengthens the median PSA doubling time in men who had increasing PSA levels after radical prostatectomy. Furthermore, exisulind has shown significant antineoplastic activity in prostate cancer cell lines in vitro and in nude mouse xenograft models. Because preclinical studies have suggested synergistic interactions between docetaxel and exisulind, a phase I/II clinical trial combining these agents has been initiated in patients with HRPC. The primary objective of this study is to determine PSA response and measurable disease response rate of the combination therapy; secondary objectives include toxicity assessment and determination of time to disease progression, duration of response, and overall survival. Accrual is ongoing. Copyright © 2001 by W.B. Saunders Company.
引用
收藏
页码:56 / 61
页数:6
相关论文
共 30 条
[1]   Eligibility and response guidelines for phase II clinical trials in androgen-independent prostate cancer: Recommendations from the prostate-specific antigen working group [J].
Bubley, GJ ;
Carducci, M ;
Dahut, W ;
Dawson, N ;
Daliani, D ;
Eisenberger, M ;
Figg, WD ;
Freidlin, B ;
Halabi, S ;
Hudes, G ;
Hussain, M ;
Kaplan, R ;
Myers, C ;
Oh, W ;
Petrylak, DP ;
Reed, E ;
Roth, B ;
Sartor, O ;
Scher, H ;
Simons, J ;
Sinibaldi, V ;
Small, EJ ;
Smith, MR ;
Trump, DL ;
Vollmer, R ;
Wilding, G .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (11) :3461-3467
[2]  
CHAN D, 1999, P AN M AM SOC CLIN, V18, pA488
[3]  
CHAN DC, 2000, 9 WORLD C LUNG CANC
[4]  
Friedland D, 1999, SEMIN ONCOL, V26, P19
[5]   TREATMENT OF COLONIC AND RECTAL ADENOMAS WITH SULINDAC IN FAMILIAL ADENOMATOUS POLYPOSIS [J].
GIARDIELLO, FM ;
HAMILTON, SR ;
KRUSH, AJ ;
PIANTADOSI, S ;
HYLIND, LM ;
CELANO, P ;
BOOKER, SV ;
ROBINSON, CR ;
OFFERHAUS, GJA .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (18) :1313-1316
[6]   Exsulind (sulindac sulfone) suppresses growth of human prostate cancer in a nude mouse xenograft model by increasing apoptosis [J].
Goluboff, ET ;
Shabsigh, A ;
Saidi, JA ;
Weinstein, IB ;
Mitra, N ;
Heitjan, D ;
Piazza, GA ;
Pamukcu, R ;
Buttyan, R ;
Olsson, CA .
UROLOGY, 1999, 53 (02) :440-445
[7]  
GOLUBOFF ET, 2000, J UROLOGY, V163, P705
[8]   Cancer statistics, 2001 [J].
Greenlee, RT ;
Hill-Harmon, MB ;
Murray, T ;
Thun, M .
CA-A CANCER JOURNAL FOR CLINICIANS, 2001, 51 (01) :15-36
[9]   INACTIVATION OF BCL-2 BY PHOSPHORYLATION [J].
HALDAR, S ;
JENA, N ;
CROCE, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (10) :4507-4511
[10]  
Haldar S, 1996, CANCER RES, V56, P1253