Progression-Free Survival as a Predictor of Overall Survival in Men With Castrate-Resistant Prostate Cancer

被引:87
作者
Halabi, Susan [1 ]
Vogelzang, Nicholas J.
Ou, San-San
Owzar, Kouros
Archer, Laura
Small, Eric J.
机构
[1] Duke Univ, Med Ctr, Dept Biostat & Bioinformat, Durham, NC 27705 USA
关键词
LEUKEMIA GROUP-B; PHASE-II; CLINICAL-TRIALS; WORKING GROUP; END-POINTS; DOCETAXEL; ESTRAMUSTINE; MITOXANTRONE; CARCINOMA; ANTIGEN;
D O I
10.1200/JCO.2008.18.9159
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To explore whether progression-free survival (PFS) or biochemical PFS can be used as a predictor of overall survival (OS) and to investigate the dependence between PFS and OS in men with castrate-resistant prostate cancer. Patients and Methods Data from nine Cancer and Leukemia Group B trials that enrolled 1,296 men from 1991 to 2004 were pooled. Men were eligible if they had prostate cancer that had progressed during androgen deprivation therapy and did not receive prior treatment with chemotherapy, immunotherapy, or other nonhormonal therapy. Landmark analyses of PFS at 3 and 6 months from randomization/registration were performed to minimize lead time bias. The proportional hazards model was used to assess the significance effect of PFS rate at 3 and at 6 months in predicting OS. In addition, biochemical progression using the definitions of Prostate-Specific Antigen Working Group (PSAW) Criteria PSAWG1 and PSAWG2 were analyzed as time-dependent covariates in predicting OS. Results The median survival time among men who experienced progression at 3 months was 9.2 months (95% CI, 8.0 to 10.0 months) compared with 17.8 months in men who did not experience progression at 3 months (95% CI, 16.2 to 20.4 months; P < .0001). Compared with men who did not progress at 3 and at 6 months, the adjusted hazard ratios for death were 2.0 (95% CI, 1.7 to 2.4; P < .001) and 1.9 (95% CI, 1.6 to 2.4; P < .001) for men who experienced progression at 3 and 6 months, respectively. In addition, biochemical progression at 3 months predicted OS. The association between PFS and OS was 0.30 (95% confidence limits = 0.26, 0.32). Conclusion PFS at 3 and 6 months and biochemical progression at 3 months predict OS. These observations require prospective validation.
引用
收藏
页码:2766 / 2771
页数:6
相关论文
共 31 条
[1]   Randomised phase III study of intravenous vinorelbine plus hormone therapy versus hormone therapy alone in hormone-refractory prostate cancer [J].
Abratt, RP ;
Brune, D ;
Dirnopoulos, MA ;
Kliment, J ;
Breza, J ;
Selvaggi, FP ;
Beuzeboc, P ;
Demkow, T ;
Oudard, S .
ANNALS OF ONCOLOGY, 2004, 15 (11) :1613-1621
[2]   A test for partial correlation with censored astronomical data [J].
Akritas, MG ;
Siebert, J .
MONTHLY NOTICES OF THE ROYAL ASTRONOMICAL SOCIETY, 1996, 278 (04) :919-924
[3]   ANALYSIS OF SURVIVAL BY TUMOR RESPONSE [J].
ANDERSON, JR ;
CAIN, KC ;
GELBER, RD .
JOURNAL OF CLINICAL ONCOLOGY, 1983, 1 (11) :710-719
[4]   A contemporary prognostic nomogram for men with hormone-refractory metastatic prostate cancer: A TAX327 study analysis [J].
Armstrong, Andrew J. ;
Garrett-Mayer, Elizabeth S. ;
Yang, Yi-Chun Ou ;
de Wit, Ronald ;
Tannock, Ian F. ;
Eisenberger, Mario .
CLINICAL CANCER RESEARCH, 2007, 13 (21) :6396-6403
[5]   Prostate-specific antigen and pain surrogacy analysis in metastatic hormone-refractory prostate cancer [J].
Armstrong, Andrew J. ;
Garrett-Mayer, Elizabeth ;
Yang, Yi-Chun Ou ;
Carducci, Michael A. ;
Tannock, Ian ;
de Wit, Ronald ;
Eisenberger, Mario .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (25) :3965-3970
[6]   Low Power Memory Storage and Transfer Organization for the MPEG-4 Full Pel Motion Estimation on a Multimedia Processor [J].
Brockmeyer, Erik ;
Nachtergaele, Lode ;
Catthoor, Francky V. M. ;
Bormans, Jan ;
De Man, Hugo J. .
IEEE TRANSACTIONS ON MULTIMEDIA, 1999, 1 (02) :202-216
[7]   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
[8]   A phase 3 randomized controlled trial of the efficacy and safety of atrasentan in men with metastatic hormone-refractory prostate cancer [J].
Carducci, Michael A. ;
Saad, Fred ;
Abrahamsson, Per-Anders ;
Dearnaley, David R. ;
Schulman, Claude C. ;
North, Scott A. ;
Sleep, Darryl J. ;
Isaacson, Jeffrey D. ;
Nelson, Joel B. .
CANCER, 2007, 110 (09) :1959-1966
[9]  
COX DR, 1972, J R STAT SOC B, V187, P220
[10]   A phase II clinical trial of sorafenib in androgen-independent prostate cancer [J].
Dahut, William L. ;
Scripture, Charity ;
Posadas, Edwin ;
Jain, Lokesh ;
Gulley, James L. ;
Arlen, Philip M. ;
Wright, John J. ;
Yu, Yunkai ;
Cao, Liang ;
Steinberg, Seth M. ;
Aragon-Ching, Jeanny B. ;
Venitz, Juergen ;
Jones, Elizabeth ;
Chen, Clara C. ;
Figg, William D. .
CLINICAL CANCER RESEARCH, 2008, 14 (01) :209-214