Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer: Updated survival in the TAX 327 study

被引:881
作者
Berthold, Dominik R.
Pond, Gregory R.
Soban, Freidele
de Wit, Ronald
Eisenberger, Mario
Tannock, Ian F.
机构
[1] Princess Margaret Hosp, Toronto, ON M5G 2M9, Canada
[2] Univ Toronto, Toronto, ON, Canada
[3] Erasmus Univ, Med Ctr, Rotterdam, Netherlands
[4] Johns Hopkins Univ, Sydney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
关键词
D O I
10.1200/JCO.2007.12.4008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The TAX 327 study compared docetaxel administered every 3 weeks (D3), weekly docetaxel (D1), and mitoxantrone (M), each with prednisone (P), in 1,006 men with metastatic hormone-resistant prostate cancer (HRPC). The original analysis, undertaken in August 2003 when 557 deaths had occurred, showed significantly better survival and response rates for pain, prostate-specific antigen (PSA), and quality of life for D3P when compared with MP. Here, we report an updated analysis of survival. Methods Investigators were asked to provide the date of death or last follow-up for all participants who were alive in August 2003. Results By March 2007, data on 310 additional deaths were obtained (total = 867 deaths). The survival benefit of D3P compared with MP has persisted with extended follow-up (P = .004). Median survival time was 19.2 months (95% CI, 17.5 to 21.3 months) in the D3P arm, 17.8 months (95% CI, 16.2 to 19.2 months) in the D1P arm, and 16.3 months (95% CI, 14.3 to 17.9 months) in the MP arm. More patients survived >= 3 years in the D3P and D1P arms (18.6% and 16.6%, respectively) compared with the MP arm (13.5%). Similar trends in survival between treatment arms were seen for men greater than and less than 65 years of age, for those with and without pain at baseline, and for those with baseline PSA greater than and less than the median value of 115 ng/mL. Conclusion The present analysis confirms that survival of men with metastatic HRPC is significantly longer after treatment with D3P than with MP. Consistent results are observed across subgroups of patients.
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页码:242 / 245
页数:4
相关论文
共 7 条
  • [1] BERTHOLD DR, IN PRESS CLIN CANC R
  • [2] Measuring quality of life in men with prostate cancer using the functional assessment of cancer therapy prostate instrument
    Esper, P
    Mo, F
    Chodak, G
    Sinner, M
    Cella, D
    Pienta, KJ
    [J]. UROLOGY, 1997, 50 (06) : 920 - 928
  • [3] Hydrocortisone with or without mitoxantrone in men with hormone-refractory prostate cancer: Results of the Cancer and Leukemia Group B 9182 study
    Kantoff, PW
    Halabi, S
    Conaway, M
    Picus, J
    Kirshner, J
    Hars, V
    Trump, D
    Winer, EP
    Vogelzang, NJ
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (08) : 2506 - 2513
  • [4] MCGILL PAIN QUESTIONNAIRE - MAJOR PROPERTIES AND SCORING METHODS
    MELZACK, R
    [J]. PAIN, 1975, 1 (03) : 277 - 299
  • [5] Docetaxel and estramustine compared with mitoxantrone and prednisone for advanced refractory prostate cancer
    Petrylak, DP
    Tangen, CM
    Hussain, MHA
    Lara, PN,J
    Jones, JA
    Taplin, ME
    Burch, PA
    Berry, D
    Moinpour, C
    Kohli, M
    Benson, MC
    Small, EJ
    Raghavan, D
    Crawford, ED
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (15) : 1513 - 1520
  • [6] Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: A Canadian randomized trial with palliative end points
    Tannock, IF
    Osoba, D
    Stockler, MR
    Ernst, DS
    Neville, AJ
    Moore, MJ
    Armitage, GR
    Wilson, JJ
    Venner, PM
    Coppin, CML
    Murphy, KC
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (06) : 1756 - 1764
  • [7] Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer
    Tannock, IF
    de Wit, R
    Berry, WR
    Horti, J
    Pluzanska, A
    Chi, KN
    Oudard, S
    Theodore, C
    James, ND
    Turesson, I
    Rosenthal, MA
    Eisenberger, MA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (15) : 1502 - 1512