Sipuleucel-T Immunotherapy for Castration-Resistant Prostate Cancer.

被引:4258
作者
Kantoff, Philip W. [1 ]
Higano, Celestia S. [2 ]
Shore, Neal D. [3 ]
Berger, E. Roy [4 ]
Small, Eric J. [5 ]
Penson, David F. [6 ]
Redfern, Charles H. [7 ]
Ferrari, Anna C. [8 ]
Dreicer, Robert [9 ]
Sims, Robert B. [10 ]
Xu, Yi [10 ]
Frohlich, Mark W. [10 ]
Schellhammer, Paul F. [11 ]
Ahmed, T.
Amin, A.
Arseneau, J.
Barth, N.
Bernstein, G.
Bracken, B.
Burch, P.
Caggiano, V.
Chin, J.
Chodak, G.
Chu, F.
Corman, J.
Curti, B.
Dawson, N.
Deeken, J. F.
Dubernet, T.
Fishman, M.
Flanigan, R.
Gailani, F.
Garbo, L.
Gardner, T.
Gelmann, E.
George, D.
Godfrey, T.
Gomella, L.
Guerra, M.
Hall, S.
Hanson, J.
Israeli, R.
Jancis, E.
Jewett, M. A. S.
Kassabian, V.
Katz, J.
Klotz, L.
Koeneman, K.
Koh, H.
Kratzke, R.
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Lank Ctr Genitourinary Oncol, Boston, MA 02115 USA
[2] Univ Washington, Sch Med, Seattle, WA USA
[3] Carolina Urol Res Ctr, Myrtle Beach, SC USA
[4] SUNY Stony Brook, Sch Med, Stony Brook, NY 11794 USA
[5] Univ Calif San Francisco, Urol Oncol Program, San Francisco, CA 94143 USA
[6] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[7] Sharp Healthcare, San Diego, CA USA
[8] NYU, Ctr Clin Canc, Langone Med Ctr, New York, NY USA
[9] Cleveland Clin, Taussig Canc Inst, Cleveland, OH 44106 USA
[10] Dendreon Corp, Seattle, WA USA
[11] Eastern Virginia Med Sch, Norfolk, VA 23501 USA
关键词
MITOXANTRONE PLUS PREDNISONE; RANDOMIZED CONTROLLED-TRIAL; SURROGATE MARKER; DENDRITIC CELLS; CLINICAL-TRIALS; PHASE-III; SURVIVAL; MEN; DOCETAXEL; LEUKEMIA;
D O I
10.1056/NEJMoa1001294
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Sipuleucel-T, an autologous active cellular immunotherapy, has shown evidence of efficacy in reducing the risk of death among men with metastatic castration-resistant prostate cancer. Methods: In this double-blind, placebo-controlled, multicenter phase 3 trial, we randomly assigned 512 patients in a 2:1 ratio to receive either sipuleucel-T (341 patients) or placebo (171 patients) administered intravenously every 2 weeks, for a total of three infusions. The primary end point was overall survival, analyzed by means of a stratified Cox regression model adjusted for baseline levels of serum prostate-specific antigen (PSA) and lactate dehydrogenase. Results: In the sipuleucel-T group, there was a relative reduction of 22% in the risk of death as compared with the placebo group (hazard ratio, 0.78; 95% confidence interval [CI], 0.61 to 0.98; P=0.03). This reduction represented a 4.1-month improvement in median survival (25.8 months in the sipuleucel-T group vs. 21.7 months in the placebo group). The 36-month survival probability was 31.7% in the sipuleucel-T group versus 23.0% in the placebo group. The treatment effect was also observed with the use of an unadjusted Cox model and a log-rank test (hazard ratio, 0.77; 95% CI, 0.61 to 0.97; P=0.02) and after adjustment for use of docetaxel after the study therapy (hazard ratio, 0.78; 95% CI, 0.62 to 0.98; P=0.03). The time to objective disease progression was similar in the two study groups. Immune responses to the immunizing antigen were observed in patients who received sipuleucel-T. Adverse events that were more frequently reported in the sipuleucel-T group than in the placebo group included chills, fever, and headache. Conclusions: The use of sipuleucel-T prolonged overall survival among men with metastatic castration-resistant prostate cancer. No effect on the time to disease progression was observed. (Funded by Dendreon; ClinicalTrials.gov number, NCT00065442.) N Engl J Med 2010;363:411-22.
引用
收藏
页码:411 / 422
页数:12
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