Phase II study of pomegranate juice for men with rising prostate-specific antigen following surgery or radiation for prostate cancer

被引:294
作者
Pantuck, Allan J.
Leppert, John T.
Zomorodian, Nazy
Aronson, William
Hong, Jenny
Barnard, R. James
Seeram, Navindra
Liker, Harley
Wang, Hejing
Elashoff, Robert
Heber, David
Aviram, Michael
Ignarro, Louis
Belldegrun, Arie
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Urol, Ctr Hlth Sci 66 118, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Physiol Sci, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Biomath, Los Angeles, CA 90095 USA
[5] Technion Israel Inst Technol, Rambam Med Ctr, Haifa, Israel
关键词
D O I
10.1158/1078-0432.CCR-05-2290
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Phytochemicals in plants may have cancer preventive benefits through antioxidation and via gene-nutrient interactions, We sought to determine the effects of pomegranate juice (a major source of antioxidants) consumption on prostate-specific antigen (PSA) progression in men with a rising PSA following primary therapy. Experimental Design: A phase II, Simon two-stage clinical trial for men with rising PSA after surgery or radiotherapy was conducted. Eligible patients had a detectable PSA >0.2 and <5 ng/mL and Gleason score <= 7. Patients were treated with 8 ounces of pomegranate juice daily (Wonderful variety, 570 mg total polyphenol gallic acid equivalents) until disease progression. Clinical end points included safety and effect on serum PSA, serum-induced proliferation and apoptosis of LNCaP cells, serum lipid peroxidation, and serum nitric oxide levels. Results: The study was fully accrued after efficacy criteria were met. There were no serious adverse events reported and the treatment was well tolerated. Mean PSA doubling time significantly increased with treatment from a mean of 15 months at baseline to 54 months posttreatment (P<0.001). In vitro assays comparing pretreatment and posttreatment patient serum on the growth of LNCaP showed a 12% decrease in cell proliferation and a 17% increase in apoptosis (P=0.0048 and 0.0004, respectively), a 23% increase in serum nitric oxide (P=0.0085), and significant (P<0.02) reductions in oxidative state and sensitivity to oxidation of serum lipids after versus before pomegranate juice consumption. Conclusions: We report the first clinical trial of pomegranate juice in patients with prostate cancer. The statistically significant prolongation of PSA doubling time, coupled with corresponding laboratory effects on prostate cancer in vitro cell proliferation and apoptosis as well as oxidative stress, warrant further testing in a placebo-controlled study.
引用
收藏
页码:4018 / 4026
页数:9
相关论文
共 66 条
[41]   Effects of ligand activation of peroxisome proliferator-activated receptor γ in human prostate cancer [J].
Mueller, E ;
Smith, M ;
Sarraf, P ;
Kroll, T ;
Aiyer, A ;
Kaufman, DS ;
Oh, W ;
Demetri, G ;
Figg, WD ;
Zhou, XP ;
Eng, C ;
Spiegelman, BM ;
Kantoff, PW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (20) :10990-10995
[42]   Deletion of the p66Shc longevity gene reduces systemic and tissue oxidative stress, vascular cell apoptosis, and early atherogenesis in mice fed a high-fat diet [J].
Napoli, C ;
Martin-Padura, I ;
de Nigris, F ;
Giorgio, M ;
Mansueto, G ;
Somma, P ;
Condorelli, M ;
Sica, G ;
De Rosa, G ;
Pelicci, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (04) :2112-2116
[43]   Intensive lifestyle changes may affect the progression of prostate cancer [J].
Ornish, D ;
Weidner, G ;
Fair, WR ;
Marlin, R ;
Pettengill, EB ;
Raisin, CJ ;
Dunn-Emke, S ;
Crutchfield, L ;
Jacobs, FN ;
Barnard, RJ ;
Aronson, WJ ;
McCormac, P ;
McKnight, DJ ;
Fein, JD ;
Dnistrian, AM ;
Weinstein, J ;
Ngo, TH ;
Mendell, NR ;
Carroll, PR .
JOURNAL OF UROLOGY, 2005, 174 (03) :1065-1069
[44]   Prostate carcinogenesis and inflammation: emerging insights [J].
Palapattu, GS ;
Sutcliffe, S ;
Bastian, PJ ;
Platz, EA ;
De Marzo, AM ;
Isaacs, WB ;
Nelson, WG .
CARCINOGENESIS, 2005, 26 (07) :1170-1181
[45]   Adenocarcinoma of the prostate: Innovations in management [J].
Petrovich, Z ;
Baert, L ;
Bagshaw, MA ;
Brady, LW ;
Elgamal, A ;
Goethuys, H ;
Heilman, HP ;
Kirkels, WJ ;
Lieskovsky, G ;
Perez, CA ;
VanPoppel, H ;
Williams, RD .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1997, 20 (02) :111-119
[46]  
Pianetti S, 2002, CANCER RES, V62, P652
[47]   Natural history of progression after PSA elevation following radical prostatectomy [J].
Pound, CR ;
Partin, AW ;
Eisenberger, MA ;
Chan, DW ;
Pearson, JD ;
Walsh, PC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (17) :1591-1597
[48]   Why do we expect carotenoids to be antioxidants in vivo? [J].
RiceEvans, CA ;
Sampson, J ;
Bramley, PM ;
Holloway, DE .
FREE RADICAL RESEARCH, 1997, 26 (04) :381-398
[49]   Prostate-specific antigen kinetics as a measure of the biologic effect of granulocyte-macrophage colony-stimulating factor in patients with serologic progression of prostate cancer [J].
Rini, BI ;
Weinberg, V ;
Bok, R ;
Small, EJ .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (01) :99-105
[50]   Randomized, double-blind, placebo-controlled crossover study in men with prostate cancer and rising PSA:: Effectiveness of a dietary supplement [J].
Schröder, FH ;
Roobol, MJ ;
Boevé, ER ;
de Mutsert, R ;
Zuijdgeest-Van Leeuwen, SD ;
Kersten, I ;
Wildhagen, MF ;
van Helvoort, A .
EUROPEAN UROLOGY, 2005, 48 (06) :922-931