Intermittent hormone therapy versus continuous hormone therapy for locally advanced prostate cancer: a meta-analysis

被引:13
作者
Dong, ZhiLong [1 ]
Wang, Hanzhang [2 ]
Xu, MengMeng [3 ]
Li, Yang [1 ]
Hou, MingLi [4 ]
Wei, YanLing [1 ]
Liu, Xingchen [1 ]
Wang, ZhiPing [5 ]
Xie, XiaoDong [6 ]
机构
[1] Lanzhou Univ, Hosp 2, Lanzhou 730000, Gansu, Peoples R China
[2] Tulane Univ, Sch Publ Hlth & Trop Med, New Orleans, LA USA
[3] Duke Univ, Med Ctr, Med Scientist Training Program, Durham, NC USA
[4] Second Peoples Hosp Gansu Prov, Lanzhou, Gansu, Peoples R China
[5] Lanzhou Univ, Inst Urol, Hosp 2, Lanzhou 730000, Gansu, Peoples R China
[6] Lanzhou Univ, Sch Basic Med Sci, Key Lab Preclin Study New Drugs Gansu Prov, Lanzhou 730000, Gansu, Peoples R China
基金
中国博士后科学基金;
关键词
Hormone therapy; meta-analysis; prostate cancer; ANDROGEN SUPPRESSION; DEPRIVATION; MORTALITY; BLOCKADE;
D O I
10.3109/13685538.2015.1065245
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Few randomized studies have compared intermittent hormone therapy (IHT) with continuous hormone therapy (CHT) for the treatment of locally advanced prostate cancer (PCa). Here, we report the results of a meta-analysis of a randomized controlled trial, evaluating the effectiveness of IHT versus CHT for patients with locally advanced PCa. Types of intervention were IHT versus CHT. The primary endpoint of this study is overall mortality and the secondary endpoints are any progression of disease, quality of life (QOL) and adverse effects between two groups. Six randomized controlled trials totaling 2996 patients were included. Results are as follows: after hormone therapy, patients undergoing IHT demonstrated no significant difference from those undergoing CHT in terms of the overall mortality (OR=1.0, 95% CI [0.86, 1.17]) and disease progression (OR=1.16, 95% CI [0.86, 1.57]). Men treated with IHT also reported better QOL, fewer adverse effects and considerable economic benefit for the individual and the community. With no difference in overall mortality and incidence of progression, current clinical studies confirm that both therapeutic methods were safe and effective. However, our study also takes into account QOL. When these secondary measures are considered, IHT may be a better option over CHT as patients report a more affordable treatment with improved QOL and fewer adverse effects.
引用
收藏
页码:233 / 237
页数:5
相关论文
共 20 条
  • [1] AKAKURA K, 1993, CANCER, V71, P2782, DOI 10.1002/1097-0142(19930501)71:9<2782::AID-CNCR2820710916>3.0.CO
  • [2] 2-Z
  • [3] Cancer incidence and mortality in the European Union: Cancer registry data and estimates of national incidence for 1990
    Black, RJ
    Bray, F
    Ferlay, J
    Parkin, DM
    [J]. EUROPEAN JOURNAL OF CANCER, 1997, 33 (07) : 1075 - 1107
  • [4] Intermittent androgen suppression in the treatment of metastatic prostate cancer
    Bouchot, O
    Lenormand, L
    Karam, G
    Prunet, D
    Gaschignard, N
    Malinovsky, JM
    Buzelin, JM
    [J]. EUROPEAN UROLOGY, 2000, 38 (05) : 543 - 549
  • [5] Estimates of cancer incidence and mortality in Europe in 1995
    Bray, F
    Sankila, R
    Ferlay, J
    Parkin, DM
    [J]. EUROPEAN JOURNAL OF CANCER, 2002, 38 (01) : 99 - 166
  • [6] BRUCHOVSKY N, 1990, CANCER RES, V50, P2275
  • [7] Intermittent Androgen Deprivation for Locally Advanced and Metastatic Prostate Cancer: Results from a Randomised Phase 3 Study of the South European Uroncological Group
    Calais da Silva, Fernando E. C.
    Bono, Aldo V.
    Whelan, Peter
    Brausi, Maurizio
    Marques Queimadelos, Anton
    Portillo Martin, Jose A.
    Kirkali, Ziya
    Calais da Silva, Fernando M. V.
    Robertson, Chris
    [J]. EUROPEAN UROLOGY, 2009, 55 (06) : 1269 - 1277
  • [8] Intermittent androgen suppression in the management of prostate cancer
    Crook, JM
    Szumacher, E
    Malone, S
    Huan, S
    Segal, R
    [J]. UROLOGY, 1999, 53 (03) : 530 - 534
  • [9] de Leval Jean, 2002, Clin Prostate Cancer, V1, P163, DOI 10.3816/CGC.2002.n.018
  • [10] Intermittent androgen deprivation: Update of cycling characteristics in patients without clinically apparent metastatic prostate cancer
    Grossfeld, GD
    Chaudhary, UB
    Reese, DM
    Carroll, PR
    Small, EJ
    [J]. UROLOGY, 2001, 58 (02) : 240 - 245