Risks and benefits of hormonal manipulation as monotherapy or adjuvant treatment in localised prostate cancer

被引:22
作者
Abrahamsson, PA [1 ]
Anderson, J
Boccon-Gibod, L
Schulman, C
Studer, UE
Wirth, M
机构
[1] Lund Univ, Malmo Univ Hosp, Dept Urol, S-20502 Malmo, Sweden
[2] Royal Hallamshire, Sheffield, S Yorkshire, England
[3] Hop Bichat Claude Bernard, Paris, France
[4] Univ Clin Brussels, Erasme Hosp, Brussels, Belgium
[5] Univ Bern, Bern, Switzerland
[6] Tech Univ Dresden, Hosp Carl Gustav, Dresden, Germany
关键词
prostate cancer; androgen ablation; survival; immediate therapy; deferred therapy; side-effects; anti-androgen mono-therapy;
D O I
10.1016/j.eururo.2005.09.005
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
A round table meeting was held to discuss the role of hormonal therapy in localised prostate cancer. The findings of the group were that immediate hormonal therapy does not provide an overall survival advantage in localised and locally advanced prostate cancer. Bicalutamide can prolong disease free survival in patients with locally advanced prostate cancer, however it is important to underline that at this time it has not been shown to influence disease specific nor overall survival. It remains also unproven that early treatment is superior to treatment at progression. However, a trend towards decreased survival with bicalutamide was observed in low risk patients such as those with localised disease. In patients receiving bicalutamide, there were increased cardiovascular side-effects, in addition to the high incidence of gynaecomastia. Early hormonal therapy has to be balanced against such side-effects and the inevitable appearance of hormone refractory disease in patients who progress after hormonal therapy. Consequently, patients with localised, low risk disease are not considered appropriate candidates for hormonal therapy used either as mono-therapy or in the adjuvant setting. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:900 / 905
页数:6
相关论文
共 22 条
  • [1] Adib RS, 1997, BRIT J UROL, V79, P235
  • [2] Structural basis for antagonism and resistance of bicalutamide in prostate cancer
    Bohl, CE
    Gao, WQ
    Miller, DD
    Bell, CE
    Dalton, JT
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (17) : 6201 - 6206
  • [3] BYAR DP, 1973, CANCER, V32, P1126, DOI 10.1002/1097-0142(197311)32:5<1126::AID-CNCR2820320518>3.0.CO
  • [4] 2-C
  • [5] Molecular determinants of resistance to antiandrogen therapy
    Chen, CD
    Welsbie, DS
    Tran, C
    Baek, SH
    Chen, R
    Vessella, R
    Rosenfeld, MG
    Sawyers, CL
    [J]. NATURE MEDICINE, 2004, 10 (01) : 33 - 39
  • [6] Switch from antagonist to agonist of the androgen receptor blocker bicalutamide is associated with prostate tumour progression in a new model system
    Culig Z.
    Hoffmann J.
    Erdel M.
    Eder I.E.
    Hobisch A.
    Hittmair A.
    Bartsch G.
    Utermann G.
    Schneider M.R.
    Parczyk K.
    Klocker H.
    [J]. British Journal of Cancer, 1999, 81 (2) : 242 - 251
  • [7] Antiandrogens in prostate cancer endocrine therapy
    Culig, Z
    Bartsch, G
    Hobisch, A
    [J]. CURRENT CANCER DRUG TARGETS, 2004, 4 (05) : 455 - 461
  • [8] Hormone-refractory prostate cancer: a multi-step and multi-event process
    de la Taille, A
    Vacherot, F
    Salomon, L
    Druel, C
    de Medina, SGD
    Abbou, C
    Buttyan, R
    Chopin, D
    [J]. PROSTATE CANCER AND PROSTATIC DISEASES, 2001, 4 (04) : 204 - 212
  • [9] Legal pitfalls in the diagnosis of prostate cancer
    Dunn, IB
    Kirk, D
    [J]. BJU INTERNATIONAL, 2000, 86 (03) : 304 - 307
  • [10] Garnick M., 2004, European Urology Supplements, V3, P57, DOI 10.1016/S1569-9056(04)90218-7