Literature DB >> 9854195

Intermittent androgen suppression for prostate cancer: rationale and clinical experience.

M Gleave1, N Bruchovsky, S L Goldenberg, P Rennie.   

Abstract

The rationale behind intermittent androgen suppression (IAS) is based on: (1) observations that androgen ablation is palliative, not curative, in most patients with prostate cancer, and that quality of life must be considered; (2) the assumption that immediate androgen ablation is superior to delayed therapy in improving survival; (3) the hypothesis that if tumour cells surviving androgen withdrawal are forced into a normal pathway of differentiation by androgen replacement, then apoptotic potential might be restored and progression to androgen independence delayed. Several centres have now tested the feasibility of IAS therapy in non-randomized groups of prostate cancer patients using serum of prostate-specific antigen levels as trigger points. Clinical data suggest that prostate cancer is amenable to control by IAS and offers clinicians an opportunity to improve patients' quality of life by balancing the benefits of immediate androgen ablation (delayed progression and prolonged survival) while reducing treatment-related side effects and expense. Whether time to progression and survival is affected in a beneficial or adverse way is being studied in randomized, prospective protocols.

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Year:  1998        PMID: 9854195     DOI: 10.1159/000052297

Source DB:  PubMed          Journal:  Eur Urol        ISSN: 0302-2838            Impact factor:   20.096


  12 in total

1.  Targeting the binding function 3 (BF3) site of the human androgen receptor through virtual screening.

Authors:  Nathan A Lack; Peter Axerio-Cilies; Peyman Tavassoli; Frank Q Han; Ka Hong Chan; Clementine Feau; Eric LeBlanc; Emma Tomlinson Guns; R Kiplin Guy; Paul S Rennie; Artem Cherkasov
Journal:  J Med Chem       Date:  2011-11-18       Impact factor: 7.446

2.  Hormonal therapy for prostate cancer.

Authors:  Michael K Brawer
Journal:  Rev Urol       Date:  2006

3.  Hormonal therapy in prostate cancer: historical approaches.

Authors:  E David Crawford
Journal:  Rev Urol       Date:  2004

4.  Inhibition of 5alpha-reductase enhances testosterone-induced expression of U19/Eaf2 tumor suppressor during the regrowth of LNCaP xenograft tumor in nude mice.

Authors:  Shubham Gupta; Yujuan Wang; Raquel Ramos-Garcia; Daniel Shevrin; Joel B Nelson; Zhou Wang
Journal:  Prostate       Date:  2010-10-01       Impact factor: 4.104

5.  5α-Reductase inhibition coupled with short off cycles increases survival in the LNCaP xenograft prostate tumor model on intermittent androgen deprivation therapy.

Authors:  Laura E Pascal; Khalid Z Masoodi; Katherine J O'Malley; Daniel Shevrin; Jeffrey R Gingrich; Rahul A Parikh; Zhou Wang
Journal:  J Urol       Date:  2014-10-31       Impact factor: 7.450

6.  Bipolar androgen therapy: the rationale for rapid cycling of supraphysiologic androgen/ablation in men with castration resistant prostate cancer.

Authors:  Samuel R Denmeade; John T Isaacs
Journal:  Prostate       Date:  2010-10-01       Impact factor: 4.104

Review 7.  Intermittent androgen deprivation.

Authors:  N A Dawson
Journal:  Curr Oncol Rep       Date:  2000-09       Impact factor: 5.075

8.  5α-reductase inhibition suppresses testosterone-induced initial regrowth of regressed xenograft prostate tumors in animal models.

Authors:  Khalid Z Masoodi; Raquel Ramos Garcia; Laura E Pascal; Yujuan Wang; Hei M Ma; Katherine O'Malley; Kurtis Eisermann; Daniel H Shevrin; Holly M Nguyen; Robert L Vessella; Joel B Nelson; Rahul A Parikh; Zhou Wang
Journal:  Endocrinology       Date:  2013-05-13       Impact factor: 4.736

Review 9.  Prostate cancer: 9. Treatment of advanced disease.

Authors:  M E Gleave; N Bruchovsky; M J Moore; P Venner
Journal:  CMAJ       Date:  1999-01-26       Impact factor: 8.262

10.  Management of patients with advanced prostate cancer: recommendations of the St Gallen Advanced Prostate Cancer Consensus Conference (APCCC) 2015.

Authors:  S Gillessen; A Omlin; G Attard; J S de Bono; E Efstathiou; K Fizazi; S Halabi; P S Nelson; O Sartor; M R Smith; H R Soule; H Akaza; T M Beer; H Beltran; A M Chinnaiyan; G Daugaard; I D Davis; M De Santis; C G Drake; R A Eeles; S Fanti; M E Gleave; A Heidenreich; M Hussain; N D James; F E Lecouvet; C J Logothetis; K Mastris; S Nilsson; W K Oh; D Olmos; A R Padhani; C Parker; M A Rubin; J A Schalken; H I Scher; A Sella; N D Shore; E J Small; C N Sternberg; H Suzuki; C J Sweeney; I F Tannock; B Tombal
Journal:  Ann Oncol       Date:  2015-06-03       Impact factor: 32.976

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