Literature DB >> 16632343

Adverse effects to quality of life arising from treatment can recover with intermittent androgen suppression in men with prostate cancer.

N A Spry1, L Kristjanson, B Hooton, L Hayden, G Neerhut, H Gurney, T Corica, E Korbel, S Weinstein, K McCaul.   

Abstract

Health-related quality of life (HQOL) research is a means of broadening the assessment of treatment effects. This longitudinal study investigated the dynamic change to quality of life (QOL) and testosterone dependant physiology in men commencing an intermittent maximal androgen blockade program (IMAB). Two hundred and fifty men were accrued to the multi-centre study of IMAB (Flutamide 250 mg TDS, Leuprolide 22.5 mg depot) ceasing treatment after 9 months if PSA <4 ng/ml, and restarting when PSA >20 ng/ml. QOL was assessed every 3 months for 30 months using the EORTC QLQ-C30 and EORTC QLQ-PR25 module. Data completion for the whole study was 90%. At baseline, our cohort was less symptomatic and had better function than the EORTC reference cohort, which may be related to a shift in clinical practice with time. Testosterone suppression (AS) lead to a significant reduction in global HQOL and deterioration in most function and symptom scales. During the off period, there was a trend of progressive improvement in HQOL that paralleled testosterone recovery but was slower than the rate of deterioration during the treatment phase. Maximum recovery of HQOL occurred most frequently by months 9-12. Testosterone recovery was slower and less complete in older men, and lead to concomitant poorer HOQL recovery. Whilst the magnitude of mean change to scale scores was small, there was a consistent and simultaneous deterioration during maximal androgen blockade (MAB) and improvement during androgen recovery. Older men are more likely to show an impaired testosterone recovery, and this was paralleled by a slower HQOL recovery. Newer methods of analysis to describe results in a way that has meaning to the individual patient are warranted.

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Year:  2006        PMID: 16632343     DOI: 10.1016/j.ejca.2006.01.029

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  27 in total

1.  Comparison of maximal and more maximal intermittent androgen blockade during 5-year treatment of advanced prostate cancer T3NxMx-1.

Authors:  Slawomir A Dutkiewicz
Journal:  Int Urol Nephrol       Date:  2011-09-20       Impact factor: 2.370

Review 2.  The role of intermittent androgen deprivation therapy in the management of biochemically recurrent or metastatic prostate cancer.

Authors:  Jasbir Jaswal; Juanita Crook
Journal:  Curr Urol Rep       Date:  2015-03       Impact factor: 3.092

3.  Sexuality and exercise in men undergoing androgen deprivation therapy for prostate cancer.

Authors:  K Hamilton; S K Chambers; M Legg; J L Oliffe; P Cormie
Journal:  Support Care Cancer       Date:  2014-07-10       Impact factor: 3.603

4.  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

5.  Influence of serum testosterone on urinary continence and sexual activity in patients undergoing radical prostatectomy for clinically localized prostate cancer.

Authors:  M Gacci; G Corona; G Apolone; A Apolone; M Lanciotti; N Tosi; S Giancane; L Masieri; S Serni; M Maggi; M Carini
Journal:  Prostate Cancer Prostatic Dis       Date:  2010-03-09       Impact factor: 5.554

6.  A phase III clinical trial of exercise modalities on treatment side-effects in men receiving therapy for prostate cancer.

Authors:  Robert U Newton; Dennis R Taaffe; Nigel Spry; Robert A Gardiner; Gregory Levin; Bradley Wall; David Joseph; Suzanne K Chambers; Daniel A Galvão
Journal:  BMC Cancer       Date:  2009-06-29       Impact factor: 4.430

7.  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 8.  Exercise in prevention and management of cancer.

Authors:  Robert U Newton; Daniel A Galvão
Journal:  Curr Treat Options Oncol       Date:  2008-08-13

Review 9.  Exercise therapy for sexual dysfunction after prostate cancer.

Authors:  Prue Cormie; Robert U Newton; Dennis R Taaffe; Nigel Spry; Daniel A Galvão
Journal:  Nat Rev Urol       Date:  2013-10-08       Impact factor: 14.432

10.  A randomized controlled trial of an exercise intervention targeting cardiovascular and metabolic risk factors for prostate cancer patients from the RADAR trial.

Authors:  Daniel A Galvão; Nigel Spry; Dennis R Taaffe; James Denham; David Joseph; David S Lamb; Greg Levin; Gillian Duchesne; Robert U Newton
Journal:  BMC Cancer       Date:  2009-12-02       Impact factor: 4.430

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