What implications do the tolerability profiles of antiandrogens and other commonly used prostate cancer treatments have on patient care?
- PMID: 16896883
- PMCID: PMC12161115
- DOI: 10.1007/s00432-006-0134-4
What implications do the tolerability profiles of antiandrogens and other commonly used prostate cancer treatments have on patient care?
Abstract
Purpose: Increased awareness of prostate cancer has led to earlier initiation of therapy, and the potential for a longer duration of treatment has led to a stronger emphasis on tolerability. Historically, the mainstay of treatment of hormone-sensitive prostate cancer has been castration-based therapy, but antiandrogens are now emerging as an alternative. This article reviews the tolerability profiles of antiandrogens as well as other existing treatments for prostate cancer and examines their implications on patient care.
Methods: A search of online literature databases was conducted to identify recent articles and studies (1990-2006) that have reported adverse effects associated with treatment approaches for men with prostate cancer. The therapies reviewed here include castration, antiandrogens, a combination of castration and antiandrogens (CAB), estrogens, and chemotherapy.
Results: Castration offers significant clinical benefits when used as monotherapy or as adjuvant therapy; however, it is associated with loss of bone mineral density, and a reduction in physical activity and sexual function, which can have a negative impact on quality of life. Detrimental effects on muscle mass, fat deposition, and cognitive function have also been reported. Recent data suggest that the non-steroidal antiandrogen, bicalutamide, confers a significant overall survival benefit when used as adjuvant to radiotherapy in patients with locally advanced disease. However, the survival data for bicalutamide are not as extensive as those available for LHRH agonists. Although they do not appear to have a significant impact on sexual and physical activity, non-steroidal antiandrogens are frequently associated with gynecomastia and breast pain, and some are associated with diarrhea. Estrogens have been used in patients with androgen-independent prostate cancer; however, cardiovascular toxicity has restricted their use. In patients whose prostate cancer has become hormone-refractory, treatment options include chemotherapeutic agents, such as docetaxel and mitoxantrone.
Conclusions: It is important for physicians to discuss the adverse effects of all the available treatment options with patients so that a therapy can be selected to meet their expectations in terms of overall survival and tolerability.
Similar articles
-
Antiandrogen treatments in locally advanced prostate cancer: are they all the same?J Cancer Res Clin Oncol. 2006 Aug;132 Suppl 1(Suppl 1):S17-26. doi: 10.1007/s00432-006-0133-5. J Cancer Res Clin Oncol. 2006. PMID: 16845534 Free PMC article. Review.
-
A rapid and systematic review of the clinical effectiveness and cost-effectiveness of paclitaxel, docetaxel, gemcitabine and vinorelbine in non-small-cell lung cancer.Health Technol Assess. 2001;5(32):1-195. doi: 10.3310/hta5320. Health Technol Assess. 2001. PMID: 12065068
-
Chemotherapy for hormone-refractory prostate cancer.Cochrane Database Syst Rev. 2006 Oct 18;(4):CD005247. doi: 10.1002/14651858.CD005247.pub2. Cochrane Database Syst Rev. 2006. PMID: 17054249
-
Cost-effectiveness of using prognostic information to select women with breast cancer for adjuvant systemic therapy.Health Technol Assess. 2006 Sep;10(34):iii-iv, ix-xi, 1-204. doi: 10.3310/hta10340. Health Technol Assess. 2006. PMID: 16959170
-
The Black Book of Psychotropic Dosing and Monitoring.Psychopharmacol Bull. 2024 Jul 8;54(3):8-59. Psychopharmacol Bull. 2024. PMID: 38993656 Free PMC article. Review.
Cited by
-
[Cardiovascular risks of androgen deprivation therapy for prostate cancer].Urologe A. 2016 May;55(5):627-31. doi: 10.1007/s00120-015-0021-1. Urologe A. 2016. PMID: 27003571 Review. German.
-
Cancer treatment-related bone disease.Crit Rev Eukaryot Gene Expr. 2009;19(1):47-60. doi: 10.1615/critreveukargeneexpr.v19.i1.20. Crit Rev Eukaryot Gene Expr. 2009. PMID: 19191756 Free PMC article. Review.
References
-
- Akaza H, Yamaguchi A, Matsuda T, Igawa M, Kumon H, Soeda A, Arai Y, Usami M, Naito S, Kanetake H, Ohashi Y (2004) Superior anti-tumor efficacy of bicalutamide 80 mg in combination with a luteinizing hormone-releasing hormone (LHRH) agonist versus LHRH agonist monotherapy as first-line treatment for advanced prostate cancer: interim results of a randomized study in Japanese patients. Jpn J Clin Oncol 34:20–28 - PubMed
-
- Aus G, Abbou CC, Bolla M, Heidenreich A, Van Poppel H, Schmid H-P, Wolff JM, Zattoni F (2005) European Association of Urology Guidelines on Prostate Cancer (accessed 19 December 2005, through http://www.uroweb.nl/files/uploaded_files/2005Prostate%20Cancer.pdf) - PubMed
-
- Boccardo F, Rubagotti A, Barichello M, Battaglia M, Carmignani G, Comeri G, Conti G, Cruciani G, Dammino S, Delliponti U, Ditonno P, Ferraris V, Lilliu S, Montefiore F, Portoghese F, Spano G, for the Italian Prostate Cancer Project (1999) Bicalutamide monotherapy versus flutamide plus goserelin in prostate cancer patients: results of an Italian Prostate Cancer Project study. J Clin Oncol 17:2027–2038 - PubMed
-
- Bolla M, Collette L, Blank L, Warde P, Dubois JB, Mirimanoff R-O, Storme G, Bernier J, Kuten A, Sternberg C, Mattelaer J, Lopez Torecilla J, Pfeffer JR, Cutajar CL, Zurlo A, Pierart M (2002) Long-term results with immediate androgen suppression and external irradiation in patients with locally advanced prostate cancer (an EORTC study): a phase III randomised trial. Lancet 360:103–108 - PubMed
-
- Bruchovsky N, Goldenberg SL, Akakura K, Rennie PS (1993) Luteinizing hormone-releasing hormone agoinsts in prostate cancer. Elimination of flare reaction by pretreatment with cyproterone acetate and low-dose diethylstilbestrol. Cancer 72:1685–1691 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical