Intermittent Androgen Deprivation Therapy for Prostate Cancer

Learning Objectives After completing this course, the reader will be able to: Explain the utility of intermittent androgen deprivation therapy in the management of patients with prostate cancer. Describe the preclinical observations leading to the development of intermittent androgen deprivation the...

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Veröffentlicht in:The oncologist (Dayton, Ohio) Ohio), 2004-06, Vol.9 (3), p.295-301
Hauptverfasser: Rashid, Mohammad H., Chaudhary, Uzair B.
Format: Artikel
Sprache:eng
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Zusammenfassung:Learning Objectives After completing this course, the reader will be able to: Explain the utility of intermittent androgen deprivation therapy in the management of patients with prostate cancer. Describe the preclinical observations leading to the development of intermittent androgen deprivation therapy. Identify the limitations in using intermittent androgen deprivation therapy for prostate cancer. Access and take the CME test online and receive 1 hour of AMA PRA category 1 credit at CME.TheOncologist.com Androgen deprivation therapy for prostate cancer is associated with several complications, including loss of libido, hot flashes, night sweats, psychological stress, osteoporosis, anemia, fatigue, loss of muscle mass, glucose intolerance, and changes in lipid profile. The natural history of prostate cancer while on such therapy is the attainment of an incurable androgen‐independent state. Early diagnosis by prostate‐specific antigen screening, longer life expectancies, and a penchant for immediate therapy pose a problem where clinicians have to balance the potential benefits of early hormonal therapy with the risks of development of these metabolic and psychological complications. Intermittent androgen deprivation offers clinicians a prospect to improve quality of life in patients with prostate cancer by harmonizing the benefits of androgen ablation with a reduction in treatment‐related side effects and expenditure. In this review we discuss the challenges and opportunities of this mode of therapy and shed light on some of the underlying molecular mechanisms.
ISSN:1083-7159
1549-490X
DOI:10.1634/theoncologist.9-3-295