Optimizing outcomes and quality of life in the hormonal treatment of prostate cancer

BJU Int. 2006 Jul;98(1):20-7. doi: 10.1111/j.1464-410X.2006.06176.x. Epub 2006 Mar 23.

Abstract

We review the effectiveness of androgen-deprivation therapy (ADT) in the management of prostate cancer, and the effect that this treatment has on a patient's quality of life (QoL), based on discussions held at a European symposium on the management of prostate cancer. The overall QoL is reduced in asymptomatic men, and there are known decreases in cognitive function, self-esteem, libido and sexual function. Hot flashes are also a frequent problem. Prolonged ADT can lead to osteoporosis and subsequently fractures. Various effective methods exist to manage and minimize these side-effects; some are specific to the side-effect, whereas other more general methods include lifestyle changes, specific drugs and added hormonal manipulations. Intermittent ADT for patients taking luteinizing hormone-releasing hormone agonists offers a promising method to reduce adverse effects, and possibly increases the time to androgen independence. Initial studies indicate that prostate-specific antigen-based progression with intermittent ADT is similar to that seen with continuous ADT, but there is a reduction in side-effects, leading to an improvement in QoL.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Androgen Antagonists / therapeutic use*
  • Anemia / chemically induced
  • Antineoplastic Agents, Hormonal / therapeutic use*
  • Bone Density / drug effects
  • Cognition Disorders / chemically induced
  • Depressive Disorder / chemically induced
  • Fractures, Bone / chemically induced
  • Humans
  • Male
  • Metabolic Diseases / chemically induced
  • Osteoporosis / chemically induced
  • Pain / chemically induced
  • Prostatic Neoplasms / drug therapy*
  • Prostatic Neoplasms / psychology
  • Quality of Life*
  • Risk Factors
  • Sexual Dysfunction, Physiological / chemically induced
  • Treatment Outcome

Substances

  • Androgen Antagonists
  • Antineoplastic Agents, Hormonal