Radiotherapy and Hormone Treatment in Prostate Cancer
- PMID: 27146591
- PMCID: PMC4985515
- DOI: 10.3238/arztebl.2016.0235
Radiotherapy and Hormone Treatment in Prostate Cancer
Abstract
Background: Prostate cancer has the highest incidence of any type of cancer in Germany; an estimated 67 000 new diagnoses of prostate cancer will be made in 2016. In the current German S3 guideline for the treatment of prostate cancer, radiotherapy-sometimes in combination with androgen deprivation therapy (ADT)-is one of the two recommended options for treatment with curative intent (the other is radical prostatectomy). There have been many publications on this subject, yet it is still often unclear in routine practice how ADT should be administered, and for how long.
Methods: This review is based on publications retrieved by a selective literature search, with special attention to controlled trials.
Results: For low risk patients, radiotherapy without ADT is indicated (evidence level 1). Patients with localized prostate cancer and an intermediate risk benefit from radiotherapy combined with a four-to-six-month course of ADT. In this situation, a higher radiation dose might be an effective substitute for ADT (evidence level 1-2). For patients at high risk, radiotherapy combined with long-term hormonal treatment is the standard therapy, as it significantly improves all oncological end points (evidence level 1). For example, in the largest randomized and controlled trial, this form of treatment reduced cancer-specific mortality from 19% to 9% . Higher radiation doses of 66-74 Gy and longer ADT can improve local control at the cost of increased urethral toxicity.
Conclusion: Androgen deprivation combined with external beam radiotherapy is a curative standard option for patients with prostate cancer who are at high risk of recurrence. The modern radiotherapeutic techniques that are now available, such as intensity-modulated radiotherapy, enable a further improvement of the risk/benefit ratio.
Comment in
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Avoid Downplaying Side Effects.Dtsch Arztebl Int. 2016 Oct 7;113(40):678. doi: 10.3238/arztebl.2016.0678a. Dtsch Arztebl Int. 2016. PMID: 27788753 Free PMC article. No abstract available.
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In Reply.Dtsch Arztebl Int. 2016 Oct 7;113(40):678-679. doi: 10.3238/arztebl.2016.0678b. Dtsch Arztebl Int. 2016. PMID: 27788754 Free PMC article. No abstract available.
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