Treatment strategies to prevent and reduce gynecomastia and/or breast pain caused by antiandrogen therapy for prostate cancer : Statement from the DEGRO working group prostate cancer.


Journal

Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]
ISSN: 1439-099X
Titre abrégé: Strahlenther Onkol
Pays: Germany
ID NLM: 8603469

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 05 02 2020
accepted: 18 02 2020
pubmed: 14 3 2020
medline: 15 12 2020
entrez: 14 3 2020
Statut: ppublish

Résumé

To provide an overview on the available treatments to prevent and reduce gynecomastia and/or breast pain caused by antiandrogen therapy for prostate cancer. The German Society of Radiation Oncology (DEGRO) expert panel summarized available evidence published and assessed the validity of the information on efficacy and treatment-related toxicity. Eight randomized controlled trials and one meta-analysis were identified. Two randomized trials demonstrated that prophylactic radiation therapy (RT) using 1 × 10 Gy or 2 × 6 Gy significantly reduced the rate of gynecomastia but not breast pain, as compared to observation. A randomized dose-finding trial identified the daily dose of 20 mg tamoxifen (TMX) as the most effective prophylactic dose and another randomized trial described that daily TMX use was superior to weekly use. Another randomized trial showed that prophylactic daily TMX is more effective than TMX given at the onset of gynecomastia. Two other randomized trials described that TMX was clearly superior to anastrozole in reducing the risk for gynecomastia and/or breast pain. One comparative randomized trial between prophylactic RT using 1 × 12 Gy and TMX concluded that prophylactic TMX is more effective compared to prophylactic RT and furthermore that TMX appears to be more effective to treat gynecomastia and/or breast pain when symptoms are already present. A meta-analysis confirmed that both prophylactic RT and TMX can reduce the risk of gynecomastia and/or breast pain with TMX being more effective; however, the rate of side effects after TMX including dizziness and hot flushes might be higher than after RT and must be taken into account. Less is known regarding the comparative effectiveness of different radiation fractionation schedules and more modern RT techniques. Prophylactic RT as well as daily TMX can significantly reduce the incidence of gynecomastia and/or breast pain. TMX appears to be an effective alternative to RT also as a therapeutic treatment in the presence of gynecomastia but its side effects and off-label use must be considered.

Identifiants

pubmed: 32166452
doi: 10.1007/s00066-020-01598-9
pii: 10.1007/s00066-020-01598-9
pmc: PMC7305090
doi:

Substances chimiques

Androgen Antagonists 0
Androgens 0
Anilides 0
Antineoplastic Agents, Hormonal 0
Estrogen Receptor Modulators 0
Nitriles 0
Tosyl Compounds 0
Tamoxifen 094ZI81Y45
Anastrozole 2Z07MYW1AZ
bicalutamide A0Z3NAU9DP

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

589-597

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Auteurs

Pirus Ghadjar (P)

Department of Radiation Oncology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany, Augustenburger Platz 1, 13353, Berlin, Germany. Pirus.ghadjar@charite.de.

Daniel M Aebersold (DM)

Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Clemens Albrecht (C)

Klinikum Nürnberg Nord, Nürnberg, Germany.

Dirk Böhmer (D)

Department of Radiation Oncology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany, Augustenburger Platz 1, 13353, Berlin, Germany.

Michael Flentje (M)

Universitätsklinikum Würzburg, Würzburg, Germany.

Ute Ganswindt (U)

Innsbruck Medical University, Innsbruck, Austria.

Stefan Höcht (S)

Xcare Praxis für Strahlentherapie Saarlouis, Xcare Gruppe, Saarlouis, Germany.

Tobias Hölscher (T)

Universitätsklinikum Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.

Arndt-Christian Müller (AC)

Universitätsklinikum Tübingen, Tübingen, Germany.

Peter Niehoff (P)

Sana Klinikum Offenbach, Offenbach, Germany.

Michael Pinkawa (M)

MediClin Robert Janker Klinik, Bonn, Germany.

Felix Sedlmayer (F)

Landeskrankenhaus, Universitätsklinikum der Paracelsus Medizinischen Privatuniversität, Salzburg, Austria.

Daniel Zips (D)

Universitätsklinikum Tübingen, Tübingen, Germany.

Thomas Wiegel (T)

Universitätsklinikum Ulm, Ulm, Germany.

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Classifications MeSH