Print page Print page
Switch language
The Capital Region of Denmark - a part of Copenhagen University Hospital

Hormone naïve metastatic prostate cancer: How to treat it?

Research output: Contribution to journalJournal articleResearchpeer-review

  1. Electronic reporting of patient-reported outcomes in a fragile and comorbid population during cancer therapy - a feasibility study

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Epigenetic Analysis of Circulating Tumor DNA in Localized and Metastatic Prostate Cancer: Evaluation of Clinical Biomarker Potential

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. The Value of 68Ga-PSMA PET/CT Following Equivocal 18F-NaF PET/CT in Prostate Cancer Patients

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Varicocele Testis

    Research output: Contribution to journalJournal articleResearchpeer-review

View graph of relations

OBJECTIVES: Recent landmark studies (GETUG-AFU 15, CHAARTED, STAMPEDE (docetaxel), LATITUDE and STAMPEDE (abiraterone)) have changed the treatment of hormone sensitive metastatic prostate cancer (mHSPC) from androgen deprivation therapy (ADT) only to combined therapy with either docetaxelor abiraterone acetate plus prednisone (AAP) together with ADT. In this Review we highlight current evidence and recommendations on how to treat men with newly diagnosed mHSPC beyond ADTMETHODS: Narrative overview of available evidence retrieved from pubmed searches, hand searches and authoritative texts.

RESULTS: Docetaxel or AAP in combination with ADT improves overall survival (OS) in men fit for combined treatment presenting with newly diagnosed mHSPC. The strongest evidence is for men with high volume mHSPC (four or more bone metastases with at least one outside the axial skeleton and/or visceral metastases) or mHSPC with high risk features (A minimum of two out of threefollowing high-risk features: Gleason score ≥ 8, ≥ 3 bone lesions or visceral metastasis) as per CHAARTED and LATITUDE criteria, respectively. While upfront docetaxel and AAP yield comparable OS improvement, docetaxel has not been shown to increase OS specifically for men with low volume/low risk mHSPC, whereas, a recent post-hoc analysis from the STAMPEDE (abiraterone)trial showed consistent overall survival benefit of AAP plus ADT independent of risk stratification. While these data are limited by their retrospective nature, they do suggest that patients with low-risk mHSPC should be offered AAP. In men with high volume/high risk mHSPC, choosing between six-cycles of docetaxel or AAP until disease progression relies on patient preference, cost and individual assessment of which drug side-effect profile is most suitable.

CONCLUSION: Offer men presenting with newly diagnosed mHSPC fit enough for combined therapy either ADT plus docetaxel or AAP.

Original languageEnglish
JournalArchivos Espanoles de Urologia
Issue number2
Pages (from-to)192-202
Number of pages11
Publication statusPublished - Mar 2019

    Research areas

  • Abiraterone Acetate/therapeutic use, Androgen Antagonists/therapeutic use, Disease-Free Survival, Humans, Male, Neoplasm Metastasis/drug therapy, Prostatic Neoplasms/drug therapy, Retrospective Studies, Taxoids/therapeutic use

ID: 56804177