Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia
Expert practical recommendations for optimising tumour and germline testing of homologous recombination repair gene mutations in metastatic prostate cancer
Abstract
With the approval of PARP inhibitors (PARPi), both as monotherapy and in combination with androgen receptor signalling inhibitors (ARSi), for metastatic castration-resistant prostate cancer (mCRPC) and their rapid development in earlier disease settings, there is an urgent need to integrate homologous recombination repair (HRR) testing into daily clinical practice to identify patients who may benefit from these therapies and to improve patient management. Alterations in HRR genes are found in approximately 15-30% of patients with mCRPC and are associated with poor prognosis. In addition, some alterations are hereditary; therefore, testing also has implications for the identification of hereditary cancer risk. The successful implementation of HRR gene testing depends not only on access to sequencing technologies but also on the establishment of a comprehensive pre- and post-analytical framework. The aim of this document is to establish a multidisciplinary expert opinion consensus on the optimisation of molecular assessment of BRCA1/2 and other HRR gene alterations in metastatic prostate cancer to support implementation in clinical practice.
Source and rights
Published by Revista espanola de patologia : publicacion oficial de la Sociedad Espanola de Anatomia Patologica y de la Sociedad Espanola de Citologia, 2026. The guideline itself is at the source linked here.
Prognia summarises this guideline for reference and education. It is not medical advice. Always check the official guideline and current local protocols before acting on it.
At a glance
- Published
- 2026
- Applies to
- 🇪🇸 Spain











