Synthetic Lethality by Co-Inhibition of Androgen Receptor and Polyadenosine Diphosphate-Ribose in Metastatic Prostate Cancer.

Mariangela Calabrese, Isabella Saporita, Fabio Turco, Silke Gillessen, Elena Castro, Ursula Maria Vogl, Rosario Francesco Di Stefano, Federica Maria Carfì, Stefano Poletto, Giovanni Farinea, Marcello Tucci, Consuelo Buttigliero

Journal: International journal of molecular sciences 2024;25(1):78

PMID: 38203248

Abstract

Androgen receptor pathway inhibitors (ARPI) and polyadenosine diphosphate-ribose inhibitors (PARPi) are part of the standard of care in patients with metastatic castration-resistant prostate cancer (mCRPC). There is biological evidence that the association of ARPI and PARPi could have a synergistic effect; therefore, several ongoing clinical trials are investigating the efficacy of this combination with preliminary results that are not perfectly concordant in identifying patients who can obtain the most benefit from this therapeutic option. The purpose of this review is to describe the PARPi mechanisms of action and to analyze the biological mechanisms behind the interplay between the androgen receptor and the PARPi system to better understand the rationale of the ARPI + PARPi combinations. Furthermore, we will summarize the preliminary results of the ongoing studies on these combinations, trying to understand in which patients to apply. Finally, we will discuss the clinical implications of this combination and its possible future perspectives.

Address: Department of Oncology, University of Turin, AOU San Luigi Gonzaga, 10043 Orbassano, Italy.; Ente Ospedaliero Cantonale-Istituto Oncologico della Svizzera Italiana, 6500 Bellinzona, Switzerland.; Department of Medical Oncology, Faculty of Biomedical Sciences, Università della Svizzera Italiana, 6900 Lugano, Switzerland.; Hospital Universitario 12 de Octubre, 28041 Madrid, Spain.; Department of Medical Oncology, Cardinal Massaia Hospital, 14100 Asti, Italy.
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