Synthetic Lethality by Co-Inhibition of Androgen Receptor and Polyadenosine Diphosphate-Ribose in Metastatic Prostate Cancer.
Mariangela CalabreseIsabella SaporitaUrsula Maria VoglSilke GillessenElena CastroUrsula Maria VoglRosario Francesco Di StefanoFederica Maria CarfìStefano PolettoGiovanni FarineaMarcello TucciConsuelo ButtiglieroPublished in: International journal of molecular sciences (2023)
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.
Keyphrases
- prostate cancer
- clinical trial
- end stage renal disease
- ejection fraction
- newly diagnosed
- healthcare
- small cell lung cancer
- chronic kidney disease
- squamous cell carcinoma
- palliative care
- prognostic factors
- radical prostatectomy
- quality improvement
- randomized controlled trial
- chronic pain
- study protocol
- patient reported
- double blind