Current HRD assays in ovarian cancer: differences, pitfalls, limitations, and novel approaches

Front Oncol. 2024 Aug 16:14:1405361. doi: 10.3389/fonc.2024.1405361. eCollection 2024.

Abstract

Ovarian carcinoma (OC) still represents an insidious and fatal malignancy, and few significant results have been obtained in the last two decades to improve patient survival. Novel targeted therapies such as poly (ADP-ribose) polymerase inhibitors (PARPi) have been successfully introduced in the clinical management of OC, but not all patients will benefit, and drug resistance almost inevitably occurs. The identification of patients who are likely to respond to PARPi-based therapies relies on homologous recombination deficiency (HRD) tests, as this condition is associated with response to these treatments. This review summarizes the genomic and functional HRD assays currently used in clinical practice and those under evaluation, the clinical implications of HRD testing in OC, and their current pitfalls and limitations. Special emphasis will be placed on the functional HRD assays under development and the use of machine learning and artificial intelligence technologies as novel strategies to overcome the current limitations of HRD tests for a better-personalized treatment to improve patient outcomes.

Keywords: PARP inhibitors; artificial intelligence; homologous recombination deficiency; ovarian cancer; platinum drug; predictive biomarkers.

Publication types

  • Review

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The research leading to this manuscript has received funding from the institutional “Ricerca Corrente” granted by the Italian Ministry of Health; Ministry of University and Research-MUR under PNRR M4C2I1.3 Heal Italia project PE00000019 CUP B43D22000710006 of Istituto di Ricerche Farmacologiche Mario Negri IRCCS – P.I. Giovanna Damia.