PARP inhibitors in older patients with ovarian and breast cancer: Young International Society of Geriatric Oncology review paper.

Gabor Liposits, Kah Poh Loh, Enrique Soto-Perez-de-Celis, Lucy Dumas, Nicolò Matteo Luca Battisti, Sindhuja Kadambi, Capucine Baldini, Susana Banerjee, Stuart M Lichtman

Journal: Journal of geriatric oncology 2020;10(2):337-345

PMID: 30333088

Abstract

Breast and ovarian cancer are common malignancies among older adults, causing significant morbidity and mortality. Although most cases of breast and ovarian cancer are sporadic, a significant proportion is caused by mutations in cancer susceptibility genes, most often breast cancer susceptibility genes (BRCA) 1 and 2. Furthermore, some breast and ovarian tumors are phenotypically similar to those with BRCA mutations, a phenomenon known as "BRCAness". BRCA mutations and "BRCAness" lead to defects in DNA repair, which may be a target for therapeutic agents such as Poly ADP-Ribose Polymerase (PARP) inhibitors. PARP inhibitors are novel medications which lead to double-strand breaks resulting in cell death due to synthetic lethality, and which have been shown to be effective in patients with advanced breast and ovarian cancers with or without BRCA mutations. Three different PARP inhibitors (olaparib, niraparib, and rucaparib) have been approved for the treatment of ovarian cancer and one (olaparib) for breast cancer harboring BRCA mutations. Here, we review the currently available evidence regarding the use of PARP inhibitors for the treatment of patients with breast and ovarian cancer, with a particular focus on the inclusion of older adults in clinical trials of these therapies. Additionally, we provide an overview of currently ongoing studies of PARP inhibitors in breast and ovarian cancer, and include recommendations for increasing the evidence-base for using these medications among older patients.

Copyright © 2018. Published by Elsevier Ltd.

Address: Department of Oncology, Region Hospital West Jutland, Gl. Landevej 61, Herning, 7400, Denmark. Electronic address: [email protected].; Division of Hematology/Oncology, James P. Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY, USA. Electronic address: [email protected].; Enrique Soto-Perez-de-Celis Department of Geriatrics, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Mexico. Electronic address: [email protected].; Gynaecology Unit, The Royal Marsden NHS Foundation Trust, Sutton, United Kingdom. Electronic address: [email protected].; Department of Medicine - Breast Unit, The Royal Marsden NHS Foundation Trust, Sutton, United Kingdom. Electronic address: [email protected].; Division of Geriatrics/Aging, Department of Medicine, University of Rochester Medical Center, Rochester, NY, USA. Electronic address: [email protected].; Drug Development Department (DITEP), Gustave Roussy, Université Paris-Saclay, Villejuif, F-94805, France. Electronic address: [email protected].; Gynaecology Unit, The Royal Marsden NHS Foundation Trust Sutton, United Kingdom. Electronic address: [email protected].; Department of Medical Oncology, Memorial Sloan Kettering Cancer Center, NY, USA. Electronic address: [email protected].
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.