Baseline risk of hematologic malignancy at initiation of frontline PARP inhibitor maintenance for BRCA1/2-associated ovarian cancer

Poly(ADP-ribose) polymerase inhibitors (PARPi) are FDA approved as frontline maintenance for BRCA-associated advanced stage high-grade ovarian cancer (HGOC), having demonstrated an unprecedented improvement in relapse-free survival. Myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) are...

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Main Authors: Anastasia Navitski (Author), Duaa H. Al-Rawi (Author), Ying Liu (Author), Maria M. Rubinstein (Author), Claire F. Friedman (Author), Raajit K. Rampal (Author), Diana L. Mandelker (Author), Karen Cadoo (Author), Roisin E. O'Cearbhaill (Author)
Format: Book
Published: Elsevier, 2021-11-01T00:00:00Z.
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Summary:Poly(ADP-ribose) polymerase inhibitors (PARPi) are FDA approved as frontline maintenance for BRCA-associated advanced stage high-grade ovarian cancer (HGOC), having demonstrated an unprecedented improvement in relapse-free survival. Myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) are rare toxicities of PARPi. We describe three patients with germline BRCA-associated (gBRCA+) HGOC and alterations in AML driver genes. Although none evidenced overt hematologic malignancy, PARPi maintenance was cautiously considered given the potential risk of MDS/AML. A better understanding of the role of clonal hematopoiesis in the subsequent development of PARPi-associated MDS/AML will improve management of this patient population.
Item Description:2352-5789
10.1016/j.gore.2021.100873