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

被引:4
|
作者
Navitski, Anastasia [1 ]
Al-Rawi, Duaa H. [2 ]
Liu, Ying [2 ,3 ,4 ]
Rubinstein, Maria M. [2 ,3 ]
Friedman, Claire F. [2 ,3 ]
Rampal, Raajit K. [3 ,5 ]
Mandelker, Diana L. [4 ]
Cadoo, Karen [6 ]
O'Cearbhaill, Roisin E. [2 ,3 ]
机构
[1] Columbia Univ, Vagelos Coll Phys & Surg, New York, NY USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, Gynecol Med Oncol Serv, 1275 York Ave, New York, NY 10065 USA
[3] Weill Cornell Med Coll, Dept Med, New York, NY USA
[4] Mem Sloan Kettering Canc Ctr, Dept Med, Clin Genet Serv, 1275 York Ave, New York, NY 10065 USA
[5] Mem Sloan Kettering Canc Ctr, Dept Med, Leukemia Serv, 1275 York Ave, New York, NY 10065 USA
[6] Trinity Coll Dublin, St Jamess Hosp, Trinity St Jamess Canc Inst, Dublin, Ireland
来源
关键词
Ovarian cancer; BRCA mutation; PARP inhibitors; Myelodysplastic syndrome; Acute myeloid leukemia;
D O I
10.1016/j.gore.2021.100873
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
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.
引用
收藏
页数:5
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