Targeted Combination of Poly(ADP-ribose) Polymerase Inhibitors and Immune Checkpoint Inhibitors Lacking Evidence of Benefit: Focus in Ovarian Cancer

被引:3
|
作者
Bailey, Morgan [1 ]
Morand, Susan [1 ]
Royfman, Rachel [1 ]
Lin, Leslie [1 ]
Singh, Aditi [1 ]
Stanbery, Laura [2 ]
Walter, Adam [2 ,3 ]
Hamouda, Danae [1 ]
Nemunaitis, John [2 ]
机构
[1] Univ Toledo, Dept Med, Toledo, OH 43614 USA
[2] Gradalis Inc, Dallas, TX 75006 USA
[3] Promedica, Dept Gynecol Oncol, Toledo, OH 43614 USA
关键词
ovarian cancer; PARP inhibitor; immunotherapy; BRCA; homologous recombination; HRD; HRP; checkpoint inhibitor; ACUTE MYELOID-LEUKEMIA; TUMOR MUTATIONAL BURDEN; REGULATORY T-CELLS; OPEN-LABEL; PARP INHIBITORS; MYELODYSPLASTIC SYNDROME; MAINTENANCE THERAPY; SYNTHETIC LETHALITY; PLATINUM-RESISTANT; ANTI-PD-1; ANTIBODY;
D O I
10.3390/ijms25063173
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The emergence of targeted therapeutics in ovarian cancer, particularly poly (ADP-ribose) polymerase inhibitors (PARPi's), has created additional opportunities for patients seeking frontline and recurrent disease management options. In particular, PARPi's have shown clinical benefits in BRCA mutant and/or homologous recombination deficient (HRD) ovarian cancer. Until recently, response was thought to be limited in BRCA wild-type, homologous recombination proficient (HRP) cancers. Therefore, attempts have been made at combination therapy involving PARPi to improve patient outcomes. Additionally, immune checkpoint inhibitors (ICIs) have demonstrated underwhelming results involving ovarian cancer. Many are searching for reliable biomarkers of immune response to increase efficacy of ICI therapy involving ovarian cancer. In this review, we examine the evidence supporting the combination of PARPi and ICIs in ovarian cancer, which is still lacking.
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页数:21
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