Determining PARP Inhibition as a Treatment Strategy in Melanoma Based on Homologous Recombination Deficiency-Related Loss of Heterozygosity

被引:2
|
作者
Zhou, Alice [1 ]
Butt, Omar [1 ]
Ansstas, Michael [1 ]
Mauer, Elizabeth [2 ]
Khaddour, Karam [3 ]
Ansstas, George [1 ]
机构
[1] Washington Univ St Louis, Div Med Oncol, Dept Internal Med, St Louis, MO USA
[2] Tempus Labs Inc, Chicago, IL USA
[3] Univ Illinois, Div Hematol & Oncol, Chicago, IL USA
关键词
METASTATIC MELANOMA; REPAIR; IMMUNOTHERAPY; BLOCKADE; PATTERNS; OLAPARIB; MUTATION; CANCER;
D O I
10.6004/jnccn.2022.7102
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
There is a lack of effective treatments for immunotherapy-refectory melanoma. Although PARP inhibitors (PARPi) are an effective treatment strategy in cancers with homologous recombination deficiency (HRD), determining HRD status is challenging in melanoma. Here, we chart the longitudinal relationship between PARPi response and HRD scores derived from genome-wide loss of heterozygosity (LOH) in 4 patients with metastaticmelanoma. When next examining 933 melanoma cases, using an updated threshold, we observed HRD-related LOH (HRD-LOH) in nearly one-third of all cases compared with,10% using traditional gene panels. Taken together, HRD-LOH in refractory melanoma is both a common occurrence and a potential biomarker for response to PARPi.
引用
收藏
页码:688 / +
页数:11
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