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基于同源重组缺陷相关杂合性丢失的 PARP 抑制作为黑色素瘤的治疗策略。

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

机构信息

Division of Medical Oncology, Department of Internal Medicine, Washington University in St. Louis, St. Louis, Missouri.

Tempus Laboratories Inc., Chicago, Illinois.

出版信息

J Natl Compr Canc Netw. 2023 Jul;21(7):688-693.e3. doi: 10.6004/jnccn.2022.7102.

Abstract

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 metastatic melanoma. 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.

摘要

免疫治疗难治性黑色素瘤缺乏有效的治疗方法。尽管聚腺苷二磷酸核糖聚合酶抑制剂(PARPi)在同源重组缺陷(HRD)的癌症中是一种有效的治疗策略,但在黑色素瘤中确定 HRD 状态具有挑战性。在这里,我们描绘了 4 名转移性黑色素瘤患者的 PARPi 反应与全基因组杂合性丢失(LOH)得出的 HRD 评分之间的纵向关系。当使用更新的阈值进一步检查 933 例黑色素瘤病例时,与使用传统基因面板时 <10%相比,我们发现近三分之一的病例存在与 HRD 相关的 LOH(HRD-LOH)。总之,难治性黑色素瘤中的 HRD-LOH 不仅是一种常见现象,也是对 PARPi 反应的潜在生物标志物。

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