ctDNA动态识别Nivolumab/Relatlimab治疗的转移性黑色素瘤患者的假进展。

IF 3.2 4区 医学 Q3 IMMUNOLOGY
Alyssa K Steimle, Steve Y Cho, Nandakumar Menon, Robert Jeraj, Alexander Birbrair, Mark R Albertini, Vincent T Ma
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引用次数: 0

摘要

假性进展已知发生在接受免疫检查点抑制剂治疗的转移性黑色素瘤患者中,并使临床决策复杂化。区分假级数和真级数的更好方法是必要的。在本病例报告中,我们展示了循环肿瘤DNA (ctDNA)如何在联合抗程序性细胞死亡蛋白1(抗pd -1)和抗淋巴细胞活化基因3(抗lag -3)治疗的转移性黑色素瘤患者的早期间隔放射反应评估中识别假进展中发挥作用。循环肿瘤DNA是一种很有前途的生物标志物,有可能可靠地评估黑色素瘤对免疫检查点抑制剂的反应,即使放射学结果具有误导性或不确定。需要进一步的研究来确定不同免疫检查点抑制剂方案的假进展率,并确定ctDNA动力学在确定这一现象中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ctDNA Dynamics Identifies Pseudoprogression in a Metastatic Melanoma Patient Treated With Nivolumab/Relatlimab.

Pseudoprogression is known to occur in patients with metastatic melanoma treated with immune checkpoint inhibitors and complicates clinical decision-making. Better methods of distinguishing pseudoprogression from true progression are necessary. In this case report, we show how circulating tumor DNA (ctDNA) plays a role in identifying pseudoprogression on early interval radiologic response assessment in a patient with metastatic melanoma treated with combination anti-programmed cell death protein 1 (anti-PD-1) and anti-lymphocyte activation gene 3 (anti-LAG-3). Circulating tumor DNA is a promising biomarker that has potential to reliably assess response to immune checkpoint inhibitors in melanoma, even when the radiologic findings are misleading or indeterminate. Further research is warranted to identify rates of pseudoprogression across various immune checkpoint inhibitor regimens and to identify the role of ctDNA dynamics to identify this phenomenon.

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来源期刊
Journal of Immunotherapy
Journal of Immunotherapy 医学-免疫学
CiteScore
6.90
自引率
0.00%
发文量
79
审稿时长
6-12 weeks
期刊介绍: Journal of Immunotherapy features rapid publication of articles on immunomodulators, lymphokines, antibodies, cells, and cell products in cancer biology and therapy. Laboratory and preclinical studies, as well as investigative clinical reports, are presented. The journal emphasizes basic mechanisms and methods for the rapid transfer of technology from the laboratory to the clinic. JIT contains full-length articles, review articles, and short communications.
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