Silverman Rebecca F, Francis Jasmine H, Robbins Melissa A, Dunkel Ira J, Abramson David H
Department of Surgery, Ophthalmic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Department of Ophthalmology, Weill Cornell-Medical Center, New York, New York; and.
Retina. 2024 Dec 1;44(12):2123-2128. doi: 10.1097/IAE.0000000000004224.
Circulating tumor DNA (ctDNA) in plasma has been identified in many cancers, including retinoblastoma at diagnosis. It has previously been shown that with treatment (enucleation or ophthalmic artery chemosurgery), all ctDNA disappears; if there is persistent plasma ctDNA after treatment, metastases develop. The purpose of this study was to determine how the ctDNA RB1 variant allele frequency changes in patients with retinoblastoma who have delayed treatment.
Circulating tumor DNA RB1 was detected, and variant allele frequency was measured at diagnosis and again before any intervention at some time later ranging from 2 days to 28 days.
Four patients with five ctDNA RB1 mutations were detected at diagnosis, and variant allele frequency was increased on reevaluation of the same RB1 mutations in ctDNA.
In this small cohort, every patient (4) and every RB1 mutation (5) plasma level VAF% increased when measured at two time periods before treatment was initiated suggesting that growing tumors demonstrate increasing plasma ctDNA.
血浆中的循环肿瘤DNA(ctDNA)已在许多癌症中被鉴定出来,包括视网膜母细胞瘤诊断时。此前已经表明,经过治疗(眼球摘除术或眼动脉化学手术),所有ctDNA都会消失;如果治疗后血浆ctDNA持续存在,则会发生转移。本研究的目的是确定视网膜母细胞瘤患者延迟治疗时ctDNA RB1变异等位基因频率如何变化。
检测循环肿瘤DNA RB1,并在诊断时以及在2天至28天内的稍后某个时间进行任何干预之前再次测量变异等位基因频率。
诊断时检测到4例有5个ctDNA RB1突变的患者,对ctDNA中相同的RB1突变进行重新评估时,变异等位基因频率增加。
在这个小队列中,在开始治疗前的两个时间段测量时,每个患者(4例)和每个RB1突变(5个)的血浆水平VAF%都增加了,这表明肿瘤生长时血浆ctDNA会增加。