Department of Dermatology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto 390-8621, Japan.
Acta Derm Venereol. 2017 Nov 15;97(10):1212-1218. doi: 10.2340/00015555-2748.
Anti-programmed cell death-1 (anti-PD-1) antibody shows high therapeutic efficacy in patients with advanced melanoma. However, assessment of its therapeutic activity can be challenging because of tumour enlargement associated with intratumoural inflammation. Because circulating tumour DNA (ctDNA) correlates with tumour burden, we assessed the value of ctDNA levels as an indicator of tumour changes. Quantification of ctDNA (BRAFmutant or NRASmutant) levels by droplet digital PCR in 5 patients with BRAF or NRAS mutant melanoma during the treatment course showed dynamic changes corresponding to radiological and clinical alterations. In 3 cases in which the anti-PD-1 antibody was effective, ctDNA levels decreased within 2-4 weeks after treatment initiation. In 2 cases in which the anti-PD-1 antibody was ineffective, ctDNA levels did not decrease after treatment initiation. ctDNA could be a useful biomarker to predict early response to treatment in patients with advanced melanoma treated with anti-PD-1 immunotherapy.
抗程序性细胞死亡蛋白 1(抗 PD-1)抗体在晚期黑色素瘤患者中显示出很高的治疗疗效。然而,由于肿瘤内炎症相关的肿瘤增大,评估其治疗活性可能具有挑战性。由于循环肿瘤 DNA(ctDNA)与肿瘤负担相关,我们评估了 ctDNA 水平作为肿瘤变化指标的价值。在 5 例 BRAF 或 NRAS 突变黑色素瘤患者的治疗过程中,通过液滴数字 PCR 定量检测 ctDNA(BRAF 突变或 NRAS 突变)水平,显示出与影像学和临床改变相对应的动态变化。在抗 PD-1 抗体有效的 3 例病例中,ctDNA 水平在治疗开始后 2-4 周内下降。在抗 PD-1 抗体无效的 2 例病例中,治疗开始后 ctDNA 水平没有下降。ctDNA 可能是一种有用的生物标志物,可预测接受抗 PD-1 免疫治疗的晚期黑色素瘤患者的早期治疗反应。