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首页> 外文期刊>Journal of Translational Medicine >Quantitative assessment of BRAF V600 mutant circulating cell-free tumor DNA as a tool for therapeutic monitoring in metastatic melanoma patients treated with BRAF/MEK inhibitors
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Quantitative assessment of BRAF V600 mutant circulating cell-free tumor DNA as a tool for therapeutic monitoring in metastatic melanoma patients treated with BRAF/MEK inhibitors

机译:定量评估BRAF V600突变体循环无细胞肿瘤DNA作为BRAF / MEK抑制剂治疗的转移性黑色素瘤患者治疗监测的工具

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摘要

Background BRAF V600 mutant circulating cell-free tumor DNA ( BRAF V600mut ctDNA) could serve as a specific biomarker in patients with BRAF V600 mutant melanoma. We analyzed the value of BRAF V600mut ctDNA from plasma as a monitoring tool for advanced melanoma patients treated with BRAF/MEK inhibitors. Methods Allele-specific quantitative PCR analysis for BRAF V600 E/E2/D/K/R/M mutations was performed on DNA extracted from plasma of patients with known BRAF V600 mutant melanoma who were treated with dabrafenib and trametinib. Results 245 plasma samples from 36 patients were analyzed. In 16 patients the first plasma sample was obtained before the first dosing of dabrafenib/trametinib. At baseline, BRAF V600mut ctDNA was detected in 75?% of patients (n?=?12/16). BRAF V600mut ctDNA decreased rapidly upon initiation of targeted therapy (p?Conclusions Quantitative analysis of BRAF V600mut ctDNA in plasma has unique features as a monitoring tool during treatment with BRAF/MEK inhibitors. Its potential as an early predictor of acquired resistance deserves further evaluation.
机译:背景BRAF V600突变型无细胞循环肿瘤DNA(BRAF V600mut ctDNA)可以作为BRAF V600突变型黑素瘤患者的特异性生物标志物。我们分析了血浆BRAF V600mut ctDNA作为BRAF / MEK抑制剂治疗的晚期黑色素瘤患者的监测工具的价值。方法对达拉非尼和曲美替尼治疗的已知BRAF V600突变型黑素瘤患者血浆中提取的DNA进行BRAF V600 E / E2 / D / K / R / M突变的等位基因特异性定量PCR分析。结果分析了36例患者的245份血浆样品。在16例患者中,在首次给予dabrafenib / trametinib之前先获得了血浆样品。基线时,在75%的患者中检出了BRAF V600mut ctDNA(n == 12/16)。靶向治疗开始后,BRAF V600mut ctDNA迅速下降(p?结论)血浆中BRAF V600mut ctDNA的定量分析具有独特的功能,可作为BRAF / MEK抑制剂治疗期间的监测工具。其作为获得性耐药的早期预测指标的潜力值得进一步评估。

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