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Quantification of tumor-derived cell free DNA(cfDNA) by digital PCR (DigPCR) in cerebrospinal fluid of patients with BRAFV600 mutated malignancies

机译:通过数字PCR(DigPCR)对BRAFV600突变的恶性肿瘤患者脑脊液中肿瘤衍生的无细胞DNA(cfDNA)进行定量

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摘要

Tumor-derived cell free DNA (cfDNA) can be detected in plasma. We hypothesized that mutated BRAF V600 cfDNA could be quantified in the cerebrospinal fluid (CSF) of patients with central nervous system (CNS) metastases. We collected CSF from patients with BRAF V600E or K-mutated melanoma (N=8) or BRAF V600E mutated Erdheim-Chester Disease (ECD) (N=3) with suspected central nervous system (CNS) involvement on the basis of neurological symptoms (10/11), MRI imaging (8/11), or both. Tumor-derived cfDNA was quantified by digital PCR in the CSF of 6/11 patients (range from 0.15-10.56 copies/μL). Conventional cytology was negative in all patients except in the two patients with markedly elevated levels of tumor-derived cfDNA. In 2 patients with serial measurements, CSF tumor-derived cfDNA levels reflected response to treatment or progressive disease. CSF tumor-derived cfDNA has the potential to serve as a diagnostic tool that complements MRI and may be more sensitive than conventional cytology.
机译:血浆中可检测到肿瘤来源的无细胞DNA(cfDNA)。我们假设突变的BRAF V600 cfDNA可以在中枢神经系统(CNS)转移患者的脑脊液(CSF)中定量。我们根据神经系统症状从怀疑患有中枢神经系统(CNS)的BRAF V600E或K突变黑素瘤(N = 8)或BRAF V600E突变Erdheim-Chester病(ECD)(N = 3)患者中收集了CSF( 10/11),MRI成像(8/11)或两者兼有。肿瘤来源的cfDNA通过数字PCR在6/11患者的CSF中定量(范围从0.15-10.56拷贝/μL)。除两名患者肿瘤来源的cfDNA水平显着升高外,所有患者的常规细胞学检查均为阴性。在进行连续测量的2例患者中,脑脊液肿瘤衍生的cfDNA水平反映了对治疗或疾病进展的反应。 CSF肿瘤来源的cfDNA有潜力作为补充MRI的诊断工具,并且可能比常规细胞学更为敏感。

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