检测脑脊液中的游离细胞肿瘤 DNA 作为脑膜黑色素瘤转移的诊断生物标志物:病例系列。

IF 3.9 3区 医学 Q2 CELL BIOLOGY Pigment Cell & Melanoma Research Pub Date : 2024-07-11 DOI:10.1111/pcmr.13186
Iris Dirven, Manon Vounckx, Jolien I. Kessels, Justine Lauwyck, Gil Awada, Anne-Marie Vanbinst, Bart Neyns
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引用次数: 0

摘要

脑膜黑色素瘤转移(LMM)与生存率低下有关。诊断主要依据临床表现、脑磁共振成像和脑脊液(CSF)分析。初次就诊时的不确定结果会延误治疗。在这一单中心病例系列中,脑脊液中 BRAFV600 和 NRASQ61 突变细胞游离肿瘤 DNA(cfDNA)的检测作为辅助诊断生物标记物进行了评估。在 12 例临床怀疑为 LMM 的患者中,使用 Idylla® 平台对 1 mL CSF 的 MRI、CSF 细胞学和 cfDNA 分析进行了回顾性分析。九名患者的磁共振成像出现异常,提示为 LMM。CSF 分析确定了三名患者(包括一名无 MRI 异常的患者)的恶性细胞。九名患者的 CSF 中检测到 BRAFV600 或 NRASQ61 突变的 cfDNA(八名患者有 MRI 异常,一名患者无 MRI 异常;所有患者的 CSF 细胞学检查均呈阳性)。随后的随访证实,所有 CSF cfDNA 分析呈阳性的患者和一名呈阴性的患者均为 LMM(敏感性 81.8%;特异性 100%)。我们的研究结果表明,使用Idylla®平台分析CSF中的BRAFV600和NRASQ61突变cfDNA有望成为LMM敏感而特异的辅助诊断生物标记物,尤其是在影像学和CSF细胞学结果不一致的情况下。110 分钟的分析有助于做出紧急治疗决定。
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Detection of cell-free tumor DNA in cerebrospinal fluid as a diagnostic biomarker for leptomeningeal melanoma metastasis: A case series

Leptomeningeal melanoma metastases (LMM) are associated with poor survival. Diagnosis is based on clinical presentation, brain MRI and cerebrospinal fluid (CSF) analysis. Inconclusive findings at initial presentation can delay treatment. In this single-center case series, detection of BRAFV600- and NRASQ61-mutant cell-free tumor DNA (cfDNA) in CSF was evaluated as a complementary diagnostic biomarker. In 12 patients with clinical suspicion of LMM, a retrospective analysis of MRI, CSF cytology and cfDNA analysis on 1 mL of CSF using the Idylla® platform was carried out. Nine patients displayed MRI abnormalities suggesting LMM. CSF analysis identified malignant cells in three patients (including one without MRI abnormalities). BRAFV600- or NRASQ61-mutant cfDNA was detected in CSF of nine patients (eight with and one without MRI abnormalities; all patients with positive CSF cytology). Subsequent follow-up confirmed LMM in all patients with positive and in one patient with a negative CSF cfDNA analysis (sensitivity 81.8%; specificity 100%). Our findings suggest that analyzing BRAFV600- and NRASQ61-mutant cfDNA in CSF using the Idylla® platform holds promise as a sensitive and specific complementary diagnostic biomarker for LMM, particularly in case of inconsistency between imaging and CSF cytology. The 110-min analysis can facilitate urgent treatment decisions.

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来源期刊
Pigment Cell & Melanoma Research
Pigment Cell & Melanoma Research 医学-皮肤病学
CiteScore
8.90
自引率
2.30%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Pigment Cell & Melanoma Researchpublishes manuscripts on all aspects of pigment cells including development, cell and molecular biology, genetics, diseases of pigment cells including melanoma. Papers that provide insights into the causes and progression of melanoma including the process of metastasis and invasion, proliferation, senescence, apoptosis or gene regulation are especially welcome, as are papers that use the melanocyte system to answer questions of general biological relevance. Papers that are purely descriptive or make only minor advances to our knowledge of pigment cells or melanoma in particular are not suitable for this journal. Keywords Pigment Cell & Melanoma Research, cell biology, melatonin, biochemistry, chemistry, comparative biology, dermatology, developmental biology, genetics, hormones, intracellular signalling, melanoma, molecular biology, ocular and extracutaneous melanin, pharmacology, photobiology, physics, pigmentary disorders
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