Tumor DNA in cerebral spinal fluid reflects clinical course in a patient with melanoma leptomeningeal brain metastases

被引:71
作者
Li, Yingmei [1 ]
Pan, Wenying [3 ]
Connolly, Ian D. [1 ]
Reddy, Sunil [4 ]
Nagpal, Seema [5 ]
Quake, Stephen [3 ,6 ]
Gephart, Melanie Hayden [2 ]
机构
[1] Stanford Univ, Dept Neurosurg, MSLS, 1201 Welch Rd,P151, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Neurosurg, MSLS, 1205 Welch Rd,R307, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Bioengn, James H Clark Ctr, 318 Campus Dr,E300, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Med, Ctr Canc, 875 Blake Wilbur Dr,CC2232, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Neurol, Ctr Canc, 875 Blake Wilbur Dr,CC2221, Stanford, CA 94305 USA
[6] Howard Hughes Med Inst, Chevy Chase, MD USA
关键词
Brain Tumor; Cell-free DNA; Cerebral spinal fluid; Droplet digital PCR; Exome sequencing; Leptomeningeal disease; Melanoma; CELL-FREE DNA; SOLID TUMORS; MUTATIONS; CANCER; VEMURAFENIB; SURVIVAL; PLASMA;
D O I
10.1007/s11060-016-2081-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cerebral spinal fluid (CSF) from brain tumor patients contains tumor cellular and cell-free DNA (cfDNA), which provides a less-invasive and routinely accessible method to obtain tumor genomic information. In this report, we used droplet digital PCR to test mutant tumor DNA in CSF of a patient to monitor the treatment response of metastatic melanoma leptomeningeal disease (LMD). The primary melanoma was known to have a BRAF (V600E) mutation, and the patient was treated with whole brain radiotherapy and BRAF inhibitors. We collected 9 CSF samples over 6 months. The mutant cfDNA fraction gradually decreased from 53 % (time of diagnosis) to 0 (time of symptom alleviation) over the first 6 time points. Three months after clinical improvement, the patient returned with severe symptoms and the mutant cfDNA was again detected in CSF at high levels. The mutant DNA fraction corresponded well with the patient's clinical response. We used whole exome sequencing to examine the mutation profiles of the LMD tumor DNA in CSF before therapeutic response and after disease relapse, and discovered a canonical cancer mutation PTEN (R130*) at both time points. The cellular and cfDNA revealed similar mutation profiles, suggesting cfDNA is representative of LMD cells. This study demonstrates the potential of using cellular or cfDNA in CSF to monitor treatment response for LMD.
引用
收藏
页码:93 / 100
页数:8
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