Skip to main content
Erschienen in: Journal of Neuro-Oncology 1/2016

09.03.2016 | Clinical Study

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

verfasst von: Yingmei Li, Wenying Pan, Ian D. Connolly, Sunil Reddy, Seema Nagpal, Stephen Quake, Melanie Hayden Gephart

Erschienen in: Journal of Neuro-Oncology | Ausgabe 1/2016

Einloggen, um Zugang zu erhalten

Abstract

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.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
2.
Zurück zum Zitat Weller M (2003) Leptomeningeal metastasis. In: Brant T (ed) Neurological disorders: course and treatment, 2nd edn. Academic Press, Amsterdam, pp 897–909CrossRef Weller M (2003) Leptomeningeal metastasis. In: Brant T (ed) Neurological disorders: course and treatment, 2nd edn. Academic Press, Amsterdam, pp 897–909CrossRef
3.
Zurück zum Zitat Nagpal S, Riess J, Wakelee H (2012) Treatment of leptomeningeal spread of NSCLC: a continuing challenge. Curr Treat Options Oncol 13(4):491–504CrossRefPubMed Nagpal S, Riess J, Wakelee H (2012) Treatment of leptomeningeal spread of NSCLC: a continuing challenge. Curr Treat Options Oncol 13(4):491–504CrossRefPubMed
4.
Zurück zum Zitat Wasserstrom WR, Glass JP, Posner JB (1982) Diagnosis and treatment of leptomeningeal metastases from solid tumors: experience with 90 patients. Cancer 49(4):759–772CrossRefPubMed Wasserstrom WR, Glass JP, Posner JB (1982) Diagnosis and treatment of leptomeningeal metastases from solid tumors: experience with 90 patients. Cancer 49(4):759–772CrossRefPubMed
5.
Zurück zum Zitat Pan W, Gu W, Nagpal S, Gephart MH, Quake SR (2015) Brain tumor mutations detected in cerebral spinal fluid. Clin Chem 61(3):514–522CrossRefPubMed Pan W, Gu W, Nagpal S, Gephart MH, Quake SR (2015) Brain tumor mutations detected in cerebral spinal fluid. Clin Chem 61(3):514–522CrossRefPubMed
6.
Zurück zum Zitat Bettegowda C, Sausen M, Leary RJ et al (2014) Detection of circulating tumor DNA in early- and late-stage human malignancies. Sci Transl Med 6(224):224ra224CrossRef Bettegowda C, Sausen M, Leary RJ et al (2014) Detection of circulating tumor DNA in early- and late-stage human malignancies. Sci Transl Med 6(224):224ra224CrossRef
7.
Zurück zum Zitat Jang NE, Baek SK, Jeong Jh et al (2013) Early detection of BCR-ABL fusion gene of cerebrospinal fluid (CSF) by RT-PCR in relapsed acute lymphoblastic leukemia with philadelphia chromosome. Lab Med 43(2):e33–e37 Jang NE, Baek SK, Jeong Jh et al (2013) Early detection of BCR-ABL fusion gene of cerebrospinal fluid (CSF) by RT-PCR in relapsed acute lymphoblastic leukemia with philadelphia chromosome. Lab Med 43(2):e33–e37
8.
Zurück zum Zitat Swinkels DW, de Kok JB, Hanselaar A, Lamers K, Boerman RH (2000) Early detection of leptomeningeal metastasis by PCR examination of tumor-derived K-ras DNA in cerebrospinal fluid. Clin Chem 46(1):132–133PubMed Swinkels DW, de Kok JB, Hanselaar A, Lamers K, Boerman RH (2000) Early detection of leptomeningeal metastasis by PCR examination of tumor-derived K-ras DNA in cerebrospinal fluid. Clin Chem 46(1):132–133PubMed
11.
Zurück zum Zitat McKenna A, Hanna M, Banks E et al (2010) The genome analysis toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20(9):1297–1303CrossRefPubMedPubMedCentral McKenna A, Hanna M, Banks E et al (2010) The genome analysis toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20(9):1297–1303CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Cibulskis K, Lawrence MS, Carter SL et al (2013) Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat Biotechnol 31(3):213–219CrossRefPubMedPubMedCentral Cibulskis K, Lawrence MS, Carter SL et al (2013) Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat Biotechnol 31(3):213–219CrossRefPubMedPubMedCentral
13.
Zurück zum Zitat Wang K, Li M, Hakonarson H (2010) ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 38(16):e164CrossRefPubMedPubMedCentral Wang K, Li M, Hakonarson H (2010) ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 38(16):e164CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat De Mattos-Arruda L, Cortes J, Santarpia L et al (2013) Circulating tumour cells and cell-free DNA as tools for managing breast cancer. Nat Rev Clin Oncol 10(7):377–389CrossRefPubMed De Mattos-Arruda L, Cortes J, Santarpia L et al (2013) Circulating tumour cells and cell-free DNA as tools for managing breast cancer. Nat Rev Clin Oncol 10(7):377–389CrossRefPubMed
15.
Zurück zum Zitat Kamat AA, Baldwin M, Urbauer D et al (2010) Plasma cell-free DNA in ovarian cancer: an independent prognostic biomarker. Cancer 116(8):1918–1925CrossRefPubMedPubMedCentral Kamat AA, Baldwin M, Urbauer D et al (2010) Plasma cell-free DNA in ovarian cancer: an independent prognostic biomarker. Cancer 116(8):1918–1925CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat Papadopoulou E, Davilas E, Sotiriou V et al (2006) Cell-free DNA and RNA in plasma as a new molecular marker for prostate and breast cancer. Ann N Y Acad Sci 1075:235–243CrossRefPubMed Papadopoulou E, Davilas E, Sotiriou V et al (2006) Cell-free DNA and RNA in plasma as a new molecular marker for prostate and breast cancer. Ann N Y Acad Sci 1075:235–243CrossRefPubMed
17.
Zurück zum Zitat Pathak AK, Bhutani M, Kumar S, Mohan A, Guleria R (2006) Circulating cell-free DNA in plasma/serum of lung cancer patients as a potential screening and prognostic tool. Clin Chem 52(10):1833–1842PubMed Pathak AK, Bhutani M, Kumar S, Mohan A, Guleria R (2006) Circulating cell-free DNA in plasma/serum of lung cancer patients as a potential screening and prognostic tool. Clin Chem 52(10):1833–1842PubMed
18.
Zurück zum Zitat Wang Y, Springer S, Zhang M et al (2015) Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord. Proc Natl Acad Sci 112(31):9704–9709CrossRefPubMedPubMedCentral Wang Y, Springer S, Zhang M et al (2015) Detection of tumor-derived DNA in cerebrospinal fluid of patients with primary tumors of the brain and spinal cord. Proc Natl Acad Sci 112(31):9704–9709CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Grommes C, Oxnard GR, Kris MG et al (2011) “Pulsatile” high-dose weekly erlotinib for CNS metastases from EGFR mutant non-small cell lung cancer. Neuro Oncol 13(12):1364–1369CrossRefPubMedPubMedCentral Grommes C, Oxnard GR, Kris MG et al (2011) “Pulsatile” high-dose weekly erlotinib for CNS metastases from EGFR mutant non-small cell lung cancer. Neuro Oncol 13(12):1364–1369CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Schulze B, Meissner M, Wolter M, Rodel C, Weiss C (2014) Unusual acute and delayed skin reactions during and after whole-brain radiotherapy in combination with the BRAF inhibitor vemurafenib. Two case reports. Strahlenther Onkol 190(2):229–232CrossRefPubMed Schulze B, Meissner M, Wolter M, Rodel C, Weiss C (2014) Unusual acute and delayed skin reactions during and after whole-brain radiotherapy in combination with the BRAF inhibitor vemurafenib. Two case reports. Strahlenther Onkol 190(2):229–232CrossRefPubMed
21.
Zurück zum Zitat Chapman PB, Hauschild A, Robert C et al (2011) Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med 364(26):2507–2516CrossRefPubMedPubMedCentral Chapman PB, Hauschild A, Robert C et al (2011) Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med 364(26):2507–2516CrossRefPubMedPubMedCentral
22.
Zurück zum Zitat Falchook GS, Long GV, Kurzrock R et al (2012) Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial. Lancet 379(9829):1893–1901CrossRefPubMedPubMedCentral Falchook GS, Long GV, Kurzrock R et al (2012) Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial. Lancet 379(9829):1893–1901CrossRefPubMedPubMedCentral
23.
Zurück zum Zitat Fennira F, Pages C, Schneider P et al (2014) Vemurafenib in the French temporary authorization for use metastatic melanoma cohort: a single-centre trial. Melanoma Res 24(1):75–82CrossRefPubMed Fennira F, Pages C, Schneider P et al (2014) Vemurafenib in the French temporary authorization for use metastatic melanoma cohort: a single-centre trial. Melanoma Res 24(1):75–82CrossRefPubMed
24.
Zurück zum Zitat Sosman JA, Kim KB, Schuchter L et al (2012) Survival in BRAF V600-mutant advanced melanoma treated with vemurafenib. N Engl J Med 366(8):707–714CrossRefPubMedPubMedCentral Sosman JA, Kim KB, Schuchter L et al (2012) Survival in BRAF V600-mutant advanced melanoma treated with vemurafenib. N Engl J Med 366(8):707–714CrossRefPubMedPubMedCentral
25.
Zurück zum Zitat Wilgenhof S, Neyns B (2014) Complete cytologic remission of V600E BRAF-mutant melanoma-associated leptomeningeal carcinomatosis upon treatment with dabrafenib. J Clin Oncol 33:e109CrossRefPubMed Wilgenhof S, Neyns B (2014) Complete cytologic remission of V600E BRAF-mutant melanoma-associated leptomeningeal carcinomatosis upon treatment with dabrafenib. J Clin Oncol 33:e109CrossRefPubMed
26.
Zurück zum Zitat Tsao H, Goel V, Wu H, Yang G, Haluska FG (2004) Genetic interaction between NRAS and BRAF mutations and PTEN/MMAC1 inactivation in melanoma. J Invest Dermatol 122(2):337–341CrossRefPubMedPubMedCentral Tsao H, Goel V, Wu H, Yang G, Haluska FG (2004) Genetic interaction between NRAS and BRAF mutations and PTEN/MMAC1 inactivation in melanoma. J Invest Dermatol 122(2):337–341CrossRefPubMedPubMedCentral
27.
28.
Zurück zum Zitat Paraiso KH, Xiang Y, Rebecca VW et al (2011) PTEN loss confers BRAF inhibitor resistance to melanoma cells through the suppression of BIM expression. Cancer Res 71(7):2750–2760CrossRefPubMedPubMedCentral Paraiso KH, Xiang Y, Rebecca VW et al (2011) PTEN loss confers BRAF inhibitor resistance to melanoma cells through the suppression of BIM expression. Cancer Res 71(7):2750–2760CrossRefPubMedPubMedCentral
29.
Zurück zum Zitat Naji L, Pacholsky D, Aspenstrom P (2011) ARHGAP30 is a Wrch-1-interacting protein involved in actin dynamics and cell adhesion. Biochem Biophys Res Commun 409(1):96–102CrossRefPubMed Naji L, Pacholsky D, Aspenstrom P (2011) ARHGAP30 is a Wrch-1-interacting protein involved in actin dynamics and cell adhesion. Biochem Biophys Res Commun 409(1):96–102CrossRefPubMed
30.
Zurück zum Zitat Yang Y, Cochran DA, Gargano MD et al (2011) Regulation of flagellar motility by the conserved flagellar protein CG34110/Ccdc135/FAP50. Mol Biol Cell 22(7):976–987CrossRefPubMedPubMedCentral Yang Y, Cochran DA, Gargano MD et al (2011) Regulation of flagellar motility by the conserved flagellar protein CG34110/Ccdc135/FAP50. Mol Biol Cell 22(7):976–987CrossRefPubMedPubMedCentral
31.
Zurück zum Zitat Strauss U, Brauer AU (2013) Current views on regulation and function of plasticity-related genes (PRGs/LPPRs) in the brain. Biochim Biophys Acta 1831(1):133–138CrossRefPubMed Strauss U, Brauer AU (2013) Current views on regulation and function of plasticity-related genes (PRGs/LPPRs) in the brain. Biochim Biophys Acta 1831(1):133–138CrossRefPubMed
Metadaten
Titel
Tumor DNA in cerebral spinal fluid reflects clinical course in a patient with melanoma leptomeningeal brain metastases
verfasst von
Yingmei Li
Wenying Pan
Ian D. Connolly
Sunil Reddy
Seema Nagpal
Stephen Quake
Melanie Hayden Gephart
Publikationsdatum
09.03.2016
Verlag
Springer US
Erschienen in
Journal of Neuro-Oncology / Ausgabe 1/2016
Print ISSN: 0167-594X
Elektronische ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-016-2081-5

Weitere Artikel der Ausgabe 1/2016

Journal of Neuro-Oncology 1/2016 Zur Ausgabe

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Frühe Alzheimertherapie lohnt sich

25.04.2024 AAN-Jahrestagung 2024 Nachrichten

Ist die Tau-Last noch gering, scheint der Vorteil von Lecanemab besonders groß zu sein. Und beginnen Erkrankte verzögert mit der Behandlung, erreichen sie nicht mehr die kognitive Leistung wie bei einem früheren Start. Darauf deuten neue Analysen der Phase-3-Studie Clarity AD.

Viel Bewegung in der Parkinsonforschung

25.04.2024 Parkinson-Krankheit Nachrichten

Neue arznei- und zellbasierte Ansätze, Frühdiagnose mit Bewegungssensoren, Rückenmarkstimulation gegen Gehblockaden – in der Parkinsonforschung tut sich einiges. Auf dem Deutschen Parkinsonkongress ging es auch viel um technische Innovationen.

Demenzkranke durch Antipsychotika vielfach gefährdet

23.04.2024 Demenz Nachrichten

Wenn Demenzkranke aufgrund von Symptomen wie Agitation oder Aggressivität mit Antipsychotika behandelt werden, sind damit offenbar noch mehr Risiken verbunden als bislang angenommen.

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.