EXTH-39. DETECTION, MOLECULAR PROFILING AND CULTURE OF CSF-CTCs IN LEPTOMENINGEAL DISEASE (LMDz) IN MELANOMA TO IMPROVE DIAGNOSIS AND TREATMENT STRATEGIES. (5th November 2018)
- Record Type:
- Journal Article
- Title:
- EXTH-39. DETECTION, MOLECULAR PROFILING AND CULTURE OF CSF-CTCs IN LEPTOMENINGEAL DISEASE (LMDz) IN MELANOMA TO IMPROVE DIAGNOSIS AND TREATMENT STRATEGIES. (5th November 2018)
- Main Title:
- EXTH-39. DETECTION, MOLECULAR PROFILING AND CULTURE OF CSF-CTCs IN LEPTOMENINGEAL DISEASE (LMDz) IN MELANOMA TO IMPROVE DIAGNOSIS AND TREATMENT STRATEGIES
- Authors:
- Law, Vincent
Evernden, Brittany
Kenchappa, Rajappa
Puskas, John
Ryzhova, Elena
Smalley, Inna
Tran, Nam
Etame, Arnold
Sahebjam, Solmaz
Magliocco, Anthony
Smalley, Keiran
Forsyth, Peter - Abstract:
- Abstract: BACKGROUND: Approximately 5% of melanoma-associated brain metastasis also develops universally fatal LMDz. The aim of this study was to improve diagnosis and personalized treatment for melanoma-LMDz by enumerating CTCs from CSF. METHODS: CSF-CTCs were enriched and detected by Veridex CellSearch® System and the circulating melanoma cell kit. Cell-free DNA and cell-associated DNA were extracted, sequenced and profiled. Expanded ex-vivo CSF-CTCs and murine BRAF V600E mutant SM1 cells were labeled with viral fluorophore-NanoLuc BRET and injected into the cisterna magna of immunocomprised mice. These cells were also tested for drug sensitivity in-vitro . RESULTS: CSF-CTCs: 12 patients with definite LMDz and 8 melanoma patients without LMDz were studied. All but 1 LMDz patients (92%) had CSF-CTCs (23 CTCs/ml to 3055 CTCs/ml CSF). In contrast, only 3/8 (37%) melanoma patients without LMDz had CSF-CTCs detected, with significantly lower CTC counts per ml CSF (0.13 CTCs/ml to 0.6 CTCs/ml CSF). CSF-CTCs Profile: LMDz patients showed GNAQ Q209P mutation (uveal melanoma), NRAS Q61R mutation (nasal melanoma) and also BRAF V600E mutation. Ex vivo culture of CSF-CTCs and in-vivo injections : We successfully demonstrated ex-vivo expansion of isolated CSF-CTCs (~25% of samples). Drug treatment revealed Ceritinib could kill BRAF-inhibitor resistant melanoma-CTCs. Mice injected with SM1-GFP-NanoLuc exhibited tumor growth in ~1.5 weeks. Metastasis was detected in the brain and spinalAbstract: BACKGROUND: Approximately 5% of melanoma-associated brain metastasis also develops universally fatal LMDz. The aim of this study was to improve diagnosis and personalized treatment for melanoma-LMDz by enumerating CTCs from CSF. METHODS: CSF-CTCs were enriched and detected by Veridex CellSearch® System and the circulating melanoma cell kit. Cell-free DNA and cell-associated DNA were extracted, sequenced and profiled. Expanded ex-vivo CSF-CTCs and murine BRAF V600E mutant SM1 cells were labeled with viral fluorophore-NanoLuc BRET and injected into the cisterna magna of immunocomprised mice. These cells were also tested for drug sensitivity in-vitro . RESULTS: CSF-CTCs: 12 patients with definite LMDz and 8 melanoma patients without LMDz were studied. All but 1 LMDz patients (92%) had CSF-CTCs (23 CTCs/ml to 3055 CTCs/ml CSF). In contrast, only 3/8 (37%) melanoma patients without LMDz had CSF-CTCs detected, with significantly lower CTC counts per ml CSF (0.13 CTCs/ml to 0.6 CTCs/ml CSF). CSF-CTCs Profile: LMDz patients showed GNAQ Q209P mutation (uveal melanoma), NRAS Q61R mutation (nasal melanoma) and also BRAF V600E mutation. Ex vivo culture of CSF-CTCs and in-vivo injections : We successfully demonstrated ex-vivo expansion of isolated CSF-CTCs (~25% of samples). Drug treatment revealed Ceritinib could kill BRAF-inhibitor resistant melanoma-CTCs. Mice injected with SM1-GFP-NanoLuc exhibited tumor growth in ~1.5 weeks. Metastasis was detected in the brain and spinal cord regions. CONCLUSIONS: Though current patient size is small, this is the first report of the successful culture and drug testing of CSF-CTCs from patients with LMDz. Single cell analysis and in-vivo testing in progress. … (more)
- Is Part Of:
- Neuro-oncology. Volume 20(2018)Supplement 6
- Journal:
- Neuro-oncology
- Issue:
- Volume 20(2018)Supplement 6
- Issue Display:
- Volume 20, Issue 6 (2018)
- Year:
- 2018
- Volume:
- 20
- Issue:
- 6
- Issue Sort Value:
- 2018-0020-0006-0000
- Page Start:
- vi93
- Page End:
- vi93
- Publication Date:
- 2018-11-05
- Subjects:
- Brain Neoplasms -- Periodicals
Brain -- Tumors -- Periodicals
Brain -- Cancer -- Periodicals
Nervous system -- Cancer -- Periodicals
616.99481 - Journal URLs:
- http://neuro-oncology.dukejournals.org/ ↗
http://neuro-oncology.oxfordjournals.org/ ↗
http://www.oxfordjournals.org/content?genre=journal&issn=1522-8517 ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/neuonc/noy148.387 ↗
- Languages:
- English
- ISSNs:
- 1522-8517
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.288000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12325.xml