Journals / Turkish Neurosurgery / 2020 / Cilt: 30 - Sayı: 4

Current Clinical Practice About Pediatric Midline Gliomas in the Scope of Molecular Era

Pages
595–603
DOI
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⚡ TL;DR(Too Long; Didn't Read)

Stereotactic biopsy for midlinegliomas is a safe and effective method.

📌 3 Key Takeaways

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Objective & Hypothesis:AIM: To share our clinical experience with surgical and adjuvant treatment strategies followed during the treatment of midlinegliomas.MATERIAL and METHODS: Pediatric patients with midline gliomas who underwent surgery in our clinic between March 2016 andNovember 2019 were included.
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Key Findings & Data:Allsamples were analyzed for ATRX, BRAFV600E, IDH1/2, H3K27M, and H3G34R mutations, EGFR and PGFRA amplifications, andPTEN loss.RESULTS: There were 7 (43.8%) female and 9 (56.2%) male pediatric patients in the study.
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Conclusion & Impact:Stereotactic biopsy for midlinegliomas is a safe and effective method.
🔬Design:Research Article
📍Scope:2016 Verileri
⚙️Variables:Domain Parameters

Özet

AIM: To share our clinical experience with surgical and adjuvant treatment strategies followed during the treatment of midlinegliomas.MATERIAL and METHODS: Pediatric patients with midline gliomas who underwent surgery in our clinic between March 2016 andNovember 2019 were included. Tissue samples were obtained through surgical excision, open biopsy, or stereotactic biopsy. Allsamples were analyzed for ATRX, BRAFV600E, IDH1/2, H3K27M, and H3G34R mutations, EGFR and PGFRA amplifications, andPTEN loss.RESULTS: There were 7 (43.8%) female and 9 (56.2%) male pediatric patients in the study. Eight patients had thalamic, 5 patientshad pontine, 2 patients had medulla oblongata and one patient had brachium pontis tumors. Presenting symptoms were headache,disequilibrium, ophthalmoplegia, and panic attack. Eleven tumors showed H3K27M mutation and were diagnosed as diffuse midlinegliomas. BRAFV600E, ATRX mutations, PTEN loss, and EGFR amplifications were other molecular alterations detected within tumorsamples. Patients with H3K27M mutant tumors had a shorter life span. Five patients were enrolled in an ONC201 trial.CONCLUSION: Although most midline gliomas are not amenable to gross total excision, obtaining tissue samples is mandatoryfor determining patients’ exact diagnoses, tailored treatment plans, and eligibility for clinical trials. Stereotactic biopsy for midlinegliomas is a safe and effective method.

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Cite This Article

TANRIKULU, B., ÖZEK, M. M. (2020). Current Clinical Practice About Pediatric Midline Gliomas in the Scope of Molecular Era. Turkish Neurosurgery, Cilt: 30 - Sayı: 4, 595–603. https://ajindex.com/articles/404318

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References (1)

  1. Albright AL, Packer RJ, Zimmerman R, Rorke LB, Boyett J, Hammond GD: Magnetic resonance scans should replace biopsies for the diagnosis of diffuse brain stem gliomas: A report from the Children’s Cancer Group. Neurosurgery 33:1026-1029; discussion 1029-1030, 1993 2. Bilginer B, Narin F, Isikay I, Oguz KK, Soylemezoglu F, Akalan N: Thalamic tumors in children. Childs Nerv Syst 30:1493- 1498, 2014 3. Chamberlain MC: Salvage therapy with BRAF inhibitors for recurrent pleomorphic xanthoastrocytoma: A retrospective case series. J Neurooncol 114:237-240, 2013 4. Chi AS, Tarapore RS, Hall MD, Shonka N, Gardner S, Umemura Y, Sumrall A, Khatib Z, Mueller S, Kline C, Zaky W, Khatua S, Weathers SP, Odia Y, Niazi TN, Daghistani D, Cherrick I, Korones D, Karajannis MA, Kong XT, Minturn J, Waanders A, Arillaga-Romany I, Batchelor T, Wen PY, Merdinger K, Schalop L, Stogniew M, Allen JE, Oster W, Mehta MP: Pediatric and adult H3 K27M-mutant diffuse midline glioma treated with the selective DRD2 antagonist ONC201. J Neurooncol 145:97- 105, 2019 5. Choux M, Lena G, Do L: Brainstem tumors. In: Choux M DrC, Hockley AD (eds), Pediatric Neurosurgery. NewYork: Churchill Livingstone, 1999:471-491 6. Dahiya S, Emnett RJ, Haydon DH, Leonard JR, Phillips JJ, Perry A, Gutmann DH: BRAF-V600E mutation in pediatric and adult glioblastoma. Neuro Oncol 16:318-319, 2014 7. Dellaretti M, Touzet G, Reyns N, Dubois F, Gusmao S, Pereira JL, Blond S: Correlation among magnetic resonance imaging findings, prognostic factors for survival, and histological diagnosis of intrinsic brainstem lesions in children. J Neurosurg Pediatr 8:539-543, 2011 8. Di Rocco C, Iannelli A: Bilateral thalamic tumors in children. Childs Nerv Syst 18:440-444, 2002 9. Eisner W, Schmid UD, Reulen HJ, Oeckler R, OlteanuNerbe V, Gall C, Kothbauer K: The mapping and continuous monitoring of the intrinsic motor nuclei during brain stem surgery. Neurosurgery 37:255-265, 1995 10. Epstein F, McCleary EL: Intrinsic brain-stem tumors of childhood: surgical indications. J Neurosurg 64:11-15, 1986 11. Fisher PG, Breiter SN, Carson BS, Wharam MD, Williams JA, Weingart JD, Foer DR, Goldthwaite PT, Tihan T, Burger PC: A clinicopathologic reappraisal of brain stem tumor classification. Identification of pilocystic astrocytoma and fibrillary astrocytoma as distinct entities. Cancer 89:1569- 1576, 2000 12. Fontebasso AM, Bechet D, Jabado N: Molecular biomarkers in pediatric glial tumors: A needed wind of change. Curr Opin Oncol 25:665