INTRODUCTION: TP53 mutations remain a poor prognotic factor and account for a high proportion of the treatment failure in SHH subgroup medulloblatoma. Poor survival of patients with P53 mutant medulloblastoma may be related to radiation/chemotherapy resistance. Lithium, an activator of the WNT pathway, sensitizes TP53 mutant medulloblastoma to radiation. CASE REPORT: a 12-yo boy presented with left localized hemispheric medulloblastoma. After a complete excision of the tumour he was randomized and treated according to COG ACNS0331 and received a standard-dose craniospinal radiation with a boost to the entire posterior fossa, followed by maintenance chemotherapy. Patient was considered in complete remission. 15 months post-end of treatment, MRI showed a local recurrence. After 2 cycles of temozolomide, irinotecan and bevacizumab chemotherapy, patient had tumor progression. He then underwent a complete resection of the tumour. Pathology showed anaplastic type, SHH/TP53 mutant medulloblastoma. Due to the expected poor survival and the lack of known and consensual curative treatment, the patient was treated with a combination of therapeutic dose of lithium and focal radiation therapy to a dose of 54 Gy. One year later, the patient remains asymptomatic and, in complete remission. CONCLUSION: Lithium combined to radiation therapy may represent an interesting therapeutic avenue for higher risk groups of medulloblastoma in a context of a pilot study.
. 2016 May 30;18(Suppl 3):iii101. doi: 10.1093/neuonc/now076.21
MB-23: RECURRENT SHH/TP53 MUTANT MEDULLOBLASTOMA TREATED WITH A COMBINATION OF LITHIUM AND RADIATION THERAPY
Anne-Sophie Carret
1, Louis Crevier
2, Yvan Samson
1, Benjamin Ellezam
3, Anne-Marie Charpentier
4
Anne-Sophie Carret
1Department of Pediatrics, Division of Hematology-Oncology, CHU Sainte-Justine/Université de Montréal, Montreal, QC, Canada
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Louis Crevier
2Department of Neurosurgery, CHU Sainte-Justine/Université de Montréal, Montreal, QC, Canada
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Yvan Samson
1Department of Pediatrics, Division of Hematology-Oncology, CHU Sainte-Justine/Université de Montréal, Montreal, QC, Canada
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Benjamin Ellezam
3Department of Pathology, CHU Sainte-Justine/Université de Montréal, Montreal, QC, Canada
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Anne-Marie Charpentier
4Department of Radiation Oncology, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada
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1Department of Pediatrics, Division of Hematology-Oncology, CHU Sainte-Justine/Université de Montréal, Montreal, QC, Canada
2Department of Neurosurgery, CHU Sainte-Justine/Université de Montréal, Montreal, QC, Canada
3Department of Pathology, CHU Sainte-Justine/Université de Montréal, Montreal, QC, Canada
4Department of Radiation Oncology, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada
Issue date 2016 Jun.
© the author(s) 2016. published by oxford university press on behalf of the society for neuro-oncology. all rights reserved. for permissions, please e-mail: journals.permissions@oup.com
PMCID: PMC4903580
