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Neuro-Oncology logoLink to Neuro-Oncology
. 2016 May 30;18(Suppl 3):iii108. doi: 10.1093/neuonc/now076.49

MB-51: TANDEM HEMATOPOIETIC STEM CELL TRANSPLANT USING SYNGENEIC CELLS

Victor Zecchin 1, Nasjla Saba 1, Andrea Cappellano 1, Sergio Cavalheiro 1, Patricia Dastoli 1, Ana Cristina Mendonca 1, Renata Guimaraes 1, Virginio Fernandes Junior 1, Cintia Monteiro 1, Adriane Ibanez 1, Leticia Ribeiro 1
PMCID: PMC4903608

INTRODUCTION: Survival of central nervous system (CNS) embryonal tumors in infants remains dismal with better outcome being achieved with hematopoietic stem cell transplant (HSCT) consolidation. Tandem HSCT has been studied as a low toxicity alternative with promising survival rates; however it requires larger hematopoietic stem-cell harvesting. OBJECTIVE: To describe a patient submitted to three sequential tandem HSCT, receiving autologous stem cells rescue for the first two procedures and syngeneic for the third. METHODS: Case report with medical records review. RESULTS: Female, 3.9 years old, R0M0 desmoplastic medulloblastoma submitted to modifying HIT-SKK protocol. Relapse occurred at primary site two months after the end of treatment. The patient underwent second surgery followed by tandem HSCT. Peripheral stem-cell harvesting was performed after cisplatin/etoposide chemotherapy, but a low dose cell count was obtained (6,4x10[6] CD34+ cells/kg). To avoid treatment delay for the 3rd transplant, marrow stem-cells were harvested from an identical twin sister. Conditioning treatment was performed according COG99703 protocol (Carboplatin 17mg/kg/day and Thiotepa 6.5mg/kg/day 2 days). The period between 1st and 2nd HSCT was 25 days and 20 days between 2nd and 3rd. Engraftment occurred at D + 10 on the 1st and 2nd HSCT and D + 9 in the 3rd HSCT. Number of infused CD34+ cells for 1st HSCT was 2.53x10(6)/kg, for 2nd 3,08x10(6)/kg and for 3rd (syngeneic cells) 10,3x10(6)/kg. The patient is now three months after HSCT and craniospinal radiotherapy (24Gy). CONCLUSION: Syngeneic transplant seem to be a reasonable strategy for patients unable to harvest enough progenitor cells.


Articles from Neuro-Oncology are provided here courtesy of Society for Neuro-Oncology and Oxford University Press

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