Dose intensive melphalan and cyclophosphamide with autologous hematopoietic stem cells for recurrent medulloblastoma or germinoma
Purpose To determine the response, toxicity, and survival for children with progressive or recurrent medulloblastoma and germinoma using a single myeloablative course of chemotherapy supported by autologous hematopoietic stem cells. Patients and Methods Subjects were in second remission or had minim...
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Published in | Pediatric Blood & Cancer Vol. 51; no. 5; pp. 675 - 678 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.11.2008
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Subjects | |
Online Access | Get full text |
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Summary: | Purpose
To determine the response, toxicity, and survival for children with progressive or recurrent medulloblastoma and germinoma using a single myeloablative course of chemotherapy supported by autologous hematopoietic stem cells.
Patients and Methods
Subjects were in second remission or had minimal residual disease at the time of study entry. The conditioning regimen consisted of cyclophosphamide 6,000 mg/m2 plus melphalan 180 mg/m2.
Results
Twenty‐nine evaluable pediatric patients were accrued. The most frequent major toxicities were myelosuppression, infections, and stomatitis, but no toxic deaths were recorded. Best responses were: CR = 6, CCR = 13, PR = 6, SD = 2, and PD = 2. There were 6 medulloblastoma and 3 germinoma survivors with a median follow‐up of 7.5 years (range = 2.8–10). Two germinoma survivors received radiotherapy after autografting for presumptive progressive disease.
Conclusion
Myeloablative chemotherapy consisting of cyclophosphamide and melphalan was tolerable in the relapsed brain tumor setting with 19/29 cases achieving CR or CCR status and 9/29 becoming long‐term survivors. Pediatr Blood Cancer 2008;51:675–678. © 2008 Wiley‐Liss, Inc. |
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Bibliography: | A preliminary report was presented at the 39th Annual Congress of the International Society of Paediatric Oncology in Mumbai, India on November 1, 2007. ark:/67375/WNG-T6GDZ732-C istex:47EBB8F0AD3C0D7DAC91D7E743BD892E45E6E51C Children's Oncology Group - No. CA98543 ArticleID:PBC21655 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1545-5009 1545-5017 1096-911X |
DOI: | 10.1002/pbc.21655 |