High-dose busulfan-thiotepa with autologous stem cell transplantation followed by posterior fossa irradiation in young children with classical or incompletely resected medulloblastoma

Background The aim of the study is to evaluate the outcome of young children with high risk localized medulloblastomas (newly diagnosed classical or incompletely resected) treated by high‐dose busulfan–thiotepa with autologous stem cell rescue (ASCT) followed by focal radiation therapy (RT). Procedu...

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Veröffentlicht in:Pediatric blood & cancer 2014-05, Vol.61 (5), p.907-912
Hauptverfasser: Bergthold, Guillaume, Kababri, Maria El, Varlet, Pascale, Dhermain, Frederic, Sainte-Rose, Christian, Raquin, Marie-Anne, Kieffer, Virginie, Goma, Gisele, Grill, Jacques, Valteau-Couanet, Dominique, Dufour, Christelle
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container_issue 5
container_start_page 907
container_title Pediatric blood & cancer
container_volume 61
creator Bergthold, Guillaume
Kababri, Maria El
Varlet, Pascale
Dhermain, Frederic
Sainte-Rose, Christian
Raquin, Marie-Anne
Kieffer, Virginie
Goma, Gisele
Grill, Jacques
Valteau-Couanet, Dominique
Dufour, Christelle
description Background The aim of the study is to evaluate the outcome of young children with high risk localized medulloblastomas (newly diagnosed classical or incompletely resected) treated by high‐dose busulfan–thiotepa with autologous stem cell rescue (ASCT) followed by focal radiation therapy (RT). Procedure Between September 1994 and January 2010, 19 children younger than 5 years old at diagnosis fulfilling the above inclusion criteria were treated at the Institute Gustave Roussy. After conventional chemotherapy, they received busulfan at a dose of 600 mg/m2 and thiotepa at a dose of 900 mg/m2 followed by ASCT. Focal RT was delivered at least 70 days after ASCT. Results The median follow‐up was 40.5 months (range, 14.5–191.2 months). The 3‐year event‐free survival (EFS) and OS were 68% (95% CI 45–84%) and 84% (95% CI 61–94%), respectively. Acute toxicity consisted mainly in hepatic veno‐occlusive disease (6/19 patients) and bone marrow aplasia (all patients). No toxic death occurred. The Full Scale Intellectual Quotient tended to decrease over time at a mean rate of 0.9 point per year from the date of diagnosis. Conclusions This intensive treatment resulted in a high overall survival rate in young children with newly diagnosed non‐metastatic classic or incompletely resected MB. In spite of a high incidence of hepatic veno‐occlusive disease (32%), the acute toxicity was manageable. Delayed neuropsychological side effects remain main concerns. These results should to be confirmed in a larger cohort. Pediatr Blood Cancer 2014;61:907–912. © 2014 Wiley Periodicals, Inc.
doi_str_mv 10.1002/pbc.24954
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Procedure Between September 1994 and January 2010, 19 children younger than 5 years old at diagnosis fulfilling the above inclusion criteria were treated at the Institute Gustave Roussy. After conventional chemotherapy, they received busulfan at a dose of 600 mg/m2 and thiotepa at a dose of 900 mg/m2 followed by ASCT. Focal RT was delivered at least 70 days after ASCT. Results The median follow‐up was 40.5 months (range, 14.5–191.2 months). The 3‐year event‐free survival (EFS) and OS were 68% (95% CI 45–84%) and 84% (95% CI 61–94%), respectively. Acute toxicity consisted mainly in hepatic veno‐occlusive disease (6/19 patients) and bone marrow aplasia (all patients). No toxic death occurred. The Full Scale Intellectual Quotient tended to decrease over time at a mean rate of 0.9 point per year from the date of diagnosis. Conclusions This intensive treatment resulted in a high overall survival rate in young children with newly diagnosed non‐metastatic classic or incompletely resected MB. In spite of a high incidence of hepatic veno‐occlusive disease (32%), the acute toxicity was manageable. Delayed neuropsychological side effects remain main concerns. These results should to be confirmed in a larger cohort. 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Procedure Between September 1994 and January 2010, 19 children younger than 5 years old at diagnosis fulfilling the above inclusion criteria were treated at the Institute Gustave Roussy. After conventional chemotherapy, they received busulfan at a dose of 600 mg/m2 and thiotepa at a dose of 900 mg/m2 followed by ASCT. Focal RT was delivered at least 70 days after ASCT. Results The median follow‐up was 40.5 months (range, 14.5–191.2 months). The 3‐year event‐free survival (EFS) and OS were 68% (95% CI 45–84%) and 84% (95% CI 61–94%), respectively. Acute toxicity consisted mainly in hepatic veno‐occlusive disease (6/19 patients) and bone marrow aplasia (all patients). No toxic death occurred. The Full Scale Intellectual Quotient tended to decrease over time at a mean rate of 0.9 point per year from the date of diagnosis. Conclusions This intensive treatment resulted in a high overall survival rate in young children with newly diagnosed non‐metastatic classic or incompletely resected MB. In spite of a high incidence of hepatic veno‐occlusive disease (32%), the acute toxicity was manageable. Delayed neuropsychological side effects remain main concerns. These results should to be confirmed in a larger cohort. 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Kababri, Maria El ; Varlet, Pascale ; Dhermain, Frederic ; Sainte-Rose, Christian ; Raquin, Marie-Anne ; Kieffer, Virginie ; Goma, Gisele ; Grill, Jacques ; Valteau-Couanet, Dominique ; Dufour, Christelle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4264-d418537d07eb98066830743693b047fdf7309c39aaa0e70f5a94897c53bc73103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Busulfan - administration &amp; dosage</topic><topic>Cerebellar Neoplasms - surgery</topic><topic>Cerebellar Neoplasms - therapy</topic><topic>Child, Preschool</topic><topic>childhood</topic><topic>Combined Modality Therapy</topic><topic>Cranial Irradiation</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hematology</topic><topic>high-dose chemotherapy</topic><topic>Humans</topic><topic>Infant</topic><topic>Infratentorial Neoplasms - surgery</topic><topic>Infratentorial Neoplasms - therapy</topic><topic>Male</topic><topic>medulloblastoma</topic><topic>Medulloblastoma - surgery</topic><topic>Medulloblastoma - therapy</topic><topic>Neuropsychological Tests</topic><topic>Oncology</topic><topic>Pediatrics</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Stem Cell Transplantation</topic><topic>Thiotepa - administration &amp; dosage</topic><topic>Transplantation, Autologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bergthold, Guillaume</creatorcontrib><creatorcontrib>Kababri, Maria El</creatorcontrib><creatorcontrib>Varlet, Pascale</creatorcontrib><creatorcontrib>Dhermain, Frederic</creatorcontrib><creatorcontrib>Sainte-Rose, Christian</creatorcontrib><creatorcontrib>Raquin, Marie-Anne</creatorcontrib><creatorcontrib>Kieffer, Virginie</creatorcontrib><creatorcontrib>Goma, Gisele</creatorcontrib><creatorcontrib>Grill, Jacques</creatorcontrib><creatorcontrib>Valteau-Couanet, Dominique</creatorcontrib><creatorcontrib>Dufour, Christelle</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Pediatric blood &amp; cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bergthold, Guillaume</au><au>Kababri, Maria El</au><au>Varlet, Pascale</au><au>Dhermain, Frederic</au><au>Sainte-Rose, Christian</au><au>Raquin, Marie-Anne</au><au>Kieffer, Virginie</au><au>Goma, Gisele</au><au>Grill, Jacques</au><au>Valteau-Couanet, Dominique</au><au>Dufour, Christelle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-dose busulfan-thiotepa with autologous stem cell transplantation followed by posterior fossa irradiation in young children with classical or incompletely resected medulloblastoma</atitle><jtitle>Pediatric blood &amp; cancer</jtitle><addtitle>Pediatr Blood Cancer</addtitle><date>2014-05</date><risdate>2014</risdate><volume>61</volume><issue>5</issue><spage>907</spage><epage>912</epage><pages>907-912</pages><issn>1545-5009</issn><eissn>1545-5017</eissn><abstract>Background The aim of the study is to evaluate the outcome of young children with high risk localized medulloblastomas (newly diagnosed classical or incompletely resected) treated by high‐dose busulfan–thiotepa with autologous stem cell rescue (ASCT) followed by focal radiation therapy (RT). Procedure Between September 1994 and January 2010, 19 children younger than 5 years old at diagnosis fulfilling the above inclusion criteria were treated at the Institute Gustave Roussy. After conventional chemotherapy, they received busulfan at a dose of 600 mg/m2 and thiotepa at a dose of 900 mg/m2 followed by ASCT. Focal RT was delivered at least 70 days after ASCT. Results The median follow‐up was 40.5 months (range, 14.5–191.2 months). The 3‐year event‐free survival (EFS) and OS were 68% (95% CI 45–84%) and 84% (95% CI 61–94%), respectively. Acute toxicity consisted mainly in hepatic veno‐occlusive disease (6/19 patients) and bone marrow aplasia (all patients). No toxic death occurred. The Full Scale Intellectual Quotient tended to decrease over time at a mean rate of 0.9 point per year from the date of diagnosis. Conclusions This intensive treatment resulted in a high overall survival rate in young children with newly diagnosed non‐metastatic classic or incompletely resected MB. In spite of a high incidence of hepatic veno‐occlusive disease (32%), the acute toxicity was manageable. Delayed neuropsychological side effects remain main concerns. These results should to be confirmed in a larger cohort. Pediatr Blood Cancer 2014;61:907–912. © 2014 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>24470384</pmid><doi>10.1002/pbc.24954</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Busulfan - administration & dosage
Cerebellar Neoplasms - surgery
Cerebellar Neoplasms - therapy
Child, Preschool
childhood
Combined Modality Therapy
Cranial Irradiation
Dose-Response Relationship, Drug
Female
Follow-Up Studies
Hematology
high-dose chemotherapy
Humans
Infant
Infratentorial Neoplasms - surgery
Infratentorial Neoplasms - therapy
Male
medulloblastoma
Medulloblastoma - surgery
Medulloblastoma - therapy
Neuropsychological Tests
Oncology
Pediatrics
Prognosis
Retrospective Studies
Stem Cell Transplantation
Thiotepa - administration & dosage
Transplantation, Autologous
title High-dose busulfan-thiotepa with autologous stem cell transplantation followed by posterior fossa irradiation in young children with classical or incompletely resected medulloblastoma
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