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Article: Autologous hematopoietic stem cell transplantation for high-risk brain tumors in children
Title | Autologous hematopoietic stem cell transplantation for high-risk brain tumors in children |
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Authors | |
Keywords | Autologous hematopoietic stem cell transplantation Brain tumor Children Relapse |
Issue Date | 2008 |
Publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0167-594X |
Citation | Journal Of Neuro-Oncology, 2008, v. 86 n. 3, p. 337-347 How to Cite? |
Abstract | Autologous hematopoietic stem cell transplant (AHSCT) has been advocated as a form of salvage therapy for children with high-risk or relapsed brain tumors but only limited data are available currently. We report the outcomes of pediatric brain tumors treated with AHSCT in a quaternary referral center in Hong Kong over 10 years (June 1996-May 2006). Thirteen patients with medulloblastoma (n = 9), cerebral primitive neuroectodermal tumor (n = 1), ependymoma (n = 1), germ cell tumor (n = 1) and cerebellar rhabdoid (n = 1) were transplanted because of tumor residual (n = 1) or recurrence (n = 12). Uniform upfront treatment protocols were adopted according to specific tumor types. Prior to AHSCT, 8 patients (61.5%) achieved complete remission and 5 (38.5%) were in partial remission. Conditioning employed thiotepa 300 mg/m2, etoposide 250 mg/m2 and carboplatin 500 mg/m2 daily for 3 days. Toxicity included mucositis and neutropenic fever in all patients, grade 4 hepatic toxicity in 4 patients (including hepatic veno-occlusive disease in 2 patients) and grade 4 renal toxicity in 1 patient. The 5-year event-free survival was 53.9%. Five patients died of disease recurrence or progression 8-21 months after transplant with a median disease-free period of 8 months post-transplant. One died of transplant-related complications in the early post-transplant period. Seven survived for a median of 5.4 years (maximum follow-up of 9.8 years), with six having Lansky-Karnofsky performance score above 80. All survivors had complete remission before transplant though 2 had leptomeningeal spread. We conclude that AHSCT can achieve long-term survival in children with recurrent brain tumor. However, those with macroscopic residual tumor before transplant cannot be salvaged. © Springer Science+Business Media, LLC. 2007. |
Persistent Identifier | http://hdl.handle.net/10722/79946 |
ISSN | 2023 Impact Factor: 3.2 2023 SCImago Journal Rankings: 1.131 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Cheuk, DKL | en_HK |
dc.contributor.author | Lee, TL | en_HK |
dc.contributor.author | Chiang, AKS | en_HK |
dc.contributor.author | Ha, SY | en_HK |
dc.contributor.author | Chan, GCF | en_HK |
dc.date.accessioned | 2010-09-06T08:00:36Z | - |
dc.date.available | 2010-09-06T08:00:36Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Journal Of Neuro-Oncology, 2008, v. 86 n. 3, p. 337-347 | en_HK |
dc.identifier.issn | 0167-594X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/79946 | - |
dc.description.abstract | Autologous hematopoietic stem cell transplant (AHSCT) has been advocated as a form of salvage therapy for children with high-risk or relapsed brain tumors but only limited data are available currently. We report the outcomes of pediatric brain tumors treated with AHSCT in a quaternary referral center in Hong Kong over 10 years (June 1996-May 2006). Thirteen patients with medulloblastoma (n = 9), cerebral primitive neuroectodermal tumor (n = 1), ependymoma (n = 1), germ cell tumor (n = 1) and cerebellar rhabdoid (n = 1) were transplanted because of tumor residual (n = 1) or recurrence (n = 12). Uniform upfront treatment protocols were adopted according to specific tumor types. Prior to AHSCT, 8 patients (61.5%) achieved complete remission and 5 (38.5%) were in partial remission. Conditioning employed thiotepa 300 mg/m2, etoposide 250 mg/m2 and carboplatin 500 mg/m2 daily for 3 days. Toxicity included mucositis and neutropenic fever in all patients, grade 4 hepatic toxicity in 4 patients (including hepatic veno-occlusive disease in 2 patients) and grade 4 renal toxicity in 1 patient. The 5-year event-free survival was 53.9%. Five patients died of disease recurrence or progression 8-21 months after transplant with a median disease-free period of 8 months post-transplant. One died of transplant-related complications in the early post-transplant period. Seven survived for a median of 5.4 years (maximum follow-up of 9.8 years), with six having Lansky-Karnofsky performance score above 80. All survivors had complete remission before transplant though 2 had leptomeningeal spread. We conclude that AHSCT can achieve long-term survival in children with recurrent brain tumor. However, those with macroscopic residual tumor before transplant cannot be salvaged. © Springer Science+Business Media, LLC. 2007. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0167-594X | en_HK |
dc.relation.ispartof | Journal of Neuro-Oncology | en_HK |
dc.rights | Pediatric Blood & Cancer. Copyright © John Wiley & Sons, Inc. | en_HK |
dc.subject | Autologous hematopoietic stem cell transplantation | en_HK |
dc.subject | Brain tumor | en_HK |
dc.subject | Children | en_HK |
dc.subject | Relapse | en_HK |
dc.title | Autologous hematopoietic stem cell transplantation for high-risk brain tumors in children | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1545-5009&volume=&spage=&epage=&date=2006&atitle=Autologous+hematopoietic+stem+cell+transplantation+for+high+risk+brain+tumors+in+children.+ | en_HK |
dc.identifier.email | Chiang, AKS:chiangak@hkucc.hku.hk | en_HK |
dc.identifier.email | Chan, GCF:gcfchan@hkucc.hku.hk | en_HK |
dc.identifier.authority | Chiang, AKS=rp00403 | en_HK |
dc.identifier.authority | Chan, GCF=rp00431 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1007/s11060-007-9478-0 | en_HK |
dc.identifier.pmid | 17906911 | - |
dc.identifier.scopus | eid_2-s2.0-38049048723 | en_HK |
dc.identifier.hkuros | 145791 | en_HK |
dc.identifier.hkuros | 142312 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-38049048723&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 86 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 337 | en_HK |
dc.identifier.epage | 347 | en_HK |
dc.identifier.isi | WOS:000252157400011 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Cheuk, DKL=8705936100 | en_HK |
dc.identifier.scopusauthorid | Lee, TL=8508917400 | en_HK |
dc.identifier.scopusauthorid | Chiang, AKS=7101623534 | en_HK |
dc.identifier.scopusauthorid | Ha, SY=7202501115 | en_HK |
dc.identifier.scopusauthorid | Chan, GCF=16160154400 | en_HK |
dc.identifier.issnl | 0167-594X | - |