Treatment of high-risk neuroblastoma

Although high-dose chemotherapy and autologous stem cell transplantation (HDCT/autoSCT) have improved the prognosis for patients with high-risk neuroblastoma (NB), event-free survival rates remain in the range of 30 to 40%, which is unsatisfactory. To further improve outcomes, several clinical trial...

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Main Author: Ki Woong Sung
Format: Article
Language:English
Published: Korean Pediatric Society 2012-04-01
Series:Korean Journal of Pediatrics
Subjects:
Online Access:http://kjp.or.kr/upload/pdf/kjped-55-115.pdf
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spelling doaj-b9c0f05a9ebe4a61b9fae2a4f65f4c412020-11-24T23:08:22ZengKorean Pediatric SocietyKorean Journal of Pediatrics1738-10612092-72582012-04-0155411512010.3345/kjp.2012.55.4.1152012550401Treatment of high-risk neuroblastomaKi Woong Sung0Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.Although high-dose chemotherapy and autologous stem cell transplantation (HDCT/autoSCT) have improved the prognosis for patients with high-risk neuroblastoma (NB), event-free survival rates remain in the range of 30 to 40%, which is unsatisfactory. To further improve outcomes, several clinical trials, including tandem HDCT/autoSCT, high-dose 131I-metaiodobenzylguanidine treatment, and immunotherapy with NB specific antibody, have been undertaken and pilot studies have reported encouraging results. Nonetheless, about half of high-risk NB patients still experience treatment failure and have no realistic chance for cure with conventional treatment options alone after relapse. Therefore, a new modality of treatment is warranted for these patients. In recent years, several groups of investigators have examined the feasibility and effectiveness of reduced-intensity allogeneic stem cell transplantation (RI alloSCT) for the treatment of relapsed/progressed NB. Although a graft-versus-tumor effect has not yet been convincingly demonstrated in the setting of relapsed NB, the strategy of employing RI alloSCT has provided hope that treatment-related mortality will be reduced and a therapeutic benefit will emerge. However, alloSCT for NB is still investigational and there remain many issues to be elucidated in many areas. At present, alloSCT is reserved for specific clinical trials testing the immunomodulatory effect against NB.http://kjp.or.kr/upload/pdf/kjped-55-115.pdfNeuroblastomaHigh-dose chemotherapyAllogeneic stem cell transplantation
collection DOAJ
language English
format Article
sources DOAJ
author Ki Woong Sung
spellingShingle Ki Woong Sung
Treatment of high-risk neuroblastoma
Korean Journal of Pediatrics
Neuroblastoma
High-dose chemotherapy
Allogeneic stem cell transplantation
author_facet Ki Woong Sung
author_sort Ki Woong Sung
title Treatment of high-risk neuroblastoma
title_short Treatment of high-risk neuroblastoma
title_full Treatment of high-risk neuroblastoma
title_fullStr Treatment of high-risk neuroblastoma
title_full_unstemmed Treatment of high-risk neuroblastoma
title_sort treatment of high-risk neuroblastoma
publisher Korean Pediatric Society
series Korean Journal of Pediatrics
issn 1738-1061
2092-7258
publishDate 2012-04-01
description Although high-dose chemotherapy and autologous stem cell transplantation (HDCT/autoSCT) have improved the prognosis for patients with high-risk neuroblastoma (NB), event-free survival rates remain in the range of 30 to 40%, which is unsatisfactory. To further improve outcomes, several clinical trials, including tandem HDCT/autoSCT, high-dose 131I-metaiodobenzylguanidine treatment, and immunotherapy with NB specific antibody, have been undertaken and pilot studies have reported encouraging results. Nonetheless, about half of high-risk NB patients still experience treatment failure and have no realistic chance for cure with conventional treatment options alone after relapse. Therefore, a new modality of treatment is warranted for these patients. In recent years, several groups of investigators have examined the feasibility and effectiveness of reduced-intensity allogeneic stem cell transplantation (RI alloSCT) for the treatment of relapsed/progressed NB. Although a graft-versus-tumor effect has not yet been convincingly demonstrated in the setting of relapsed NB, the strategy of employing RI alloSCT has provided hope that treatment-related mortality will be reduced and a therapeutic benefit will emerge. However, alloSCT for NB is still investigational and there remain many issues to be elucidated in many areas. At present, alloSCT is reserved for specific clinical trials testing the immunomodulatory effect against NB.
topic Neuroblastoma
High-dose chemotherapy
Allogeneic stem cell transplantation
url http://kjp.or.kr/upload/pdf/kjped-55-115.pdf
work_keys_str_mv AT kiwoongsung treatmentofhighriskneuroblastoma
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