Nationwide survey of pediatric hypodiploid acute lymphoblastic leukemia in Japan

Background Ploidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia (ALL). Children with hypodiploid ALL have poor outcomes despite current intensive chemotherapy. Little has been investigated with regard to hypodiploid ALL in Japanese children. Methods We retrospe...

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Published inPediatrics international Vol. 61; no. 11; pp. 1103 - 1108
Main Authors Ishimaru, Sae, Okamoto, Yasuhiro, Imai, Chihaya, Sakaguchi, Hirotoshi, Taki, Tomohiko, Hasegawa, Daisuke, Cho, Yuko, Kakuda, Harumi, Sano, Hideki, Manabe, Atsushi, Imamura, Toshihiko, Kato, Motohiro, Arakawa, Yuki, Shimonodan, Hidemi, Sato, Atsushi, Suenobu, Souichi, Inukai, Takeshi, Watanabe, Arata, Kawano, Yoshifumi, Kikuta, Atsushi, Horibe, Keizo, Ohara, Akira, Koh, Katsuyoshi
Format Journal Article
LanguageEnglish
Published Australia Blackwell Publishing Ltd 01.11.2019
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Abstract Background Ploidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia (ALL). Children with hypodiploid ALL have poor outcomes despite current intensive chemotherapy. Little has been investigated with regard to hypodiploid ALL in Japanese children. Methods We retrospectively collected clinical data on hypodiploid ALL cases from the registries of prospective multicenter trials conducted by the four independent clinical study groups in Japan between 1997 and 2012. Results A total of 117 ALL patients with hypodiploidy were analyzed in this study. There were 101, eight, and eight patients with 45, 44, and fewer than 44 chromosomes, respectively. The 5 year overall survival rates differed significantly: 86.0%, 87.5%, and 62.5% for patients with 45, 44, and fewer than 44 chromosomes, respectively (P = 0.037). Of the eight patients with 44 chromosomes, seven were alive, including five patients who maintained complete remission without undergoing hematopoietic stem cell transplantation (HSCT). Of the eight patients with fewer than 44 chromosomes, six were good responders to prednisolone and none had induction failure, but the relapse rate was high (5/8). No patients had central nervous system relapse. Four patients underwent HSCT after relapse, but only one survived. Conclusions Outcomes of Japanese ALL patients with fewer than 44 chromosomes were poor, as previously reported in other countries. Although the sample size was small, patients with 44 chromosomes had better prognoses than those previously reported. Further studies including international collaboration are needed to improve outcomes for pediatric ALL patients with fewer than 44 chromosomes.
AbstractList Ploidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia (ALL). Children with hypodiploid ALL have poor outcomes despite current intensive chemotherapy. Little has been investigated with regard to hypodiploid ALL in Japanese children. We retrospectively collected clinical data on hypodiploid ALL cases from the registries of prospective multicenter trials conducted by the four independent clinical study groups in Japan between 1997 and 2012. A total of 117 ALL patients with hypodiploidy were analyzed in this study. There were 101, eight, and eight patients with 45, 44, and fewer than 44 chromosomes, respectively. The 5 year overall survival rates differed significantly: 86.0%, 87.5%, and 62.5% for patients with 45, 44, and fewer than 44 chromosomes, respectively (P = 0.037). Of the eight patients with 44 chromosomes, seven were alive, including five patients who maintained complete remission without undergoing hematopoietic stem cell transplantation (HSCT). Of the eight patients with fewer than 44 chromosomes, six were good responders to prednisolone and none had induction failure, but the relapse rate was high (5/8). No patients had central nervous system relapse. Four patients underwent HSCT after relapse, but only one survived. Outcomes of Japanese ALL patients with fewer than 44 chromosomes were poor, as previously reported in other countries. Although the sample size was small, patients with 44 chromosomes had better prognoses than those previously reported. Further studies including international collaboration are needed to improve outcomes for pediatric ALL patients with fewer than 44 chromosomes.
Background Ploidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia (ALL). Children with hypodiploid ALL have poor outcomes despite current intensive chemotherapy. Little has been investigated with regard to hypodiploid ALL in Japanese children. Methods We retrospectively collected clinical data on hypodiploid ALL cases from the registries of prospective multicenter trials conducted by the four independent clinical study groups in Japan between 1997 and 2012. Results A total of 117 ALL patients with hypodiploidy were analyzed in this study. There were 101, eight, and eight patients with 45, 44, and fewer than 44 chromosomes, respectively. The 5 year overall survival rates differed significantly: 86.0%, 87.5%, and 62.5% for patients with 45, 44, and fewer than 44 chromosomes, respectively (P = 0.037). Of the eight patients with 44 chromosomes, seven were alive, including five patients who maintained complete remission without undergoing hematopoietic stem cell transplantation (HSCT). Of the eight patients with fewer than 44 chromosomes, six were good responders to prednisolone and none had induction failure, but the relapse rate was high (5/8). No patients had central nervous system relapse. Four patients underwent HSCT after relapse, but only one survived. Conclusions Outcomes of Japanese ALL patients with fewer than 44 chromosomes were poor, as previously reported in other countries. Although the sample size was small, patients with 44 chromosomes had better prognoses than those previously reported. Further studies including international collaboration are needed to improve outcomes for pediatric ALL patients with fewer than 44 chromosomes.
Abstract Background Ploidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia ( ALL ). Children with hypodiploid ALL have poor outcomes despite current intensive chemotherapy. Little has been investigated with regard to hypodiploid ALL in Japanese children. Methods We retrospectively collected clinical data on hypodiploid ALL cases from the registries of prospective multicenter trials conducted by the four independent clinical study groups in Japan between 1997 and 2012. Results A total of 117 ALL patients with hypodiploidy were analyzed in this study. There were 101, eight, and eight patients with 45, 44, and fewer than 44 chromosomes, respectively. The 5 year overall survival rates differed significantly: 86.0%, 87.5%, and 62.5% for patients with 45, 44, and fewer than 44 chromosomes, respectively ( P = 0.037). Of the eight patients with 44 chromosomes, seven were alive, including five patients who maintained complete remission without undergoing hematopoietic stem cell transplantation ( HSCT ). Of the eight patients with fewer than 44 chromosomes, six were good responders to prednisolone and none had induction failure, but the relapse rate was high (5/8). No patients had central nervous system relapse. Four patients underwent HSCT after relapse, but only one survived. Conclusions Outcomes of Japanese ALL patients with fewer than 44 chromosomes were poor, as previously reported in other countries. Although the sample size was small, patients with 44 chromosomes had better prognoses than those previously reported. Further studies including international collaboration are needed to improve outcomes for pediatric ALL patients with fewer than 44 chromosomes.
BackgroundPloidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia (ALL). Children with hypodiploid ALL have poor outcomes despite current intensive chemotherapy. Little has been investigated with regard to hypodiploid ALL in Japanese children.MethodsWe retrospectively collected clinical data on hypodiploid ALL cases from the registries of prospective multicenter trials conducted by the four independent clinical study groups in Japan between 1997 and 2012.ResultsA total of 117 ALL patients with hypodiploidy were analyzed in this study. There were 101, eight, and eight patients with 45, 44, and fewer than 44 chromosomes, respectively. The 5 year overall survival rates differed significantly: 86.0%, 87.5%, and 62.5% for patients with 45, 44, and fewer than 44 chromosomes, respectively (P = 0.037). Of the eight patients with 44 chromosomes, seven were alive, including five patients who maintained complete remission without undergoing hematopoietic stem cell transplantation (HSCT). Of the eight patients with fewer than 44 chromosomes, six were good responders to prednisolone and none had induction failure, but the relapse rate was high (5/8). No patients had central nervous system relapse. Four patients underwent HSCT after relapse, but only one survived.ConclusionsOutcomes of Japanese ALL patients with fewer than 44 chromosomes were poor, as previously reported in other countries. Although the sample size was small, patients with 44 chromosomes had better prognoses than those previously reported. Further studies including international collaboration are needed to improve outcomes for pediatric ALL patients with fewer than 44 chromosomes.
Author Okamoto, Yasuhiro
Shimonodan, Hidemi
Kakuda, Harumi
Koh, Katsuyoshi
Imamura, Toshihiko
Kato, Motohiro
Inukai, Takeshi
Imai, Chihaya
Sakaguchi, Hirotoshi
Cho, Yuko
Manabe, Atsushi
Sano, Hideki
Taki, Tomohiko
Arakawa, Yuki
Ohara, Akira
Ishimaru, Sae
Horibe, Keizo
Kikuta, Atsushi
Suenobu, Souichi
Sato, Atsushi
Watanabe, Arata
Hasegawa, Daisuke
Kawano, Yoshifumi
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  organization: Kyoto Prefectural University of Medicine
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  givenname: Motohiro
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  organization: National Center for Child Health and Development
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  givenname: Yuki
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  organization: Miyazaki Prefectural Miyazaki Hospital
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  givenname: Atsushi
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  organization: Miyagi Children's Hospital
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  givenname: Souichi
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  fullname: Suenobu, Souichi
  organization: Oita University
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  organization: University of Yamanashi
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  givenname: Arata
  surname: Watanabe
  fullname: Watanabe, Arata
  organization: Nakadori General Hospital
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  givenname: Yoshifumi
  surname: Kawano
  fullname: Kawano, Yoshifumi
  organization: Kagoshima University
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  givenname: Atsushi
  surname: Kikuta
  fullname: Kikuta, Atsushi
  organization: Fukushima Medical University Hospital
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  givenname: Keizo
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  organization: National Hospital Organization Nagoya Medical Center
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  fullname: Ohara, Akira
  organization: Toho University School of Medicine
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  givenname: Katsuyoshi
  surname: Koh
  fullname: Koh, Katsuyoshi
  organization: Saitama Children's Medical Center
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Issue 11
Keywords hematopoietic stem cell transplantation
hypodiploid
acute lymphoblastic leukemia
child
Language English
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Snippet Background Ploidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia (ALL). Children with hypodiploid ALL have poor outcomes...
Ploidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia (ALL). Children with hypodiploid ALL have poor outcomes despite...
Abstract Background Ploidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia ( ALL ). Children with hypodiploid ALL have...
BackgroundPloidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia (ALL). Children with hypodiploid ALL have poor outcomes...
BACKGROUNDPloidy is a highly significant prognostic factor for pediatric acute lymphoblastic leukemia (ALL). Children with hypodiploid ALL have poor outcomes...
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SubjectTerms Acute lymphoblastic leukemia
Adolescent
Central nervous system
Chemotherapy
Child
Child, Preschool
Children
Chromosomes
Clinical trials
Combined Modality Therapy
Female
Hematopoietic Stem Cell Transplantation
Hematopoietic stem cells
Humans
hypodiploid
Hypodiploidy
Incidence
Infant
International cooperation
Japan - epidemiology
Leukemia
Lymphatic leukemia
Male
Patients
Pediatrics
Ploidy
Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis
Precursor Cell Lymphoblastic Leukemia-Lymphoma - epidemiology
Precursor Cell Lymphoblastic Leukemia-Lymphoma - therapy
Prednisolone
Prognosis
Prospective Studies
Registries
Remission
Remission Induction - methods
Stem cell transplantation
Stem cells
Surveys and Questionnaires
Survival Rate - trends
Transplantation
Title Nationwide survey of pediatric hypodiploid acute lymphoblastic leukemia in Japan
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fped.14006
https://www.ncbi.nlm.nih.gov/pubmed/31519067
https://www.proquest.com/docview/2318340268
https://search.proquest.com/docview/2290834468
Volume 61
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