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Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+)ALL04

Incorporation of imatinib into chemotherapeutic regimens has improved the prognosis of children with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph(+)ALL). We investigated a role of imatinib immediately before hematopoietic stem cell transplantation (HSCT). Children with Ph(+)ALL...

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Autores principales: Manabe, Atsushi, Kawasaki, Hirohide, Shimada, Hiroyuki, Kato, Itaru, Kodama, Yuichi, Sato, Atsushi, Matsumoto, Kimikazu, Kato, Keisuke, Yabe, Hiromasa, Kudo, Kazuko, Kato, Motohiro, Saito, Tomohiro, Saito, Akiko M, Tsurusawa, Masahito, Horibe, Keizo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430261/
https://www.ncbi.nlm.nih.gov/pubmed/25641907
http://dx.doi.org/10.1002/cam4.383
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author Manabe, Atsushi
Kawasaki, Hirohide
Shimada, Hiroyuki
Kato, Itaru
Kodama, Yuichi
Sato, Atsushi
Matsumoto, Kimikazu
Kato, Keisuke
Yabe, Hiromasa
Kudo, Kazuko
Kato, Motohiro
Saito, Tomohiro
Saito, Akiko M
Tsurusawa, Masahito
Horibe, Keizo
author_facet Manabe, Atsushi
Kawasaki, Hirohide
Shimada, Hiroyuki
Kato, Itaru
Kodama, Yuichi
Sato, Atsushi
Matsumoto, Kimikazu
Kato, Keisuke
Yabe, Hiromasa
Kudo, Kazuko
Kato, Motohiro
Saito, Tomohiro
Saito, Akiko M
Tsurusawa, Masahito
Horibe, Keizo
author_sort Manabe, Atsushi
collection PubMed
description Incorporation of imatinib into chemotherapeutic regimens has improved the prognosis of children with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph(+)ALL). We investigated a role of imatinib immediately before hematopoietic stem cell transplantation (HSCT). Children with Ph(+)ALL were enrolled on JPLSG Ph(+)ALL 04 Study within 1 week of initiation of treatment for ALL. Treatment regimen consisted of Induction phase, Consolidation phase, Reinduction phase, 2 weeks of imatinib monotherapy phase, and HSCT phase (Etoposide+CY+TBI conditioning). Minimal residual disease (MRD), the amount of BCR–ABL transcripts, was measured with the real-time PCR method. The study was registered in UMIN-CTR: UMIN ID C000000290. Forty-two patients were registered and 36 patients (86%) achieved complete remission (CR). Eight of 17 patients (47%) who had detectable MRD at the beginning of imatinib monotherapy phase showed disappearance or decrease in MRD after imatinib treatment. Consequently, 26 patients received HSCT in the first CR and all the patients had engraftment and no patients died because of complications of HSCT. The 4-year event-free survival rates and overall survival rates among all the 42 patients were 54.1 ± 7.8% and 78.1 ± 6.5%, respectively. Four of six patients who did achieve CR and three of six who relapsed before HSCT were salvaged with imatinib-containing chemotherapy and subsequently treated with HSCT. The survival rate was excellent in this study although all patients received HSCT. A longer use of imatinib concurrently with chemotherapy should eliminate HSCT in a subset of patients with a rapid clearance of the disease.
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spelling pubmed-44302612015-05-18 Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+)ALL04 Manabe, Atsushi Kawasaki, Hirohide Shimada, Hiroyuki Kato, Itaru Kodama, Yuichi Sato, Atsushi Matsumoto, Kimikazu Kato, Keisuke Yabe, Hiromasa Kudo, Kazuko Kato, Motohiro Saito, Tomohiro Saito, Akiko M Tsurusawa, Masahito Horibe, Keizo Cancer Med Cancer Research Incorporation of imatinib into chemotherapeutic regimens has improved the prognosis of children with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph(+)ALL). We investigated a role of imatinib immediately before hematopoietic stem cell transplantation (HSCT). Children with Ph(+)ALL were enrolled on JPLSG Ph(+)ALL 04 Study within 1 week of initiation of treatment for ALL. Treatment regimen consisted of Induction phase, Consolidation phase, Reinduction phase, 2 weeks of imatinib monotherapy phase, and HSCT phase (Etoposide+CY+TBI conditioning). Minimal residual disease (MRD), the amount of BCR–ABL transcripts, was measured with the real-time PCR method. The study was registered in UMIN-CTR: UMIN ID C000000290. Forty-two patients were registered and 36 patients (86%) achieved complete remission (CR). Eight of 17 patients (47%) who had detectable MRD at the beginning of imatinib monotherapy phase showed disappearance or decrease in MRD after imatinib treatment. Consequently, 26 patients received HSCT in the first CR and all the patients had engraftment and no patients died because of complications of HSCT. The 4-year event-free survival rates and overall survival rates among all the 42 patients were 54.1 ± 7.8% and 78.1 ± 6.5%, respectively. Four of six patients who did achieve CR and three of six who relapsed before HSCT were salvaged with imatinib-containing chemotherapy and subsequently treated with HSCT. The survival rate was excellent in this study although all patients received HSCT. A longer use of imatinib concurrently with chemotherapy should eliminate HSCT in a subset of patients with a rapid clearance of the disease. BlackWell Publishing Ltd 2015-05 2015-01-31 /pmc/articles/PMC4430261/ /pubmed/25641907 http://dx.doi.org/10.1002/cam4.383 Text en © 2015 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Research
Manabe, Atsushi
Kawasaki, Hirohide
Shimada, Hiroyuki
Kato, Itaru
Kodama, Yuichi
Sato, Atsushi
Matsumoto, Kimikazu
Kato, Keisuke
Yabe, Hiromasa
Kudo, Kazuko
Kato, Motohiro
Saito, Tomohiro
Saito, Akiko M
Tsurusawa, Masahito
Horibe, Keizo
Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+)ALL04
title Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+)ALL04
title_full Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+)ALL04
title_fullStr Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+)ALL04
title_full_unstemmed Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+)ALL04
title_short Imatinib use immediately before stem cell transplantation in children with Philadelphia chromosome-positive acute lymphoblastic leukemia: Results from Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) Study Ph(+)ALL04
title_sort imatinib use immediately before stem cell transplantation in children with philadelphia chromosome-positive acute lymphoblastic leukemia: results from japanese pediatric leukemia/lymphoma study group (jplsg) study ph(+)all04
topic Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430261/
https://www.ncbi.nlm.nih.gov/pubmed/25641907
http://dx.doi.org/10.1002/cam4.383
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