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High event-free survival rate with minimum-dose-anthracycline treatment in childhood acute promyelocytic leukaemia: a nationwide prospective study by the Japanese Paediatric Leukaemia/Lymphoma Study Group.
Takahashi, Hiroyuki; Watanabe, Tomoyuki; Kinoshita, Akitoshi; Yuza, Yuki; Moritake, Hiroshi; Terui, Kiminori; Iwamoto, Shotaro; Nakayama, Hideki; Shimada, Akira; Kudo, Kazuko; Taki, Tomohiko; Yabe, Miharu; Matsushita, Hiromichi; Yamashita, Yuka; Koike, Kazutoshi; Ogawa, Atsushi; Kosaka, Yoshiyuki; Tomizawa, Daisuke; Taga, Takashi; Saito, Akiko M; Horibe, Keizo; Nakahata, Tatsutoshi; Miyachi, Hayato; Tawa, Akio; Adachi, Souichi.
Affiliation
  • Takahashi H; Department of Paediatrics, Toho University, Tokyo, Japan.
  • Watanabe T; Department of Nutritional Science, Faculty of Psychological and Physical Science, Aichi Gakuin University, Nisshin, Japan.
  • Kinoshita A; Department of Paediatrics, St. Marianna University School of Medicine, Kawasaki, Japan.
  • Yuza Y; Department of Haematology-Oncology, Tokyo Metropolitan Children's Medical Centre, Tokyo, Japan.
  • Moritake H; Division of Paediatrics, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
  • Terui K; Department of Paediatrics, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
  • Iwamoto S; Department of Paediatrics, Mie University Graduate School of Medicine, Tsu, Japan.
  • Nakayama H; Department of Paediatrics, National Hospital Organization, Fukuoka-Higashi Medical Centre, Fukuoka, Japan.
  • Shimada A; Department of Paediatrics, Okayama University Graduate School of Medicine, Okayama, Japan.
  • Kudo K; Department of Paediatrics, Fujita Health University, Toyoake, Japan.
  • Taki T; Department of Molecular Diagnostics and Therapeutics, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Yabe M; Department of Laboratory Medicine, Tokai University School of Medicine, Isehara, Japan.
  • Matsushita H; Department of Laboratory Medicine, Tokai University School of Medicine, Isehara, Japan.
  • Yamashita Y; Clinical Research Centre, National Hospital Organization Nagoya Medical Centre, Nagoya, Japan.
  • Koike K; Department of Paediatric Haematology and Oncology, Ibaraki Children's Hospital, Mito, Japan.
  • Ogawa A; Department of Paediatrics, Niigata Cancer Centre Hospital, Niigata, Japan.
  • Kosaka Y; Department of Haematology/Oncology, Hyogo Prefectural Children's Hospital, Kobe, Japan.
  • Tomizawa D; Division of Leukaemia and Lymphoma, Children's Cancer Centre, National Centre for Child Health and Development, Tokyo, Japan.
  • Taga T; Department of Paediatrics, Shiga University of Medical Science, Otsu, Japan.
  • Saito AM; Clinical Research Centre, National Hospital Organization Nagoya Medical Centre, Nagoya, Japan.
  • Horibe K; Clinical Research Centre, National Hospital Organization Nagoya Medical Centre, Nagoya, Japan.
  • Nakahata T; Centre for iPS cell research and application, Kyoto University, Kyoto, Japan.
  • Miyachi H; Department of Laboratory Medicine, Tokai University School of Medicine, Isehara, Japan.
  • Tawa A; Department of Paediatrics, National Hospital Organization, Osaka Medical Centre, Osaka, Japan.
  • Adachi S; Human Health Science, Kyoto University, Kyoto, Japan.
Br J Haematol ; 174(3): 437-43, 2016 08.
Article in En | MEDLINE | ID: mdl-27029412
ABSTRACT
We evaluated the efficacy of treatment using reduced cumulative doses of anthracyclines in children with acute promyelocytic leukaemia (APL) in the Japanese Paediatric Leukaemia/Lymphoma Study Group AML-P05 study. All patients received two and three subsequent courses of induction and consolidation chemotherapy respectively, consisting of all-trans retinoic acid (ATRA), cytarabine and anthracyclines, followed by maintenance therapy with ATRA. Notably, a single administration of anthracyclines was introduced in the second induction and all consolidation therapies to minimize total doses of anthracycline. The 3-year event-free (EFS) and overall survival rates for 43 eligible children were 83·6% [95% confidence interval (CI) 68·6-91·8%] and 90·7% (95% CI 77·1-96·4%), respectively. Although two patients died of intracranial haemorrhage or infection during induction phases, no cardiac adverse events or treatment-related deaths were observed during subsequent phases. Patients not displaying M1 marrow after the first induction therapy, or those under 5 years of age at diagnosis, showed inferior outcomes (3-year EFS rate; 33·3% (95% CI 19·3-67·6%) and 54·6% (95% CI 22·9-78·0%), respectively). In conclusion, a single administration of anthracycline during each consolidation phase was sufficient for treating childhood APL. In younger children, however, conventional ATRA and chemotherapy may be insufficient so that alternative therapies should be considered.
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Full text: 1 Database: MEDLINE Main subject: Leukemia, Promyelocytic, Acute / Anthracyclines Type of study: Observational_studies Country/Region as subject: Asia Language: En Journal: Br J Haematol Year: 2016 Type: Article Affiliation country: Japan

Full text: 1 Database: MEDLINE Main subject: Leukemia, Promyelocytic, Acute / Anthracyclines Type of study: Observational_studies Country/Region as subject: Asia Language: En Journal: Br J Haematol Year: 2016 Type: Article Affiliation country: Japan