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A risk-stratified therapy for infants with acute lymphoblastic leukemia: a report from the JPLSG MLL-10 trial.
Tomizawa, Daisuke; Miyamura, Takako; Imamura, Toshihiko; Watanabe, Tomoyuki; Moriya Saito, Akiko; Ogawa, Atsushi; Takahashi, Yoshihiro; Hirayama, Masahiro; Taki, Tomohiko; Deguchi, Takao; Hori, Toshinori; Sanada, Masashi; Ohmori, Shigeru; Haba, Masami; Iguchi, Akihiro; Arakawa, Yuki; Koga, Yuhki; Manabe, Atsushi; Horibe, Keizo; Ishii, Eiichi; Koh, Katsuyoshi.
Afiliación
  • Tomizawa D; Division of Leukemia and Lymphoma, Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
  • Miyamura T; Department of Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan.
  • Imamura T; Department of Pediatrics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Kyoto, Japan.
  • Watanabe T; Department of Nutritional Science, Faculty of Psychological and Physical Science, Aichi Gakuin University, Nisshin, Japan.
  • Moriya Saito A; Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
  • Ogawa A; Department of Pediatrics, Niigata Cancer Center Hospital, Niigata, Japan.
  • Takahashi Y; Department of Pediatrics, Aomori Prefectural Central Hospital, Aomori, Japan.
  • Hirayama M; Department of Pediatrics, Mie University Graduate School of Medicine, Tsu, Japan.
  • Taki T; Department of Medical Technology, Kyorin University Faculty of Health Sciences, Tokyo, Japan.
  • Deguchi T; Department of Pediatrics, Mie University Graduate School of Medicine, Tsu, Japan.
  • Hori T; Division of Cancer Immunodiagnostics, Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
  • Sanada M; Department of Pediatrics, Aichi Medical University, Nagakute, Japan.
  • Ohmori S; Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
  • Haba M; Department of Pharmacy, Shinshu University Hospital, Matsumoto, Japan.
  • Iguchi A; Department of Pharmacy, Faculty of Pharmacy, Chiba Institute of Science, Choshi, Japan.
  • Arakawa Y; Department of Pediatrics, Hokkaido University, Sapporo, Japan.
  • Koga Y; Department of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
  • Manabe A; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; and.
  • Horibe K; Department of Pediatrics, Hokkaido University, Sapporo, Japan.
  • Ishii E; Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
  • Koh K; Department of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.
Blood ; 136(16): 1813-1823, 2020 10 15.
Article en En | MEDLINE | ID: mdl-32845001
ABSTRACT
The prognosis for infants with acute lymphoblastic leukemia (ALL), particularly those with KMT2A gene rearrangement (KMT2A-r), is dismal. Continuous efforts have been made in Japan to investigate the role of hematopoietic stem cell transplantation (HSCT) for infants with KMT2A-r ALL, but improvement in outcome was modest. In the Japanese Pediatric Leukemia/Lymphoma Study Group MLL-10 trial, infants with ALL were stratified into 3 risk groups (low risk [LR], intermediate risk [IR], and high risk [HR]) according to KMT2A status, age, and presence of central nervous system leukemia. Children's Oncology Group AALL0631 modified chemotherapy with the addition of high-dose cytarabine in early intensification was introduced to KMT2A-r patients, and the option of HSCT was restricted to HR patients only. The role of minimal residual disease (MRD) was also evaluated. Ninety eligible infants were stratified into LR (n = 15), IR (n = 19), or HR (n = 56) risk groups. The 3-year event-free survival (EFS) rate for patients with KMT2A-r ALL (IR + HR) was 66.2% (standard error [SE], 5.6%), and for those with germline KMT2A (KMT2A-g) ALL (LR), the 3-year EFS rate was 93.3% (SE, 6.4%). The 3-year EFS rate was 94.4% (SE, 5.4%) for IR patients and 56.6% (SE, 6.8%) for HR patients. In multivariable analysis, female sex and MRD ≥0.01% at the end of early consolidation were significant factors for poor prognosis. Risk stratification and introduction of intensive chemotherapy in this study were effective and were able to eliminate HSCT for a subset of infants with KMT2A-r ALL. Early clearance of MRD seems to have translated into favorable outcomes and should be incorporated into risk stratifications in future trials. This trial was registered at the University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR) as #UMIN000004801.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Blood Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Blood Año: 2020 Tipo del documento: Article