Risk-adjusted therapy for pediatric non-T cell ALL improves outcomes for standard risk patients: results of JACLS ALL-02.


Journal

Blood cancer journal
ISSN: 2044-5385
Titre abrégé: Blood Cancer J
Pays: United States
ID NLM: 101568469

Informations de publication

Date de publication:
27 02 2020
Historique:
received: 29 11 2019
accepted: 07 02 2020
revised: 01 02 2020
entrez: 29 2 2020
pubmed: 29 2 2020
medline: 31 10 2020
Statut: epublish

Résumé

This study was a second multicenter trial on childhood ALL by the Japan Childhood Leukemia Study Group (JACLS) to improve outcomes in non-T ALL. Between April 2002 and March 2008, 1138 children with non-T ALL were enrolled in the JACLS ALL-02 trial. Patients were stratified into three groups using age, white blood cell count, unfavorable genetic abnormalities, and treatment response: standard risk (SR), high risk (HR), and extremely high risk (ER). Prophylactic cranial radiation therapy (PCRT) was abolished except for CNS leukemia. Four-year event-free survival (4yr-EFS) and 4-year overall survival (4yr-OS) rates for all patients were 85.4% ± 1.1% and 91.2% ± 0.9%, respectively. Risk-adjusted therapy resulted in 4yr-EFS rates of 90.4% ± 1.4% for SR, 84.9% ± 1.6% for HR, and 66.5% ± 4.0% for ER. Based on NCI risk classification, 4yr-EFS rates were 88.2% in NCI-SR and 76.4% in NCI-HR patients, respectively. Compared to previous trial ALL-97, 4yr-EFS of NCI-SR patients was significantly improved (88.2% vs 81.2%, log rank p = 0.0004). The 4-year cumulative incidence of isolated (0.9%) and total (1.5%) CNS relapse were significantly lower than those reported previously. In conclusion, improved EFS in NCI-SR patients and abolish of PCRT was achieved in ALL-02.

Identifiants

pubmed: 32107374
doi: 10.1038/s41408-020-0287-4
pii: 10.1038/s41408-020-0287-4
pmc: PMC7046744
doi:

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

23

Références

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Auteurs

Daiichiro Hasegawa (D)

Department of Hematology/Oncology, Hyogo Prefectural Children's Hospital, Kobe, Japan.

Toshihiko Imamura (T)

Department of Pediatrics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Kyoto, Japan. imamura@koto.kpu-m.ac.jp.
Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan. imamura@koto.kpu-m.ac.jp.

Keiko Yumura-Yagi (K)

Yumura Clinic, Osaka, Japan.

Yoshihiro Takahashi (Y)

Department of Pediatrics, Aomori Prefectural Central Hospital, Aomori, Japan.

Ikuya Usami (I)

Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Department of Pediatric Hematology and Oncology, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan.

So-Ichi Suenobu (SI)

Division of General Pediatrics and Emergency Medicine, Department of Pediatrics, Oita University, Oita, Japan.

Shinichiro Nishimura (S)

Department of Pediatrics, Hiroshima University Hospital, Hiroshima, Japan.

Nobuhiro Suzuki (N)

Department of Pediatrics, Hokkaido Medical Center for Child Health and Rehabilitation, Sapporo, Japan.

Yoshiko Hashii (Y)

Department of Pediatrics, Osaka University, Suita, Japan.

Takao Deguchi (T)

Department of Pediatrics, Mie University, Tsu, Japan.

Akiko Moriya-Saito (A)

Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

Koji Kato (K)

Department of Hematology Oncology, Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.

Yoshiyuki Kosaka (Y)

Department of Hematology/Oncology, Hyogo Prefectural Children's Hospital, Kobe, Japan.

Masahiro Hirayama (M)

Department of Pediatrics, Mie University, Tsu, Japan.

Akihiro Iguchi (A)

Department of Pediatrics, Hokkaido University Hospital, Sapporo, Japan.

Hirohide Kawasaki (H)

Department of Pediatrics Kansai Medical University, Hirakata, Japan.

Hiroki Hori (H)

Department of Pediatrics, Mie University, Tsu, Japan.

Atsushi Sato (A)

Department of Hematology/Oncology, Miyagi Children's Hospital, Sendai, Japan.

Tooru Kudoh (T)

Saiseikai Nishiotaru Hospital, Otaru, Japan.

Tatsutoshi Nakahata (T)

Department of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.

Megumi Oda (M)

Department of Pediatrics, Okayama University, Okayama, Japan.

Junichi Hara (J)

Department of Pediatric Hematology/Oncology, Osaka City General Hospital, Osaka, Japan.

Keizo Horibe (K)

Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

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