Evidence map›Paper›PMID 32845001›Full record

ArticleBlood2020

A risk-stratified therapy for infants with acute lymphoblastic leukemia: a report from the JPLSG MLL-10 trial.

Daisuke Tomizawa, Takako Miyamura, Toshihiko Imamura, Tomoyuki Watanabe, Akiko Moriya Saito, Atsushi Ogawa, Yoshihiro Takahashi, Masahiro Hirayama, Tomohiko Taki, Takao Deguchi and 11 more

Erratum issuedOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Blood, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
11.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 97 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Targeting IMPDH to inhibit SAMHD1 inCell cycle (Georgetown, Tex.) · 2026
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  6. Synergistic adverse prognosis ofFrontiers in cell and developmental biology · 2026
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  8. Haematologica · 2025
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  9. Article
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  11. Only InfantInternational journal of molecular sciences · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Infant Acute Lymphoblastic Leukemia-New Therapeutic Opportunities.International journal of molecular sciences · 2024
    Review
  19. Article
  20. Advancing Diagnostics and Therapy to Reach Universal Cure in Childhood ALL.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 16 institutions in 1 country.

Daisuke TomizawaDivision of Leukemia and Lymphoma, Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
Takako MiyamuraDepartment of Pediatrics, Osaka University Graduate School of Medicine, Suita, Japan.
Toshihiko ImamuraDepartment of Pediatrics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Kyoto, Japan.
Tomoyuki WatanabeDepartment of Nutritional Science, Faculty of Psychological and Physical Science, Aichi Gakuin University, Nisshin, Japan.
Akiko Moriya SaitoClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Atsushi OgawaDepartment of Pediatrics, Niigata Cancer Center Hospital, Niigata, Japan.
Yoshihiro TakahashiDepartment of Pediatrics, Aomori Prefectural Central Hospital, Aomori, Japan.
Masahiro HirayamaDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Japan.
Tomohiko TakiDepartment of Medical Technology, Kyorin University Faculty of Health Sciences, Tokyo, Japan.
Takao DeguchiDepartment of Pediatrics, Mie University Graduate School of Medicine, Tsu, Japan.
Toshinori HoriDepartment of Pediatrics, Aichi Medical University, Nagakute, Japan.
Masashi SanadaClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Shigeru OhmoriDepartment of Pharmacy, Shinshu University Hospital, Matsumoto, Japan.
Masami HabaDepartment of Pharmacy, Faculty of Pharmacy, Chiba Institute of Science, Choshi, Japan.
Akihiro IguchiDepartment of Pediatrics, Hokkaido University, Sapporo, Japan.
Yuki ArakawaDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Yuhki KogaDepartment of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; and.
Atsushi ManabeDepartment of Pediatrics, Hokkaido University, Sapporo, Japan.
Keizo HoribeClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Eiichi IshiiDepartment of Pediatrics, Ehime University Graduate School of Medicine, Toon, Japan.
Katsuyoshi KohDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
National Hospital Organization · JPHokkaido University · JPMie University · JPSaitama Children's Medical Center · JPAichi Gakuin University · JPAichi Medical University · JPAomori Prefectural Central Hospital · JPChiba Institute of Science · JPEhime University · JPKyorin University · JPKyoto Prefectural University of Medicine · JPKyushu University · JPNational Center For Child Health and Development · JPNiigata Cancer Center Hospital · JPShinshu University Hospital · JPThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Age FactorsAntineoplastic Combined Chemotherapy ProtocolsClinical Decision-MakingClinical Trials as TopicDisease ManagementFemaleHematopoietic Stem Cell TransplantationHumansInfantJapanMaleMulticenter Studies as TopicNeoplasm, ResidualPrecursor Cell Lymphoblastic Leukemia-LymphomaPrognosisTreatment Outcome

Identifiers

PMID32845001
OpenAlexW3042129338

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.