Evidence map›Paper›PMID 34500465›Full record

ArticleBlood advances2021

Hematopoietic stem cell transplantation for infants with high-risk KMT2A gene-rearranged acute lymphoblastic leukemia.

Takayuki Takachi, Tomoyuki Watanabe, Takako Miyamura, Akiko Moriya Saito, Takao Deguchi, Toshinori Hori, Tomomi Yamada, Shigeru Ohmori, Masami Haba, Yuki Aoki and 11 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Infant Acute Lymphoblastic Leukemia-New Therapeutic Opportunities.International journal of molecular sciences · 2024
    Review
  7. Updates inBiomedicines · 2023
    Review
  8. Article
  9. Article
  10. Updates in infant acute lymphoblastic leukemia and the potential for targeted therapy.Hematology. American Society of Hematology. Education Program · 2022
    Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 16 institutions in 1 country.

Takayuki TakachiDepartment of Hematology and Oncology, Shizuoka Children's Hospital, Shizuoka, Japan.ORCID 0000-0001-9813-8873
Tomoyuki WatanabeDepartment of Health and Nutrition, Faculty of Psychological and Physical Science, Aichi Gakuin University, Nisshin, Japan.ORCID 0000-0002-2627-8102
Takako MiyamuraDepartment of Pediatrics, Graduate School of Medicine, Osaka University, Suita, Japan.ORCID 0000-0002-3226-556X
Akiko Moriya SaitoClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.ORCID 0000-0003-3723-8445
Takao DeguchiDepartment of Pediatrics, Graduate School of Medicine, Mie University, Tsu, Japan.ORCID 0000-0001-9932-4299
Toshinori HoriDepartment of Pediatrics, School of Medicine, Aichi Medical University, Nagakute, Japan.
Tomomi YamadaDepartment of Pediatrics, School of Medicine, Aichi Medical University, Nagakute, Japan.
Shigeru OhmoriDepartment of Pharmacy, Shinshu University Hospital, Matsumoto, Japan.
Masami HabaDepartment of Biopharmaceutics, Faculty of Pharmacy, Chiba Institute of Science, Choshi, Japan.
Yuki AokiDepartment of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-7056-9898
Sae IshimaruDepartment of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.ORCID 0000-0002-5437-8821
Shinya SasakiDepartment of Pediatrics, Graduate School of Medicine, Hirosaki University, Hirosaki, Japan.
Junjiro OhshimaDepartment of Pediatrics, Hokkaido University, Sapporo, Japan.
Akihiro IguchiDepartment of Pediatrics, Hokkaido University, Sapporo, Japan.ORCID 0000-0002-1367-3883
Yoshiyuki TakahashiDepartment of Pediatrics, Graduate School of Medicine, Nagoya University, Nagoya, Japan.
Nobuyuki HyakunaDepartment of Pediatrics, University of the Ryukyus Hospital, Nishihara, Japan.ORCID 0000-0003-1241-852X
Atsushi ManabeDepartment of Pediatrics, Hokkaido University, Sapporo, Japan.ORCID 0000-0002-6698-2348
Keizo HoribeClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.ORCID 0000-0002-6251-6059
Eiichi IshiiDepartment of Pediatrics, Graduate School of Medicine, Ehime University, Toon, Japan.
Katsuyoshi KohDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan; and.ORCID 0000-0002-0476-4978
Daisuke TomizawaDivision of Leukemia and Lymphoma, Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.ORCID 0000-0003-1520-7007
Hokkaido University · JPAichi Medical University · JPNational Hospital Organization · JPTokyo National Hospital · JPAichi Gakuin University · JPChiba Institute of Science · JPEhime University · JPHirosaki University · JPMie University · JPNagoya University · JPNational Center For Child Health and Development · JPSaitama Children's Medical Center · JPShinshu University Hospital · JPShizuoka Children's Hospital · JPThe University of Osaka · JPUniversity of the Ryukyus · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of allogeneic hematopoietic stem cell transplantation (HSCT) for infants with acute lymphoblastic leukemia (ALL) and KMT2A gene rearrangement (KMT2A-r) is controversial in terms of both its efficacy and potential for acute and late toxicities. In Japanese Pediatric Leukemia/Lymphoma Study Group trial MLL-10, by introducing intensive chemotherapy, indication of HSCT was restricted to patients with high-risk (HR) features only (KMT2A-r and either age <180 days or presence of central nervous system leukemia). Of the 56 HR patients, 49 achieved complete remission. Forty-three patients received HSCT in first remission including 38 patients receiving protocol-specified HSCT with conditioning consisting of individualized targeted doses of busulfan, etoposide, and cyclophosphamide. Three-year event-free survival (EFS) of 56.8% (95% confidence interval [CI], 42.4% to 68.8%) and overall survival of 80.2% (95% CI, 67.1% to 88.5%) were accomplished. Univariable analysis showed that Interfant-HR criteria and flow cytometric minimal residual disease (MRD; ≥0.01%), both at the end of induction and at the end of consolidation (EOC), were significantly associated with poorer EFS. In the multivariable analysis, positive MRD at EOC was solely associated with poor EFS (P < .001). Rapid pretransplant MRD clearance and tailored HSCT strategy in the MLL-10 trial resulted in a favorable outcome for infants with HR KMT2A-r ALL. However, considering the high rate of potentially life-threatening toxicities and the risk of late effects, its indication should be further restricted or even eliminated in the future by introducing more effective therapeutic modalities with minimal toxicities. This trial was registered at the University Hospital Medical Information Network Clinical Trials Registry (UMIN-CTR) as #UMIN000004801.

Indexed as

Hematopoietic Stem Cell TransplantationPrecursor Cell Lymphoblastic Leukemia-LymphomaHistone-Lysine N-MethyltransferaseHumansMyeloid-Lymphoid Leukemia ProteinPrognosisHistone-Lysine N-MethyltransferaseMyeloid-Lymphoid Leukemia Protein

Identifiers

PMID34500465
PMCPMC8679679
OpenAlexW3198686952

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.