Evidence map›Paper›PMID 26781613›Full record

Trial reportInternational journal of hematology2016

Residual disease detected by multidimensional flow cytometry shows prognostic significance in childhood acute myeloid leukemia with intermediate cytogenetics and negative FLT3-ITD: a report from the Tokyo Children's Cancer Study Group.

Dai Keino, Akitoshi Kinoshita, Daisuke Tomizawa, Hiroyuki Takahashi, Kohmei Ida, Hidemitsu Kurosawa, Kazutoshi Koike, Setsuo Ota, Noriyuki Iwasaki, Junya Fujimura and 12 more

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in International journal of hematology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
–field-weighted citation impact, top 99% 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

5 citing papers in PubMed, 2 syntheses or guidelines pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. MRD-directed and risk-adapted individualized stratified treatment of AML.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2023
    Article
  5. 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

22 authors at 16 institutions in 1 country.

Dai KeinoDepartment of Pediatrics, St.Marianna University School of Medicine, 2-16-1 Sugao Miyamae-ku, Kawasaki, Kanagawa, 216-8511, Japan. d2keino@marianna-u.ac.jp.
Akitoshi KinoshitaDepartment of Pediatrics, St.Marianna University School of Medicine, 2-16-1 Sugao Miyamae-ku, Kawasaki, Kanagawa, 216-8511, Japan.
Daisuke TomizawaDivision of Leukemia and Lymphoma, Childern's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
Hiroyuki TakahashiDepartment of Pediatrics, Toho University, Tokyo, Japan.
Kohmei IdaDepartment of Pediatrics, Teikyo University Mizonokuchi Hospital, Kawasaki, Kanagawa, Japan.
Hidemitsu KurosawaDepartment of Pediatrics, Dokkyo Medical University, Mibu, Tochigi, Japan.
Kazutoshi KoikeDivision of Pediatric Hematology and Oncology, Ibaraki Children's Hospital, Mito, Ibaraki, Japan.
Setsuo OtaDepartment of Pediatrics, Teikyo University Chiba Medical Center, Chiba, Japan.
Noriyuki IwasakiDepartment of Hematology/Oncology, Kanagawa Children's Medical Center, Yokohama, Kanagawa, Japan.
Junya FujimuraDepartment of Pediatrics and Adolescent Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Yuki YuzaDepartment of Hematology/Oncology, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan.
Chikako KiyotaniDivision of Leukemia and Lymphoma, Childern's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
Shohei YamamotoDepartment of Pediatrics, Showa University Fujigaoka Hospital, Yokohama, Kanagawa, Japan.
Tomoo OsumiDivision of Leukemia and Lymphoma, Childern's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.
Takahiro UedaDepartment of Pediatrics, Nippon Medical School, Tokyo, Japan.
Shinji MochizukiDivision of Stem Cell Processing, Center for Stem Cell Biology and Regenerative Medicine, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Keiichi IsoyamaDepartment of Pediatrics, Showa University Fujigaoka Hospital, Yokohama, Kanagawa, Japan.
Ryoji HanadaDepartment of Hematology/Oncology, Saitama Children's Medical Center, Saitama, Japan.
Akio TawaDepartment of Pediatrics, National Hospital Organization Osaka Medical Center, Osaka, Japan.
Atsushi ManabeDepartment of Pediatrics, St. Luke's International Hospital, Tokyo, Japan.
Yoichi ToguchiReproCELL Incorporated, Yokohama, Japan.
Akira OharaDepartment of Pediatrics, Toho University, Tokyo, Japan.
National Center For Child Health and Development · JPShowa University Fujigaoka Hospital · JPSt. Marianna University School of Medicine · JPToho University · JPDokkyo Medical University · JPIbaraki Children's Hospital · JPJuntendo University · JPKanagawa Children's Medical Center · JPNippon Medical School · JPOsaka National Hospital · JPSaitama Children's Medical Center · JPSt. Luke's International Hospital · JPTeikyo University · JPTeikyo University Chiba Medical Center · JPThe University of Tokyo · JPTokyo Metropolitan Children's Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Residual disease (RD) after induction chemotherapy may predict clinical outcome in acute myeloid leukemia (AML). In the present study, we investigated the prognostic significance of RD detected by multidimensional flow cytometry (MDF) among 34 children treated for AML in a clinical trial (JPLSG AML-05) in Japan. Bone marrow samples were analyzed at the points of the end of the first induction course (BMA-1) and second induction course (BMA-2) by MDF. RD was evaluated by detecting the immature cells showing abnormal antigen expression pattern; CD34(+), CD15(+), CD7(+). Thirteen (39.4 %) of 34 patients at BMA-1 and 8 (27.6 %) of 34 at BMA-2 had RD levels ≥0.1 %. There was no significant difference in 3y-EFS and 3y-OS between patients with RD levels ≥0.1 % and those with RD levels <0.1 % (53.8 versus 70.0 %, P = 0.30 and 50.0 versus 66.7 %, P = 0.27, respectively). However, IR cytogenetics and negative FLT3-ITD patients with RD levels ≥0.1 % exhibited significantly lower 3y-EFS and 3y-OS than those with RD levels <0.1 % (33.3 versus 83.3 %, P = 0.02 and 20.0 versus 76.9 %, P = 0.005, respectively). Our study suggests that RD shows prognostic relevance in pediatric patients with IR cytogenetics and negative FLT3-ITD AML.

Indexed as

AdolescentBone MarrowChildChild, PreschoolChromosome AberrationsCytogenetic AnalysisFemaleFlow Cytometryfms-Like Tyrosine Kinase 3Gene DuplicationHumansInduction ChemotherapyInfantLeukemia, Myeloid, AcuteMaleNeoplasm, Residualfms-Like Tyrosine Kinase 3Acute myeloid leukemiaChildrenFLT3-ITDMultidimensional flow cytometryResidual disease

Identifiers

PMID26781613
OpenAlexW2289669711

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.