Evidence map›Paper›PMID 35258855›Full record

ArticleInternational journal of hematology2022

JACLS ALL-02 SR protocol reduced-intensity chemotherapy produces excellent outcomes in patients with low-risk childhood acute lymphoblastic leukemia.

Yoshihiro Takahashi, Hisashi Ishida, Toshihiko Imamura, Kosuke Tamefusa, Souichi Suenobu, Ikuya Usami, Keiko Yumura-Yagi, Daiichiro Hasegawa, Shinichiro Nishimura, Nobuhiro Suzuki and 14 more

Abstract read
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In one paragraph

Article in International journal of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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

24 authors at 18 institutions in 1 country.

Yoshihiro Takahashi *Department of Pediatrics, Aomori Prefectural Central Hospital, Aomori, Japan.
Hisashi Ishida *Department of Pediatrics, Okayama University Hospital, Okayama, Japan.
Toshihiko ImamuraDepartment of Pediatrics, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, 465, Kajiichou, Hirokouji Kawaramachidori, Kamigyo-ku, Kyoto, 602-8566, Japan. imamura@koto.kpu-m.ac.jp.ORCID http://orcid.org/0000-0002-5727-4470
Kosuke TamefusaDepartment of Pediatrics, Okayama University Hospital, Okayama, Japan.
Souichi SuenobuDivision of General Pediatrics and Emergency Medicine, Department of Pediatrics, Oita University Faculty of Medicine, Oita, Japan.
Ikuya UsamiDepartment of Pediatric Hematology and Oncology, Hyogo Prefectural Amagasaki General Medical Center, Hyogo, Japan.
Keiko Yumura-YagiYumura Clinic, Osaka, Japan.
Daiichiro HasegawaDepartment of Hematology/Oncology, Hyogo Prefectural Kobe Children's Hospital, Kobe, Japan.
Shinichiro NishimuraDepartment of Pediatrics, Hiroshima University Hospital, Hiroshima, Japan.
Nobuhiro SuzukiDepartment of Pediatrics, Hokkaido Medical Center for Child Health and Rehabilitation, Sapporo, Japan.
Yoshiko HashiiDepartment of Pediatrics, Osaka University, Suita, Japan.
Takao DeguchiDepartment of Pediatrics, Mie University, Tsu, Japan.
Akiko Moriya-SaitoClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Yoshiyuki KosakaDepartment of Hematology/Oncology, Hyogo Prefectural Kobe Children's Hospital, Kobe, Japan.
Koji KatoDepartment of Hematology Oncology, Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Ryoji KobayashiDepartment of Pediatrics, Sapporo Hokuyu Hospital, Sapporo, Japan.
Hirohide KawasakiDepartment of Pediatrics, Kansai Medical University, Hirakata, Japan.
Hiroki HoriDepartment of Pediatrics, Mie University, Tsu, Japan.
Atsushi SatoDepartment of Hematology/Oncology, Miyagi Children's Hospital, Sendai, Japan.
Toru KudoSaiseikai Nishiotaru Hospital, Otaru, Japan.
Tatsutoshi NakahataDepartment of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
Megumi OdaDepartment of Pediatrics, Okayama University Hospital, Okayama, Japan.
Junichi HaraDepartment of Pediatric Hematology/Oncology, Osaka City General Hospital, Osaka, Japan.
Keizo HoribeClinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.
Okayama University Hospital · JPKobe Children's Hospital · JPMie University · JPNational Hospital Organization · JPAomori Prefectural Central Hospital · JPHiroshima University Hospital · JPHyogo Prefectural Amagasaki General Medical Center · JPKansai Medical University · JPKawamura Hospital · JPKyoto Prefectural University of Medicine · JPKyoto University · JPMiyagi Children's Hospital · JPNational Hospital Organization Hokkaido Medical Center · JPOita University · JPOsaka City General Hospital · JPOtaru Municipal Hospital · JPSapporo Hokuyu Hospital · JPThe University of Osaka · JP

Funding

Ministry of Health, Labour and Welfare H14-Koka (Gan)- 031Ministry of Health, Labour and Welfare H15-Koka (Gan)-024Ministry of Health, Labour and Welfare H16-GanRinsho-004Ministry of Health, Labour and Welfare H17-GanRinsho-004.
6 · The paper itself

Abstract

Acute lymphoblastic leukemia (ALL) is the most common childhood cancer. As overall cure rates of childhood ALL have improved, reduction of overall treatment intensity while still ensuring excellent outcomes is imperative for low-risk patients. We report the outcomes of patients treated following the standard-risk protocol from the prospective Japan Association of Childhood Leukemia Study (JACLS) ALL-02 study, which was conducted between 2002 and 2008 for patients with newly diagnosed ALL aged 1-18 years. Of 1138 patients with B-cell precursor ALL, 388 (34.1%) were allocated to this protocol. Excellent outcomes were achieved despite the overall treatment intensity being lower than that of most contemporary protocols: 4 years event-free survival (EFS) was 92.3% and 4 years overall survival 98.2%. Patients with high hyperdiploidy (HHD) involving triple trisomy (trisomy of chromosomes 4, 10, and 17) or ETV6-RUNX1 had even better outcomes (4 years EFS 97.6% and 100%, respectively). Unique characteristics of this protocol include a selection of low-risk patients with a low initial WBC count and good early treatment response and reduction of cumulative doses of chemotherapeutic agents while maintaining dose density. In Japan, we are currently investigating the feasibility of this protocol while incorporating minimal residual disease into the patient stratification strategy.

Indexed as

Precursor Cell Lymphoblastic Leukemia-LymphomaTrisomyAntineoplastic Combined Chemotherapy ProtocolsDisease-Free SurvivalHumansInfantNeoplasm, ResidualPrognosisProspective StudiesTreatment OutcomeAcute lymphoblastic leukemiaChildrenReduced intensityStandard risk

Identifiers

PMID35258855
OpenAlexW4220853535

What OpenQuestion holds

Textmetadata
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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.