Evidence map›Paper›PMID 31611626›Full record

ArticleLeukemia2020

T-cell acute lymphoblastic leukemia in patients 1-45 years treated with the pediatric NOPHO ALL2008 protocol.

P Quist-Paulsen, N Toft, M Heyman, J Abrahamsson, L Griškevičius, H Hallböök, Ó G Jónsson, K Palk, G Vaitkeviciene, K Vettenranta and 10 more

2 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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.

NCT05289687 phase2recruitingnot on this mapstarted 2023, after this paper: background citation

A Phase II Study of Daratumumab-Hyaluronidase for Chemotherapy-Relapsed/Refractory Minimal Residual Disease (MRD) in T Cell Acute Lymphoblastic Leukemia (T-ALL

TypeinterventionalSponsorEastern Cooperative Oncology GroupRan2023 to 2027Enrolled20ConditionsT-cell Acute Lymphoblastic LeukemiaArmsDaratumumab / Hyaluronidase Injection
NCT06742463 phase2recruitingnot on this mapstarted 2024, after this paper: background citation

Venetoclax Combined With HAG Regimen in Treating Adult Relapse/Refractory Acute T Cell Lymphoblastic Leukemia/Lymphoma: A Phase II, Single Arm and Multicenter Study

TypeinterventionalSponsorFirst Affiliated Hospital of Zhejiang UniversityRan2024 to 2028Enrolled50ConditionsAcute T Lymphpblastic Leukemia/LymphomaArmsVenetoclax, homoharringtonine, Cytarabine (Ara-C), G-CSF
3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. Transplant in ALL: who, when, and how?Hematology. American Society of Hematology. Education Program · 2024
    Review
  10. Article
  11. Article
  12. Future of Treatment of Adolescents and Young Adults With ALL: A Vision for Collaboration and Equity.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Review
  13. Frontiers in oncology · 2024
    Article
  14. Outcome for Children and Young Adults With T-Cell ALL and Induction Failure in Contemporary Trials.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Optimal approach to T-cell ALL.Hematology. American Society of Hematology. Education Program · 2022
    Review
  20. 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

20 authors.

P Quist-PaulsenDepartment of Hematology, St. Olav's Hospital, Trondheim University Hospital, Trondheim, Norway. Petter.Quist-Paulsen@ntnu.no.
N ToftDepartment of Hematology, Herlev University Hospital, University of Copenhagen, Herlev, Denmark.
M HeymanChildhood Cancer Research Unit, Karolinska Institute, Astrid Lindgren's Childrens' Hospital, Karolinska University Hospital, Stockholm, Sweden.
J AbrahamssonDepartment of Pediatrics, Institution for Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
L GriškevičiusHematology, Oncology and Transfusion Medicine Center, Vilnius University Hospital Santaros Klinikos, Vilnius University, Vilnius, Lithuania.
H HallböökDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.
Ó G JónssonChildren's Hospital, Landspitali University Hospital, Reykjavík, Iceland.
K PalkDepartment of Hematology, North Estonia Medical Centre, Tallinn, Estonia.
G VaitkevicieneCentre for Pediatric Oncology and Hematology, Children's Hospital, Affiliate of Vilnius University Hospital Santariskiu Klinikos, Vilnius University, Vilnius, Lithuania.
K VettenrantaDivision of Hematology-Oncology and Stem Cell Transplantation, Hospital for Children and Adolescents, Helsinki University Central Hospital, Helsinki, Finland.
A ÅsbergDepartment of Pediatrics, St. Olav's Hospital, Trondheim University Hospital, Trondheim, Norway.
T L FrandsenDepartment of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark.
S OpdahlDepartment of Public Health and Nursing, Faculty of Medicine and Health Science, NTNU, Trondheim, Norway.
H V MarquartDepartment of Clinical Immunology, Section 7631, University Hospital Rigshospitalet, Copenhagen, Denmark.
S SiitonenDepartment of Clinical Chemistry, Helsinki University Central Hospital, Helsinki, Finland.
L T OsnesDepartment of Immunology, Oslo University Hospital, Oslo, Norway.
M HultdinDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
U M OvergaardDepartment of Hematology, The University Hospital Rigshospitalet, Copenhagen, Denmark.
U Wartiovaara-KauttoDepartment of Hematology, Helsinki University Hospital Comprehensive Cancer Center and University of Helsinki, Helsinki, Finland.
K SchmiegelowDepartment of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-0829-4993

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The NOPHO ALL2008 is a population-based study using an unmodified pediatric protocol in patients 1-45 years of age with acute lymphoblastic leukemia. Patients with T-ALL were given a traditional pediatric scheme if fast responding (minimal residual disease (MRD) < 0.1% day 29), or intensive block-based chemotherapy if slow responding (MRD > 0.1% day 29). Both treatment arms included pediatric doses of high-dose methotrexate and asparaginase. If MRD ≥ 5% on day 29 or ≥0.1% after consolidation, patients were assigned to allogeneic hematopoietic stem cell transplantation. The 5-year overall survival of the 278 T-ALL patients was 0.75 (95% CI 0.69-0.81), being 0.82 (0.74-0.88) for patients 1.0-9.9 years, 0.76 (0.66-0.86) for those 10.0-17.9 years, and 0.65 (0.55-0.75) for the older patients. The risk of death in first remission was significantly higher in adults (12%) compared with the 1-9 years group (4%). The MRD responses in the three age groups were similar, and only a nonsignificant increase in relapse risk was found in adults. In conclusion, an unmodified pediatric protocol in patients 1-45 years is effective in all age groups. The traditional pediatric treatment schedule was safe for all patients, but the intensive block therapy led to a high toxic death rate in adults.

Indexed as

AdolescentAdultAntineoplastic Combined Chemotherapy ProtocolsChildChild, PreschoolFemaleHematopoietic Stem Cell TransplantationHumansInfantMaleMiddle AgedPrecursor T-Cell Lymphoblastic Leukemia-LymphomaTreatment OutcomeYoung Adult

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.