Evidence map›Paper›PMID 17530023›Full record

ReviewOncogene2007

Daclizumab (anti-Tac, Zenapax) in the treatment of leukemia/lymphoma.

T A Waldmann

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 79 citations in OpenAlex.

  1. Trial
  2. Strategies to therapeutically modulate cytokine action.Nature reviews. Drug discovery · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Daclizumab: Development, Clinical Trials, and Practical Aspects of Use in Multiple Sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Antibody therapy for Adult T-cell leukemia-lymphoma.International journal of hematology · 2011
    Article
  18. Treating rheumatic patients with a malignancy.Arthritis research & therapy · 2011
    Review
  19. Immunotherapy for ovarian cancer: what's next?Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2011
    Review
  20. New strategies in peripheral T-cell lymphoma: understanding tumor biology and developing novel therapies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2010
    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

1 author at 1 institution in 1 country.

T A WaldmannMetabolism Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892-1374, USA. tawald@helix.nih.gov
Center for Cancer Research · US

Funding

IL-2:IL-15 : implications for cancer therapy (Investigator -Initiated Project)ZIASC004002 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WALDMANN, THOMAS · 2009 to 2022
$22.9M
Immunoregulatory Cell Receptor Defects--Leukemia/LymphomZ01SC004002 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI WALDMANN, THOMAS A · 1996 to 2008
$6.1M
Intramural NIH HHS
6 · The paper itself

Abstract

Daclizumab (Zenapax) identifies the alpha subunit of the interleukin-2 (IL-2) receptor and blocks the interaction of this cytokine with its growth factor receptor. The scientific basis for the choice of the IL-2 receptor alpha subunit as a target for monoclonal antibody-mediated therapy of leukemia/lymphoma is that very few normal cells express IL-2R alpha, whereas the abnormal T cells in patients with an array of lymphoid malignancies express this receptor. In 1997, daclizumab was approved by the FDA for use in the prevention of renal allograft rejection. In addition, anti-Tac provided effective therapy for select patients with T-cell malignancies and an array of inflammatory autoimmune disorders. Finally, therapy with this antibody armed with (90)Y has led to clinical responses in the majority of patients with adult T-cell leukemia. These insights concerning the IL-2/IL-2 receptor system facilitated the development of effective daclizumab antibody therapy for select patients with leukemia/lymphoma.

Indexed as

ImmunotherapyAnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedDaclizumabHumansImmunoglobulin GInterleukin-2 Receptor alpha SubunitLeukemiaLymphomaRadioisotopesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedDaclizumabImmunoglobulin GInterleukin-2 Receptor alpha SubunitRadioisotopes

Identifiers

PMID17530023
OpenAlexW2022360666

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.