Evidence map›Paper›PMID 24233555›Full record

ReviewImmunologic research2013

CD30: from basic research to cancer therapy.

Hiromi Muta, Eckhard R Podack

Open access · greenAbstract readReview
In one paragraph

Review in Immunologic research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. CD30Hematology/oncology clinics of North America · 2017
    Review
  18. Article
  19. 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

2 authors at 2 institutions in 2 countries.

Hiromi Muta
Eckhard R Podack
Kyushu University · JPUniversity of Miami · US

Funding

MOLECULAR MECHANISMS OF CD30+ LYMPHOMA GROWTHR01CA080228 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PODACK, ECKHARD R · 1999 to 2002
$632k
NCI NIH HHS R01 CA080228
6 · The paper itself

Abstract

The FDA recently approved an agonistic anti-CD30 drug conjugate, Brentuximab vedotin, for the treatment for CD30-positive lymphomas. The potent clinical activity of Brentuximab vedotin in Hodgkin's lymphoma and anaplastic large-cell lymphoma was greeted with great enthusiasm by oncologists as it provided a new treatment modality for these diseases. In this review, we will describe how we obtained the hybridoma by pursuing a basic research experiment unrelated to CD30. I will also review what we know about the normal biological functions of CD30 that were studied primarily in murine models of disease but also in patients. The picture emerging is that one of the primary functions of CD30 is the control of memory cells providing costimulation and trafficking information or inducing apoptosis in a microenvironment and cytokine milieu-dependent manner.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsBrentuximab VedotinCD30 LigandCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesColitisCytotoxicity, ImmunologicDisease Models, AnimalDrug Screening Assays, AntitumorGene Expression Regulation, NeoplasticGraft vs Host DiseaseHLA AntigensHumansImmunoconjugatesAntibodies, MonoclonalAntineoplastic AgentsBrentuximab VedotinCD30 LigandHLA AntigensImmunoconjugatesKi-1 Antigen

Identifiers

PMID24233555
PMCPMC3992519
OpenAlexW2021330461

What OpenQuestion holds

Textmetadata
LicenceTDM
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.