Evidence map›Paper›PMID 16049514›Full record

ArticleLeukemia2005

Signaling via the anti-CD30 mAb SGN-30 sensitizes Hodgkin's disease cells to conventional chemotherapeutics.

C G Cerveny, C-L Law, R S McCormick, J S Lenox, K J Hamblett, L E Westendorf, A K Yamane, J M Petroziello, J A Francisco, A F Wahl

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03576378 (A Phase Ib/II Trial of Combined SGN-35), which is not on this map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-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.

NCT03576378 phase1 / phase2unknown statusnot on this mapstarted 2018, after this paper: background citation

A Phase Ib/II Trial of Combined SGN-35 (BrentuximabVedotin) Therapy With Cyclophosphamide, Procarbazine, Prednisone, Etoposide and Mitoxantrone (BrEPEM) for Older Patients With Untreated Hodgkin Lymphoma (HL)

TypeinterventionalSponsorGrupo Español de Linfomas y Transplante Autólogo de Médula ÓseaRan2018 to 2024Enrolled41ConditionsHodgkin LymphomaArmsBrentuximabVedotin (BV)
3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 62 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Role of CD30 targeting in malignant lymphoma.Current treatment options in oncology · 2014
    Review
  10. Review
  11. Article
  12. Article
  13. Anti-CD30 Antibodies for Hodgkin lymphoma.Current hematologic malignancy reports · 2010
    Review
  14. Article
  15. Article
  16. Immunotherapies for Hodgkin's lymphoma.Critical reviews in oncology/hematology · 2008
    Review
  17. 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

10 authors at 2 institutions in 1 country.

C G CervenyDepartment of Molecular Oncology and Immunology, Seattle Genetics, Inc., Bothell, WA 98021,USA.
C-L Law
R S McCormick
J S Lenox
K J Hamblett
L E Westendorf
A K Yamane
J M Petroziello
J A Francisco
A F Wahl
Molecular Oncology (United States) · USSeagen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SGN-30, a monoclonal antibody with activity against CD30+ malignancies, is currently in phase II clinical evaluation for treatment of Hodgkin's disease (HD) and anaplastic large cell lymphoma. The mechanisms underlying SGN-30's antitumor activity were investigated using cDNA array of L540 cells. SGN-30 treatment activated NF-kappaB and modulation of several messages including the growth regulator p21WAF1/CIP1 (p21) and cellular adhesion marker ICAM-1. p21 protein levels increased coincident with growth arrest and Annexin V/PI staining in treated HD cells. To determine if SGN-30-induced growth arrest would sensitize tumor cells to chemotherapeutics used against HD, L540cy and L428 cells were exposed to SGN-30 in combination with a panel of cytotoxic agents and resultant interactions quantified by the Combination Effects Method. Interactions between SGN-30 and all cytotoxic agents examined were additive or better. These in vitro data translated to increased efficacy of SGN-30 and bleomycin against L540cy tumor xenografts. In addition to direct cell killing, SGN-30 affects growth arrest and drug sensitization through growth regulating and proapoptotic machinery. Importantly, these data suggest that SGN-30 can enhance the efficacy of standard chemotherapies used to treat patients with CD30+ malignancies.

Indexed as

AnimalsAntibodies, MonoclonalApoptosisBleomycinCell CycleCell Line, TumorDrug Therapy, CombinationHodgkin DiseaseHumansKi-1 AntigenMiceMice, SCIDNF-kappa BOligonucleotide Array Sequence AnalysisSensitivity and SpecificitySignal TransductionAntibodies, MonoclonalBleomycinKi-1 AntigenNF-kappa BSGN-30 monoclonal antibody

Identifiers

PMID16049514
OpenAlexW2043530090

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.