Evidence map›Paper›PMID 31218098›Full record

ArticleAmerican journal of cancer research2019

The potential of brentuximab vedotin, alone or in combination with current clinical therapies, in the treatment of testicular germ cell tumors.

Marc Yeste-Velasco, Tianyu Guo, Xueying Mao, Elzbieta Stankiewicz, Glenda Scandura, Haibo Li, Claire S Wang, Sakunthala Kudahetti, Tim Oliver, Daniel Berney and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. 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
0.9field-weighted citation impact, top 23% 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, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

12 authors at 2 institutions in 1 country.

Marc Yeste-VelascoCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
Tianyu GuoCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
Xueying MaoCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
Elzbieta StankiewiczCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
Glenda ScanduraCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
Haibo LiSt George's University of London London, UK.
Claire S WangGonville and Caius College, University of Cambridge UK.
Sakunthala KudahettiCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
Tim OliverCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
Daniel BerneyCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
Jonathan ShamashCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
Yong-Jie LuCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London London, UK.
St George's, University of London · GBUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Testicular germ cell tumors (TGCTs) are the commonest tumors in young men. With the advancement of chemotherapies, most TGCTs are successfully cured, even when diagnosed at an advanced and metastatic stage. However, a proportion of often young patients, median age 35-40, with advanced disease are not cured and will inevitably die. Therefore, there is an unmet need in this small population of young patients who are candidates for experimental approaches. We investigated a new therapeutic option for this group of patients, aiming to significantly improve their outcome. In recent years, many targeted therapies have been developed which demonstrated high efficacy and low toxicity. Brentuximab vedotin, a monomethyl auristatin E conjugated CD30 antibody, targets CD30 to kill cancer cells. As a large proportion of TGCTs express CD30, in particular embryonal carcinomas, we investigated

Indexed as

brentuximab vedotinCD30 expressionchemotherapycisplatindrug combinationTesticular germ cell tumor

Identifiers

PMID31218098
PMCPMC6556605
OpenAlexW3022987649

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.