Evidence map›Paper›PMID 34031784›Full record

Trial reportInvestigational new drugs2021

Phase II trial of brentuximab vedotin in relapsed/refractory germ cell tumors.

Ryan Ashkar, Darren R Feldman, Nabil Adra, Mohammad Abu Zaid, Samuel A Funt, Sandra K Althouse, Susan M Perkins, Christin I Snow, Kayla M Lazzara, Lina M Sego and 4 more

Open access · greenAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Investigational new drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Frequent CD30 Expression in an Emerging Group of Mesenchymal Tumors With NTRK, BRAF, RAF1, or RET Fusions.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2023
    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

14 authors at 4 institutions in 1 country.

Ryan Ashkar *Indiana University Simon Comprehensive Cancer Center, Indianapolis, IN, USA.
Darren R Feldman *Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Nabil AdraIndiana University Simon Comprehensive Cancer Center, Indianapolis, IN, USA. nadra@iu.edu.ORCID 0000-0001-8905-8329
Mohammad Abu ZaidIndiana University Simon Comprehensive Cancer Center, Indianapolis, IN, USA.
Samuel A FuntMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Sandra K AlthouseDepartment of Biostatistics, Indiana University School of Medicine, Indianapolis, IN, USA.
Susan M PerkinsDepartment of Biostatistics, Indiana University School of Medicine, Indianapolis, IN, USA.
Christin I SnowIndiana University Simon Comprehensive Cancer Center, Indianapolis, IN, USA.
Kayla M LazzaraIndiana University Simon Comprehensive Cancer Center, Indianapolis, IN, USA.
Lina M SegoIndiana University Simon Comprehensive Cancer Center, Indianapolis, IN, USA.
David I QuinnUniversity of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
Nasser H HannaIndiana University Simon Comprehensive Cancer Center, Indianapolis, IN, USA.
Lawrence H EinhornIndiana University Simon Comprehensive Cancer Center, Indianapolis, IN, USA.
Costantine AlbanyIndiana University Simon Comprehensive Cancer Center, Indianapolis, IN, USA.
Indiana University Health · USIndiana University School of MedicineMemorial Sloan Kettering Cancer Center · USUniversity of Southern California · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Background CD-30 is highly expressed in some patients with non-seminomatous germ-cell tumors. Brentuximab vedotin is an antibody-drug conjugate directed to CD-30. We report a phase 2 trial of brentuximab vedotin in patients with chemo-refractory GCT. Patients and methods This is a single arm, two cohort phase 2 trial investigating brentuximab vedotin 1.8 mg/kg IV every 3 weeks until disease progression or intolerable toxicities in patients with relapsed GCT who have no curative options. Patients with mGCT who progressed after first line cisplatin-based chemotherapy and after at least 1 salvage regimen (high-dose or standard-dose chemotherapy) were eligible. CD30 expression was assessed and two cohorts defined: CD30 positive and CD30 negative/unknown. Results 18 patients were enrolled. Median age 34.7 (range, 23-56). All patients had non-seminoma. Median AFP 4.9 (range, 1-219,345) and hCG 282 (range, 0.6-172,064). Five patients had late relapse (> 2 years). Median number of previous chemotherapy regimens was 3 (range, 2-7). Ten patients received prior high-dose chemotherapy. Seven patients had positive CD30 staining. There were two grade 3 treatment-related adverse events. No partial or complete responses were observed. 6 patients achieved radiographic stable disease (range, 9-14.9 weeks), 5 had elevated AFP or hCG at trial entry and all 5 had transient > 50% decline in baseline AFP/hCG: 4 had CD30 -ve and 2 had CD30 + ve staining; 10 patients had progression of disease as their best response; 2 were not evaluable for response. Conclusion Brentuximab vedotin does not appear to have clinically meaningful single-agent activity in patients with refractory GCT.

Indexed as

AdultAntineoplastic Agents, ImmunologicalBrentuximab VedotinFemaleHumansKi-1 AntigenMaleMiddle AgedNeoplasms, Germ Cell and EmbryonalTesticular NeoplasmsAntineoplastic Agents, ImmunologicalBrentuximab VedotinKi-1 AntigenBrentuximab vedotinGerm cell tumorRelapsed testicular cancerTesticular cancer

Identifiers

PMID34031784
PMCPMC9534326
OpenAlexW3163953040

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.