Evidence map›Paper›PMID 37377225›Full record

ArticleHistology and histopathology2024

Optimizing assessment of CD30 expression in Hodgkin lymphoma by controlling for low expression.

Shoib Sarwar, Margaret E Tome, Dean Billheimer, Catherine Spier, Catharine L Smith, Daniel Persky, Monika Schmelz

Open access · greenAbstract read
In one paragraph

Article in Histology and histopathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Shoib SarwarDepartment of Pathology, University of Arizona, Tucson, AZ, USA.
Margaret E TomeDepartment of Pathology, University of Arizona, Tucson, AZ, USA.
Dean BillheimerDepartment of Epidemiology and Biostatistics, University of Arizona, Tucson, AZ, USA.
Catherine SpierDepartment of Pathology, University of Arizona, Tucson, AZ, USA.
Catharine L SmithPharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, AZ, USA.
Daniel PerskyUniversity of Arizona Cancer Center, Tucson, AZ, USA.
Monika SchmelzDepartment of Pathology, University of Arizona, Tucson, AZ, USA. schmelz@arizona.edu.
University of Arizona · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
SOUTHWEST ENVIRONMENTAL HEALTH SCIENCES CENTERP30ES006694 · NIEHS · UNIVERSITY OF ARIZONA · PI George S Watts · 1994 to 2026
$36.7M
NCI NIH HHS P30 CA023074NIEHS NIH HHS P30 ES006694
6 · The paper itself

Abstract

Since the approval of brentuximab vedotin (BV), assessment of CD30 status by immunohistochemistry gained increasing importance in the clinical management of patients diagnosed with CD30-expressing lymphomas, including classical Hodgkin lymphoma (CHL). Paradoxically, patients with low or no CD30 expression respond to BV. This discrepancy may be due to lack of standardization in CD30 staining methods. In this study, we examined 29 cases of CHL and 4 cases of nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) for CD30 expression using a staining protocol that was designed to detect low CD30 expression levels, and an evaluation system similar to the Allred scoring system used for breast cancer evaluation. For CHL, 10% of cases had low scores and 3% were CD30 negative, with 3 cases in which the majority of tumor cells showed very weak staining. Unexpectedly, one of four cases of NLPHL was positive. We demonstrate intra-patient heterogeneity in CD30 expression levels and staining patterns in tumor cells. Three CHL cases with weak staining may have been missed without the use of control tissue for low expression. Thus, standardization of CD30 immunohistochemical staining with use of known low-expressing controls may aid in proper CD30 assessment and subsequent therapeutic stratification of patients.

Indexed as

Hodgkin DiseaseBrentuximab VedotinCD30 LigandDiagnosis, DifferentialHumansImmunohistochemistryStaining and LabelingBrentuximab VedotinCD30 LigandTNFSF8 protein, human

Identifiers

PMID37377225
PMCPMC12147386
OpenAlexW4382344097

What Socratic holds

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LicenceCC BY
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 Socratic graph.