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


Journal

Histology and histopathology
ISSN: 1699-5848
Titre abrégé: Histol Histopathol
Pays: Spain
ID NLM: 8609357

Informations de publication

Date de publication:
21 Jun 2023
Historique:
medline: 28 6 2023
pubmed: 28 6 2023
entrez: 28 6 2023
Statut: aheadofprint

Résumé

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.

Identifiants

pubmed: 37377225
pii: HH-18-644
doi: 10.14670/HH-18-644
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

18644

Subventions

Organisme : NCI NIH HHS
ID : P30 CA023074
Pays : United States

Informations de copyright

©The Author(s) 2023. Open Access. This article is licensed under a Creative Commons CC-BY International License.

Auteurs

Shoib Sarwar (S)

Department of Pathology, University of Arizona, Tucson, AZ, USA.

Margaret E Tome (ME)

Department of Pathology, University of Arizona, Tucson, AZ, USA.
Department of Pharmacology, University of Arizona, Tucson, AZ, USA.

Dean Billheimer (D)

Department of Epidemiology and Biostatistics, University of Arizona, Tucson, AZ, USA.

Catherine Spier (C)

Department of Pathology, University of Arizona, Tucson, AZ, USA.

Catharine L Smith (CL)

Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, AZ, USA.

Daniel Persky (D)

University of Arizona Cancer Center, Tucson, AZ, USA.

Monika Schmelz (M)

Department of Pathology, University of Arizona, Tucson, AZ, USA. schmelz@arizona.edu.

Classifications MeSH