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Potential application and prevalence of the CD30 (Ki-1) antigen among solid tumors: A focus review of the literature.

Authors :
Berger, Garrett K.
Gee, Kevin
Votruba, Cassandra
McBride, Ali
Anwer, Faiz
Source :
Critical Reviews in Oncology/Hematology. May2017, Vol. 113, p8-17. 10p.
Publication Year :
2017

Abstract

Background CD30 (Ki-1) is a cell membrane protein derived from the tumor necrosis factor (TNF) receptor family. The CD30 antigen has been associated primarily with Hodgkin lymphoma (HL) and systemic anaplastic large cell lymphoma (sALCL). Brentuximab vedotin (BV) is an antibody-drug conjugate targeting the CD30 antigen. FDA approval for BV includes relapsed and refractory HL and sALCL. The CD30 antigen also has been identified in many solid tumors, predominantly of germ cell origins and early clinical data is promising. Objective Perform a focus literature review evaluating the prevalence of the CD30 antigen among nonlymphomatous tumors with a potential correlate for CD30 targeted therapy. Eligibility criteria Inclusion criteria: all retrospective reviews and case reports citing CD30 positivity or negativity in non-lymphomatous malignancies in which data were presented based on location. Exclusion criteria: studies with hematopoetic malignancies, cutaneous malignancies, non-human populations, and non-english publications. Included studies A total of 119 articles met these criteria and are summarized in this manuscript. Conclusion The CD30 antigen has shown variable prevalence among non-hematopoetic tumors, most notably among germ cell tumors and mesothelioma. With additional, preclinical and properly powered clinical studies, CD30 targeted therapy such as that of BV, alone or in combination with other agents may prove to be a strong candidate in the treatment of various CD30 + malignancies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10408428
Volume :
113
Database :
Academic Search Index
Journal :
Critical Reviews in Oncology/Hematology
Publication Type :
Academic Journal
Accession number :
122548571
Full Text :
https://doi.org/10.1016/j.critrevonc.2017.02.021