The absence of CD20 messenger RNA in recurrent cutaneous B-cell lymphoma following rituximab therapy.

TitleThe absence of CD20 messenger RNA in recurrent cutaneous B-cell lymphoma following rituximab therapy.
Publication TypeJournal Article
Year of Publication2005
AuthorsRawal YB, Nuovo GJ, Frambach GE, Porcu P, Baiocchi RA, Magro CM
JournalJ Cutan Pathol
Volume32
Issue9
Pagination616-21
Date Published2005 Oct
ISSN0303-6987
KeywordsAdult, Aged, Aged, 80 and over, Antibodies, Monoclonal, Antibodies, Monoclonal, Murine-Derived, Antigens, CD20, Antineoplastic Agents, Biomarkers, Tumor, Female, Humans, Immunohistochemistry, Lymphoma, B-Cell, Male, Middle Aged, Neoplasm Recurrence, Local, Reverse Transcriptase Polymerase Chain Reaction, Rituximab, RNA, Messenger, Skin Neoplasms
Abstract

BACKGROUND: Rituximab has been used to treat relapsed low-grade or advanced non-Hodgkin's lymphoma since 1997, targeting the CD20 antigen expressed by B cells. Single-agent rituximab therapy is safe and well tolerated. Recurrences showing a loss of CD20 expression following rituximab therapy have been reported.

METHODS: Four patients with CD20-positive cutaneous B-cell lymphoma received rituximab therapy with subsequent recurrences. The biopsies were assessed for cytoplasmic CD20 expression; CD20 messenger RNA was also assessed where tissue was available.

RESULTS: Cutaneous relapses occurring within 1.5-3 months following the last dose of rituximab were CD20 negative. In three cases, subsequent relapses showed renewed expression of CD20. Those biopsies demonstrating a loss of surface and cytoplasmic CD20 by immunohistochemistry also showed no evidence of messenger RNA for CD20 using an in situ polymerase chain reaction-based methodology.

CONCLUSIONS: Rituximab may be associated with the emergence of CD20-negative B-cell clones, potentially rendering a tumor insensitive to this drug. Conversely, following cessation of the drug, a re-expression of CD20 within the neoplastic cells may occur allowing therapeutic intervention with this monoclonal antibody. The loss of CD20 expression appears to be a direct effect of the drug on CD20 messenger RNA synthesis.

DOI10.1111/j.0303-6987.2005.00305.x
Alternate JournalJ Cutan Pathol
PubMed ID16176299
Related Faculty: 
Cynthia M. Magro, M.D.

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