The Absence of CD20 Messenger RNA in Recurrent Cutaneous B-cell Lymphoma Following Rituximab Therapy
Document Type
Article
Publication Date
10-2005
Publisher
Wiley
Source Publication
Journal of Cutaneous Pathology
Source ISSN
0303-6987
Original Item ID
DOI: 10.1111/j.0303-6987.2005.00305.x
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.
Recommended Citation
Rawal, Yeshwant B.; Nuovo, Gerard J.; Frambach, Gwyn E.; Porcu, Pierluigi; Baiocchi, Robert A.; and Magro, Cynthia M., "The Absence of CD20 Messenger RNA in Recurrent Cutaneous B-cell Lymphoma Following Rituximab Therapy" (2005). School of Dentistry Faculty Research and Publications. 536.
https://epublications.marquette.edu/dentistry_fac/536
Comments
Accepted version. Journal of Cutaneous Pathology, Vol. 32, No. 9 (October 2005): 616-621. DOI. © 2005 Wiley. Used with permission.