Therapy of B-Cell Lymphoma with Anti-CD20 Antibodies Can Result in the Loss of CD20 Antigen Expression
Rituximab is a chimeric antibody with human γ-1 and κ constant regions and murine variable regions. It recognizes the CD20 antigen, a pan B-cell marker. Therapeutic trials in patients with B-cell non-Hodgkin’s lymphoma (NHL) have shown significant efficacy with a primary response rate of 50%, and a...
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Veröffentlicht in: | Clinical cancer research 1999-03, Vol.5 (3), p.611-615 |
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Zusammenfassung: | Rituximab is a chimeric antibody with human γ-1 and κ constant regions and murine variable regions. It recognizes the CD20
antigen, a pan B-cell marker. Therapeutic trials in patients with B-cell non-Hodgkin’s lymphoma (NHL) have shown significant
efficacy with a primary response rate of 50%, and a secondary response rate of 44% after repeat treatments in prior responders.
The selection for proliferating tumor cells that no longer express CD20 may compromise repeated treatment. We have identified
a patient who developed a transformed NHL that lost CD20 protein expression after two courses of therapy with rituximab. In
a pretreatment lymph node biopsy, 83% of B cells (as defined by CD19 and surface immunoglobulin) expressed surface CD20. A
biopsy from the recurrent tumor after two courses of rituximab revealed a diffuse large cell NHL where 0% of B cells expressed
CD20 with no evidence of bound rituximab. Cytoplasmic staining showed no CD20 protein. Sequencing of immunoglobulin heavy
chain cDNA identified identical variable sequences in the initial and recurrent lymphomas, confirming the association between
the two tumors. Literature and database review suggests that approximately 98% of diffuse large cell lymphomas express CD20,
which suggests that these tumors rarely survive without CD20. This is the first identified case of loss of CD20 expression
in a lymphoma that has relapsed after rituximab therapy, although several other cases have since been identified. Considering
the significant number of patients treated with anti-CD20 antibodies, this may occur only rarely and is unlikely to preclude
recurrent therapy with anti-CD20 antibodies in the majority of patients. However, because many patients have relapsed after
anti-CD20 antibody therapy and have not been biopsied to identify clones with down-regulated CD20 antigen, we do not currently
know the true frequency of this phenomenon. When possible, patients should undergo evaluation for CD20 expression before repeated
courses of anti-CD20 therapy. |
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ISSN: | 1078-0432 1557-3265 |