Combined therapy with rituximab plus cyclophosphamide/Vincristine/Prednisone for Sjogren's syndrome - associated B-Cell non-Hodgkin's lymphoma

被引:6
作者
Carbone, J. [1 ]
Perez-Fernandez, R. [1 ,2 ]
Munoz, A. [2 ]
Sabin, P. [2 ]
Carreno, L. [3 ]
Fernandez-Cruz, E.
机构
[1] Univ Hosp Gregorio Maraon, Dept Immunol, Madrid 28007, Spain
[2] Univ Hosp Gregorio Maraon, Dept Oncol, Madrid 28007, Spain
[3] Univ Hosp Gregorio Maraon, Dept Rheumatol, Madrid 28007, Spain
关键词
Sjogren's syndrome; non-Hodgkin's; lymphoma NHL; rituximab; cyclophosphamide; vincristine; prednisone; CVP; autoimmunity; immunodeficiency;
D O I
10.1007/s12016-007-8025-2
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Sjogren's syndrome (SS) is characterized by an increased risk of developing non-Hodgkin's lymphoma (NHL). Optimal treatment for NEL-complicating SS is not clearly established. NEL, which expresses the CD20 antigen on tumor cell surfaces, is a disease entity candidate to treatment with anti-CD20 monoclonal antibodies. We report clinical and immunological data of a patient with SS and NEL who was treated with a regimen consisting of cyclophosphamide/vincristine/prednisone (CVP) plus rituximab. A 68-year-old women had a 26-year history of SS and autoimmune thyroiditis. The clinical course of SS was complicated with severe splenomegaly. An increased percentage of CD19+ B cells (up to 30%) was detected in peripheral blood during follow-up. Clonal rearrangement of immunoglobulin heavy chain was detected. Low-grade B marginal zone lymphoma was diagnosed (peripheral blood immunophenotype: CD19 + CD20 + CD23 + sIg + Kappa; bone marrow immunophenotype: 25% lymphocytes; CD 19 + CD20 + CD79A/BCL2+). She received a total of six cycles of CVP plus rituximab (375 mg/m(2)). Therapy was well tolerated, and B lymphocytes were depleted from the peripheral blood. Splenomegaly normalized.
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页码:80 / 84
页数:5
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