Abstract

B-cell lymphoma in children accounts for about 10% of all pediatric malignancies. Chemotherapy has been very successful leading to an over-all 5-year survival between 80 and 90% depending on lymphoma type and extent of disease. Therapeutic toxicity remains high calling for better targeted and thus less toxic therapies. Therapeutic antibodies have become a standard element of B-cell lymphoma therapy in adults. Clinical experience in pediatric lymphoma patients is still very limited. This review outlines the rationale for antibody treatment of B-cell lymphomas in children and describes potential target structures on B-cell lymphoma cells. It summarizes the clinical experience of antibody therapy of B-cell lymphoma in children and gives an outlook on new developments and challenges for antibody therapy of pediatric B-cell lymphoma.

Highlights

  • B-cell lymphoma in children accounts for about 10% of all pediatric malignancies

  • The optimal B-cell lymphoma target antigen should be expressed on the cell surface, so it can be reached by the antibody

  • The anti-CD21 antibody-131Iconjugate 131I-OKB7 was evaluated in a phase I study in 18 adult lymphoma patients

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Summary

Introduction

B-cell lymphoma in children accounts for about 10% of all pediatric malignancies. Chemotherapy has been very successful leading to an over-all 5-year survival between 80 and 90% depending on lymphoma type and extent of disease.Therapeutic toxicity remains high calling for better targeted and less toxic therapies. A CD19 antibody-drug conjugate (SAR3419) has recently been tested in a phase I trial in adult lymphoma patients (Younes et al, 2012a). High CD21 expression on lymphomas has been shown to inhibit internalization of anti-CD19 antibodies into lymphoma cells leading to reduced efficacy of anti-CD19-drug conjugates (Ingle et al, 2008).

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