Abstract
Malignancies of B-cell origin constitute a diverse set of neoplasms that vary in B-cell subtype of origin and underlying genetic drivers. In addition, they vary widely in clinical outcome. Follicular non-Hodgkin’s lymphoma (FL) or chronic lymphocytic leukemia (CLL), are indolent and incurable diseases with a median survival of 8–10 years whereas the more aggressive diseases such as diffuse large cell lymphoma (DCBL) and Mantle cell lymphoma (MCL) can have a median survival of 6 months if left untreated. Diffuse large B-cell lymphoma (DLBCL) is the most common type of NHL accounting for approximately 30–40 % of all NHL diagnosis followed by follicular lymphoma (20–25 % of NHL diagnosis) and MCL (6–10 % NHL diagnosis). B-cell chronic lymphocytic leukemia (B-CLL) is the most common of the chronic leukemias in adults with approximately 15,000 new cases per year in the United States [1]. These diseases are quite diverse; however, most of them are treated with the anti-CD20 chimeric monoclonal antibody rituximab (Rituxan®, MabThera®) in combination with cytotoxic chemotherapy. Although durable responses can be achieved in some patients, approximately half of patients with aggressive NHL will ultimately experience progressive or relapsed disease. In addition, indolent B-cell malignancies remain incurable despite longer durations of response with current therapies. Thus, there is still a need for treatments that can significantly extend disease-free and overall survival in these patients, with at least acceptable if not superior safety profiles.
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Polson, A.G. (2013). Antibody–Drug Conjugates for the Treatment of B-Cell Malignancies. In: Phillips, G. (eds) Antibody-Drug Conjugates and Immunotoxins. Cancer Drug Discovery and Development. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-5456-4_8
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