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Accelerated therapeutic progress in diffuse large B cell lymphoma
Authors:Qingqing Cai  Jason Westin  Kai Fu  Madhav Desai  Liang Zhang  Huiqiang Huang  Wenqi Jiang  Rong Liang  Zhengzi Qian  Richard E. Champlin  Michael Wang
Affiliation:1. Department of Medical Oncology, Cancer Center, Sun Yat-sen University, Guangzhou, China
2. State Key Laboratory of Oncology in Southern China, Guangzhou, China
3. Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Unit 429, 1515 Holcombe Blvd, Houston, TX, 77030, USA
4. Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA
5. Department of Leukemia, Xi’an The Fourth Military Medical University, Xi’an, China
6. Department of Medical Oncology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China
7. Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
Abstract:Diffuse large B cell lymphoma (DLBCL) is the most common non-Hodgkin lymphoma in the world. Clinically, biologically, and pathologically, DLBCL is a heterogeneous entity with a range of potential outcomes. Immunochemotherapy regimens, consisting of the chimeric monoclonal anti-CD20 antibody rituximab in combination with chemotherapy, have improved the outcomes. Relapsed DLBCL is generally treated with salvage immunochemotherapy followed by high-dose therapy and autologous stem cell transplantation; however, DLBCL is not yet curable in up to a third of patients. The real promise for cure lies in novel agents and their rational combinations. The improved understanding of DLBCL subtypes and gene expression profiling has led to the identification of targeted drugs that may allow for subtype specific therapy. We have summarized the existing data on the prognostic factors and the treatment of DLBCL, including the use of novel agents such as lenalidomide, carfilzomib, and ibrutinib. We also share our thoughts on the direction of future clinical trials.
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