Diffuse Large B-Cell Lymphoma: Optimizing Therapy for Relapsed/Refractory Disease

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Matthew J. Matasar
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Despite a growing therapeutic arsenal to treat relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL), outcomes remain poor. Only approximately half of patients with this disease are eligible to receive curative autologous stem cell transplant, and of those, only half will be cured. Moreover, for patients who are transplant-ineligible, there are few effective options. Dr. Matthew J. Matasar discussed the current unmet needs in the treatment of patients with R/R DLBCL, treatment strategies in the second- and third-line settings, and emerging therapeutic options.

Disclosures: Dr. Matasar has disclosed receiving consulting fees from Bayer HealthCare, Daiichi-Sankyo Co., Genentech, Inc., Juno Therapeutics, Inc., Merck & Co., Inc., Roche Laboratories, Inc., Rocket Medical, Seattle Genetics, Inc., Takeda Pharmaceuticals North America, Inc., and Teva Pharmaceutical Industries Ltd.; receiving grant/research support from Bayer HealthCare, Genentech, Inc., GlaxoSmithKline, IGM Biosciences, Immunovaccine Technologies, Janssen Pharmaceutica Products, LP, Pharmacyclics, Roche Laboratories, Inc., Rocket Medical, and Seattle Genetics, Inc.; receiving honoraria from Bayer HealthCare, Genentech, Inc., GlaxoSmithKline, Immunovaccine Technologies, Janssen Pharmaceutica Products, LP, Pharmacyclics, Roche Laboratories, Inc., Seattle Genetics, Inc., and Takeda Pharmaceuticals North America, Inc.; and having ownership/partnership/principal in Merck & Co. Inc.

Correspondence: Matthew J. Matasar, MD, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10065. Email: matasarm@mskcc.org
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