This roundtable series explores the use of later-line therapies in patients with diffuse large B-cell lymphoma discussed in virtual live events.
Part 2: Shah Discusses Challenges in Using Lenalidomide Plus Tafasitamab for Patients With DLBCL
October 28th 2021Looking at the combination of lenalidomide plus tafasitamab for patients with diffuse large B-cell lymphoma shows promise for patients' treatment, but challenges remain that clinicians need to address.
Part 3: Polatuzumab Vedotin Plus Bendamustine and Rituximab Shows Promise in Patients With DLBCL
November 1st 2021The efficacy and data for the combination of polatuzumab vedotin plus bendamustine and rituximab for patients with diffuse large B-cell lymphoma show effective outcomes for patients that clinicians can use when discussing treatment options.
Part 3: Kline Discusses the Use of Tafasitamab in Certain Patients with R/R DLBCL
November 16th 2021While antibody-drug conjugates have shown promise in patients with relapsed/refractory diffuse large B-cell lymphoma, there are other options that can help patients before moving on to CAR T-cell therapy.
Part 3: Third-Line Use of Loncastuximab for Relapsed/Refractory DLBCL
December 6th 2021During a live virtual event, Beth A. Christian, MD, discussed data on third-line loncastuximab tesirine treatment in patients with diffuse large B-cell lymphoma and how to sequence treatments for patients who may receive CAR T-cell therapy.
Part 2: Loncastuximab as a Third-Line Therapy for Relapsed/Refractory DLBCL
December 15th 2021During a live virtual event, Paolo Caimi, MD, discussed the toxicity and dosage of loncastuximab tesirine as a third-line therapy for diffuse large B-cell lymphoma before receiving chimeric antigen receptor T-cell therapy.
Part 2: Selecting a Non-CAR T-Cell Treatment in Third-Line R/R DLBCL
June 6th 2022During a live virtual event, Jason Westin, MD, discussed with participants the choice of third-line treatment for relapsed/refractory diffuse large B-cell lymphoma for a patient who declines chimeric antigen receptor T-cell therapy.