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Bispecific Antibodies in Diffuse Large B-Cell Lymphoma and Follicular Lymphoma: Proactive Toxicity Recognition and Management in Clinical Practice

Tuesday, December 15, 2026 | 1:00 PM and 8:00 PM ETVirtual

Program Description

Bispecific antibody (BsAb) therapy has expanded treatment options in diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL). However, its distinct toxicities, primarily cytokine release syndrome (CRS) and immune effector cell–associated neurotoxicity syndrome (ICANS), require proactive recognition and management. Safe administration relies on structured dosing schedules, monitoring protocols, and clear escalation pathways. As toxicity mitigation evolves, so must practical guidance used to develop protocols, coordinate monitoring, and support timely intervention. Building on the clinical evidence reviewed in webinar 1, this session focuses on practical management of BsAb toxicities, covering the recognition and grading of CRS and ICANS using American Society for Transplantation and Cellular Therapy (ASTCT) criteria, mitigation and monitoring strategies, site-of-care decisions, and evidence-based protocol development aligned with published guidelines to support the safe integration of these therapies into practice.

Target audience: Oncology Pharmacist
Type of activity: Application
Release date: December 15, 2026
Expiration date: February 15, 2027
Time to complete activity: 1 hour
Learner level: Foundational, Intermediate
Fee: Free

Educational Objectives

At the completion of this activity, pharmacists will be able to:

  • Apply the American Society for Transplantation and Cellular Therapy (ASTCT) grading criteria to classify the clinical presentation of bispecific antibody (BsAb)–associated cytokine release syndrome (CRS) and immune effector cell–associated neurotoxicity syndrome (ICANS).
  • Evaluate current site-level BsAb toxicity management approaches against published guidelines and evidence-based standards.
  • Develop BsAb toxicity management protocols based on regimen selection and patient comorbidities.