
Opinion|Videos|February 20, 2025
Outpatient CAR T Therapy and Expanding Access
Panelists discuss strategies for managing transitions of care for chimeric antigen receptor (CAR) T-cell therapy patients, including monitoring for long-term toxicities as well as the feasibility and logistics of administering CAR T therapy in the outpatient vs inpatient setting.
Advertisement
Episodes in this series

Video content above is prompted by the following:
- Dr. O’Dwyer to Dr. Molina: As your patients transition back to the community setting following their initial CAR T-cell infusion and monitoring phase, what steps do you take in the transitions of care process? Do you continue to monitor these patients, and how do you communicate with community providers to ensure they monitor for potential long-term CAR T-cell toxicities?
- Dr. O’Dwyer to Dr. Shaughnessy: At your institution, are patients receiving CAR T-cell therapy in the outpatient or inpatient setting? How feasible is it to administer CAR T-cell therapy in the outpatient setting?
- Resource link:
Othman T et al. Outpatient brexu-cel MCL and ALL safe and feasible. ASH 2024 poster abstract or see Appendix 9
Advertisement
Related to this article

Teclistamab plus talquetamab met the primary PFS end point and improved overall survival in relapsed/refractory multiple myeloma in MonumenTAL-6.

The FDA has granted priority review to a supplemental application for talazoparib plus enzalutamide in HRR-altered mCSPC.

Camizestrant plus a CDK4/6 inhibitor was approved in the European Union for ER-positive, HER2-negative advanced breast cancer with an emergent ESR1 mutation.

The FDA is reviewing data for daraxonrasib in previously treated pancreatic cancer under the Commissioner’s National Priority Voucher program.

Johannes Schetelig, MD, MSc, discusses phase 3 data for post-transplant cyclophosphamide vs ATLG as GVHD prophylaxis in hematologic malignancies.

Matthew Galsky, MD, discusses the FDA approval of perioperative pembrolizumab plus enfortumab vedotin in MIBC.

The FDA has approved zidesamtinib in patients with locally advanced/metastatic ROS1+ NSCLC who received a prior ROS1 kinase inhibitor.
Advertisement
Advertisement
Trending on OncLive
1
FDA Accepts NDA for Daraxonrasib in Previously Treated Metastatic Pancreatic Cancer
2
FDA Approves Zidesamtinib in Pretreated ROS1+ NSCLC
3
Teclistamab Plus Talquetamab Yields Significant Survival Benefits in Earlier-Line R/R Myeloma
4
European Commission Approves Camizestrant Plus CDK4/6 Inhibition for Emergent ESR1-Mutated Advanced Breast Cancer
5

