CD19-directed chimeric antigen receptor (CAR) T-cell therapies have proven to be an important treatment option for certain hematological malignancies.1 However, many physicians apply the autologous stem cell transplantation (ASCT) eligibility criteria to CAR T-cell therapy referral, limiting the number of patients who could potentially benefit from access to treatment.1
Patient identification, timing of referral, and transitioning to post-treatment monitoring are key factors highlighted by experts that may improve CAR T-cell therapy referral.1 Age, performance status, disease status, cardiovascular function, pulmonary function, renal function, hepatic function, infections, and psychological health should not preclude patients from receiving referrals or further evaluation for CAR T-cell therapy.1 Timely referral should be made by the patient’s primary oncologist to specialists as soon as the disease becomes relapsed or refractory, and close collaboration between CAR T-cell therapy specialists and other medical disciplines allows CAR T-cell therapy to remain a feasible option for patients despite comorbidities.1
This infographic summarises the expert recommendations for unique CAR T-cell therapy patient eligibility and highlights referral practices with fewer restrictions compared with the ASCT eligibility criteria. To read the published paper please click here.
After reading this infographic, participants should be better able to:
Shadman M, Ahmed S, Byrne MT, et al. Who Is Eligible for CAR T-Cell Therapy? Expert Perspectives on Overcoming Referral Barriers. Transplant Cell Ther. 2025;doi 10.1016/j.jtct.2025.10.025: 23 Oct [Epub ahead of print]
This activity is sponsored by Bristol Myers Squibb.
Bristol Myers Squibb provided financial support and has had input into the detailed project scope. This activity is provided by Touch Medical Communications (TMC) for touchONCOLOGY.
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Bristol Myers Squibb provided financial support and has had input into the detailed project scope. This activity is provided by Touch Medical Communications (TMC) for touchONCOLOGY.
Unapproved products or unapproved uses of approved products may be discussed; these situations may reflect the approval status in one or more jurisdictions. TMC has advised the sponsor to ensure that they disclose any such references made to unlabelled or unapproved use. No endorsement by TMC of any unapproved products or unapproved uses is either made or implied by mention of these products or uses in TMC activities. TMC accepts no responsibility for errors or omissions.
HE-US-2500780
Date of preparation: November 2025
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