An international survey on the management of patients receiving CAR T-cell therapy for haematological malignancies on behalf of the Chronic Malignancies Working Party of EBMT

• Published in: Current research in translational medicine Vol. 67; no. 3; pp. 79 - 88
• Main Authors: Hayden, P.J., Sirait, T., Koster, L., Snowden, J.A., Yakoub-Agha, I.
• Format: Journal Article
• Language: English
• Published: France Elsevier Masson SAS 01-08-2019; Elsevier-Masson SAS
• Series: Current Research in Translational Medicine
• Subjects: CAR T; CAR T-cells; Life Sciences; Long-term follow-up; Patient eligibility; Patient selection; Long-term follow-up; CAR T-cells; Patient eligibility; Patient selection; CAR T
• ISSN: 2452-3186; 2452-3186
• DOI: 10.1016/j.retram.2019.05.002

Two chimeric antigen receptor (CAR) T-cell therapies - Tisagenlecleucel (Kymriah™) and Axicabtagene ciloleucel (Yescarta™) - have been approved for commercial use. In order to inform forthcoming EBMT guidelines on the management of adults and children undergoing autologous CAR T-cell therapy, we undertook a survey of experienced clinicians.
An online survey with a dual focus on (1) ‘real world’ patient eligibility criteria and (2) models of care for patient follow-up was sent to experienced physicians.
There were 41 respondents (10 countries) and 93% worked in FACT-JACIE-accredited transplant centres. Most felt that a history of malignancy (57%), prior allo-HCT for B-NHL (78%–81%) and prior treatment with anti-CD19/CD3 BiTE antibodies (76%–86%) do not constitute contra-indications to CAR T therapy. Clinicians were divided as to whether CNS involvement represented an exclusion criterion. There was agreement that patients with viral infections (HIV, Hepatitis B or Hepatitis C) are not eligible. There is no common model of care for long-term follow-up. Most respondents believed that patients should attend the hospital two (43%) to three (33%) times weekly during the first month following discharge. A majority (69%) of respondents work in centres where there is an MDT meeting with a specific focus on follow-up following CAR T Therapy. Follow-up care is currently delivered either in HCT or haematology-oncology outpatient clinics.
The responses reveal wide variation in perceived patient eligibility criteria and highlight the need for consensus guidelines. The findings also illustrate the embryonic nature of current follow-up arrangements.