Dr Karl M. Kilgore (Avalere, a healthcare consulting firm in Washington DC, USA) reported on 207 CAR T-cell recipients receiving Medicare (median age 71 years; 60% men; 87% Caucasian) [1]. In mid-2017, the 2 different CD19-directed CAR T-cell therapies tisagenlecleucel and axicabtagene ciloleucel were approved for the treatment of patients with relapsed or refractory large B-cell lymphoma who had already had ≥2 prior systemic therapies. The first claims came in October 2017, and the current study followed patients receiving either of these CAR T products until 30 September 2018. “This study provides the first real-world look at patients’ CAR T experience, using the first Medicare fee-for-service claims subsequent to product FDA approvals,” Dr Kilgore said.
Over 78% of this cohort had Charlson Comorbidity Index scores greater than 2 (range 2-15), indicating a complex group of patients. Half of the patients (51%) had one or more chronic condition, e.g. heart disease, chronic obstructive pulmonary disease, and chronic kidney disease.
The results showed that 73% of these patients remained alive at the end of 6-month follow-up. Hospital time after CAR T was reduced by 17% compared with the 6-month period prior to CAR T infusion. Median length of stay was 7 days in the pre-index period and 5 days in the post-index period. In addition, the number of visits to the emergency room decreased by nearly a third after the infusion as compared with that same period prior to infusion; accordingly, healthcare costs were 39% lower in the 6 months after infusion than the 6 months preceding infusion.
The investigators concluded that longer follow-up and a more comprehensive cost analysis is warranted, but the current data from this study indicate that age limitations for CAR T trials may not be necessary.
1. Kilgore K, et al. Abstract 793, ASH 2019, 7-10 December, Orlando, USA.
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Table of Contents: ASH 2019
Featured articles
Late-Breaking Abstracts
Likely new standard of care: Blinatumomab for children with relapsed B-ALL
Pivotal phase 3 trial in cold agglutinin disease: sutimlimab can stop haemolysis
Oral azacitidine improves overall survival in patients with AML in remission
BCL11A as a novel target in gene therapy for sickle cell disease
Adding daratumumab to carfilzomib/dexamethasone prolongs PFS and OS in R/R MM
Long-term data of ropeginterferon alpha-2b in polycythaemia vera
Anti-CD70 is safe with hypomethylating agents in AML
MRD assessment to guide pre-emptive treatment decisions
Luspatercept effective for myelofibrosis-associated anaemia
Arsenic, ATRA, and ascorbic acid in acute promyelocytic leukaemia maintenance
Updated results ECOG-ACRIN E2906: decitabine maintenance after alloSCT
Sickle Cell Disease
Arginine supplements help against sickle cell disease pain
Abatacept prevents graft-versus-host disease in sickle cell patients after alloSCT
Plenary Scientific Session
HOVON-96: Better outcomes with cyclophosphamide after transplantation
Erythroferrone and skeletal changes associated with thalassaemia
Experimental model for limitations of haematopoietic stem cells propagation
Mosunetuzumab: complete remissions in non-Hodgkin lymphoma
Inclusive Medicine
Socioeconomic disparities and survival in paediatric AML
Oral selinexor/pomalidomide/dexamethasone shows activity in heavily pre-treated multiple myeloma
CAR T-cell therapy successful in older non-Hodgkin’s lymphoma patients
Mild renal impairment in African Americans does not affect OS in AML
ALCYONE: New overall survival results for myeloma
Venous Thromboembolism
Rivaroxaban is safe and effective for paediatric venous thromboembolism
Aspirin plus DOAC is not better than a DOAC alone
20-Year follow-up of imatinib in chronic myeloid leukaemia after failure with interferon
CAR T and Beyond
BCMA-targeted CAR T therapy yields 100% response in relapsed/refractory MM
Anti-BCMA/anti-CD38 in refractory multiple myeloma
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