CD34<b>+</b>-selected stem cell boost can safely improve cytopenias following CAR T-cell therapy

Khushnuma Mullanfiroze(NHS Blood and Transplant), Arina Lazareva(NHS Blood and Transplant), Jan Chu(NHS Blood and Transplant), Lindsey Williams(NHS Blood and Transplant), Saskia Burridge(NHS Blood and Transplant), Juliana Silva(NHS Blood and Transplant), Robert Chiesa(NHS Blood and Transplant), Kanchan Rao(NHS Blood and Transplant), Giovanna Lucchini(NHS Blood and Transplant), Sara Ghorashian(Great Ormond Street Hospital), Maeve O’Reilly(Royal London Hospital), Ben Carpenter(Royal London Hospital), Victoria Grandage(Royal London Hospital), Rachael Hough(Royal London Hospital), Claire Roddie(Royal London Hospital), Persis Amrolia(NHS Blood and Transplant)
Blood Advances
July 5, 2022
Cited by 48Open Access
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Abstract

2] For example, in the ELIANA study, 41% and 53% of patients demonstrated grade 3 to 4 thrombocytopenia and neutropenia, respectively, persisting beyond day 30. Impaired hematological recovery after CAR T-cell therapy can lead to susceptibility to opportunistic infections, bleeding, and/or transfusion dependence, causing significant morbidity and mortality. Pre-CAR T-cell therapy lymphodepletion causes cytopenia that generally recovers in most patients within a month after CAR T-cell therapy. However, a proportion of patients develop persistent cytopenia, particularly neutropenia, associated with bone marrow (BM) hypoplasia that can persist for several months after CAR T-cell therpay. We hypothesized that for those patients who have undergone allogeneic SCT before CAR T-cell therapy and develop persistent cytopenia after CAR-T cell therapy, an unconditioned CD34 1 -selected stem-cell boost (SCB) from the SCT donor could be used to improve the cytopenia, similar to its use in those who have poor graft function after SCT. A cohort of 101 pediatric and young adults from 2 centers in the United Kingdom with r/r B-ALL were treated with CAR T-cell therapy from May 2016 through December 2021. Of those patients, 2 were not evaluable for assessment of cytopenias after day 128 of CAR infusion (1 died on post-infusion day 4, and 1 had a morphological relapse on day 28). Of the 99 evaluable patients, 52 had undergone SCT before CAR therapy and 23 (44.2%) of them developed grade 3 to 4 cytopenia. Of the 47 patients who did not undergo an SCT, 23 (48.9%) developed grade 3 to 4 cytopenia. The difference in the rate of cytopenia between the 2 groups was not significant (P 5 .5999).


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