| Literature DB >> 34748664 |
Maro Ohanian1, Jose A Cancelas2, Robertson Davenport3, Vinod Pullarkat4, Tor Hervig5, Catherine Broome6, Kelly Marek1, Mary Kelly1, Zartash Gul7, Neeta Rugg2, Shawnagay Nestheide2, Bridget Kinne7, Zbigniew Szczepiorkowski8, Hagop Kantarjian1, Joan Pehta9, Ruth Biehl10, Anna Yu10, Fleur Aung11, Ben Antebi10, Glen Michael Fitzpatrick10.
Abstract
Thrombosomes are trehalose-stabilized, freeze-dried group O platelets with a 3-year shelf life. They can be stockpiled, rapidly reconstituted, and infused regardless of the recipient's blood type. Thrombosomes thus represent a potential alternative platelet transfusion strategy. The present study assessed the safety and potential early signals of efficacy of Thrombosomes in bleeding thrombocytopenic patients. We performed an open-label, phase 1 study of single doses of allogeneic Thrombosomes at three dose levels in three cohorts, each consisting of eight patients who had hematologic malignancies, thrombocytopenia, and bleeding. Adverse events, dose-limiting toxicities (DLTs), World Health Organization (WHO) bleeding scores, and hematology values were assessed. No DLTs were reported. The median age was 59 years (24-71). Most patients had AML (58%) or ALL (29%), followed by MDS (8%) and myeloproliferative neoplasm (4%). The WHO scores of 22 patients who were actively bleeding at a total of 27 sites at baseline either improved (n = 17 [63%]) or stabilized (n = 10 [37%]) through day 6. Twenty-four hours after infusion, 12 patients (50%) had a clinically significant platelet count increase. Of eight patients who received no platelet transfusions for 6 days after Thrombosomes infusion, 5 had a clinically significant increase in platelet count of ≥5000 platelets/μL and 2 had platelet count normalization. Thrombosomes doses up to 3.78 × 108 particles/kg demonstrated safety in 24 bleeding, thrombocytopenic patients with hematological malignancies. Thrombosomes may represent an alternative to conventional platelets to treat bleeding. A phase 2 clinical trial in a similar patient population is underway.Entities:
Mesh:
Year: 2021 PMID: 34748664 DOI: 10.1002/ajh.26403
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047