脱敏(药物)
医学
队列
内科学
CD38
抗体
药效学
肾移植
移植
药代动力学
胃肠病学
免疫学
干细胞
受体
生物
川地34
遗传学
作者
Flavio Vincenti,Oriol Bestard,Amarpali Brar,Josep M. Cruzado,Daniel Serón,A. Osama Gaber,Nicole Ali,Anat R. Tambur,Helen Lee,Giovanni Abbadessa,Jo-Anne Paul,Markus Dudek,Ruby Siegel,Alba Torija,Dorothée Sémiond,Lucie Lépine,Nils Ternès,Robert A. Montgomery,Mark D. Stegall
出处
期刊:Journal of The American Society of Nephrology
日期:2023-12-26
标识
DOI:10.1681/asn.0000000000000287
摘要
Background Patients with calculated panel reactive antibody (cPRA) ≥80.00%, particularly those with cPRA ≥99.90%, are considered highly sensitized and underserved by the Kidney Allocation System. Desensitization removes circulating reactive antibodies and/or suppresses antibody production to increase chances of a negative crossmatch. CD38 is expressed highly on plasma cells, thus is a potential target for desensitization. Methods This was an open-label single-arm Phase 1/2 study investigating the safety, pharmacokinetics, and preliminary efficacy of isatuximab in patients awaiting kidney transplantation. There were two cohorts, Cohorts A and B, which enrolled cPRA ≥99.90% and 80.00%–<99.90%, respectively. Results 23 patients (12 Cohort A, 11 Cohort B) received isatuximab 10 mg/kg weekly for 4 weeks then every 2 weeks for 8 weeks. Isatuximab was well tolerated with pharmacokinetic and pharmacodynamic profiles that indicated similar exposure to multiple myeloma trials. It resulted in decreases in CD38 + plasmablasts, plasma cells, and NK cells; and significant reductions in HLA-specific IgG-producing memory B cells. Overall response rate, based on a pre-defined composite desensitization end-point, was 83.3% and 81.8% in Cohorts A and B. Most responders had decreases in anti-HLA antibodies that were maintained for 26 weeks after the last dose. Overall cPRA values were minimally impacted, however, with only 9/23 patients (39%) having cPRA decreases to target levels. By study cut-off (median follow-up 68 weeks), 6 patients received transplant offers, of which 4 were accepted. Conclusions In this open-label trial, isatuximab was well tolerated and resulted in a durable decrease in anti-HLA antibodies with partial desensitization activity.
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