| Literature DB >> 34988692 |
Kaito Harada1, Shohei Mizuno2, Shingo Yano3, Akiyoshi Takami2, Hiroto Ishii3, Kazuhiro Ikegame4, Yuho Najima5, Shinichi Kako6, Takashi Ashida7, Souichi Shiratori8, Shuichi Ota9, Makoto Onizuka10, Kentaro Fukushima11, Takahiro Fukuda12, Tatsuo Ichinohe13, Yoshiko Atsuta14,15, Masamitsu Yanada16.
Abstract
Although haploidentical donor lymphocyte infusion (DLI) is a valid treatment option for relapsed acute myeloid leukemia (AML), the incidence and risk factors for graft-versus-host disease (GVHD) and the efficacy of haploidentical DLI have not been fully evaluated. We retrospectively analyzed the outcomes after haploidentical DLI for 84 patients with AML using a nationwide database and additional questionnaires. The median number of DLI cycles and infused CD3+ cell dose was 1 and 1.0 × 106/kg, respectively. The infused CD3+ cell count of 5.0 × 105/kg or higher was associated with acute GVHD (grade II-IV, 32.1% vs. 10.5%, p = 0.03; grade III-IV, 21.4% vs. 5.3%, p = 0.10). Patients who developed grade III-IV acute GVHD more frequently succumbed to treatment-related mortality (46.7% vs. 15.8% at 1 year, p = 0.002), although the relapse-related mortality was significantly low (40.0% vs. 72.2% at 1 year, p = 0.025). The overall response to DLI was significantly higher in the preemptive DLI group (47.4%) than in the therapeutic group (13.9%, p = 0.002). In the multivariate analysis, preemptive DLI was the predictive factor for overall response (odds ratio, 5.58; p = 0.003). Our results indicated the substantial risk of acute GVHD after haploidentical DLI with CD3+ cell count of 5.0×105/kg or higher and the favorable outcomes after preemptive DLI.Entities:
Keywords: Acute myeloid leukemia; Cell therapy; Donor lymphocyte infusion; Haploidentical stem cell Transplantation
Mesh:
Year: 2022 PMID: 34988692 DOI: 10.1007/s00277-021-04731-5
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673