Possible prognostic impact of WT1 mRNA expression at day + 30 after haploidentical peripheral blood stem cell transplantation with posttransplant cyclophosphamide for patients with myeloid neoplasm: a multicenter study from the Okayama Hematological Study Group

Int J Hematol. 2022 Apr;115(4):515-524. doi: 10.1007/s12185-022-03290-3. Epub 2022 Feb 4.

Abstract

Background: Previous studies have revealed that relapse of myeloid neoplasms after allogeneic hematopoietic stem cell transplantation (allo-HSCT) could be predicted by monitoring Wilms' tumor 1 (WT1) mRNA expression. However, only a few studies have investigated patients who received human leukocyte antigen-haploidentical stem cell transplantation with posttransplant cyclophosphamide (PTCY-haplo). In this study, we investigated the relationship between WT1 mRNA levels and clinical outcomes in the PTCY-haplo group, and compared them with those in the conventional graft-versus-host disease prophylaxis group (conventional group).

Methods: We retrospectively analyzed 130 patients who received their first allo-HSCT between April 2017 and December 2020, including 26 who received PTCY-haplo.

Results: The WT1 mRNA expression level at day + 30 after allo-HSCT associated with increased risk of 1-year cumulative incidence of relapse (CIR) was ≥ 78 copies/μg RNA in the conventional group (p < 0.01) and ≥ 50 copies/μg RNA in the PTCY-haplo group (p = 0.03).

Conclusions: The appropriate cutoff level of WT1 mRNA at day + 30 after allo-HSCT for predicting prognosis in patients treated with PTCY-haplo may be < 50 copies/μg RNA.

Keywords: Allogeneic hematopoietic stem cell transplantation; Minimal residual disease; Myeloid neoplasm; Posttransplant cyclophosphamide; Wilms’ tumor 1.

Publication types

  • Multicenter Study

MeSH terms

  • Cyclophosphamide / therapeutic use
  • Graft vs Host Disease* / drug therapy
  • Graft vs Host Disease* / etiology
  • Graft vs Host Disease* / prevention & control
  • Hematopoietic Stem Cell Transplantation* / adverse effects
  • Humans
  • Neoplasms* / drug therapy
  • Peripheral Blood Stem Cell Transplantation*
  • Prognosis
  • RNA, Messenger / genetics
  • Retrospective Studies
  • WT1 Proteins / genetics

Substances

  • RNA, Messenger
  • WT1 Proteins
  • WT1 protein, human
  • Cyclophosphamide