Abstract | INTRODUCTION: METHODS: For this purpose, WT1 gene expression and the CMML-related abnormal immunophenotype were examined using real-time quantitative polymerase chain reaction and FCM, respectively. RESULTS: In total, 59 patients with CMML who underwent allo-HSCT were enrolled in this study. Thirteen cases (22.0%) developed hematological relapse, and 15 patients (25.4%) expired during the follow-up period. Thirty-four patients (37.6%) were positive for WT1 (WT1+), and 44 patients (74.6%) were positive for FCM prior to allo-HSCT. After allo-HSCT, there were 21 WT1+ patients (35.6%) and 10 patients (16.9%) who were positive in FCM (FCM+). Post-transplant WT1+ (post-WT1 0.6+; 50.7% vs. 7.6%, p < .001) and post-transplant FCM+ (post-FCM+; 90.0% vs. 8.8%, p < .001) indicated a higher 3-year cumulative incidence of relapse (CIR) compared with the WT1- or FCM-patients. Multivariate analysis of event-free survival (EFS), overall survival (OS), and CIR showed that the FCM status after transplantation was an independent prognostic factor for relapse (p < .05). CONCLUSION: Both FCM and WT1 after HSCT were identified as important predictors of recurrence of CMML following transplantation and may be useful in guiding interventions against disease relapse.
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Authors | Xinan Pan, Mengge Gao, Yuqian Sun, Yang Zhou, Ke Wang, Yu Wang, Lanping Xu, Xiaohui Zhang, Xiaojun Huang, Xiao-Su Zhao |
Journal | International journal of laboratory hematology
(Int J Lab Hematol)
Vol. 44
Issue 3
Pg. 510-517
(Jun 2022)
ISSN: 1751-553X [Electronic] England |
PMID | 35061336
(Publication Type: Journal Article)
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Copyright | © 2022 John Wiley & Sons Ltd. |
Chemical References |
- WT1 Proteins
- WT1 protein, human
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Topics |
- Flow Cytometry
- Hematopoietic Stem Cell Transplantation
- Humans
- Leukemia, Myeloid, Acute
(pathology)
- Leukemia, Myelomonocytic, Chronic
(diagnosis, genetics, therapy)
- Leukemia, Myelomonocytic, Juvenile
- Neoplasm, Residual
(diagnosis)
- Prognosis
- Recurrence
- Transplantation, Homologous
- WT1 Proteins
(genetics)
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