Effect of Pre- and Peri-Transplant Measurable Residual Disease Clearance in Patients with Myelodysplastic Neoplasm; A Referral Center Experience

Measurable residual disease (MRD) has emerged as a potential prognostic marker for allogeneic stem cell transplant (HSCT) outcomes in various hematologic malignancies . However, the MRD status in myelodysplastic neoplasm (MDS) or myelodysplastic/myeloproliferative neoplasm (MDS/MPN), can be difficult to interpret due to heterogenous disease biology and unique limitations in each MRD measuring techniques. In comparison to B-cell acute lymphoblastic leukemia whose clearance of pre-HSCT MRD is considered essential, the data in MDS or MDS/MPN is less clear. As post-HSCT disease surveillance becomes more standardized, we also evaluated the effect of peri-HSCT MRD status on relapse-free and overall survival (RFS and OS) outcomes. We reviewed records of adult patients who underwent HSCT for MDS or MDS/MPN at our institution between 2012-2023 and report the outcomes of patients between those who had undetectable MRD (MRD-) vs detectable MRD (MRD+) pre-HSCT and conducted a conditional analysis of outcomes based on MRD status at day+90 post-HSCT. We identified 38 and 55 patients in MRD- and MRD+ cohorts respectively. Baseline patient characteristics were similar between the cohorts, including age, Revised and Molecular International Prognostic Scores (IPSS-R & IPSS-M), and HSCT-related factors. The MRD+ cohort had inferior RFS (HR: 1.84, 95% CI: 1.09-3.12, p=0.02) but a statistically significant difference in OS was not evidenced (HR: 1.52, 95% CI: 0.88-2.61, p=0.14). After adjusting for % blasts at diagnosis, and conditioning intensity, MRD+ patients were found to be at 1.92 times increased risk of relapse or death (95% CI: 1.12-3.28, p=0.02). Additionally, increasing IPSS-M score was associated with poorer RFS (HR: 1.27, 95% CI: 1.01-1.59, p=0.04) and OS (HR: 1.52, 95% CI: 1.20-1.91, p<0.01). On a conditional analysis of patients who were alive and in remission until day +90 post-HSCT, the pre-HSCT MRD status did not confer a statistically significant difference in RFS and OS if patients were able to achieve an MRD- status by day +90 post-HSCT. Pre- and peri-HSCT MRD testing may offer valuable survival prognostic information in patients with MDS and MDS/MPN and should be considered part of routine disease surveillance.

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Journal
Transplantation and Cellular Therapy
Published
2025-02-01
DOI
https://doi.org/10.1016/j.jtct.2025.01.660
Primary Topic
Acute Myeloid Leukemia Research
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article
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article

Effect of Pre- and Peri-Transplant Measurable Residual Disease Clearance in Patients with Myelodysplastic Neoplasm; A Referral Center Experience

Kittika Poonsombudlert, Ratdanai Yodsuwan, Andrew J. Vegel, Sarah L. Mott et al.
Transplantation and Cellular Therapy
Acute Myeloid Leukemia Research
article

Effect of Pre- and Peri-Transplant Measurable Residual Disease Clearance in Patients with Myelodysplastic Neoplasm; A Referral Center Experience

Kittika Poonsombudlert, Ratdanai Yodsuwan, Andrew J. Vegel, Sarah L. Mott, Grerk Sutamtewagul, Aditya Ravindra, Prajwal Dhakal, Margarida Magalhaes‐Silverman
article en

Abstract

Measurable residual disease (MRD) has emerged as a potential prognostic marker for allogeneic stem cell transplant (HSCT) outcomes in various hematologic malignancies . However, the MRD status in myelodysplastic neoplasm (MDS) or myelodysplastic/myeloproliferative neoplasm (MDS/MPN), can be difficult to interpret due to heterogenous disease biology and unique limitations in each MRD measuring techniques. In comparison to B-cell acute lymphoblastic leukemia whose clearance of pre-HSCT MRD is considered essential, the data in MDS or MDS/MPN is less clear. As post-HSCT disease surveillance becomes more standardized, we also evaluated the effect of peri-HSCT MRD status on relapse-free and overall survival (RFS and OS) outcomes. We reviewed records of adult patients who underwent HSCT for MDS or MDS/MPN at our institution between 2012-2023 and report the outcomes of patients between those who had undetectable MRD (MRD-) vs detectable MRD (MRD+) pre-HSCT and conducted a conditional analysis of outcomes based on MRD status at day+90 post-HSCT. We identified 38 and 55 patients in MRD- and MRD+ cohorts respectively. Baseline patient characteristics were similar between the cohorts, including age, Revised and Molecular International Prognostic Scores (IPSS-R & IPSS-M), and HSCT-related factors. The MRD+ cohort had inferior RFS (HR: 1.84, 95% CI: 1.09-3.12, p=0.02) but a statistically significant difference in OS was not evidenced (HR: 1.52, 95% CI: 0.88-2.61, p=0.14). After adjusting for % blasts at diagnosis, and conditioning intensity, MRD+ patients were found to be at 1.92 times increased risk of relapse or death (95% CI: 1.12-3.28, p=0.02). Additionally, increasing IPSS-M score was associated with poorer RFS (HR: 1.27, 95% CI: 1.01-1.59, p=0.04) and OS (HR: 1.52, 95% CI: 1.20-1.91, p<0.01). On a conditional analysis of patients who were alive and in remission until day +90 post-HSCT, the pre-HSCT MRD status did not confer a statistically significant difference in RFS and OS if patients were able to achieve an MRD- status by day +90 post-HSCT. Pre- and peri-HSCT MRD testing may offer valuable survival prognostic information in patients with MDS and MDS/MPN and should be considered part of routine disease surveillance.

Transplantation and Cellular TherapyVol. 31(2)
University of Iowa Hospitals and Clinics (US), University of Iowa Health Care (US)
Zero hunger
Openalex Percentile: Top 95%
Acute Myeloid Leukemia Research
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