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. 2008 Oct 1;112(7):2681-6.
doi: 10.1182/blood-2008-05-153700. Epub 2008 Jul 7.

Validation of a flow cytometric scoring system as a prognostic indicator for posttransplantation outcome in patients with myelodysplastic syndrome

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Validation of a flow cytometric scoring system as a prognostic indicator for posttransplantation outcome in patients with myelodysplastic syndrome

Bart L Scott et al. Blood. .

Abstract

A total of 152 patients with myelodysplastic syndrome (MDS) receiving a first stem cell transplant had marrow cells prospectively analyzed to calculate the flow cytometric scoring system (FCSS) score. The FCSS scores were retrospectively compared with patient outcomes in both univariate and multivariate models. The cumulative incidence of posttransplantation relapse at 3 years was 15%, 10%, and 36% for patients with mild, moderate, and severe FCSS scores, respectively, with the hazard for relapse of 2.8 (P = .02) for severe scores in comparison to patients with mild or normal FCSS scores. In multivariate analyses, the FCSS score was associated with relapse even after accounting for International Prognostic Scoring System (IPSS) score or for marrow myeloblast percentage. Among patients with intermediate-1 risk by IPSS, severe FCSS scores were associated with an increased hazard of relapse (3.8; P = .02) compared with patients with normal/mild/moderate FCSS scores. Among patients with less than 5% marrow myeloblasts, myeloblast dyspoiesis was associated with an increased hazard of relapse (3.7; P = .02). This analysis confirmed that FCSS scores are predictive of posttransplantation outcomes in patients with MDS even after adjusting for risk factors such as marrow myeloblast percentage and IPSS score.

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Figures

Figure 1
Figure 1
Outcome probabilities. Probability of disease-free survival by FCSS (A) and probability of relapse by FCSS (B).
Figure 2
Figure 2
Probability of relapse by FCSS. (A) Patients with intermediate-1 risk disease. (B) Patients with intermediate-2 risk disease.
Figure 3
Figure 3
Probability of relapse in patients with less than 5% marrow myeloblasts that did or did not have evidence of myeloid dyspoiesis as assessed by flow cytometry.

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