4.6 Article

A predictive algorithm using clinical and laboratory parameters may assist in ruling out and in diagnosing MDS

Journal

BLOOD ADVANCES
Volume 5, Issue 16, Pages 3066-3075

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ELSEVIER
DOI: 10.1182/bloodadvances.2020004055

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Funding

  1. Novartis Pharmacy B.V. Oncology Europe
  2. Amgen Limited
  3. Celgene International
  4. Janssen Pharmaceutica
  5. Takeda Pharmaceuticals International

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The study proposes a noninvasive web-based application utilizing gradient boosted models to help exclude or diagnose myelodysplastic syndrome (MDS). By utilizing demographic, clinical, and laboratory variables, the application can accurately predict or exclude MDS in 86% of patients with unexplained anemia. The developed application shows stability and accuracy in predicting MDS and provides physicians with a convenient noninvasive diagnostic tool.
We present a noninvasive Web-based app to help exclude or diagnose myelodysplastic syndrome (MDS), a bone marrow (BM) disorder with cytopenias and leukemic risk, diagnosed by BM examination. A sample of 502 MDS patients from the European MDS (EUMDS) registry (n > 2600) was combined with 502 controls (all BM proven). Gradient-boosted models (GBMs) were used to predict/exclude MDS using demographic, clinical, and laboratory variables. Area under the receiver operating characteristic curve (AUC), sensitivity, and specificity were used to evaluate the models, and performance was validated using 100 times fivefold cross-validation. Model stability was assessed by repeating its fit using different randomly chosen groups of 502 EUMDS cases. AUC was 0.96 (95% confidence interval, 0.95-0.97). MDS is predicted/excluded accurately in 86% of patients with unexplained anemia. A GBM score (range, 0-1) of less than 0.68 (GBM < 0.68) resulted in a negative predictive value of 0.94, that is, MDS was excluded. GBM >= 0.82 provided a positive predictive value of 0.88, that is, MDS. The diagnosis of the remaining patients (0.68 <= GBM < 0.82) is indeterminate. The discriminating variables: age, sex, hemoglobin, white blood cells, platelets, mean corpuscular volume, neutrophils, monocytes, glucose, and creatinine. A Web-based app was developed; physicians could use it to exclude or predict MDS noninvasively in most patients without a BM examination. Future work will add peripheral blood cytogenetics/genetics, EUMDS-based prospective validation, and prognostication.

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