TY - JOUR
T1 - Do we Need to Perform Bone Marrow Examination in all Subjects Suspected of MDS? Evaluation and Validation of Non-Invasive (Web-Based) Diagnostic Algorithm
AU - Oster, Howard S.
AU - Polakow, Ariel M.
AU - Gat, Roi
AU - Goldschmidt, Noa
AU - Ben-Ezra, Jonathan
AU - Mittelman, Moshe
N1 - Publisher Copyright:
© 2025 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2025
Y1 - 2025
N2 - Background: Bone marrow examination (BME) is the gold standard of diagnosing myelodysplastic syndromes (MDS). Problems: it is invasive, painful, causing possible bleeding, inaccurate (aspirate hemodilution), and subjective (inter-observer interpretation discordance). We developed non-invasive diagnostic tools: A logistic regression formula [LeukRes 2018], then a web algorithm using 10 variables (age, gender, Hb, MCV, WBC, ANC, monocytes, PLT, glucose, creatinine) to diagnose/exclude MDS [BldAdv 2021]. Here, we perform external validation of the model. Methods: From the TASMC BM registry (2019–22) we identified and compared the model performance between MDS patients and controls (> 50 year with unexplained anemia, not MDS), all BME diagnosed, and not used in model building. Results: The model was accurate and predicted MDS in 63% of 103 patients, and excluded (correctly) in 83% of 101 controls. It miss-classified in 11%/7% respectively, and was indeterminate in 26%/10% respectively. The positive predictive value (PPV), NPV, sensitivity, and specificity (excluding the indeterminate group) were 90%, 88%, 86%, and 92%, respectively. Subgroup (Lower/higher risk, LR/HR) analysis results were similar. Conclusions: The MDS diagnostic model was validated and can be used, mainly for MDS exclusion, especially in suspected LR-MDS, avoiding BME in some patients. In the future incorporating peripheral blood genetics and morphometry can further improve the model.
AB - Background: Bone marrow examination (BME) is the gold standard of diagnosing myelodysplastic syndromes (MDS). Problems: it is invasive, painful, causing possible bleeding, inaccurate (aspirate hemodilution), and subjective (inter-observer interpretation discordance). We developed non-invasive diagnostic tools: A logistic regression formula [LeukRes 2018], then a web algorithm using 10 variables (age, gender, Hb, MCV, WBC, ANC, monocytes, PLT, glucose, creatinine) to diagnose/exclude MDS [BldAdv 2021]. Here, we perform external validation of the model. Methods: From the TASMC BM registry (2019–22) we identified and compared the model performance between MDS patients and controls (> 50 year with unexplained anemia, not MDS), all BME diagnosed, and not used in model building. Results: The model was accurate and predicted MDS in 63% of 103 patients, and excluded (correctly) in 83% of 101 controls. It miss-classified in 11%/7% respectively, and was indeterminate in 26%/10% respectively. The positive predictive value (PPV), NPV, sensitivity, and specificity (excluding the indeterminate group) were 90%, 88%, 86%, and 92%, respectively. Subgroup (Lower/higher risk, LR/HR) analysis results were similar. Conclusions: The MDS diagnostic model was validated and can be used, mainly for MDS exclusion, especially in suspected LR-MDS, avoiding BME in some patients. In the future incorporating peripheral blood genetics and morphometry can further improve the model.
KW - diagnostic model
KW - gradient boosted model
KW - myelodysplastic syndromes
KW - validation
UR - http://www.scopus.com/inward/record.url?scp=85214110521&partnerID=8YFLogxK
U2 - 10.1111/ejh.14379
DO - 10.1111/ejh.14379
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AN - SCOPUS:85214110521
SN - 0902-4441
VL - 114
SP - 672
EP - 678
JO - European Journal of Haematology
JF - European Journal of Haematology
IS - 4
ER -