In Reply

In Reply.—We thank Dr Chin-Yee and colleagues for their interest in our study. They point out some practical issues with applying the machine learning (ML) algorithm we describe for JAK2 decision support. These include hemoglobin (Hgb) cutoffs, erythropoietin (EPO) availability, and the model’s generalizability when trained on a predominantly male population.Inclusion criteria were based on Hgb concentrations above high-normal reference ranges. These cutoffs are somewhat different from those endorsed by the World Health Organization (WHO), which are intended as diagnostic criteria for polycythemia vera (PV) and optimized to differentiate PV from essential thrombocythemia.1 First, Hgb was not used as a training parameter. Additionally, platelets and relative distribution width (RDW)—which are not affected by Hgb—had the greatest impact on model performance, while red blood cell count had marginal effect. WHO Hgb criteria were used to standardize comparisons between the algorithm and rule-based systems. Under these conditions, algorithm performance was comparable (88.5% potential reduction in JAK2 testing) to cases selected by reference range criteria (90.3%) and exceeded rule-based systems (50.0% to 62.3%).2We agree that the availability of EPO results has practical limitations as shown by this parameter—among all others—having the highest number of missing values: 26.8% for training/validation and 31.8% for out-of-sample data sets.2 EPO, which ranked third in impact on model performance, was not used in rule-based systems, nor was RDW, which ranked second. Use of these parameters in the algorithm likely contributed to better performance when compared to rule-based systems. However, it’s worth noting that 92% of false positives seen in the independent data set were associated with low EPO levels, which substantially lowered the algorithm’s positive predictive power.2 Additional comparisons between the ML algorithm described in our article, which lacks EPO inputs, or other models trained with only blood count parameters against current or new rule-based systems that might be improved by including RDW, could help identify the most effective and practical JAK2 decision support approach.The validation data sets were highly overweighted with male cases (96.6%)2 and less so (205 of 285; 72.9%) for the JAKPOT study cited. The subset of out-of-sample cases used to compare the algorithm to JAKPOT rules had a similar proportion of males, 71%.2 Despite a male-dominant training set, there were only marginal differences in algorithm performance between male and female cases in the out-of-sample data set. See Table 1 and Figure 4 in Schifman et al.2 However, the sample size was low, and further evaluations with other defined populations and larger data sets will be necessary to resolve this concern as well as better delineate differences between the effectiveness of ML and rule-based systems for JAK2 decision support.

Authors

Institutions

Publication Details

Journal
Archives of Pathology & Laboratory Medicine
Published
2025-11-21
DOI
https://doi.org/10.5858/arpa.2025-0305-le
Primary Topic
Myeloproliferative Neoplasms: Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

In Reply

Ron B. Schifman
Archives of Pathology & Laboratory Medicine
Myeloproliferative Neoplasms: Diagnosis and Treatment
article

In Reply

Ron B. Schifman
article en

Abstract

In Reply.—We thank Dr Chin-Yee and colleagues for their interest in our study. They point out some practical issues with applying the machine learning (ML) algorithm we describe for JAK2 decision support. These include hemoglobin (Hgb) cutoffs, erythropoietin (EPO) availability, and the model’s generalizability when trained on a predominantly male population.Inclusion criteria were based on Hgb concentrations above high-normal reference ranges. These cutoffs are somewhat different from those endorsed by the World Health Organization (WHO), which are intended as diagnostic criteria for polycythemia vera (PV) and optimized to differentiate PV from essential thrombocythemia.1 First, Hgb was not used as a training parameter. Additionally, platelets and relative distribution width (RDW)—which are not affected by Hgb—had the greatest impact on model performance, while red blood cell count had marginal effect. WHO Hgb criteria were used to standardize comparisons between the algorithm and rule-based systems. Under these conditions, algorithm performance was comparable (88.5% potential reduction in JAK2 testing) to cases selected by reference range criteria (90.3%) and exceeded rule-based systems (50.0% to 62.3%).2We agree that the availability of EPO results has practical limitations as shown by this parameter—among all others—having the highest number of missing values: 26.8% for training/validation and 31.8% for out-of-sample data sets.2 EPO, which ranked third in impact on model performance, was not used in rule-based systems, nor was RDW, which ranked second. Use of these parameters in the algorithm likely contributed to better performance when compared to rule-based systems. However, it’s worth noting that 92% of false positives seen in the independent data set were associated with low EPO levels, which substantially lowered the algorithm’s positive predictive power.2 Additional comparisons between the ML algorithm described in our article, which lacks EPO inputs, or other models trained with only blood count parameters against current or new rule-based systems that might be improved by including RDW, could help identify the most effective and practical JAK2 decision support approach.The validation data sets were highly overweighted with male cases (96.6%)2 and less so (205 of 285; 72.9%) for the JAKPOT study cited. The subset of out-of-sample cases used to compare the algorithm to JAKPOT rules had a similar proportion of males, 71%.2 Despite a male-dominant training set, there were only marginal differences in algorithm performance between male and female cases in the out-of-sample data set. See Table 1 and Figure 4 in Schifman et al.2 However, the sample size was low, and further evaluations with other defined populations and larger data sets will be necessary to resolve this concern as well as better delineate differences between the effectiveness of ML and rule-based systems for JAK2 decision support.

Archives of Pathology & Laboratory MedicineVol. 149(12)
University of Arizona (US), Southern Arizona VA Health Care System (US)
Openalex Percentile: Top 49%
Myeloproliferative Neoplasms: Diagnosis and Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.