Back

Molecular classifier vs cytology diagnostic accuracy in Bethesda III/IV nodules. Rapid review

Pardal-Refoyo, J. L.

2025-04-28 otolaryngology
10.1101/2025.04.27.25326507 medRxiv
Show abstract

IntroductionThyroid nodules with indeterminate cytology (Bethesda III and IV) present a diagnostic challenge, as conventional cytology offers limited predictive value and can lead to unnecessary surgeries. Recently, validated molecular classifiers have been developed with the aim of improving the stratification of the risk of malignancy in these nodules and optimizing clinical decision-making. Objectives To evaluate and compare the diagnostic yield of validated commercial molecular systems, including ThyroSeq and Afirma, versus conventional cytology in Bethesda III and IV thyroid nodules, using the result of postsurgical histopathology as a reference. MethodA structured review of prospective studies, randomized controlled trials, retrospective cohorts, and meta-analyses that analyzed the performance of commercial molecular classifiers in Bethesda III and IV nodules was conducted. We included studies that reported sensitivity, specificity, positive and negative predictive value, and that used postoperative histopathology as a reference standard. The sample volume of individual studies ranges from several hundred to more than six thousand nodules using pooled analyses. ResultsThe selected studies show that molecular classifiers such as ThyroSeq v3 and Afirma GSC achieve a high sensitivity and negative predictive value ([≥]94% and [≥]96%, respectively), outperforming conventional cytology. Specificity and positive predictive value show greater variability between studies and clinical settings. The use of these classifiers has made it possible to reduce the number of unnecessary surgeries on benign nodules. ConclusionsThe available evidence supports that validated molecular classifiers increase diagnostic accuracy in thyroid nodules with indeterminate cytology, reduce unnecessary surgical interventions, and improve clinical decision-making compared to conventional cytology, using histopathology as a standard reference.

Matching journals

The top 4 journals account for 50% of the predicted probability mass.

1
Communications Medicine
85 papers in training set
Top 0.1%
17.6%
2
Journal of Clinical Medicine
91 papers in training set
Top 0.1%
14.8%
3
Frontiers in Oncology
95 papers in training set
Top 0.1%
12.8%
4
PLOS ONE
4510 papers in training set
Top 18%
10.2%
50% of probability mass above
5
Cancers
200 papers in training set
Top 1%
4.9%
6
Frontiers in Immunology
586 papers in training set
Top 2%
4.3%
7
Scientific Reports
3102 papers in training set
Top 31%
4.0%
8
Nature Communications
4913 papers in training set
Top 44%
2.6%
9
American Journal of Respiratory and Critical Care Medicine
39 papers in training set
Top 0.4%
2.1%
10
Diagnostics
48 papers in training set
Top 0.7%
2.1%
11
npj Digital Medicine
97 papers in training set
Top 2%
1.9%
12
Frontiers in Endocrinology
53 papers in training set
Top 1%
1.7%
13
Ophthalmology Science
20 papers in training set
Top 0.2%
1.7%
14
European Journal of Nuclear Medicine and Molecular Imaging
19 papers in training set
Top 0.1%
1.7%
15
eBioMedicine
130 papers in training set
Top 2%
1.5%
16
ERJ Open Research
44 papers in training set
Top 0.6%
1.2%
17
BMC Cancer
52 papers in training set
Top 2%
1.2%
18
British Journal of Cancer
42 papers in training set
Top 1%
1.1%
19
Cureus
67 papers in training set
Top 4%
0.9%
20
Frontiers in Medicine
113 papers in training set
Top 6%
0.8%
21
Cells
232 papers in training set
Top 6%
0.8%
22
Frontiers in Neurology
91 papers in training set
Top 5%
0.8%
23
PeerJ
261 papers in training set
Top 17%
0.6%
24
iScience
1063 papers in training set
Top 37%
0.6%