RAS-mutated cytologically indeterminate thyroid nodules: Prevalence of malignancy and behavior under active surveillance Journal Article


Authors: Sfreddo, H. J.; Koh, E. S.; Zhao, K.; Swartzwelder, C. E.; Untch, B. R.; Marti, J. L.; Roman, B. R.; Dublin, J.; Wang, R. S.; Xia, R.; Cohen, J. M.; Xu, B.; Ghossein, R.; Givi, B.; Boyle, J. O.; Tuttle, R. M.; Fagin, J. A.; Wong, R. J.; Morris, L. G.
Article Title: RAS-mutated cytologically indeterminate thyroid nodules: Prevalence of malignancy and behavior under active surveillance
Abstract: Background: Genomic profiling is now available for risk stratification of cytologically indeterminate thyroid nodules (ITNs). Mutations in RAS genes (HRAS, NRAS, KRAS) are found in both benign and malignant thyroid nodules, although isolated RAS mutations are rarely associated with aggressive tumors. Because the long-term behavior of RAS-mutant ITNs is not well understood, most undergo immediate surgery. In this multicenter retrospective cohort study, we characterize tumor growth kinetics of RAS-mutant ITNs followed with active surveillance (AS) using serial ultrasound (US) scans and examine the histopathologic diagnoses of those surgically resected. Methods: US and histopathologic data were analyzed retrospectively from two cohorts: (1) RAS-mutant ITNs managed with AS at three institutions (2010-2023) and (2) RAS-mutant ITNs managed with immediate surgery at two institutions (2016-2020). AS cohort subjects had ≥3 months of follow-up and two or more US scans. Cumulative incidence of nodule growth was determined by the Kaplan-Meier method and growth by ≥72% change in tumor volume. Pathological diagnoses for the immediate surgery cohort were analyzed separately. Results: Sixty-two patients with 63 RAS-mutated ITNs under AS had a median diameter of 1.7 cm (interquartile range [IQR] 1.2-2.6) at time of diagnosis. During a median AS period of 23 months (IQR 9.5-53.5 months), growth was observed in 12 of 63 nodules (19.0%), with a cumulative incidence of 1.9% (1 year), 23.0% (3 years), and 28.0% (5 years). Most nodules (81.0%) demonstrated stability. Surgery was ultimately performed in 6 nodules, of which 1 (16.7%) was malignant. In the cohort of 209 RAS-mutant ITNs triaged to immediate surgery, 33% were malignant (23.9% American Thyroid Association [ATA] low-risk cancers, 7.2% ATA intermediate-risk, and 1.9% ATA high-risk. During a median follow-up of 6.9 (IQR 4.4-7.1) years, there were no disease-specific deaths in these patients. Conclusions: We describe the behavior of RAS-mutant ITNs under AS and find that most demonstrate stability over time. Of the resected RAS-mutant nodules, most were benign; of the cancers, most were ATA low-risk. Immediate surgical resection of all RAS-mutant ITNs appears to be a low-value practice. Further research is needed to help define cases most appropriate for AS or immediate surgery. Copyright 2024, Mary Ann Liebert, Inc., publishers.
Keywords: adult; controlled study; aged; cancer surgery; retrospective studies; gene mutation; major clinical study; genetics; clinical trial; follow up; tumor volume; prevalence; cohort analysis; diagnostic imaging; retrospective study; radiation exposure; cancer cytodiagnosis; active surveillance; watchful waiting; multicenter study; thyroid neoplasms; kaplan meier method; tumor growth; thyroid nodule; race difference; vocal cord paralysis; thyroid tumor; oncogene ras; thyroid surgery; hypoparathyroidism; cumulative incidence; intermediate risk patient; clinical outcome; thyroid nodules; total thyroidectomy; tumor doubling time; hemithyroidectomy; humans; human; male; female; article; ultrasound guided fine needle aspiration; cytologically indeterminate thyroid nodules; ras gene mutation; thyroseq
Journal Title: Thyroid
Volume: 34
Issue: 4
ISSN: 1050-7256
Publisher: Mary Ann Liebert, Inc  
Date Published: 2024-04-01
Start Page: 450
End Page: 459
Language: English
DOI: 10.1089/thy.2023.0544
PUBMED: 38407967
PROVIDER: scopus
PMCID: PMC11971614
DOI/URL:
Notes: The MSK Cancer Center Support Grant (P30 CA008748) is acknowledged in the PubMed record and PDF. Corresponding MSK author is Luc G.T. Morris -- Source: Scopus
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MSK Authors
  1. James A Fagin
    181 Fagin
  2. Ronald A Ghossein
    483 Ghossein
  3. Jay O Boyle
    148 Boyle
  4. Robert M Tuttle
    482 Tuttle
  5. Richard J Wong
    415 Wong
  6. Luc Morris
    279 Morris
  7. Babak Givi
    24 Givi
  8. Brian Untch
    65 Untch
  9. Benjamin Raphael Roman
    75 Roman
  10. Bin   Xu
    227 Xu
  11. Jean-Marc Cohen
    13 Cohen
  12. Karena Zhao
    5 Zhao
  13. Elizabeth Sunyoung Koh
    3 Koh