TY - JOUR
T1 - [18F]FDG-PET/CT to prevent futile surgery in indeterminate thyroid nodules
T2 - a blinded, randomised controlled multicentre trial
AU - de Koster, Elizabeth J.
AU - de Geus-Oei, Lioe-Fee
AU - Brouwers, Adrienne H.
AU - van Dam, Eveline W. C. M.
AU - Dijkhorst-Oei, Lioe-Ting
AU - van Engen-van Grunsven, Adriana C. H.
AU - van den Hout, Wilbert B.
AU - Klooker, Tamira K.
AU - Netea-Maier, Romana T.
AU - Snel, Marieke
AU - EfFECTS trial study group
AU - Oyen, Wim J. G.
AU - Vriens, Dennis
N1 - Funding Information: The EfFECTS trial was supported by a project grant from the Dutch Cancer Society (KUN 2014–6514). Funding Information: The authors like to thank all the patients who participated in the EfFECTS trial, all members of the EfFECTS trial consortium, and all others who were involved in any of the study procedures. In particular, we like to thank Dr. B. Küsters (BK), a pathologist at the Radboud university medical centre, Nijmegen, the Netherlands, for his assistance with the central review of cytology and histopathology samples, and Prof. dr. O.M. Dekkers, a clinical epidemiologist and endocrinologist at the Leiden University Medical Center, Leiden, the Netherlands, and Prof. dr. H. Putter, a statistician at the Leiden University Medical Center, Leiden, the Netherlands, for their expertise and guidance during the execution of the trial. Publisher Copyright: © 2021, The Author(s).
PY - 2022/5
Y1 - 2022/5
N2 - Purpose: To assess the impact of an [ 18F]FDG-PET/CT-driven diagnostic workup to rule out malignancy, avoid futile diagnostic surgeries, and improve patient outcomes in thyroid nodules with indeterminate cytology. Methods: In this double-blinded, randomised controlled multicentre trial, 132 adult euthyroid patients with scheduled diagnostic surgery for a Bethesda III or IV thyroid nodule underwent [ 18F]FDG-PET/CT and were randomised to an [ 18F]FDG-PET/CT-driven or diagnostic surgery group. In the [ 18F]FDG-PET/CT-driven group, management was based on the [ 18F]FDG-PET/CT result: when the index nodule was visually [ 18F]FDG-positive, diagnostic surgery was advised; when [ 18F]FDG-negative, active surveillance was recommended. The nodule was presumed benign when it remained unchanged on ultrasound surveillance. In the diagnostic surgery group, all patients were advised to proceed to the scheduled surgery, according to current guidelines. The primary outcome was the fraction of unbeneficial patient management in one year, i.e., diagnostic surgery for benign nodules and active surveillance for malignant/borderline nodules. Intention-to-treat analysis was performed. Subgroup analyses were performed for non-Hürthle cell and Hürthle cell nodules. Results: Patient management was unbeneficial in 42% (38/91 [95% confidence interval [CI], 32–53%]) of patients in the [ 18F]FDG-PET/CT-driven group, as compared to 83% (34/41 [95% CI, 68–93%]) in the diagnostic surgery group (p < 0.001). [ 18F]FDG-PET/CT-driven management avoided 40% (25/63 [95% CI, 28–53%]) diagnostic surgeries for benign nodules: 48% (23/48 [95% CI, 33–63%]) in non-Hürthle cell and 13% (2/15 [95% CI, 2–40%]) in Hürthle cell nodules (p = 0.02). No malignant or borderline tumours were observed in patients under surveillance. Sensitivity, specificity, negative and positive predictive value, and benign call rate (95% CI) of [ 18F]FDG-PET/CT were 94.1% (80.3–99.3%), 39.8% (30.0–50.2%), 95.1% (83.5–99.4%), 35.2% (25.4–45.9%), and 31.1% (23.3–39.7%), respectively. Conclusion: An [ 18F]FDG-PET/CT-driven diagnostic workup of indeterminate thyroid nodules leads to practice changing management, accurately and oncologically safely reducing futile surgeries by 40%. For optimal therapeutic yield, application should be limited to non-Hürthle cell nodules. Trial registration number: This trial is registered with ClinicalTrials.gov: NCT02208544 (5 August 2014), https://clinicaltrials.gov/ct2/show/NCT02208544.
AB - Purpose: To assess the impact of an [ 18F]FDG-PET/CT-driven diagnostic workup to rule out malignancy, avoid futile diagnostic surgeries, and improve patient outcomes in thyroid nodules with indeterminate cytology. Methods: In this double-blinded, randomised controlled multicentre trial, 132 adult euthyroid patients with scheduled diagnostic surgery for a Bethesda III or IV thyroid nodule underwent [ 18F]FDG-PET/CT and were randomised to an [ 18F]FDG-PET/CT-driven or diagnostic surgery group. In the [ 18F]FDG-PET/CT-driven group, management was based on the [ 18F]FDG-PET/CT result: when the index nodule was visually [ 18F]FDG-positive, diagnostic surgery was advised; when [ 18F]FDG-negative, active surveillance was recommended. The nodule was presumed benign when it remained unchanged on ultrasound surveillance. In the diagnostic surgery group, all patients were advised to proceed to the scheduled surgery, according to current guidelines. The primary outcome was the fraction of unbeneficial patient management in one year, i.e., diagnostic surgery for benign nodules and active surveillance for malignant/borderline nodules. Intention-to-treat analysis was performed. Subgroup analyses were performed for non-Hürthle cell and Hürthle cell nodules. Results: Patient management was unbeneficial in 42% (38/91 [95% confidence interval [CI], 32–53%]) of patients in the [ 18F]FDG-PET/CT-driven group, as compared to 83% (34/41 [95% CI, 68–93%]) in the diagnostic surgery group (p < 0.001). [ 18F]FDG-PET/CT-driven management avoided 40% (25/63 [95% CI, 28–53%]) diagnostic surgeries for benign nodules: 48% (23/48 [95% CI, 33–63%]) in non-Hürthle cell and 13% (2/15 [95% CI, 2–40%]) in Hürthle cell nodules (p = 0.02). No malignant or borderline tumours were observed in patients under surveillance. Sensitivity, specificity, negative and positive predictive value, and benign call rate (95% CI) of [ 18F]FDG-PET/CT were 94.1% (80.3–99.3%), 39.8% (30.0–50.2%), 95.1% (83.5–99.4%), 35.2% (25.4–45.9%), and 31.1% (23.3–39.7%), respectively. Conclusion: An [ 18F]FDG-PET/CT-driven diagnostic workup of indeterminate thyroid nodules leads to practice changing management, accurately and oncologically safely reducing futile surgeries by 40%. For optimal therapeutic yield, application should be limited to non-Hürthle cell nodules. Trial registration number: This trial is registered with ClinicalTrials.gov: NCT02208544 (5 August 2014), https://clinicaltrials.gov/ct2/show/NCT02208544.
KW - Indeterminate
KW - Thyroid carcinoma
KW - Thyroid cytology
KW - Thyroid nodule
KW - Thyroid surgery
KW - [ F]FDG-PET/CT
KW - [F]FDG-PET/CT
UR - http://www.scopus.com/inward/record.url?scp=85122254683&partnerID=8YFLogxK
U2 - https://doi.org/10.1007/s00259-021-05627-2
DO - https://doi.org/10.1007/s00259-021-05627-2
M3 - Article
C2 - 34981165
VL - 49
SP - 1970
EP - 1984
JO - European Journal of Nuclear Medicine and Molecular Imaging
JF - European Journal of Nuclear Medicine and Molecular Imaging
SN - 1619-7070
IS - 6
ER -