TY - JOUR
T1 - Thyroidectomy without radioiodine in patients with low-risk thyroid cancer
T2 - 5 years of follow-up of the prospective randomised ESTIMABL2 trial
AU - Leboulleux, Sophie
AU - Bournaud, Claire
AU - Chougnet, Cecile N.
AU - Lamartina, Livia
AU - Zerdoud, Slimane
AU - Do Cao, Christine
AU - Catargi, Bogdan
AU - Dygai, Inna
AU - Kelly, Antony
AU - Barge, Marie Luce
AU - Vera, Pierre
AU - Rusu, Daniela
AU - Schneegans, Olivier
AU - Roux, Julie
AU - Raymond, Perrine
AU - Benisvy, Danielle
AU - Eberle, Marie Claude
AU - Bidault, Sophie
AU - Nascimento, Camila
AU - Bastie, Delphine
AU - Giraudet, Anne Laure
AU - Bardet, Stéphane
AU - Le Moullec, Nathalie
AU - Roudaut, Nathalie
AU - Drui, Delphine
AU - Godbert, Yann
AU - Zalzali, Mohamad
AU - Drutel, Anne
AU - Morel, Olivier
AU - Velayoudom, Fritz Line
AU - Al Ghuzlan, Abir
AU - Schlumberger, Martin
AU - Buffet, Camille
AU - Borget, Isabelle
N1 - Publisher Copyright:
© 2025 Elsevier Ltd
PY - 2025/1/1
Y1 - 2025/1/1
N2 - Background: ESTIMABL2, a multicentre randomised phase 3 trial in patients with low-risk differentiated thyroid cancer (ie, pT1am or pT1b, N0 [no evidence of regional nodal involvement] or Nx [involvement of regional lymph nodes that cannot be assessed in the absence of neck dissection]), showed the non-inferiority of a follow-up strategy without radioactive iodine (131I) administration compared with a postoperative 131I administration at 3 years post-randomisation. Here, we report a pre-specified analysis after 5 years of follow-up. Methods: Patients treated with total thyroidectomy with or without prophylactic neck lymph node dissection, without postoperative suspicious findings on neck ultrasonography, were randomly assigned to the no-radioiodine group or to the radioiodine group (1·1 GBq-30 mCi after recombinant human thyrotropin-stimulating hormone). Follow-up consisted of annual thyroglobulin and thyroglobulin antibody determinations during levothyroxine treatment and neck ultrasonography in odd-numbered years. An event was defined as abnormal foci of 131I uptake on the post-treatment whole-body-scan requiring subsequent treatment, abnormal neck ultrasonography, elevated thyroglobulin levels, increasing titres or appearance of thyroglobulin antibody (using the same laboratory assay), or a combination of these definitions. Non-inferiority of the proportion of patients without an event in one group compared with the other at 5 years after randomisation was shown if this proportion and its CI did not differ by more than –5%. This study was registered on ClinicalTrials.gov (NCT01837745) and is completed. Findings: Of the 776 patients (n=642 [82·7%] female and n=134 [17·3%] male, median age 52·9 years [IQR 42·6–63·1]) enrolled, 698 were evaluable at 5 years. The proportions of patients without events were 93·2% in the no-radioiodine group and 94·8% in the radioiodine group, for a difference of –1·6% (90% CI –4·5 to 1·4). Events consisted of structural or functional abnormalities (n=11) and biological abnormalities (n=31). Interpretation: The non-inferiority of a follow-up strategy compared with postoperative 131I administration in low risk differentiated thyroid cancer was confirmed at 5 years. There is no loss of opportunity in following these patients without postoperative ablation. Funding: Programme de Recherche Hospitalier Clinique.
AB - Background: ESTIMABL2, a multicentre randomised phase 3 trial in patients with low-risk differentiated thyroid cancer (ie, pT1am or pT1b, N0 [no evidence of regional nodal involvement] or Nx [involvement of regional lymph nodes that cannot be assessed in the absence of neck dissection]), showed the non-inferiority of a follow-up strategy without radioactive iodine (131I) administration compared with a postoperative 131I administration at 3 years post-randomisation. Here, we report a pre-specified analysis after 5 years of follow-up. Methods: Patients treated with total thyroidectomy with or without prophylactic neck lymph node dissection, without postoperative suspicious findings on neck ultrasonography, were randomly assigned to the no-radioiodine group or to the radioiodine group (1·1 GBq-30 mCi after recombinant human thyrotropin-stimulating hormone). Follow-up consisted of annual thyroglobulin and thyroglobulin antibody determinations during levothyroxine treatment and neck ultrasonography in odd-numbered years. An event was defined as abnormal foci of 131I uptake on the post-treatment whole-body-scan requiring subsequent treatment, abnormal neck ultrasonography, elevated thyroglobulin levels, increasing titres or appearance of thyroglobulin antibody (using the same laboratory assay), or a combination of these definitions. Non-inferiority of the proportion of patients without an event in one group compared with the other at 5 years after randomisation was shown if this proportion and its CI did not differ by more than –5%. This study was registered on ClinicalTrials.gov (NCT01837745) and is completed. Findings: Of the 776 patients (n=642 [82·7%] female and n=134 [17·3%] male, median age 52·9 years [IQR 42·6–63·1]) enrolled, 698 were evaluable at 5 years. The proportions of patients without events were 93·2% in the no-radioiodine group and 94·8% in the radioiodine group, for a difference of –1·6% (90% CI –4·5 to 1·4). Events consisted of structural or functional abnormalities (n=11) and biological abnormalities (n=31). Interpretation: The non-inferiority of a follow-up strategy compared with postoperative 131I administration in low risk differentiated thyroid cancer was confirmed at 5 years. There is no loss of opportunity in following these patients without postoperative ablation. Funding: Programme de Recherche Hospitalier Clinique.
UR - http://www.scopus.com/inward/record.url?scp=85211321953&partnerID=8YFLogxK
U2 - 10.1016/S2213-8587(24)00276-6
DO - 10.1016/S2213-8587(24)00276-6
M3 - Article
C2 - 39586309
AN - SCOPUS:85211321953
SN - 2213-8587
VL - 13
SP - 38
EP - 46
JO - The Lancet Diabetes and Endocrinology
JF - The Lancet Diabetes and Endocrinology
IS - 1
ER -