Context
Anti‐thyroglobulin antibodies (anti‐Tg), present in 20%‐25% of differentiated thyroid cancer (DTC) patients, interfere with thyroglobulin measurements posing a challenge in the follow‐up.
Objectives
The aim of this study was to identify clinical‐histological factors that may affect anti‐Tg persistence and disease outcome in DTC with positive anti‐Tg.
Methods
We retrospectively studied 234 DTC patients, with positive anti‐Tg at diagnosis (females: 82.1%, age at diagnosis: 46.0 ± 14.4 yrs, median follow‐up: 5 yrs (1.5‐32 yrs). 221/234 (94.4%) received radioiodine (RAI) ablation. Patients were divided into two subgroups: those whose anti‐Tg became undetectable (anti‐Tg‐NEG) and those whose anti‐Tg remained positive (anti‐Tg‐POS) at the end of the follow‐up period.
Results
Anti‐Tg‐POS patients (n = 80, 34.2%) compared to anti‐Tg‐NEG (n = 154, 65.8%) had more frequently lymph node infiltration (36.3% vs 20.1%, P = .01), extrathyroidal extension (ETE, 35.0% vs 22.1%, P = .04), poorly differentiated DTC and increased tumour size (P ≤ .004). They received higher total RAI dose (P < .001). In most cases, additional RAI administration and/or additional surgeries did not lead to anti‐Tg elimination. These had more frequently structural disease persistence/progression compared to anti‐Tg‐NEG (remission: 78.8% vs 95.5%, persistence: 13.8% vs 3.9%, progression: 7.5% vs 0.6%, P < .001). In Kaplan‐Meier analysis, the probability of disease progression was higher in anti‐Tg‐POS. In Cox proportional hazard analysis, the predictors of disease progression were size (P = .002) and ETE (P = .006).
Conclusions
Worse histological features are more frequent in patients with anti‐Tg persistence during follow‐up. Further additional RAI administration and/or surgeries do not affect anti‐Tg elimination in most cases. Anti‐Tg persistence correlates with structural persistence although tumour size and extrathyroidal extension are the main predictors of disease progression.