Molecular characterisation and clinical correlation of papillary thyroid microcarcinoma

Purpose Papillary thyroid microcarcinoma (mPTC) is defined as a papillary thyroid cancer sized 10 mm or less. Despite their generally indolent clinical course and good prognosis, a subset of mPTCs shows potentially aggressive behaviour. Methods To search for predictors of clinical outcome of mPTCs, we retrospectively evaluated the genetic tumour profile of 100 patients (23 M/77 F, mean age +/- SD 53.8 +/- 13.4 years) with histologically confirmed mPTCs through analysis of BRAF, NRAS and TERT promoter mutations as well as RET/PTC translocations. Results Mean follow-up period was 8.4 +/- 3.6 years. In 55 cases, mPTC were detected incidentally after surgery. Capsular invasion, bilateralism and multifocality were found in 11/100, 17/100 and 24/100 cases, respectively, while lymph-nodes metastases were present at diagnosis in 9/100 cases. After 3.5 +/- 2.0 years, tumour relapse occurred in 6/100 cases and was locoregional in five (two in the thyroid bed, three in laterocervical lymph-nodes), while lung metastasis occurred in one case. Biochemical persistence of disease was seen in 1/100 case. Mutations occurred in 55/100 cases; BRAF(V600E)was the most frequently detected (49/100) and was associated with higher tumour size, bilateralism and follicular variant but not with capsular invasion. RET/PTC rearrangements were found in 2/100 cases, NRAS(Q61R)in 4/100, while no mutations of TERT promoter gene were detected. Despite the observed association between BRAF(V600E)mutation and unfavourable histopathological features, we found no direct association with tumour recurrence, distant metastases and mortality. Conclusion In our study, the search for the most frequent genetic alterations as prognostic markers in mPTCs would not have changed the therapeutic strategy.

Automated summary

Despite the generally indolent clinical course and good prognosis of mPTCs, a subset may exhibit potentially aggressive behavior, leading to relapse and metastasis. The most frequently detected mutation in mPTCs is BRAF(V600E), which is associated with unfavorable histopathological features but not directly linked to tumor recurrence and distant metastasis. Further research is needed to explore the specific genetic alterations that could serve as prognostic markers in mPTCs.