Although it has been accepted that patients with PTC have a favorable prognosis 7, cervical LNM are common, with an incidence between 30% and 80%. Liu FH and Grant CS reported that the risk of recurrence ranges from 5–21% in PTC patients with cervical LNM. 8,9However, there were other studies showed that cervical LNM did not affect recurrence and survival. The extent of cervical LNM seems to play an important role in predicting the prognosis of PTC. For example, several reports identified that LNR (the number of metastatic LN divided by the number of harvested LN) appears to predict the rate of recurrence in PTC. 10,11A certain LNR has been reported to show significantly worse prognosis for PTC patients. Schneider, et al6 showed that PTC patients with a total LNR over 0.7 or LNR over 0.86 in central compartment had significantly worse disease-free survival rates. However, there were few studies on the risk factors for LNR, and even less for a high LNR. The aim of this study is to determine the risk factors for a high LNR (over 0.8) in central compartment for PTC patients.
It is generally agreed that the LNR is affected by the patient’s individual clinicopathologic characteristics in malignancies such as gender, age, tumor size, multifocality, extra-thyroid invasion and so on. It would be beneficial to identify the subset of patients with PTC who have aggressive pathological features so that a full treatment protocol could be provided.
The present study revealed that male gender, younger age (< 40 years), larger tumor (≥ 1 cm) and co-existence of chronic lymphocytic thyroiditis were independent risk factors for high LNR.
Although women have been shown to be more susceptible to PTC than men, male gender has been suggested as an important risk factor for LNM in previous reports 12.13. Our previous study also showed male sex was an independent indicator for LNM in papillary thyroid microcarcinoma. In this study, male gender had 3.79 times higher risk of high LNR than female.
Although age is a significant factor in PTC staging systems and old age correlates with a poor prognosis, young age was found to be an independent risk factor for high LNR in present study. The relationship between age and LNM rates has been studied before. Jing Wang et al 14analyzed a total of 46,077 PTC patients from the SEER database, and identified that in each T stage, LNM rates were inversely associated with age at diagnosis, which was validated by multivariate logistic regression analysis (p < 0.001). In addition, the study also showed that the subset of patients 30 or younger had the highest LNR compared with other subsets (p < 0.001). Our study also showed younger age (< 40 years) is a predictive risk factor for high LNR.
Several studies had revealed that lymph node metastasis increased with the increase in tumor size, and larger tumor size was an independent predictor for CLNM.15–17Our research showed that tumor size ≥ 1 cm was independently predictive of high LNR in CLNM.
Zeng et al 18found that coexisting chronic lymphocytic thyroiditis (CLT)was an independent predictive factor for LLNM. Conversely, a meta-analysis by Lee et al 19suggested that PTCs with coexisting CLT had a significant negative association with LNM (odds ratio[OR]1.3, P = .041); Borowczyk M et al20 reported that CLT plays a protective role in preventing the spread of the differential thyroid cancer. In his study, in CLT group, the prevalence of pT1 was greater than for pT2-pT4 DTC (P = 0.0003; OR = 1.69, 95% CI 1.27–2.24) compared to controls (68.3 vs. 56.1%, respectively). The thyroid capsule infiltration without extrathyroidal invasion (P < 0.0001; OR = 0.21, 95% CI 0.14–0.31) was more frequent in CLT group, unlike extracapsular invasion, which was significantly more often present in patients with DTC but without CLT (P = 0.004; OR = 1.66; 95% CI 1.17–2.34) as well as nodal involvement (P = 0.048; OR = 0.65, 95% CI 0.42–0.99). Myshunina TM 21also found that the presence of CLT in papillary carcinoma patients showed a certain positive impact on the course of the disease, in particular, primary tumor growth, invasion, and metastasis. To further investigate the mechanism, Pilli T et al 22demonstrated that CLT has a positive prognostic value in PTC patients, and the imbalance between cytotoxic and regulatory T lymphocytes in the peri-tumoral without the background of CLT may affect the tumor-specific immune response favoring a more aggressive behavior of cancer. Lubin D 23 demonstrated that PTC arising in a background of CLT shows increased PD-L1 (programmed death-ligand 1) expression, which is retained with metastasis. The results of present study showed that PTC patients with coexisting CLT had a negative association with high LNR.
This study has several potential limitations. First, this was a retrospective study and conducted in a single institution. Furthermore, Some clinicopathologic risk factors such as histological subtype,
BRAF gene mutation were not provided because they were not routinely reported in the pathological report. Finally, the number of cases enrolled is still not large enough.
In conclusion, a high LNR may be predicted by clinical features such as male gender, young age and co-existence of CLT. Our findings may help to guide clinicians in the selection of candidates suitable for Prophylactic CLND.