1. Introduction
Thyroid cancer is the most common endocrine cancer, and its incidence is increasing worldwide [
1,
2]. Nearly 20% of papillary thyroid cancer (PTC) patients who have no evidence of disease after initial treatment present with recurrence of disease during subsequent follow-up [
3,
4,
5,
6]. Although most recurrences in PTC are not fatal, they can be a great burden for patients, especially in a population with a high incidence rate for PTC, like Saudi Arabia [
7].
The timing of recurrence in PTC varies considerably, being influenced by classical prognostic factors and adjuvant radioactive iodine (RAI) treatment strategies [
8,
9,
10,
11]. The average time to recurrence has been reported in the literature as being anywhere from 6 months to decades later [
12,
13,
14]. However, it is only recently that clinical studies have begun to lay emphasis on late relapse in PTCs, with very little being known regarding the pattern of recurrence occurring beyond 10 years of follow-up [
15]. Furthermore, most of the studies analyzing long-term outcomes in PTC have often focused on mortality rather than recurrence [
16,
17]. However, survival in PTCs is usually excellent and hence less informative about the natural history of disease after long-term follow-up [
18,
19,
20]. The American Thyroid Association (ATA), in 2015, announced new treatment guidelines for differentiated thyroid cancer based on risk of recurrence [
21]. Utilization of the ATA risk stratification has allowed for a more individualized approach to patient treatment [
22,
23,
24,
25]. Thus, it is important to understand changes in the risk of recurrence over time and to assess how clinical factors affect these changes. A better description of recurrence patterns, leading to a greater understanding of time-specific risk, could result in a more tailored therapeutic approach.
The purpose of this study was to analyze the hazard of recurrence after surgery for PTC patients from this ethnicity, where the prevalence of PTC is high in comparison to other populations, and to clarify the changes in hazard rate for recurrence over time in PTC patients. We also estimated the hazard rate of recurrence in RAI ablation patients from the entire cohort and with reference to the ATA risk categories. Finally, the risk factors for early and late recurrence were explored, offering unique opportunities to better define patterns of PTC recurrence.
3. Discussion
Risk analysis of tumor recurrence is highly important for the detection of recurrence, especially in PTC patients. In most of the existing studies, risk of recurrence has been analyzed by survival curves rather than using the hazard functions [
26,
27]. While survival curves only provide information on the cumulative time distribution of recurrence-free rate, hazard functions can depict the recurrence rate at any point in time among the remaining at-risk individuals [
28].
In our study, the overall recurrence rate was relatively high. Although the majority (78%) of patients had received radioactive iodine (RAI), nearly one-fifth (18.4%) of patients suffered from disease recurrence in this study. This relatively high percentage is in concordance with other populations [
13,
29,
30]. Interestingly, a recent study from a Japanese PTC cohort showed a similar recurrent rate despite only 1.5% of patients receiving RAI therapy [
15]. The relatively high incidence of recurrence in this cohort could be due to the uniqueness of PTC in this population in that nearly 50% of patients presented with high-risk disease and only 15% had low-risk disease, which is not seen in most modern studies of western populations and could be attributed to genetics or differences in presentation and access to healthcare. Another reason for the high incidence of recurrence could be due to referral bias since patients with advanced disease are referred to our hospital from all over Saudi Arabia. Previous studies from Saudi Arabia have also reported a higher incidence of advanced disease [
31,
32], suggesting that thyroid cancer from Saudi Arabia could be more aggressive than in other parts of the world.
The annual hazard curve of recurrence for the entire cohort showed a double-peaked pattern, with the first major surge reaching a peak during the second year after surgery, followed by another peak between 13 and 14 years. The annual hazard curves exhibited double-peaked distribution for high- and intermediate-risk patients and single-peaked distribution for low-risk patients. The recurrence peak for high- and intermediate-risk patients emerged earlier than low-risk patients, which suggests the importance of high surveillance and follow-up to detect early recurrence in this subset of patients. Furthermore, since low-risk PTC patients had a very low hazard of recurrence beyond 10 years of initial surgery, long-term follow-up may not be necessary for this group of patients. The double-peaked pattern of recurrence hazard in our study is in line with the tumor dormancy theory [
33,
34], which hypothesizes that micro-metastatic foci may exist in varying biological steady states, with most of them remaining dormant. However, this steady state may be disrupted by surgery, stimulating the switch from dormancy to growth, hence causing a sudden acceleration of metastatic process resulting in recurrence [
35].
This double-peaked recurrence hazard pattern has been previously observed in several cancers [
36,
37,
38,
39]. Despite limited studies on the hazard of recurrence in thyroid cancer, a recent study by Dong et al. [
15] in a cohort of 400 Japanese PTC patients showed triple-peaked annual hazard of recurrence with surges at 12, 22 and 29 years after initial surgery. Several factors might contribute to the difference in annual hazard curves between our study and Dong’s study. Sample size, follow-up timing, risk stratification, adjuvant RAI therapy given and ethnic differences might help in explaining these differences.
Little is known about the hazard of recurrence with respect to RAI status. Our data showed that patients receiving RAI therapy had a significantly reduced annual hazard of recurrence compared to those who did not receive RAI, particularly in high- and intermediate-risk patients (
p = 0.0001). This highlights the clinical importance of giving RAI in intermediate-risk PTC patients. Giving RAI in intermediate-risk PTC has been a subject of controversy. On the one hand, studies have shown that RAI therapy could reduce recurrence and hence should be considered in intermediate-risk PTC patients [
21,
40], whereas others have suggested that RAI ablation may not have a beneficial role in decreasing the risk of recurrence in intermediate-risk PTC patients [
41,
42].
The present study is unique in that it explored the risk factors that could predict early and late recurrence using Cox regression analysis. This analysis revealed that PTC patients who were male, aged ≥55 years, with T3-4 tumors and lymph node metastasis were at high risk for early recurrence, whereas only age and lymph node metastasis were predictors of late recurrence. Our data suggest that a subset of patients who are male with T3-4 tumors might need more intensive surveillance in the initial 5 years following surgery, whereas those patients who are aged ≥55 years and have lymph node metastasis will have to be followed up for a longer period of time.
4. Materials and Methods
4.1. Patient Selection
One thousand four-hundred and sixty-six consecutive unselected PTC patients diagnosed between 1988 and 2015 at King Faisal Specialist Hospital and Research Centre (Riyadh, Saudi Arabia) were available to be included in the study. Cases were identified based on clinical history followed by fine needle aspiration cytology for confirmation. However, patients aged ≤18 years (n = 84), with a history of previous thyroidectomy (n = 144) or who were never free of disease (n = 37) were excluded from the study. After exclusion, 1201 patients were eligible and included in this study. The Institutional Review Board of the hospital approved this study and the Research Advisory Council (RAC) provided waiver of consent under project RAC # 2110 031.
4.2. Clinico-Pathological Data
The baseline clinico-pathological data were collected from case records and have been summarized in
Table 1. Extra-thyroidal extension was further classified as follows: ExT0, no extra-thyroidal extension; ExT1 (microscopic extra-thyroidal extension), microscopic invasion of tumor into perithyroidal soft tissues; ExT2 (gross extra-thyroidal extension), macroscopic invasion of tumor into perithyroidal soft tissues. Staging of PTC was performed using the eighth edition of American Joint Committee on Cancer (AJCC) staging system. Patients were stratified into low, intermediate and high risk based on 2015 ATA guidelines [
21]. Thyroidectomies were divided into either total thyroidectomy or less than total thyroidectomy (subtotal, lobectomy). Overall, 78.0% (937/1201) of patients received radioactive iodine therapy following surgery. Low-risk patients received a mean cumulative RAI dosage of 110.2 mCi (SD = ±44.6 mCi), intermediate-risk patients received 135.6 ± 74.8 mCi and high-risk patients received 187.8 ± 136.4 mCi. Based on the ATA guidelines, tall cell, hobnail, columnar cell, diffuse sclerosing and insular variants were classified as aggressive variants, whereas classical and follicular variants were classified as non-aggressive variants.
4.3. Classification of Recurrence
Recurrence was defined as any newly detected tumor or metastatic lymph node based on ultrasound and/or imaging studies in patients who had been previously free of disease following initial treatment. Recurrence was classified according to the site, as follows: “local recurrence” if only the residual thyroid gland tissue or thyroid bed was involved; “regional recurrence” if central or lateral neck lymph nodes were involved; “distant recurrence” if disease was seen in soft tissues or lymph nodes at distant sites and visceral metastasis in other organs such as the lungs, liver, bones and brain. Biochemical recurrences were not considered for this study.
4.4. Follow-Up and Study Endpoints
Following initial surgery, low-risk PTC patients were followed up annually, intermediate-risk patients were followed up at 6-month intervals and high-risk patients were followed up at 3-month intervals. At each follow-up, neck ultrasound, thyroid function tests, thyroglobulin levels and thyroglobulin antibodies were performed. In addition, for high-risk patients, radioiodine scan and PET CT scan were performed at each follow-up to identify tumor recurrence. A biopsy confirmation (fine needle aspiration or histopathology) of tumor recurrence was obtained in 51.1% (113/221) cases. The remaining 48.9% (108/221) of cases were diagnosed by imaging studies alone. The median follow-up was 9.5 years (range 0.02–30.01 years). The primary study endpoint for our analysis was recurrence-free survival (RFS). RFS was defined as the time (in years) from date of initial surgery to the occurrence of any tumor recurrence (local, regional or distant). In the case of no recurrence, date of last follow-up was the study endpoint.
4.5. DNA Isolation and Sanger Sequencing Analysis
DNA samples were extracted from formalin-fixed and paraffin-embedded (FFPE) PTC tumor tissues utilizing Gentra DNA Isolation Kit (Gentra, Minneapolis, MN, USA) according to the manufacturer’s protocols, as elaborated in previous studies [
43].
Sequencing of entire coding and splicing regions of exon 15 in BRAF gene, exon 2 and 3 in HRAS and NRAS genes among 1201 PTC samples was carried out using Sanger sequencing technology. Primer 3 online software was utilized to design the primers (available upon request, Primer3web v4.1.0,
https://primer3.ut.ee/). PCR and Sanger sequencing analysis were carried out as described previously [
44]. Reference sequences were downloaded from the NCBI GenBank and sequencing results were compared with the reference sequences by Mutation Surveyor V4.04 (Soft Genetics, LLC, State College, PA, USA).
4.6. Statistical Analysis
Annual hazard rates were estimated using the maximum likelihood estimate from piece-wise exponential model and Kernel smoothing method was used for graphical representation. To determine the independent prognostic factors for early and late recurrence, Cox proportional hazards regression model was used. Covariates for Cox regression analysis were selected if they were statistically significant on univariate analysis. All the variables were significant on univariate analysis, except for multifocality and histology. However, these two variables were included since they are integral to the ATA risk stratification of PTCs. Two-sided tests were used for statistical analyses, with a limit of significance defined as p value < 0.05. Statistical analyses were performed using Stata v9.0 (StataCorp Ltd., College Station, TX, USA) and SPSS v20.0 (SPSS, Chicago, IL, USA).