Original Research ARTICLE
Patients Aged ≥55 Years With Stage T1-2N1M1 Differentiated Thyroid Cancer Should Be Downstaged in the Eighth Edition AJCC/TNM Cancer Staging System
- 1Department of Plastic Surgery, Zhongnan Hospital of Wuhan University, Wuhan, China
- 2Department of Pediatrics, St. John Hospital and Medical Center, Detroit, MI, United States
- 3Department of Cardiovascular Surgery, Tongji Medical College, Union Hospital, Huazhong University of Science and Technology, Wuhan, China
- 4Department of Ophthalmology, Zhongnan Hospital of Wuhan University, Wuhan, China
Objectives: Since the eighth edition of the American Joint Committee on Cancer tumor-node-metastasis (AJCC/TNM) cancer staging system introduced some significant changes, we investigated whether patients with stage T1-2N1M1 differentiated thyroid cancer (DTC) should be placed in stage IVB, with the goal of providing suggestions for improved survival prediction.
Materials and Methods: We divided 30,234 DTC patients aged ≥55 years enrolled from the Surveillance, Epidemiology, and End Results (SEER) database into different stage groups based on the new stage system but in a more thorough manner. Univariate and multivariate Cox regression analyses were conducted to explore the clinicopathological factors associated with cancer-specific survival. Survival of different stage groups was assessed by mortality rates per 1,000 person-years, Cox proportional hazards regression analyses, and Kaplan-Meier analyses with log-rank tests and the propensity score matching method.
Results: Univariate and multivariate analyses demonstrated that age at diagnosis, T stage, lymph node metastasis, distant metastasis, histological types, extrathyroidal extension, and radiation therapy were associated with cancer-specific survival. Patients with stage T1-2N1M1 had a lower cancer-specific mortality rate per 1,000 person-years (28.081, 95% confidence interval [CI]: 12.616–62.505) and all-cause mortality rate per 1,000 person-years (70.203, 95% CI: 42.323–116.448) than those with low-level stages such as stage T4aN1M0, stage IVA, and stage T1-2N0M1. Cox proportional hazards regression analyses suggested that patients with stage T4bN1M0 belonging to stage IVA (hazard ratio: 2.529, 95% CI: 1.018–6.278, p = 0.046) had a significantly higher risk of cancer-specific mortality than those with stage T1-2N1M1. Kaplan-Meier analyses with log-rank tests suggested that the cancer-specific survival curve of patients with stage T1-2N1M1 had a more modest decline than that of stage T4bN1M0 (p = 0.0125), and the cancer-specific survival curve and all-cause survival curve of patients with stage T1-2N1M1 were not different from those of stage T3N1M0, stage T4aN0M0, stage T4aN1M0, stage T4bN0M0, and stage T1-2N0M1 (all, p > 0.05). The analysis yielded similar results after propensity score matching for other clinicopathological characteristics.
Conclusion: Patients aged ≥55 years with stage T1-2N1M1 DTC according to the eighth edition AJCC/TNM cancer staging system should be downstaged and those with stage T4bN1M0 upstaged accordingly.
Thyroid cancer is the most common malignant endocrine cancer, and its incidence has rapidly increased in the world in recent years (1, 2). Differentiated thyroid cancer (DTC), composed of papillary thyroid cancer (PTC) and follicular thyroid cancer, constitutes almost 86% of all thyroid cancer cases (3, 4).
There are a variety of cancer staging systems for DTC, all of which are aimed at discriminating among different prognostic groups. For example, the 10-year cancer-specific survival (CSS) rate for stage I based on the eighth edition of the American Joint Committee on Cancer tumor-node-metastasis (AJCC/TNM) cancer staging system is almost 99%. In contrast, the 10-year CSS rates for stages IVB and IVC range from 64% to 73% (5, 6). The eighth edition of AJCC/TNM cancer staging system (AJCC/TNM-8) was introduced in clinical practice on January 1, 2017. In this revision, the age cutoff value was revised from 45 to 55 years, and the descriptors of the T and N stages were changed from those contained in the seventh edition (7, 8). As a result, nearly 30% of DTC patients were downstaged following the introduction of the new edition (8).
Several surveys about the new TNM classification system have indicated that its prognostic value for survival is better than that of the seventh edition (5, 9). However, it is unclear whether the prognosis of DTC patients worsens with increasing stage; thus, it is important to thoroughly evaluate how well the new cancer staging system edition correlates with the survival of DTC patients. As is well known, age at diagnosis is considered an independent predictor of DTC prognosis, and it does not significantly influence CSS until patients are aged 50–60 years (10–12). Taking this into consideration, older DTC patients with poorer prognoses require more accurate and detailed cancer staging. The study aimed to refine the new TNM cancer staging system for older DTC patients.
Materials and Methods
The protocol of this retrospective study was approved by the Ethics Review Board of Zhongnan Hospital of Wuhan University. The need for informed consent was waived because of the retrospective nature of the study. The Surveillance, Epidemiology and End Results (SEER) database of the National Cancer Institute (https://seer.cancer.gov/), which contains demographic, pathological and treatment characteristics on cancer patients, was used as the source of data. We recruited patients aged ≥55 years with DTC from the Surveillance, Epidemiology, and End Results (SEER) database of the National Cancer Institute (https://seer.cancer.gov/) by using its official software “SEERStat” version 8.3.4. and code C73.9 from the International Classification of Diseases for Oncology (i.e., thyroid, papillary). The eligible diagnoses were as follows: “papillary carcinoma,” “papillary adenocarcinoma,” “follicular carcinoma,” “follicular adenocarcinoma,” “papillary carcinoma, follicular variant,” and “papillary & follicular adenocarcinoma.” Patients with missing data on survival or AJCC staging information (version 8) were excluded. In total, this study included 30,234 patients with DTC from 2004 to 2013. All included patients were followed up until December 2013, and the median follow-up time was 42 months. The median follow-up time of each staging group is listed in the Supplementary Materials.
More Detailed Cancer Staging Groups
Based on the AJCC/TNM-8 categories, patients were divided into stage I, stage II, stage III, stage IVA, and stage IVB. For a more detailed evaluation of the ability to predict survival, stage II patients were divided into stage T1N1M0, stage T2N1M0, stage T3N0M0, and stage T3N1M0; stage III patients were divided into stage T4aN0M0 and stage T4aN1M0; stage IVA patients were divided into stage T4bN0M0 and stage T4bN1M0; and stage IVB patients were divided into stage T1-2N0M1, stage T1-2N1M1, stage T3-4N0M1, and stage T3-4N1M1.
Quantitative variables are expressed as median (interquartile range), while categorical variables are presented as percentages. We explored the clinicopathological factors associated with cancer-specific mortality (CSM) using univariate and multivariate Cox regression analyses and compared the CSM and all-cause mortality (ACM) rates per 1,000 person-years of the same or adjacent AJCC/TNM-8 stage groups. Cox proportional hazards regression analyses were then used to assess the effect of the different stage groups on CSM and ACM, with adjustment for demographic, pathological, and treatment characteristics. Finally, Kaplan-Meier analyses with log-rank tests were performed with propensity score matching applied to minimize selection bias. Moreover, the relative excess risk (RERI), attributable proportion (AP), and synergy index (SI) were used to evaluate the synergic effect.
All p-values were two-sided, with p < 0.05 considered statistically significant. Statistical analyses were performed using SPSS version 24.0 (IBM Corp., Armonk, NY), GraphPad Prism version 6 (GraphPad Software Inc., La Jolla, CA) and Stata/SE version 15 (Stata Corp., College Station, TX).
Demographic and Clinical Characteristics
The demographic and clinical characteristics of 30,234 patients with DTC enrolled in this study are summarized in Table 1. According to the AJCC/TNM-8 classification system, 22,925 patients (75.8%) were classified as stage I; 4,977 (16.5%) stage II patients included 2,370 patients with stage T1-2N1M0, 2,109 patients with stage T3N0M0, and 498 patients with stage T3N1M0; 1,084 (3.6%) stage III patients included 517 patients with stage T4aN0M0 and 567 patients with stage T4aN1M0; 597 (2.0%) stage IVA patients included 260 patients with stage T4bN0M0 and 337 patients with stage T4bN1M0; and 651 (2.2%) stage IVB patients included 139 patients with stage T1-2N0M1, 56 patients with stage T1-2N1M1, 175 patients with stage T3-4N0M1, and 281 patients with stage T3-4N1M1. In addition, while 1,999 (6.6%) patients had T4 tumors, 4,109 (13.6%) patients had lymph node metastasis (LNM), and 651 (2.2%) patients had distant metastasis (DM).
Risk Factors for Cancer-Specific Mortality in DTC
Based on the results of the univariate Cox regression analyses, the CSM of DTC patients was associated with age at diagnosis, year at diagnosis, sex, race, T stage, LNM, DM, histological types, extrathyroidal extension (ETE), radiation therapy, and surgery (all, p < 0.001). The multivariate Cox regression analyses demonstrated that the CSM of DTC patients was associated with age at diagnosis, T stage, LNM, DM, histological types, ETE, and radiation therapy (all, p < 0.05). Consequently, T stage, LNM, and DM were associated with CSM of DTC patients according to univariate and multivariate Cox regression analyses. The multivariate Cox regression model showed that the CSM rate of DTC patients with T4a or T4b stage tumors was significantly higher than that of patients with T1 stage after adjusting for other clinicopathological characteristics (hazard ratio [HR]: 7.714, 95% confidence interval [CI]: 4.640–12.824; HR: 13.479, 95% CI: 8.094–22.447, respectively). The CSM rate of DTC patients with LNM or DM was also notably higher than that of patients without them (HR: 1.988, 95% CI: 1.608–2.459; HR: 4.670, 95% CI: 3.768–5.789, respectively) (Table 2).
CSM and ACM Rates per 1,000 Person-Years
During the follow-up until December 2013, the CSM rates per 1,000 person-years for DTC patients of the detailed stage groups are shown in Table 3. The CSM for stages T3N0M0, T3N1M0, T4aN0M0, T4aN1M0, T4bN0M0, and T4bN1M0 gradually increased. However, the CSM for stage T1-2N0M1 (61.051, 95% CI: 41.868–89.024) was even lower than that for stage T4bN1M0 (76.981, 95% CI: 62.238–95.216), and the CSM for stage T1-2N1M1 (28.081, 95% CI: 12.616–62.505) was even lower than that for stage T4aN1M0 (41.667, 95% CI: 33.645–51.602) and stage IVA. Notably, the CSM for stage T4bN1M0 (76.981, 95% CI: 62.238–95.216) was more than twice that for stage T1-2N1M1. Furthermore, during the follow-up period, the ACM rates per 1,000 person-years for patients of these stage groups yielded similar results (Table 3).
HRs of Different Stage Groups for CSM and ACM Rates
Table 4 displays the HRs for cancer-specific death for stage T1-2N1M1 vs. other stages. The HR of stage T4bN1M0 was 2.837 (95% CI: 1.241–6.484, p = 0.013). After adjustment for demographic data (age at diagnosis, year at diagnosis, sex, and race), the HR of stage T4bN1M0 was 2.372 (95% CI: 1.037–5.427, p = 0.041). After adjustment for demographic data and pathological factors (multifocality and histological subtypes), the HR of stage T4bN1M0 was 2.623 (95% CI: 1.063–6.476, p = 0.036). After adjustment for demographic data, pathological factors, and therapeutic factors (surgery and radiation therapy), the HR of stage T4bN1M0 was 2.529 (95% CI: 1.018–6.278, p = 0.046) (Table 4). In addition, all 95% CIs of HRs of the other stage groups (stages T3N1M0, T4aN0M0, T4aN1M0, T4bN0M0, and T1-2N0M1) included 1. Therefore, there were no significant differences in the risk of cancer-specific death between stage T1-2N1M1 and the other lower stages. Similar results were noted for all-cause death, and the HRs for all-cause death for T1-2N1M1 vs. other stages are displayed in Table S1.
Kaplan-Meier Analysis and Propensity Score Matching Method
Kaplan-Meier analysis of survival was performed between DTC patients with stage T1-2N1M1 and stages T3N1M0, T4aN0M0, T4aN1M0, T4bN0M0, T4bN1M0, and T1-2N0M1 (Figures 1–6). The CSS curve of patients with T1-2N1M1 stage showed a more modest decline than that of patients with stage T4bN1M0 (Figure 5A). However, analysis of all-cause survival showed a lack of significant difference for the two groups (Figure 5B). In addition, the cancer-specific curve and all-cause curve for stage T1-2N1M1 did not diverge from those of stages T3N1M0, T4aN0M0, T4aN1M0, T4bN0M0, and T1-2N0M1 (Figures 1–4, 6).
Figure 1. Kaplan Meier curves between older DTC patients with T1-2N1M1 stage and with T3N1M0 stage for cancer-specific mortality (A) and all-cause mortality (B).
Figure 2. Kaplan Meier curves between older DTC patients with T1-2N1M1 stage and with T4aN0M0 stage for cancer-specific mortality (A) and all-cause mortality (B).
Figure 3. Kaplan Meier curves between older DTC patients with T1-2N1M1 stage and with T4aN1M0 stage for cancer-specific mortality (A) and all-cause mortality (B).
Figure 4. Kaplan Meier curves between older DTC patients with T1-2N1M1 stage and with T4bN0M0 stage for cancer-specific mortality (A) and all-cause mortality (B).
Figure 5. Kaplan Meier curves between older DTC patients with T1-2N1M1 stage and with T4bN1M0 stage for cancer-specific mortality (A) and all-cause mortality (B).
Figure 6. Kaplan Meier curves between older DTC patients with T1-2N1M1 stage and with T1-2N0M1 stage for cancer-specific mortality (A) and all-cause mortality (B).
Moreover, we used the 1:2 propensity score matching method to match samples of the other six stages that had similar clinicopathological characteristics, including age at diagnosis, year at diagnosis, sex, race, multifocality, histological subtypes, surgery, and radiation, with those of the T1-2N1M1 subgroup. After propensity score matching for age at diagnosis, year at diagnosis, sex and race, the T1-2N1M1 subgroup did not have a significantly different CSM from that of the T3N1M0, T4aN0M0, T4aN1M0, T4bN0M0, T1-2N0M1 subgroups, but had a lower CSM than that of the T4bN1M0 subgroup (p = 0.0182) (Figure S1). After propensity score matching for age at diagnosis, year at diagnosis, sex and race, the T1-2N1M1 subgroup did not have a significantly different ACM from that of the T3N1M0, T4aN0M0, T4aN1M0, T4bN0M0, T4bN1M0, and T1-2N0M1 subgroups (Figure S2). After propensity score matching for age at diagnosis, year at diagnosis, sex, race, multifocality and histological subtypes, the T1-2N1M1 subgroup did not have a significantly different CSM or ACM from that of the T3N1M0, T4aN0M0, T4aN1M0, T4bN0M0, T4bN1M0, and T1-2N0M1 subgroups (Figures S3, S4). The analysis yielded similar results when the data were propensity score matched for age at diagnosis, year at diagnosis, sex, race, multifocality, histological subtypes, surgery, and radiation (Figures S5, S6).
Synergic Effect of T4 Stage and LNM on Survival in DTC
We classified DTC patients into 4 subtypes according to T stage and N stage (T1-3N0, T1-3N1, T4N0, and T4N1). As shown in Table 5, stage T4N1 patients had the largest risk of CSM (HR = 6.076, 95% CI: 4.150–8.895, p < 0.001), when compared with CSM of other combinations of T stage and N status and after adjustment for age at diagnosis, year at diagnosis, sex, race, M status, multifocality, histology subtypes, ETE, radiation therapy, and surgery.
Table 5. Measures for estimation of synergic effect between T stage and N stage for the cancer-specific mortality of DTC.
Based on the abovementioned results, the RERI was 12.430 (95% CI: 2.232–22.630), AP was 0.223 (95% CI: 0.064–0.381), and SI was 1.293 (95% CI: 1.050–1.592) (Table 5).
The synergic effect of T4 stage and LNM on ACM was evaluated, and similar results were found (Table S2).
In this study, we enrolled 30,234 DTC patients aged ≥55 years. Based on the AJCC/TNM-8 system, stage I, stage II, stage III, and stage IV accounted for 75.8, 16.5, 3.6, and 4.2% of patients, respectively. Shaha et al. (8) reported that DTC patients with stage I, stage II, stage III, and stage IV accounted for 84, 13, 2, and 1%, respectively, in their study, while Song et al. (13) reported proportions of 85.9, 12.2, 1.2, and 0.7%, respectively. These discrepancies might be because our age cutoff was older than that used in the other studies; thus, a larger proportion of patients in our study had a higher stage.
More importantly, we observed that DTC patients aged ≥55 years with stage T1-2N1M1 should be downstaged in the AJCC/TNM-8 cancer staging system. In our study, patients with stage T1-2N1M1 had significantly lower DSM and ACM than those with stage T4bN1M0. Moreover, patients with stage T4bN1M0 had a more than 2-fold increased risk of cancer-specific death and all-cause death compared to patients with stage T1-2N1M1. Notably, in the study conducted by Rosario (14), among 19 patients with stage T4M0 who were classified as stage I according to the AJCC/TNM-8, there were 2 deaths among patients with stage T4aN1bM0 and T4bN1bM0 because of PTC. In addition, owing to the uncommon deaths, the author called for more studies that evaluated mortality specifically in T4N1b patients aged 45–55 years.
A good cancer staging system should focus on effective discrimination and prediction of the prognoses of DTC patients. In DTC patients, the prognosis worsens as the stage increases. Minimal ETE is excluded from the definition of stage T3 in AJCC/TNM-8 because it does not lead to higher mortality (15, 16). Since patients with stage T1-2N1M1 had lower mortality than patients with stage T4bN1M0, we suggest that patients with T1-2N1M1 disease be downstaged, and patients with stage T4bN1M0 be upstaged, in terms of better distinguishing the prognoses of different DTC patients.
DM is considered an indicator of compromised survival among DTC patients. Patients with DM are recommended to undergo more aggressive treatments such as total thyroidectomy followed by radioiodine therapy and thyroid-stimulating hormone suppressive therapy (17, 18). However, the aforementioned survival results reveal that patients with stage T4bN1M0 disease should be given more aggressive treatment, even in the absence of DM.
We hypothesized that the worse prognosis of T4bN1M0 stage disease is due to the synergic effect of gross ETE beyond the strap muscles (T4 stage) and LNM in DTC patients aged ≥55 years. The RERI (12.430, 95% CI: 2.232–22.630) indicates that there would be a 12.430 relative excess risk contributed by the additive synergic effect of gross ETE beyond the strap muscles and LNM. The AP (0.223, 95% CI: 0.064–0.381) suggests that 22.3% of the increased risk of CSM was caused by the synergic effect (19). In addition, the SI (1.293, 95% CI: 1.050–1.592) was larger than 1, which also signified the existence of a synergic effect (20). Summarily, the results (RERI > 0, AP > 0, and SI > 1) verified our hypothesis.
Another finding of this study was that the 1,000 person-years CSM of T1-2N1M1 stage patients was notably lower than that of T1-2N0M1 stage patients. However, the results of univariable and multivariable Cox regression analyses suggest that the N stage at diagnosis was associated with the CSS of DTC patients. In other studies, LNM was also associated with decreased survival (21–23).
This contradictory result may be due to the fact that there are other indicators of survival besides N stage in terms of LNM. Pyo et al. conducted a meta-analysis and showed that a high metastatic lymph node ratio (≥0.44) was notably correlated with worse survival of PTC patients (24), while Wei et al. demonstrated that the number of positive lymph nodes could be a better predictor of survival of DTC patients (23). In addition, location played a critical role, and positive lymph nodes in the lateral compartment were correlated with a shorter disease-free survival than those in the central compartment according to de Meer et al. (25). Thus, when evaluating the risk of LNM, clinicians should consider the N stage and the number, ratio, and location of metastasizing lymph nodes.
Our study has some limitations. First, because it was a retrospective study, selection bias could not be avoided. Second, there were only 56 patients with stage T1-2N1M1. Most DTC patients had a good prognosis, and only a small proportion of DTC patients belonged to stage IV. However, we recruited 30,234 DTC patients aged ≥55 years to enroll as many stage IVB patients as possible. Furthermore, the propensity score matching method was utilized to validate our conclusions. However, future clinical trials focusing on this stage group of DTC patients are needed. Third, we did not consider the extent of metastatic disease in the DTC patients in this study due to lack of information.
In conclusion, DTC patients with stage T1-2N1M1 have a better prognosis than those with stage T4bN1M0 and no significantly worse prognosis than those with lower stages. Therefore, they should be downstaged, and patients with stage T4bN1M0 should be upstaged, accordingly.
Data Availability Statement
Publicly available datasets were analyzed in this study. This data can be found here: https://seer.cancer.gov/.
This study was carried out in accordance with the recommendations of guidelines of the American Thyroid Association. The need for informed consent was waived on account of the retrospective nature of the study. The protocol was approved by the Ethics Review Board of Zhongnan Hospital of Wuhan University.
LG, WZ, and ZL contributed the conception and design of the study. YH and DH organized the database. SC performed the statistical analysis and wrote the first draft of the manuscript. MW, WW, and CZ wrote sections of the manuscript. All authors contributed to the manuscript revision, read, and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2019.01093/full#supplementary-material
DTC, differentiated thyroid cancer; PTC, papillary thyroid cancer; AJCC/TNM, American Joint Committee on Cancer tumor-node-metastasis; AJCC/TNM-8, The eighth edition of AJCC/TNM cancer staging system; SEER, Surveillance, Epidemiology, and End Results; CSS, cancer-specific survival; ACS, all-cause survival; CSM, cancer-specific mortality; ACM, all-cause mortality; RERI, relative excess risk; AP, attributable proportion; SI, synergy index; LNM, lymph node metastasis; DM, metastasis; ETE, extrathyroidal extension.
5. Kim TH, Kim YN, Kim HI, Park SY, Choe JH, Kim JH, et al. Prognostic value of the eighth edition AJCC TNM classification for differentiated thyroid carcinoma. Oral Oncol. (2017) 71:81–6. doi: 10.1016/j.oraloncology.2017.06.004
6. Tam S, Boonsripitayanon M, Amit M, Fellman BM, Li Y, Busaidy NL, et al. Survival in differentiated thyroid cancer: comparing the AJCC cancer staging seventh and eighth editions. Thyroid. (2018) 28:1301–10. doi: 10.1089/thy.2017.0572
8. Shaha AR, Migliacci JC, Nixon IJ, Wang LY, Wong RJ, Morris LGT, et al. Stage migration with the new American Joint Committee on Cancer (AJCC) staging system (8th edition) for differentiated thyroid cancer. Surgery. (2019) 165:6–11. doi: 10.1016/j.surg.2018.04.078
9. Shteinshnaider M, Muallem Kalmovich L, Koren S, Or K, Cantrell D, Benbassat C. Reassessment of differentiated thyroid cancer patients using the eighth TNM/AJCC classification system: a comparative study. Thyroid. (2018) 28:201–9. doi: 10.1089/thy.2017.0265
10. Ganly I, Nixon IJ, Wang LY, Palmer FL, Migliacci JC, Aniss A, et al. Survival from differentiated thyroid cancer: what has age got to do with it? Thyroid. (2015) 25:1106–14. doi: 10.1089/thy.2015.0104
11. Mazurat A, Torroni A, Hendrickson-Rebizant J, Benning H, Nason RW, Pathak KA. The age factor in survival of a population cohort of well-differentiated thyroid cancer. Endocrine Connect. (2013) 2:154–60. doi: 10.1530/EC-13-0056
13. Song E, Lee YM, Oh HS, Jeon M, Song DE, Kim TY, et al. A relook at the T stage of differentiated thyroid carcinoma: focus on gross extrathyroidal extension. Thyroid. (2018) 29:202–8. doi: 10.1089/thy.2018.0300
14. Rosario PW. Eighth edition of AJCC staging for differentiated thyroid cancer: Is stage I appropriate for T4/N1b patients aged 45-55 years? Endocrine. (2017) 56:679–80. doi: 10.1007/s12020-017-1288-3
15. Al-Qurayshi Z, Shama MA, Randolph GW, Kandil E. Minimal extrathyroidal extension does not affect survival of well-differentiated thyroid cancer. Endocr Relat Cancer. (2017) 24:221–6. doi: 10.1530/ERC-16-0509
16. Shin JH, Ha TK, Park HK, Ahn MS, Kim KH, Bae KB, et al. Implication of minimal extrathyroidal extension as a prognostic factor in papillary thyroid carcinoma. Int J Surg. (2013) 11:944–7. doi: 10.1016/j.ijsu.2013.06.015
18. Sampson E, Brierley JD, Le LW, Rotstein L, Tsang RW. Clinical management and outcome of papillary and follicular (differentiated) thyroid cancer presenting with distant metastasis at diagnosis. Cancer. (2007) 110:1451–6. doi: 10.1002/cncr.22956
19. Knol MJ, VanderWeele TJ, Groenwold RH, Klungel OH, Rovers MM, Grobbee DE. Estimating measures of interaction on an additive scale for preventive exposures. Eur J Epidemiol. (2011) 26:433–8. doi: 10.1007/s10654-011-9554-9
21. Adam MA, Pura J, Goffredo P, Dinan MA, Reed SD, Scheri RP, et al. Presence and number of lymph node metastases are associated with compromised survival for patients younger than age 45 years with papillary thyroid cancer. J Clin Oncol. (2015) 33:2370–5. doi: 10.1200/JCO.2014.59.8391
22. Erol V, Makay O, Icoz G, Kose T, Yararbas U, Kumanlioglu K, et al. Prognostic factors of survival and recurrence pattern in differentiated thyroid cancer: a retrospective study from Western Turkey. Endocrine Regulat. (2014) 48:173–81. doi: 10.4149/endo_2014_04_173
23. Wei WJ, Lu ZW, Wen D, Liao T, Li DS, Wang Y, et al. The positive lymph node number and postoperative n-staging used to estimate survival in patients with differentiated thyroid cancer: results from the surveillance, epidemiology, and end results dataset (1988-2008). World J Surg. (2018) 42:1762–71. doi: 10.1007/s00268-017-4343-6
25. de Meer SG, Dauwan M, de Keizer B, Valk GD, Borel Rinkes IH, Vriens MR. Not the number but the location of lymph nodes matters for recurrence rate and disease-free survival in patients with differentiated thyroid cancer. World J Surg. (2012) 36:1262–7. doi: 10.1007/s00268-012-1427-1
Keywords: differentiated thyroid cancer, prognosis, SEER, cancer stage, AJCC/TNM
Citation: Liu Z, Chen S, Huang Y, Hu D, Wang M, Wei W, Zhang C, Zeng W and Guo L (2019) Patients Aged ≥55 Years With Stage T1-2N1M1 Differentiated Thyroid Cancer Should Be Downstaged in the Eighth Edition AJCC/TNM Cancer Staging System. Front. Oncol. 9:1093. doi: 10.3389/fonc.2019.01093
Received: 20 April 2019; Accepted: 04 October 2019;
Published: 18 October 2019.
Edited by:Amanda Psyrri, University General Hospital Attikon, Greece
Reviewed by:Cesare Piazza, National Tumor Institute, Italy
Ashok R. Shaha, Memorial Sloan Kettering Cancer Center, United States
Copyright © 2019 Liu, Chen, Huang, Hu, Wang, Wei, Zhang, Zeng and Guo. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
†These authors have contributed equally to this work