PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of oncotargetLink to Publisher's site
 
Oncotarget. 2017 February 7; 8(6): 10637–10649.
Published online 2016 October 25. doi:  10.18632/oncotarget.12885
PMCID: PMC5354688

The changing characteristics and molecular profiles of papillary thyroid carcinoma over time: a systematic review

Abstract

Background

The genetic alterations of papillary thyroid carcinoma (PTC) have been reported to change over the past few decades. We performed this systematic review to further examine the trends and modifications of patient demographic, clinicopathological features and molecular profiles of PTC over time.

Methods

A literature search was performed within six electronic databases to identify relevant articles. The inclusion criteria were published studies investigating BRAF mutations, RET/PTC rearrangements or RAS mutations in PTCs or classical PTCs. Two teams of reviewers independently screened titles and abstracts of all articles. Full texts of potential articles were read and extracted data were listed and stratified into an excel file according to country, city, institution, and surgical time period. Student t test and Pearson Chi-square were used to analyze the trends of demographic and clinicopathological features of PTC patients and the prevalence of each genetic alteration in individual institutions.

Results

From 3139 articles, we included 16 articles for final analysis. Our results showed an increasing trend of BRAF and a decreasing trend of RET/PTC prevalence over time in PTCs and classical PTCs, accompanied by an older age of PTC patients, an increase in proportion of PTMC and less aggressive behaviours of tumours.

Conclusions

The demographic and clinicopathological characteristics and molecular profile of PTCs have been changing over the past few decades. These modifications suggest changes in etiologies and risk factors of thyroid cancer that influence the tumorigenesis of PTCs.

Keywords: BRAF, RAS, RET/PTC, papillary, thyroid carcinoma

INTRODUCTION

Thyroid cancer is the most common endocrine malignancy and its rate has been steadily increasing all over the world [1, 2]. The incidence of thyroid cancer more than doubled over the past 30 years in the United States (US) [3]. Davies et al. reported that the incidence of thyroid cancer was relatively stable until the early 1990s, after which its incidence increased remarkably due to an increase in PTCs [4]. The underlying causes of this increase are controversial. One proposal for the increasing incidence of thyroid cancer says it may be the result of two coexisting processes: increased diagnostic scrutiny and an increased number of cases due to unrecognized thyroid specific carcinogens [5]. Morris et al., however, stated that improved detection does not fully explain the rising incidence of thyroid cancer, and instead, a true increase in the incidence of thyroid cancer might be due to unknown hormonal, dietary, genetic or environmental risk factors [6].

In PTCs, the most common mutations are BRAF mutations, which were reported in 40-90% of cases from various geographical areas [79]. The second most common genetic alteration in PTC are RET/PTC rearrangements [10]. Both single- and multi-institutional studies in Italy, Korea and the US have shown a significant and steady increase in the prevalence of BRAF mutations [1113]. On the other hand, RAS mutations have increased sharply, and RET/PTC rearrangements have steadily decreased over the years [11, 13, 14]. Marthur et al. also linked the increased BRAF mutation prevalence with increased thyroid cancer incidence [13]. However, it is still continuously debated whether the genetic background of PTC changed or not [14]. Therefore, we conducted this systematic literature review to investigate the worldwide trends of BRAF mutations, RET/PTC rearrangements and RAS mutations in PTCs.

RESULTS

Search results

We identified 3139 results from the six libraries, but only 626 articles met our selection criteria. After carefully reading full-text versions of these 626 articles, we excluded 232 more studies. Overall, we listed and stratified 394 articles containing prevalence data of at least one genetic alteration into an excel file according to country, city, institution and the time period when surgery was performed. We used this listing to facilitate further data selection for analysis as described in each section below. To avoid overlapping patient data between publications with overlapping surgical time periods of patients from the same institution, we selected studies with the larger number of patients. Our final analysis included 16 studies (Figure (Figure11).

Figure 1
Flow diagram of study selection

Trends for BRAF mutations, RET/PTC rearrangements and RAS mutations in classical PTCs from individual institutions

BRAF mutations have been reported to be associated with variants of PTCs: high prevalence in tall cell variant and classical PTCs and low prevalence in FVPTCs. In contrast, RAS mutations were reported as most commonly found in FVPTCs. Therefore, we examined the trends of BRAF mutations, RET/PTC rearrangements and RAS mutations in classical PTCs, the most common PTC variant, to avoid bias caused by other variants. We used the following criteria to select eligible data from the stratified list: (i) the study institution had available data on BRAF mutations, RET/PTC rearrangements or RAS mutations in classical PTCs from at least 2 different surgical time periods, (ii) the same detection method provided by the same manufacturer was used between the surgical time periods and (iii) patients with classical PTCs from all surgical periods received the same treatment (for example, all patients underwent total thyroidectomy) or the authors did not use any criteria that could influence the characteristics of classical PTCs during patient selection in each period.

We found appropriate BRAF data from two US institutions (University of California at San Francisco (UCSF) [13] and University of Pittsburgh [14]), an Italian multicenter study at the Endocrine Units of Pisa/Perugia/Milan [11], a Korean medical center (Seoul St. Mary's Hospital) [15, 16], an Irish institution (St. James's Hospital) [17] and an institution from Poland (Holycross Cancer Center) [18]. Prevalence of BRAF mutations in classical PTCs increased significantly in the studies from all of the institutions, except Seoul St. Mary's Hospital in Korea (Table (Table22).

Table 2
The trends of BRAF mutations prevalence of classical PTCs from individual institutions
Table 1
Characteristics of included studies

We gathered enough information to determine the trends of RET/PTC rearrangements in classical PTCs at UCSF [13] and University of Pittsburgh [14], the University of Yamanashi (Japan) [19, 20] and St. James's Hospital (Ireland) [17]. There was a decreasing trend of RET/PTC rearrangements over time in classical PTCs at all these institutions (Table (Table33).

Table 3
The trends of RET/PTC rearrangements prevalence of classical PTCs from individual institutions

We could determine the trends for RAS mutations in classical PTCs at UCSF [13] and University of Pittsburgh [14]. The prevalence of RAS mutations was low and gradually decreased from 4.1% during the 1991-1995 period to 0% during the 2001-2005 period (p = 0.369). At the University of Pittsburgh, the RAS mutation prevalence was extremely low and remained stable over four periods (Table (Table4).4). RAS mutations are rarely detected in classical PTCs and therefore it can be difficult to observe the trend. As a result of this, we decided to further analyze the change of RAS mutations in FVPTCs from individual institutions. We could only gather information to determine the trend of RAS mutations in FVPTCs from University of Pittsburgh [14]. The prevalence of RAS mutations in FVPTCs was relatively stable during the first three periods but significantly increased from 11.1% in 2000 to 44.3% in 2009.

Table 4
Trends of RAS mutations prevalence of classical PTCs from individual institutions

All individual institutions applied the same protocol for mutational tests (same tissue treatment method, same DNA extraction method and same mutational detection method from same manufacturer) between different periods.

Trends for BRAF mutations in micro PTCs from individual institutions

According to the WHO classification, micro PTCs are PTCs with a diameter ≤1cm. Data on the stratified list was eligible for selection in our review of micro PTCs if they met the same criteria as the criteria described above in classical PTCs section.

We could determine trends of the BRAF mutations in micro PTCs from four institutions. The BRAF mutation prevalence significantly increased at the Tianjin Medical University Cancer Hospital from 40.1% during 2001-2010 to 62.7% during 2013-2014, and investigators used direct sequencing for mutational analyses in both periods [21, 22]. Although the detection method for BRAF mutations was not disclosed within this study by Lu et al [22], the authors provided this information by email and confirmed that the PTC patients were recruited from Tianjin Medical University Cancer Hospital (an affiliated hospital of Tianjin Medical University). We also found the prevalence of BRAF mutations increased significantly at Samsung Medical Center [23, 24] and Holycross Cancer Center [18] (Table (Table5).5). At the University of Pittsburgh, prevalence of BRAF mutations in micro PTCs decreased from 32.3% during 1974-1985 to 18.8% during 1990-1992 and then gradually increased to 23.5% in 2000 and 38% in 2009 [14]. This change, however, was not statistically significant (p = 0.442).

Table 5
The trends of BRAF mutations prevalence of micro PTCs from individual institutions

All included institutions used the same protocol for mutational detection among different surgical periods but one exception (Samsung Medical Center) in which the DNA materials were extracted from fine-needle aspirates in the former period and from paraffin-embedded tissues in the latter. However, all PCR products in these two periods were visualized on 2% agarose gel to confirm the good DNA quality prior to DNA purification step [23, 24], thus minimized the influence of technical issues on the results of direct sequencing.

Trends of demographic and clinicopathological features and molecular profiles in PTCs over time

To avoid bias, we only included articles with consecutive or random selection of patients and no criteria used in patient selection. We evaluated these trends only within individual institutions. We also excluded articles with consecutive or random selection of patients, but which focused on particular characteristics such as classical PTCs or patients who underwent total thyroidectomy or radioiodine ablation (possible bias toward aggressive PTCs and therefore could influence the nature of the PTC cohort). Five single- or multi-institutions met our criteria: University of Pittsburgh [14], University of Padua [25, 26], multicenter study from Pisa/Perugia/Milan [11], Samsung Medical Centre [24, 27] and Holycross Cancer Center [18].

Patients’ ages at time of diagnosis increased during the most recent period at all included institutions. Another important finding is the significant increase in the proportion of micro carcinomas at all included institutions. The rates of ETE and lymph node metastasis (LNM) decreased at most of the institutions. The rate of multifocal PTCs stayed relatively stable over time (data not shown). Table Table66 describes changes in demographic data and clinicopathological features of PTCs over time.

Table 6
Modifications of demographic and clinicopathological characteristics of PTCs over time from individual institutions

Quality assessment and risk of bias analysis

The quality score ranged from 40% to 70%, as measured by the NIH Quality Assessment Tool for Observational Cohort and Cross-Sectional Studies [28]. The lowest scored was 40% (Nakazawa et al. [19]) and the highest score was 70% (Jung et al. [14]). Quality of all included articles were classified as fair, except the two studies by Smyth et al. [17] and Nakazawa et al. [19] which were regarded as low quality. Most of included studies lacked sample size justification. Quality scores for each NIH criteria are shown in Supplementary Table.

DISCUSSION

The incidence of thyroid cancer has been increasing at an amazing rate in recent decades, especially PTCs [3, 4]. There is still debate as to whether improved detection is the only reason for the increase of PTCs or whether the tumorigenesis of thyroid cancer has changed [3, 6]. From our findings, the basic nature of PTC has been changing in recent decades (Table (Table6).6). The increase in the proportion of microcarcinomas that are diagnosed is associated with the improved detection rate in recent years, especially the development of ultrasonography. The majority of microcarcinomas show indolent behaviors, which can explain our findings that PTCs manifested less aggressive behaviors in the most recent periods we analyzed.

With improved screening and detection methods, it is reasonable to believe that patients would be diagnosed at an earlier age. However, our analysis suggests the opposite result. A number of publications showed that BRAF mutations are found in a higher proportion of older patients [12, 2934], and RET/PTC rearrangements are commonly found in young patients [3537]. Our systematic review demonstrated an increased prevalence of BRAF mutations (typically older patients) accompanied by a decreased prevalence of RET/PTC rearrangements (typically young patients).

Other than the multicenter study from the endocrine units of Pisa/Perugia/Milan [11] and the study from Holycross Cancer Center [18], the male proportion of patients with thyroid cancer has been decreasing over the years, although the difference was not significant (Table (Table6).6). Recent data showed that the increased incidence in thyroid cancer has affected more women than men, which supports our findings [3, 4].

There is still the question as to why the prevalence of BRAF mutations has been increasing significantly and the prevalence of RET/PTC rearrangements has been falling over the years. It is difficult to address the possible reasons for these changes because there are no known etiologies or risk factors that could trigger or activate these genetic alterations in PTCs other than radiation-induced RET/PTC [38]. From our findings, the significant increase of BRAF mutations in classical PTCs has occurred in different geographical areas (Table (Table2).2). Interestingly, we also found a remarkable increase of BRAF mutations in micro PTCs from Kielce, Seoul and Tianjin (Table (Table5).5). Elisei et al. suggested worldwide iodine supplementation as a potential candidate for the worldwide increasing trend of BRAF mutations [39]. How iodine intake may influence BRAF mutations in PTCs, however, is still controversial. Guan et al. reported that high iodine intake was associated with a higher prevalence of the BRAF V600E mutation in Chinese PTCs [40]. To the best of our knowledge, this is the only publication that linked iodine intake with occurrence of BRAF mutations. Frasca et al. reported there was no statistical difference in BRAF V600E prevalence in Italian PTCs from iodine-sufficient vs. iodine-deficient areas [8]. Data collected from the US showed that the US population has sufficient iodine intake [41, 42]. Because of this, it is irrational to correlate the increasing trend of BRAF mutations in classical PTCs seen in California and Pittsburgh with iodine intake. In our recent study, we found no statistical significance in the prevalence of BRAF V600E, RET/PTC rearrangements or RAS mutations in papillary and follicular thyroid carcinomas from an iodine-rich country (Japan) and an iodine-deficient country (Vietnam) [20]. Research in recent decades has increased our understanding of the molecular pathogenesis of thyroid cancer [1, 10, 43]. However, the origin of BRAF mutations in thyroid cancer still needs clarification. Further experimental studies should better clarify the origin of these mutations and help determine the reasons behind the increase in BRAF mutations over the last few decades.

A significant decrease of RET/PTC rearrangements in classical PTCs has been seen over the years (Tables (Tables3).3). RET/PTC rearrangements have been strongly associated with radiation-induced PTCs [35, 44, 45]. RET/PTC rearrangements could also be detected in sporadic PTCs, but the underlying causes are unknown. A worldwide decrease in exposure to ionizing radiation in recent years, long after the Chernobyl accident or nuclear test experiments, has been proposed as a possible reason for the decrease of RET/PTC rearrangements [39]. Another hypothesis is that RET/PTC rearrangements are induced by unknown determinants that have been changing over the last decades [39]. We are in favor of the latter hypothesis because there were no nuclear accidents or atomic bomb experiments in the UK, Italy or Japan that could explain the high prevalence of RET/PTC rearrangements in sporadic PTCs in the earlier period of our review. In recent years, there has been another nuclear accident in Fukushima (Japan) in March 2011. BRAF mutations were the major genetic event (63.2%) in pediatric PTCs in Fukushima who underwent thyroidectomy in 2013 - 2014 and RET/PTC rearrangements were found in only 10.3% of cases [46]. This oncogenic profile is quite different from Chernobyl-related studies [47] but this result should be interpreted with cautions. Firstly, the thyroid equivalent doses in Fukushima (4.2 mSV) is much lower than in Chernobyl (490 mSV) [48, 49]. The second issue is that at the time of the study by Mitsutake et al. [46], the interval period from the date of accident to the onset was too short. Continuous studies are required to further investigate the trends of thyroid cancer incidence and genetic alterations in Japanese children.

At the University of Pittsburgh, the frequency of RAS mutations in PTCs remained low and stable during 1974-2000, then significantly increased in 2009 [14]. This trend was accompanied by a remarkable increase of FVPTCs in 2009 (Table (Table6).6). The incidence of FVPTC was reported to have increased nearly three-fold from 1973 to 2003 in the US [50]. Most of the increase in FVPTCs occurred after 1988 when the WHO classification changed. However, the proportion of FVPTCs did not change in Italy over the years [11]. We can only examine the trend of RAS mutations in classical PTCs from UCSF and University of Pittsburgh. The prevalence of RAS mutations did not change in classical PTCs from the University of Pittsburgh over the four periods in our review, but its prevalence in FVPTCs did increase significantly from 11.1% in 2000 to 44.3% in 2009 [14]. The authors from UCSF only selected patients with classical PTCs for their study, and they identified RAS mutations in 4%, 2.9% and 0% of cases during 1991 to 1995, 1996 to 2000 and 2001 to 2005, respectively (Table (Table4).4). Further studies should examine the trend of RAS mutations in PTCs, especially the follicular variant or follicular neoplasms (follicular thyroid adenoma and carcinoma).

Our systematic review is limited by the relatively small number of institutions that can be included. However, we must apply strict criteria as described above to avoid the potential bias caused by heterogeneities in population characteristics, detection methods and other factors that could influence the prevalence of genetic alterations. Further population-based studies with large number of cases are required to clarify these trends. In addition, we could not perform multivariate analysis for trends of mutations adjusted for the confounding factors because most of included studies did not provide those data or individual patient data. Jung et al. and Kowalska et al. investigated the trend of mutations in classical PTCs adjusted for age and sex and they found a significant increase of BRAF mutations over time [14, 18] (Table (Table22).

From our study, it is evident that the demographic and clinicopathological characteristics and the molecular profiles of PTCs have been changing over the years worldwide, suggesting the changes in tumorigenesis of PTCs. Further research on whether the genetic alterations in PTCs are primary or secondary and elucidation of molecular pathways in the pathogenesis of thyroid cancer can help us clarify the underlying causes of these modifications.

MATERIALS AND METHODS

Search strategy and study identification

We conducted an electronic search within six databases (PubMed, Scopus, ISI Web of Science, Google Scholar, WHO Global Health Library and Virtual Health Library) to identify relevant articles using the search term: (papillary thyroid AND (carcinoma OR cancer) AND (BRAF OR RAS OR RET/PTC). We did not limit the search results as to language or year of publication. Our study included publications published before June 2015. Additionally, we performed a manual search by reviewing citations within the included publications and related references presented in PubMed. Our study strictly followed the recommendation of Preferred Reporting Items for Systematic Review and Meta-analysis (PRISMA) statement [51]. We registered our study protocol at PROSPERO database: http://www.crd.york.ac.uk/prospero/display_record.asp?ID=RD42015024778.

Selection criteria

We imported search results from 6 libraries into Endnote (Thompson Reuters) and deleted duplicates. Two teams of reviewers independently screened the abstracts using the predetermined selection criteria. The inclusion criteria were (i) articles containing data regarding frequencies of BRAF mutations, RET/PTC rearrangements or RAS mutations in PTCs or classical PTCs which had been histologically confirmed, (ii) articles containing data regarding frequencies of RAS mutations in follicular variant PTCs (FVPTCs) or (iii) articles comparing the clinicopathological characteristics of PTCs between different time periods. We excluded studies that (i) did not provide the locations or institutions where the patients with PTC were recruited or treated, (ii) focused only on a histological variant (with two exceptions described in the inclusion criteria) or a clinicopathological factor (e.g. pediatric PTCs, multifocal PTCs or recurrent PTCs), (iii) involved radiation-induced PTCs unless the study had a mixed population of radiation-induced and sporadic PTCs with the sporadic PTC data reported separately, (iv) were experimental or in vitro in nature, (v) were case reports, conference presentations, posters, proceeding papers, books, theses or reviews or (vi) duplicated data. If a study's authors did not indicate where patients’ data was collected or where they were treated and all authors were from the same affiliation, the affiliation location was considered the primary place where the patients were initially treated.

Data extraction

Two teams of reviewers independently read the full text of potential articles and extracted data using a predefined data extraction form. Supervisors resolved any discrepancies during this data extraction step. We extracted the following details: name of institution, city, country, time of surgery (when the patient was admitted), patient's age and gender, patient selection method, mutational detection method, prevalence of genetic alterations in entire PTC population and each histological variant, and clinicopathological data (histological variants, size, multiplicity, extrathyroidal extension (ETE) and TNM classification). We sought missing data from potentially eligible studies via email with the authors. If the full text did not indicate when patients received surgery and the authors did not respond to our emails, we considered time before submission date of the article as a patient's surgical time period. Native speakers from a group of international doctors extracted data from articles not written in English, and this was further checked by Google Translate.

Data analysis

Our systematic literature review assessed several factors: 1) BRAF, RET/PTC and RAS mutational trends in classical PTCs from individual institutions; 2) BRAF mutational trends in micro PTCs from individual institutions; 3) modifications and trends of clinicopathological characteristics of PTCs from individual institutions. Selection and analysis of data for each section is described in detail below.

We compared the means and standard deviations (SD) of age and tumor size by using Student t test in GraphPad QuickCals at http://www.graphpad.com/quickcalcs/ttest1.cfm?Format=SD For those articles in which the authors only provided median, range and the total number of patients, we estimated mean and SD values as described by Hozo et al [52]. Pearson Chi-square was used to compare the clinicopathological features and prevalence of each mutation between different periods from the same institutions. Statistical analysis was performed with the SPSS software, version 22 (Chicago, IL). A p value ≤ 0.05 was considered statistically significant.

Quality assessment and risk of bias analysis

Two investigators independently scored the quality and risk of bias of the included studies, as measured by the Quality Assessment Tool for Observational Cohort and Cross-Sectional Studies of the National Institute of Health (NIH) [28]. Disagreements in scoring was solved by discussion and consensus. The score of all 14 items marked with “yes” were calculated into percentage (inapplicable items were not taken into account). The quality rating of included studies was classified as low, fair and good if the score percentage was lower than 50%, 50% - 75% and more than 75%, respectively.

SUPPLEMENTARY TABLE

Footnotes

CONFLICTS OF INTEREST

All authors declare that they have no conflicts of interest.

REFERENCES

1. Kondo T, Ezzat S, Asa SL. Pathogenetic mechanisms in thyroid follicular-cell neoplasia. Nat Rev Cancer. 2006;6:292–306. doi: 10.1038/nrc1836. [PubMed] [Cross Ref]
2. Kilfoy BA, Zheng T, Holford TR, Han X, Ward MH, Sjodin A, Zhang Y, Bai Y, Zhu C, Guo GL, Rothman N, Zhang Y. International patterns and trends in thyroid cancer incidence, 1973-2002. Cancer Causes Control. 2009;20:525–31. doi: 10.1007/s10552-008-9260-4. [PMC free article] [PubMed] [Cross Ref]
3. Davies L, Welch HG. Increasing incidence of thyroid cancer in the United States, 1973-2002. JAMA. 2006;295:2164–7. doi: 10.1001/jama.295.18.2164. [PubMed] [Cross Ref]
4. Davies L, Welch HG. Current thyroid cancer trends in the United States. JAMA Otolaryngol Head Neck Surg. 2014;140:317–22. doi: 10.1001/jamaoto.2014.1. [PubMed] [Cross Ref]
5. Chou A, Fraser S, Toon CW, Clarkson A, Sioson L, Farzin M, Cussigh C, Aniss A, O’Neill C, Watson N, Clifton-Bligh RJ, Learoyd DL, Robinson BG, et al. A Detailed Clinicopathologic Study of ALK-translocated Papillary Thyroid Carcinoma. Am J Surg Pathol. 2015;39:652–9. doi: 10.1097/PAS.0000000000000368. [PMC free article] [PubMed] [Cross Ref]
6. Morris LG, Myssiorek D. Improved detection does not fully explain the rising incidence of well-differentiated thyroid cancer: a population-based analysis. Am J Surg. 2010;200:454–61. doi: 10.1016/j.amjsurg.2009.11.008. [PMC free article] [PubMed] [Cross Ref]
7. Nikiforova MN, Kimura ET, Gandhi M, Biddinger PW, Knauf JA, Basolo F, Zhu ZW, Giannini R, Salvatore G, Fusco A, Santoro M, Fagin JA, Nikiforov YE. BRAF mutations in thyroid tumors are restricted to papillary carcinomas and anaplastic or poorly differentiated carcinomas arising from papillary carcinomas. J Clin Endocrinol Metab. 2003;88:5399–404. doi: 10.1210/jc.2003-030838. [PubMed] [Cross Ref]
8. Frasca F, Nucera C, Pellegriti G, Gangemi P, Attard M, Stella M, Loda M, Vella V, Giordano C, Trimarchi F, Mazzon E, Belfiore A, Vigneri R. BRAF((V600E)) mutation and the biology of papillary thyroid cancer. Endocr Relat Cancer. 2008;15:191–205. doi: 10.1677/ERC-07-0212. [PubMed] [Cross Ref]
9. Seo JY, Choi JR, Moon HJ, Kim E-K, Han KH, Kim H, Kwak JY. Clinical Implication of Highly Sensitive Detection of the BRAF(V600E) Mutation in Fine-Needle Aspirations According to the Thyroid Bethesda System in Patients With Conventional Papillary Thyroid Carcinoma. Ann Otol Rhinol Laryngol. 2015;124:392–9. doi: 10.1177/0003489414560433. [PubMed] [Cross Ref]
10. Nikiforov YE, Nikiforova MN. Molecular genetics and diagnosis of thyroid cancer. Nat Rev Endocrinol. 2011;7:569–80. doi: 10.1038/nrendo.2011.142. [PubMed] [Cross Ref]
11. Romei C, Fugazzola L, Puxeddu E, Frasca F, Viola D, Muzza M, Moretti S, Nicolosi ML, Giani C, Cirello V, Avenia N, Rossi S, Vitti P, et al. Modifications in the Papillary Thyroid Cancer Gene Profile Over the Last 15 Years. J Clin Endocrinol Metab. 2012;97:E1758–E65. doi: 10.1210/jc.2012-1269. [PubMed] [Cross Ref]
12. Hong AR, Lim JA, Kim TH, Choi HS, Yoo WS, Min HS, Won JK, Lee KE, Jung KC, Park DJ, Park YJ. The Frequency and Clinical Implications of the BRAF(V600E) Mutation in Papillary Thyroid Cancer Patients in Korea Over the Past Two Decades. Endocrinol Metab (Seoul, Korea) 2014;29:505–13. doi: 10.3803/EnM.2014.29.4.505. [PMC free article] [PubMed] [Cross Ref]
13. Mathur A, Moses W, Rahbari R, Khanafshar E, Duh Q-Y, Clark O, Kebebew E. Higher Rate of BRAF Mutation in Papillary Thyroid Cancer Over Time A Single-Institution Study. Cancer. 2011;117:4390–5. doi: 10.1002/cncr.26072. [PMC free article] [PubMed] [Cross Ref]
14. Jung CK, Little MP, Lubin JH, Brenner AV, Wells SA, Jr., Sigurdson AJ, Nikiforov YE. The Increase in Thyroid Cancer Incidence During the Last Four Decades Is Accompanied by a High Frequency of BRAF Mutations and a Sharp Increase in RAS Mutations. J Clin Endocrinol Metab. 2014;99:E276–E85. doi: 10.1210/jc.2013-2503. [PubMed] [Cross Ref]
15. Nam JK, Jung CK, Song BJ, Lim DJ, Chae BJ, Lee NS, Park WC, Kim JS, Jung SS, Bae JS. Is the BRAF(V600E) mutation useful as a predictor of preoperative risk in papillary thyroid cancer? Am J Surg. 2012;203:436–41. doi: 10.1016/j.amjsurg.2011.02.013. [PubMed] [Cross Ref]
16. Lee SH, Jung CK, Bae JS, Jung SL, Choi YJ, Kang CS. Liquid-based cytology improves preoperative diagnostic accuracy of the tall cell variant of papillary thyroid carcinoma. Diagn Cytopathol. 2014;42:11–7. doi: 10.1002/dc.23007. [PubMed] [Cross Ref]
17. Smyth P, Finn S, Cahill S, O’Regan E, Flavin R, O’Leary JJ, Sheils O. ret/PTC and BRAF act as distinct molecular, time-dependant triggers in a sporadic Irish cohort of papillary thyroid carcinoma. Int J Surg Pathol. 2005;13:1–8. doi: 10.1177/106689690501300101. [PubMed] [Cross Ref]
18. Kowalska A, Walczyk A, Kowalik A, Palyga I, Trybek T, Kopczynski J, Kajor M, Chrapek M, Pieciak L, Chlopek M, Gozdz S, Kaminski G. Increase in Papillary Thyroid Cancer Incidence Is Accompanied by Changes in the Frequency of the BRAF(V600E) Mutation: A Single-Institution Study. 2016 doi: 10.1089/thy.2015.0352. [PubMed] [Cross Ref]
19. Nakazawa T, Murata S-i, Kondo T, Niu D, Mochizuki K, Kawasaki T, Yamane T, Nakamura N, Katoh R. RET/PTC rearrangements arising from a small population of papillary thyroid carcinoma cells, possible candidate for passenger mutation. Virchows Archiv. 2009;455:35–41. doi: 10.1007/s00428-009-0789-8. [PubMed] [Cross Ref]
20. Vuong HG, Kondo T, Oishi N, Nakazawa T, Mochizuki K, Inoue T, Kasai K, Tahara I, Tran TM, Hirokawa M, Katoh R. Genetic alterations of differentiated thyroid carcinoma in iodine-rich and iodine-deficient countries. Cancer Med. 2016 doi: 10.1002/cam4.781. [PMC free article] [PubMed] [Cross Ref]
21. Zheng X, Wei S, Han Y, Li Y, Yu Y, Yun X, Ren X, Gao M. Papillary microcarcinoma of the thyroid: clinical characteristics and BRAF(V600E) mutational status of 977 cases. Ann Surg Oncol. 2013;20:2266–73. doi: 10.1245/s10434-012-2851-z. [PubMed] [Cross Ref]
22. Lu ZZ, Zhang Y, Wei SF, Li DS, Zhu QH, Sun SJ, Li M, Li LI. Outcome of papillary thyroid microcarcinoma: Study of 1,990 cases. Mol Clin Oncol. 2015;3:672–6. doi: 10.3892/mco.2015.495. [PMC free article] [PubMed] [Cross Ref]
23. Lee JI, Jang HW, Kim SW, Kim J-W, Oh YL, Chung JH. BRAF(V600E) mutation in fine-needle aspiration aspirates: Association with poorer prognostic factors in larger papillary thyroid carcinomas. Head Neck. 2013;35:548–53. doi: 10.1002/hed.22997. [PubMed] [Cross Ref]
24. Kang SY, Ahn S, Lee S-M, Jeong JY, Sung J-Y, Oh YL, Kim K-M. Shifted termination assay (STA) fragment analysis to detect BRAF V600 mutations in papillary thyroid carcinomas. Diagn Pathol. 2013;8 doi: 10.1186/1746-1596-8-121. [PMC free article] [PubMed] [Cross Ref]
25. Barzon L, Masi G, Boschin IM, Lavezzo E, Pacenti M, Ide EC, Toniato A, Toppo S, Palu G, Pelizzo MR. Characterization of a novel complex BRAF mutation in a follicular variant papillary thyroid carcinoma. Eur J Endocrinol. 2008;159:77–80. doi: 10.1530/EJE-08-0239. [PubMed] [Cross Ref]
26. Pelizzo MR, Boschin IM, Barollo S, Pennelli G, Toniato A, Zambonin L, Vianello F, Piotto A, Ide EC, Pagetta C, Sorgato N, Torresan F, Girelli ME, et al. BRAF analysis by fine needle aspiration biopsy of thyroid nodules improves preoperative identification of papillary thyroid carcinoma and represents a prognostic factor. A mono-institutional experience. Clin Chem Lab Med. 2011;49:325–9. doi: 10.1515/CCLM.2011.031. [PubMed] [Cross Ref]
27. Hwang J, Shin JH, Han B-K, Ko EY, Kang SS, Kim J-W, Chung JH. Papillary Thyroid Carcinoma With BRAF(V600E) Mutation: Sonographic Prediction. AJR Am J Roentgenol. 2010;194:W425–W30. doi: 10.2214/AJR.09.3512. [PubMed] [Cross Ref]
28. NIH Quality assessment tool for observational cohort and cross-sectional studies
29. Fugazzola L, Puxeddu E, Avenia N, Romei C, Cirello V, Cavaliere A, Faviana P, Mannavola D, Moretti S, Rossi S, Sculli M, Bottici V, Beck-Peccoz P, et al. Correlation between B-RAF(V600E) mutation and clinico-pathologic parameters in papillary thyroid carcinoma: data from a multicentric Italian study and review of the literature. Endocr Relat Cancer. 2006;13:455–64. doi: 10.1677/erc.1.01086. [PubMed] [Cross Ref]
30. Kim KH, Suh KS, Kang DW, Kang DY. Mutations of the BRAF gene in papillary thyroid carcinoma and in Hashimoto's thyroiditis. Pathol Int. 2005;55:540–5. doi: 10.1111/j.1440-1827.2005.01866.x. [PubMed] [Cross Ref]
31. Liu RT, Chen YJ, Chou FF, Li CL, Wu WL, Tsai PC, Huang CC, Cheng JT. No correlation between BRAF(V600E) mutation and clinicopathological features of papillary thyroid carcinomas in Taiwan. Clin Endocrinol. 2005;63:461–6. doi: 10.1111/j.1365-2265.2005.02367.x. [PubMed] [Cross Ref]
32. Namba H, Nakashima M, Hayashi T, Hayashida N, Maeda S, Rogounovitch TI, Ohtsuru A, Saenko VA, Kanematsu T, Yamashita S. Clinical implication of hot spot BRAF mutation, V599E, in papillary thyroid cancers. J Clin Endocrinol Metab. 2003;88:4393–7. doi: 10.1210/jc.2003-030305. [PubMed] [Cross Ref]
33. Sykorova V, Dvorakova S, Ryska A, Vcelak J, Vaclavikova E, Laco J, Kodetova D, Kodet R, Cibula A, Duskova J, Hlobilkova A, Astl J, Vesely D, et al. BRAF(V600E) mutation in the pathogenesis of a large series of papillary thyroid carcinoma in Czech Republic. J Endocrinol Invest. 2010;33:318–24. doi: 10.3275/6722. [PubMed] [Cross Ref]
34. Kebebew E, Weng J, Bauer J, Ranvier G, Clark OH, Duh Q-Y, Shibru D, Bastian B, Griffin A. The prevalence and prognostic value of BRAF mutation in thyroid cancer. Ann Surg. 2007;246:466–71. doi: 10.1097/SLA.0b013e318148563d. [PubMed] [Cross Ref]
35. Nikiforov YE, Rowland JM, Bove KE, Monforte-Munoz H, Fagin JA. Distinct pattern of ret oncogene rearrangements in morphological variants of radiation-induced thyroid papillary carcinomas in children. Cancer Res. 1997;55:5617–20. [PubMed]
36. Elisei R, Romei C, Vorontsova T, Cosci B, Veremeychik V, Kuchinskaya E, Basolo F, Demidchik EP, Miccoli P, Pinchera A, Pacini F. RET/PTC rearrangements in thyroid nodules: studies in irradiated and not irradiated, malignant and benign thyroid lesions in children and adults. J Clin Endocrinol Metab. 2001;86:3211–6. doi: 10.1210/jcem.86.7.7678. [PubMed] [Cross Ref]
37. Nakazawa T, Kondo T, Kobayashi Y, Takamura N, Murata S, Kameyama K, Muramatsu A, Ito K, Kobayashi M, Katoh R. RET gene rearrangements (RET/PTC1 and RET/PTC3) in papillary thyroid carcinomas from an iodine-rich country (Japan) Cancer. 2005;104:943–51. doi: 10.1002/cncr.21270. [PubMed] [Cross Ref]
38. Caudill CM, Zhu Z, Ciampi R, Stringer JR, Nikiforov YE. Dose-dependent generation of RET/PTC in human thyroid cells after in vitro exposure to γ-radiation: A model of carcinogenic chromosomal rearrangement induced by ionizing radiation. J Clin Endocrinol Metab. 2005;90:2364–9. doi: 10.1210/jc.2004-1811. [PubMed] [Cross Ref]
39. Elisei R. Molecular profiles of papillary thyroid tumors have been changing in the last decades: how could we explain it? J Clin Endocrinol Metab. 2014;99:412–4. doi: 10.1210/jc.2014-1130. [PubMed] [Cross Ref]
40. Guan H, Ji M, Bao R, Yu H, Wang Y, Hou P, Zhang Y, Shan Z, Teng W, Xing M. Association of High Iodine Intake with the T1799A BRAF Mutation in Papillary Thyroid Cancer. J Clin Endocrinol Metab. 2009;94:1612–7. doi: 10.1210/jc.2008-2390. [PubMed] [Cross Ref]
41. Hollowell JG, Staehling NW, Hannon WH. Trends and public health implications: iodine excretion data from National Health and Nutrition Examination Surveys I and III (1971-1974 and 1988-1994) J Clin Endocrinol Metab. 1998;83:3401–8. doi: 10.1210/jcem.83.10.5168. [PubMed] [Cross Ref]
42. Caldwell KL, Miller GA, Wang RY, Jain RB, Jones RL. Iodine status of the U.S. population. National Health and Nutrition Examination Survey 2003-2004. Thyroid. 2008;18:1207–14. doi: 10.1089/thy.2008.0161. [PubMed] [Cross Ref]
43. Xing M. Molecular pathogenesis and mechanisms of thyroid cancer. Nat Rev Cancer. 2013;13:184–99. doi: 10.1038/nrc3431. [PMC free article] [PubMed] [Cross Ref]
44. Fugazzola L, Pilotti S, Pinchera A, Vorontsova TV, Mondellini P, Bongarzone I, Greco A, Astakhova L, Butti MG, Demidchik EP, et al. Oncogenic rearrangements of the RET proto-oncogene in papillary thyroid carcinomas from children exposed to the Chernobyl nuclear accident. Cancer Res. 1995;55:5617–20. doi: [PubMed]
45. Tuttle RM, Fenton C, Lukes Y, Davis S, Kopecky K, Reinhardt B, Lushnikov E, Abrosimov A, Troshin V, Tsyb A, Francis G. Activation of the ret/PTC oncogene in papillary thyroid cancer from Russian children exposed to radiation following the Chernobyl accident. Endocr J. 2000;47:215. doi: 10.1089/thy.2008.0072. [PubMed] [Cross Ref]
46. Mitsutake N, Fukushima T, Matsuse M, Rogounovitch T, Saenko V, Uchino S, Ito M, Suzuki K, Suzuki S, Yamashita S. BRAF(V600E) mutation is highly prevalent in thyroid carcinomas in the young population in Fukushima: a different oncogenic profile from Chernobyl. Sci Rep. 2015;5:16976. doi: 10.1038/srep16976. [PMC free article] [PubMed] [Cross Ref]
47. Nikiforov YE. Genetic events in radiation-induced thyroid cancer. Genetics of Complex Thyroid Diseases. (2002:198–219.
48. Tokonami S, Hosoda M, Akiba S, Sorimachi A, Kashiwakura I, Balonov M. Thyroid doses for evacuees from the Fukushima nuclear accident. Sci Rep. 2012;2:507. doi: 10.1038/srep00507. [PMC free article] [PubMed] [Cross Ref]
49. Nikiforov YE. Radiation-induced thyroid cancer: what we have learned from chernobyl. Endocrine pathology. 2006;17:307–17. doi: 10.1007/s12022-006-0001-5. [PubMed] [Cross Ref]
50. Albores-Saavedra J, Henson DE, Glazer E, Schwartz AM. Changing Patterns in the Incidence and Survival of Thyroid Cancer with Follicular Phenotype—Papillary, Follicular, and Anaplastic: A Morphological and Epidemiological Study. Endocr Pathol. 2007;18:1–7. doi: 10.1007/s12022-007-0002-z. [PubMed] [Cross Ref]
51. Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6:e1000097. doi: 10.1371/journal.pmed.1000097. [PMC free article] [PubMed] [Cross Ref]
52. Hozo SP, Djulbegovic B, Hozo I. Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol. 2005;20:5–13. doi: 10.1186/1471-2288-5-13. [PMC free article] [PubMed] [Cross Ref]

Articles from Oncotarget are provided here courtesy of Impact Journals, LLC