Background
Over the last two decades, the discovery of molecular pathways critical to oncogenic transformation has dramatically altered our understanding of thyroid malignancy. Reports initially suggested that nearly 70 % of thyroid cancers harbor single gene mutations in the BRAF or RAS pathways, or balanced translocations of RET/PTC, or PAX8/PPARγ [1, 2]. More recently, reports confirm an oncogenic mutation in 97 % of well-differentiated papillary carcinomas [3]. Such mutations can increasingly be identified in both preoperative fine needle aspiration (FNA) cytology specimens and on post-operative histopathology. Many believe that the synergistic use of microscopic and molecular analysis is destined to improve the clinical management of this illness [4].
Mutations or translocations identified in most thyroid carcinomas are known to activate pathways regulating cellular growth, development, and/or malignant transformation, which has led to the assumption that thyroid nodules harboring such mutations are either cancerous, or at high risk for eventual malignant transformation [5‐7]. However, observational data question this assumption as absolute and suggest that all such pathways or activating mutations may not prove equally oncogenic or may require secondary molecular ‘hits’ before behaving in a malignant fashion. In particular, clinical outcomes of patients with mutations in the N-, K-, or H- isoforms of the RAS gene are highly variable [7]. In contrast to homogeneous BRAF V600E mutations which strongly associate with higher-risk papillary carcinoma, initial observations suggest RAS mutations associate with variable histology, ranging from benign disease, to low-risk malignancy, to anaplastic carcinoma [7‐10].
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However, few prospective blinded assessments of RAS-positive thyroid nodules (treated or untreated) have been performed. Such an assessment is critically important, as diagnostic testing for these mutations is now widely available. To many clinicians, identification of an activating RAS mutation may prompt a belief that malignancy has been identified [7]. This leads to downstream clinical recommendations usually favoring surgical resection. Such treatment is highly beneficial in many scenarios, but for those with benign disease, has subjected the patient to unnecessary cost, operative morbidity, and significant risk [11, 12]. Past experience involving papillary microcarcinoma provides a cautionary parallel supporting the importance of further study of RAS-positive thyroid nodules. For decades, widespread belief that all papillary carcinoma posed danger prompted recommendations for active removal of such thyroid nodules [13, 14]. This was true even when nodules were smaller than 1 cm and ultrasound confirmed the absence of abnormal adenopathy. Prospective data debunked this belief, confirming the indolent nature of these papillary microcarcinomas [15]. Expert guidelines now recommend against evaluation of most nodules <1 cm, and/or surgical treatment of sub-centimeter papillary carcinomas [16, 17].
We performed a prospective study of clinically relevant thyroid nodules, including ultrasound-guided FNA and gene mutation analysis. Blinded mutational analysis and histopathologic interpretation was performed. Our goal was not to validate the performance of a molecular diagnostic test on cytologically indeterminate nodules, as such investigations have previously been performed. Rather, we uniquely sought to evaluate the molecular profiles of a large consecutive cohort of thyroid nodules >1 cm presenting for FNA. By doing so, we sought to understand the molecular profiles detected in an unselected nodule population whether cytologically benign, indeterminate, or malignant. Furthermore, as a large proportion of our patients also participate in an on-going prospective, long-term cohort study assessing the natural history of thyroid nodules, we hypothesized that several mutation-positive nodules would also have long-term sonographic follow-up for analysis. If so, assessment for potential malignant transformation – in particular when observing the natural history of RAS-positive thyroid nodules – would be for the first time possible.
Methods
We performed a prospective, blinded study of euthyroid patients seeking care of thyroid nodules >1 cm in diameter. Patients were referred to the thyroid biopsy clinic at the Brigham and Women’s Hospital (Boston, MA, USA) between July 2010 and October 2012, and evaluated according to current clinical practice guidelines [16]. Ultrasound evaluation was performed by one of four radiologists with expertise in thyroid evaluation, using a 6–15 mHz transducer. Following informed consent, ultrasound-guided FNA was performed by one of three thyroidologists. Three needle passes from the same nodule using 25 g needles were rinsed into a liquid-based solution (CytoLyt®; Cytyc Corp., Marlborough, MA, USA), constituting a single aspiration. An additional sample was then obtained and shipped to a centralized CLIA-certified laboratory at Asuragen, Inc. (Austin, TX, USA) where mutational analysis was performed as part of the miRInform Thyroid® diagnostic test [18]. As previously described, this test evaluates 17 distinct genetic alterations, including 14 BRAF, K-, N-, or H-RAS mutations, and three PAX8-PPARγ and RET-PTC rearrangements [18]. Of 391 nodules enrolled for initial evaluation, 11 yielded insufficient nucleic acid for mutational testing. A separate consecutive group of 15 separate nodules all showed an uncharacteristic molecular result (double positive for PAX8-PPARG and RAS) suggesting external cross-contamination during processing of this series, and were therefore excluded. Three nodules were excluded as a result of a protocol deviation (one delayed shipping) or study dropout (n = 2). This resulted in a final population of 362 nodules from 318 patients.
FNA cytology was classified according to the Bethesda system for reporting thyroid cytopathology [19]. Benign cytologic results most often prompted a conservative, non-operative recommendation. Cytologically indeterminate and malignant nodules most often prompted a recommendation for surgical resection. Midway through this study, Afirma gene expression classifier (GEC) testing became available, and was applied to a minority of low-risk patients with initial atypia of undetermined significance (AUS) cytology. If Afirma testing was benign, nodules were treated similarly to those with benign cytology [20]. Following thyroidectomy, histopathology interpretation was performed, which frequently involved multi-expert review and consensus. All histopathologic interpretations were blinded to molecular results. Similarly, molecular interpretation was performed without knowledge of any clinical or pathologic findings. At study completion, results were combined and interpreted.
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The Brigham and Women’s Hospital thyroid nodule clinic has prospectively enrolled all patients evaluated between 1995–present in an ongoing clinical trial assessing the natural history of thyroid nodules [21]. We analyzed all past and present thyroid sonographic imaging in patients with RAS-positive, cytologically benign thyroid nodules. For some of the patients, a separate ultrasound-guided FNA of the target nodule had also been performed at an earlier time point before enrollment in the current study. This was usually at a separate facility or by a separate provider.
For the purposes of this study, we sought to specifically describe the histologic outcome of all thyroid nodules positive for N-, H-, and K-RAS mutations, as these mutations are common yet observations suggest a variable phenotype. For RAS-positive nodules confirmed malignant by histopathology, we documented the cancer type and specific papillary thyroid carcinoma (PTC) variant. Nodule size, as well as multifocality, lymphovascular invasion, extrathyroidal extension, and local metastatic adenopathy were similarly documented. For RAS-positive nodules with benign cytology, we reviewed all available sonographic and cytologic reports documenting thyroid nodule size, abnormal adenopathy, or other signs of malignant behavior, with a follow-up time of at least 6 months. Growth was defined as a >20 % change in the largest two nodule dimensions.
This protocol was approved by the Investigational Review Board of the Brigham and Women’s Hospital, and all patients provided written informed consent for participation and publication of individual patient data, including the data described in Tables 2 and 4. No patients received a stipend for participating in this study. ANOVA was used to compare the mean age between patients with RAS-positive benign and malignant nodules. Statistical analysis was performed using SPSS version 22 (SPSS IBM, Armonk, NY, USA), and a P value <0.05 was considered significant.
Results
We prospectively enrolled 318 patients with 362 clinically relevant thyroid nodules (>1 cm), whose baseline characteristics are shown in Table 1. Following blinded molecular analysis, 17 nodules were positive for mutations in the K-, N-, or H- RAS genes, while nine separate nodules harbored V600E BRAF mutations. Three additional nodules were positive for translocations involving the PAX8-PPARγ genes, while no RET-PTC translocations were found. Ultimately, 33 of 362 (9.1 %) nodules proved malignant following surgical resection and blinded histopathologic assessment, including eight BRAF-positive and eight RAS-positive nodules. Of the 17 RAS-positive nodules, ten were referred to surgery because of abnormal or malignant cytology, while seven did not have surgery as their biopsy was benign (six cytologically ‘benign’; one nodule cytologically AUS but subsequent ‘benign’ GEC). Of the ten RAS-positive nodules referred to surgery, eight proved histologically malignant, while two were histologically benign. In summary, 8 of 17 RAS mutation-positive nodules (47 %) were malignant by microscopic analysis, while the remainder were benign.
Table 1
Baseline characteristics of the study population and the RAS-positive subgroup
Number of patients | Number of nodules | Female (%) | Age (years) | Nodule size (cm) | Proportion malignanta | Mutations detected | |
|---|---|---|---|---|---|---|---|
Total population | 318 | 362 | 78.7 % | Range: 21.8–87.7 Median: 55.0 | Range: 1.0–6.6 Median: 1.9 | 33 nodulesb (9.1 %) | 17 RAS + 9 BRAF + 3 PAX8-PPARγ +c |
RAS-positive nodules | 17 | 17 | 88.2 % | Range: 27.1–63.5 Median: 46.0 | Range: 1.0–5.6 Median: 1.8 | 8 nodules (47.1 %)d | 8 HRAS+ (3 G12V, 2 Q61K, 2 Q61R, 1 G13R) 7 NRAS+ (6 Q61R, 1 Q61K) 2 KRAS+ (1 G12V) |
RAS-positive thyroid malignancies
Table 2 shows the characteristics of the RAS-positive thyroid malignancies. All (n = 8) were follicular variants of PTC (fvPTC), and all demonstrated very low-risk characteristics. Specifically, there was no evidence of lymphovascular invasion, extrathyroidal extension, local lymph node metastases, or distant metastases in any RAS-positive thyroid cancers. Furthermore, all were encapsulated, or partially encapsulated/well-circumscribed malignancies, and there were no disease-specific deaths. For comparison, we evaluated the histologic characteristics of the BRAF-positive thyroid malignancies. Compared to the RAS-positive malignancies, the BRAF-positive malignancies were equal in size (2.1 cm). However, they had less favorable histological characteristics as shown in Table 3. These data suggest a more indolent phenotype among many RAS-positive thyroid cancers.
Table 2
Characteristics of RAS-positive thyroid malignancies
Subject number | Sex | Age (years) | RAS mutation | Nodule size (mm) and parenchyma | FNA result | Histopathology | Encapsulated | Extrathyroidal extension | Lymph node metastases | Distant metastases |
|---|---|---|---|---|---|---|---|---|---|---|
1 | Female | 27 | HRAS G12V | 10 × 7 × 4 Solid No calcifications | Follicular neoplasm | PTC multifocal, 1.2 cm | Partially-encapsulated/well-circumscribed | No | No | No |
2 | Female | 46 | HRAS Q61R | 14 × 9 × 9 Solid No calcifications | Suspicious for papillary carcinoma | PTC follicular variant, 1.1 cm | Partially-encapsulated/well-circumscribed | No | No | No |
3 | Male | 61 | HRAS Q61R | 36 × 23 × 21 25–50 % Cystic No calcifications | Suspicious for papillary carcinoma | PTC follicular variant, 2.6 cm | Partially-encapsulated/well-circumscribed | No | No | No |
4 | Female | 33 | HRAS G13R | 20 × 18 × 16 Solid No calcifications | Suspicious for papillary carcinoma | PTC follicular variant, 1.8 cm | Encapsulated | No | No | No |
5 | Female | 44 | NRAS Q61R | 22 × 11 × 10 Solid No calcifications | Malignant – papillary carcinoma | PTC follicular variant, 1.1 cm | Partially-encapsulated/well-circumscribed | No | No | No |
6 | Female | 45 | NRAS Q61R | 18 × 14 × 7 Solid No calcifications | Malignant – papillary carcinoma | PTC follicular variant, 1.0 cm | Encapsulated | No | No | No |
7 | Female | 44 | NRAS Q61R | 18 × 14 × 12 Solid No calcifications | Follicular neoplasm | PTC follicular variant, 1.6 cm | Encapsulated | No | No | No |
8 | Female | 33 | NRAS Q61R | 31 × 23 × 18 Solid No calcifications | Atypia of undetermined significance | PTC follicular variant, 3.1 cm | Encapsulateda | No | No | No |
Table 3
Comparison of RAS-positive and BRAF-positive papillary thyroid cancers
Mutation | Positive predictive value (test specificity) | Tumor size (cm) | Histological subtype | Lymphovascular invasion | Extrathyroidal extension | Lymph node metastases |
|---|---|---|---|---|---|---|
RAS-positive cancers (n = 8) | 47 % (97.3 %) | Range: 1.0–3.6 Median: 1.9 | 8 – follicular variant PTC | 0/8 (0 %) | 0/8 (0 %) | 0/8 (0 %) |
BRAF-positive cancers (n = 8a) | 100 % (100 %) | Range: 1.0–4.8 Median: 1.4 | 6 – classical variant PTCb 1 – tall cell variant PTC 1 – follicular variant PTC | 5/8 (62.5 %) | 1/8 (12.5 %) | 1/8 (12.5 %) |
RAS-positive benign thyroid nodules
Nine RAS-positive thyroid nodules proved benign (two histologically benign; six cytologically benign; one benign GEC). Characteristics of the RAS-positive benign nodules are shown in Table 4. These nodules averaged 2.1 cm in largest dimension at study entry. While four nodules had not been previously evaluated in our thyroid nodule clinic, five nodules had undergone previous sonographic imaging and evaluation, including four with prior ultrasound-guided FNA. We therefore analyzed the repeated sonographic assessment of five RAS-positive cytologically benign nodules over time. No significant nodule growth was confirmed in all five (100 %) cases over a mean duration of 8.3 years (range: 3.1–24.0 years). Furthermore, no abnormal adenopathy or other sonographically worrisome features were identified throughout follow-up in all patients. For comparison, we randomly selected age and sex matched mutation-negative controls at a 3:1 ratio (i.e., 15 controls) and analyzed the same parameters. Over a comparable mean follow-up time of 7.5 years (range: 2.8–24.0 years), an average 4.6 mm increase in largest dimension was observed from these cytologically benign, mutation-null nodules.
Table 4
Characteristics and sonographic follow-up of RAS-positive benign nodules
Subject number | Sex | Age at study entry (years) | RAS mutation | Nodule size (mm) and parenchyma at study entry | FNA cytology at study entry | Previous or subsequent ultrasound | Duration of sonographic follow-up | Previous FNA cytology |
|---|---|---|---|---|---|---|---|---|
(date, size (mm), parenchyma) | (date, result) | |||||||
9 | Female | 52 | HRAS G12V | 11/2010, 18 × 5 × 11, <25 % Cystic | Benign | 02/2013, 16 × 11 × 9, Cystic (<25 %) | 3.9 years (no growth) | Not performed |
10/2014, 17 × 10 × 8, N/A | ||||||||
10 | Female | 52 | HRAS Q61K | 03/2012, 16 × 14 × 9, Solid | Benign | 09/2008, 17 × 12 × 11, Solid | 3.4 years (no growth) | 11/2008, Benign cytology |
11/2008, 17 × 10 × 10, N/A | ||||||||
01/2012, 16 × 15 × 9, Solid | ||||||||
11 | Female | 37 | KRAS G12V | 09/2011, 15 × 11 × 9, <25 % Cystic | Benign | - | N/A | Not performed |
12 | Female | 54 | KRAS G12V | 10/2010, 14 × 14 × 8, Solid | Benign | 07/1990, 13 × 12 × 7, N/A 10/1993, 14 × 12 × 8, N/A 05/1998, 15 × 13 × 8, Solid 06/1998, 15 × 13 × 8, Solid 10/1999, 15 × 13 × 7, Solid 07/2003, 15 × 14 × 7, Solid 07/2005, 14 × 14 × 8, Solid 10/2007, 15 × 14 × 7, Solid 01/2008, 13 × 12 × 7, Solid 08/2009, 14 × 13 × 8, Solid 09/2010, 16 × 15 × 9, Solid 07/2011, 16 × 13 × 7, Solid 01/2012, 15 × 15 × 7, Solid 01/2013, 16 × 15 × 8, Solid 07/2014, 15 × 14 × 9, Solid | 24.0 years (no growth) | 06/1998, Benign cytology |
13 | Female | 54 | NRAS Q61K | 04/2011, 15 × 12 × 11, <25 % Cystic | Benign | 05/2006, 15 × 9 × 9, Cystic (<25 %) 09/2006, 14 × 10 × 9, Cystic (<25 %) 06/2009, 12 × 11 × 11, Cystic (<25 %) 04/2011, 16 × 13 × 10, N/A 04/2012, 17 × 12 × 12, Cystic (<25 %) 06/2013, 15 × 12 × 10, Cystic (<25 %) | 7.0 years (no growth) | 09/2006, Benign cytology |
14 | Female | 30 | NRAS Q61R | 09/2011, 16 × 14 × 9, Solid | Benign | 08/2008, 13 × 13 × 8, Solid 12/2008, 13 × 13 × 9, Solid 07/2011, 15 × 14 × 8, N/A | 3.1 years (no growth) | 12/2008, Benign cytology |
15 | Female | 62 | NRAS Q61R | 01/2012, 17 × 14 × 12, Solid | AUS + Afirma GEC ‘Benign’ | N/A | N/A | 04/2012, AUS |
05/2012, Afirma GEC: ‘benign’ | ||||||||
16 | Female | 64 | HRAS G12V | 11/2010, 23 × 19 × 15, <25 % Cystic | AUS | N/A | N/A | 01/2011, Surgerya: benign histology |
17 | Male | 46 | HRAS Q61K | 03/2012, 56 × 45 × 33, Solid | Follicular neoplasm | N/A | N/A | 05/2012, Surgerya: benign histology |
Four of six RAS-positive, cytologically benign nodules had undergone a separate secondary biopsy at a time point preceding entry into this current study. All four previous aspirates (100 %) were cytologically benign when performed at mean 5.8 years prior to study entry, confirming no change in cellular morphology to the present. One other nodule demonstrated AUS at cytology on study entry, but was benign on subsequent GEC testing. This nodule was therefore considered benign. Finally, we compared the age of patients with RAS-positive thyroid nodules which proved malignant to those which proved benign. Patients with RAS-positive benign nodules were on average 13 years older (55.1 (3.7) (mean (SD)) versus 41.9 (4.0) years; P = 0.028) than patients with RAS-positive malignant nodules.
Discussion
Over the last decade, our understanding of the molecular pathways underpinning thyroid cancer has dramatically increased. This has improved care, though simultaneously fostering many clinical assumptions influenced by the population being studied. Nearly all investigations of molecular mutations have been performed on cancerous or cytologically indeterminate thyroid nodules. Importantly, this was not the goal of our study. We sought to present the first blinded, prospective analysis of RAS mutations in a general cohort of patients presenting with nodular disease, to better understand the meaning of such mutations and the natural history of RAS-positive nodules. Our data demonstrate a variable and generally low-risk phenotype among most RAS-positive nodules. RAS-positive status predicts thyroid cancer in 47 % of cases, though is also associated with a large proportion of thyroid nodules with benign histology, benign cytology, and indolent clinical characteristics during long-term conservative follow-up.
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In our population, RAS-positive thyroid cancers were uniformly low risk – all histologically confirmed to be fvPTC and encapsulated, and all without lymphovascular invasion, extrathyroidal extension, or local lymph node metastases. While many have argued that RAS-positive nodules are destined to behave in a malignant fashion, our data suggest this assumption should be viewed with caution. Several of the RAS-positive, cytologically benign thyroid nodules in our study cohort had previously been aspirated at an average of 5.8 years prior. This confirms the lack of meaningful cellular transformation over time. Furthermore, highly accurate sonographic assessment of these nodules during a mean 8-year follow-up (and up to 24 years in one patient) confirmed no growth concerning for malignant transformation. Together, these data suggest a far more indolent phenotype inherent to many RAS-positive thyroid nodules than previously described.
In the current study, all RAS-positive malignancies were fvPTCs (Table 3), while there were no RAS mutations detected in classical variant PTCs. This is interesting in the light of the results of the study of Castro et al., who showed that fvPTCs are molecularly more similar to follicular carcinoma than to classical variant PTCs [22]. This included a higher percentage of RAS mutations in fvPTCs than generally reported in classical variant PTCs.
The ability of activated mutant RAS to induce thyroid neoplasia in vitro has been well established [23‐25]. Furthermore, the cellular pathways stimulated by mutated RAS, including the MAPK and PI3/AKT signaling pathways, have been linked to thyroid tumorigenesis [23, 26]. However, the RAS gene encodes a family of three isoforms, NRAS, HRAS, and KRAS, with numerous different mutations described. Some studies have demonstrated a tight association between mutated RAS and follicular thyroid carcinoma, while others confirm a high prevalence of RAS mutations in benign adenomas or fvPTC [7]. These findings confirm that the MAPK and PI3/AKT cellular pathways are intimately involved in cellular growth and differentiation, but also demonstrate that numerous genetic and epigenetic factors likely contribute to the clinical phenotype. This is exemplified by recent analysis of the thyroid cancer genome atlas [3]. Our data support such findings, while broadening our understanding specific to RAS-positivity in a large population, inclusive of mostly benign nodules.
Other published data support our findings. It is again important to note that most investigations have studied RAS mutations only in populations with malignant or indeterminate cytology [2, 27‐29]. Similar to us, however, Moses and colleagues performed a blinded and prospective mutational analysis of 417 patients presenting with nodular disease [9]. In this cohort, 21 RAS-positive nodules were identified (4.6 % prevalence), very similar to the 4.7 % detected in our population. While 12 RAS mutations were identified among their 194 patients with abnormal cytology, nine additional RAS mutations were identified in the remaining 257 benign nodules. In total, 6 of 21 (29 %) RAS-positive nodules proved histologically malignant. This rate is comparable to our finding of 47 %. Unlike our investigation, however, no previous sonographic analysis or FNA were performed. Nonetheless, these data independently support our conclusion that RAS mutations are commonly detected in benign nodules.
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While the number of samples in the current study is too limited from which to draw firm conclusions regarding the distribution of RAS mutation subtypes in benign or malignant nodules, it is noteworthy that two KRAS mutations were detected in benign nodules, while none were detected in malignant nodules. Interestingly, Radkay and colleagues have also studied 204 FNA cases with RAS mutations (mostly indeterminate cytology) with corresponding surgical resection pathological specimens, similarly demonstrating that mutations in KRAS were associated with a significantly lower risk of carcinoma (41.7 %) compared to nodules with HRAS (95.5 %) and NRAS (86.8 %) mutations [29].
It is unclear why RAS-positive thyroid nodules behave in a less virulent manner, though several hypotheses can be considered. One possibility is that the different RAS mutations affect downstream protein function to variable degrees. This hypothesis is supported by parallel evidence observed in medullary thyroid carcinoma patients with activating RET mutations, in which over 50 unique mutations are described [30]. These data confirm that different genetic mutations in the same oncogene lead to variable malignant risk. Separately, it is increasingly likely that a two-hit hypothesis is necessary for malignant transformation in many RAS-positive nodules, especially those associated with aggressive disease [31]. Further investigation is required to better address these hypotheses.
Importantly, we do not advocate performing RAS-mutational testing on all thyroid nodules at time of presentation for several reasons. First, FNA cytology proved more accurate than RAS-analysis, as all thyroid malignancies were identified in nodules with indeterminate or malignant cytology. Second, such an approach has not been shown to be cost-effective nor to produce an improved health outcome. We realize, however, that some may nonetheless argue that detection of RAS-mutational status is important beyond simply its use in cytologically indeterminate FNAs. RAS-positive nodules indeed carry a higher risk for malignancy compared to RAS-negative nodules, and RAS-positive status may also affect prognostic and therapeutic decisions once malignant [8].
Our data do lend preliminary support for surgical removal of RAS-positive nodules in younger individuals with non-benign cytology, but question this approach in RAS-positive benign nodules. The majority of our study cohort with cytologically benign, yet RAS-positive nodules have been closely followed by clinical and sonographic assessment. During a follow-up that ranged from 3–24 years, no significant growth or malignant transformation was documented. Furthermore, repeat aspiration confirmed the presence of consistently benign cytology. Thus, any recommendation for thyroidectomy must balance the presumed benefits of such a procedure against its known risks [11, 12].
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We acknowledge limitations to our study. Notably, we recruited patients from a single institution. However, the fact that our clinic evaluates >95 % of all patients seeking thyroid nodule care in our healthcare system improves generalizability of these results and limits selection bias. We similarly acknowledge the lack of universal long-term follow up of all RAS-positive nodules. Though our data depict no growth via highly accurate sonographic follow-up of five such patients, it is possible such benign nodules would indeed transform into malignant processes over enough time. Importantly, however, our study also confirmed an impressive low-risk histologic profile to most RAS-positive malignancies. Thus, if an observational strategy was followed, repeat sonographic follow-up or repeat FNA may allow the patient and physician to arguably detect any future malignancy while still at a treatable stage. Further prospective study of this hypothesis is required. Finally, one may argue that our study should have been restricted to nodules with indeterminate cytology as this population is in whom mutational testing is currently recommended. However, that was not the goal of our study as we sought to investigate RAS-status in all nodules regardless of cytology results. We believe this approach provided us the unique opportunity to investigate the natural history and malignant risk of clinically relevant RAS-positive nodules in an unbiased fashion.
Conclusions
In summary, our data depict the blinded, prospective evaluation of RAS-mutational status in a population of patients presenting with clinically relevant thyroid nodules, and demonstrate a more indolent and variable phenotype than previously described. RAS-positive thyroid nodules, especially in older individuals, frequently demonstrate a benign phenotype. These data therefore support the utility of FNA cytology in guiding the clinical management of RAS-positive nodules. Cytologically benign nodules, even if RAS-positive, may be candidates for a non-operative observational strategy of repeated sonographic evaluation or FNA. Even if malignant, most RAS-positive thyroid nodules appear to be low-risk histologically, and thus are likely to be highly treatable.
Acknowledgements
This analysis and investigation was supported by funding from the Brigham and Women’s Hospital and by the NIH T32 DK007529 training grant, and included no industry support. Molecular testing was performed by Asuragen, Inc. as part of a separate research investigation funded to the Brigham and Women’s Hospital.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Competing interests
EKA has served as a consultant for Veracyte, Inc. DTR and EKA have previously served on the Scientific Advisory Board of Asuragen, Inc. The other authors declare that they have no conflicts of interest. Molecular testing was performed by Asuragen, Inc. as part of a separate research investigation. The company had no role in the design of this study or decision to submit it for publication.
Authors’ contributions
MM and EKA designed and performed the study, analyzed the data, evaluated the results, and drafted and edited the manuscript. NK, TEA, EM, MIK, MCF, CBB, ESC, JAB, JFK, DTR, NLC, AAG, and FDM collected, analyzed and interpreted the data, and edited the manuscript. All authors read and approved the final manuscript.