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Malignancy risk of hyperfunctioning thyroid nodules compared with non-toxic nodules: systematic review and a meta-analysis
Thyroid Research volume 14, Article number: 3 (2021)
Hyperfunctioning or hot nodules are thought to be rarely malignant. As such, current guidelines recommend that hot nodules be excluded from further malignancy risk stratification. The objective of this systematic review and meta-analysis is to compare the malignancy risk in hot nodules and non-toxic nodules in observational studies.
Ovid MEDLINE Daily and Ovid MEDLINE, EMBASE, Scopus, and Web of Science databases were searched. Observational studies which met all of the following were included: (1) use thyroid scintigraphy for nodule assessment, (2) inclusion of both hyperfunctioning and non-functioning nodules based on scintigraphy, (3) available postoperative histopathologic nodule results, (4) published up to November 12, 2020 in either English or French. The following data was extracted: malignancy outcomes include malignancy rate, mapping of the carcinoma within the hot nodule, inclusion of microcarcinomas, and presence of gene mutations.
Among the seven included studies, overall incidence of malignancy in all hot thyroid nodules ranged from 5 to 100% in comparison with non-toxic nodules, 3.8–46%. Odds of malignancy were also compared between hot and non-toxic thyroid nodules, separated into solitary nodules, multiple nodules and combination of the two. Pooled odds ratio (OR) of solitary thyroid nodules revealed a single hot nodule OR of 0.38 (95% confidence interval (CI) 0.25, 0.59), toxic multinodular goiter OR of 0.51 (95% CI 0.34, 0.75), and a combined hot nodule OR of 0.45 (95% CI 0.31, 0.65). The odds of malignancy are reduced by 55% in hot nodules; however, the incidence was not zero.
Odds of malignancy of hot nodules is reduced compared with non-toxic nodules; however, the incidence of malignancy reported in hot nodules was higher than expected. These findings highlight the need for further studies into the malignancy risk of hot nodules.
Autonomously hyperfunctioning thyroid nodules represent approximately 5–10% of all thyroid nodules. These so-called “hot nodules” are defined by increased radiotracer uptake compared to surrounding thyroid parenchyma on scintigraphy. Hot nodules can exist as a single hot nodule or as toxic multi-nodular goiters (TMNG). The degree of autonomous hyperfunction in hot nodules is variable, and some hot nodules may not produce sufficient levels of thyroid hormones to suppress TSH levels at initial presentation [1,2,3,4]. Clinical care pathways for the management of thyroid nodules recommend measurement of serum thyrotropin (TSH) followed by scintigraphy in patients with the presence of thyroid nodules and subnormal TSH levels . Scintigraphy use in patients with normal TSH levels has been questioned  and is more commonly utilized in Europe .
Compared to non-toxic nodules, hot nodules are traditionally believed to have an exceptionally low rate of malignancy. This has led to widely-adopted recommendations by several guideline groups not to perform fine needle aspiration biopsy on these lesions irrespective of their size [1,2,3,4,5,6,7]. However, recent studies have challenged the presumed low-risk of malignancy in hot nodules, suggesting that the incidence of cancer has been underestimated [6,7,8,9,10]. In 22 patients who underwent thyroid surgery irrespective of functional nodule status, Ashcraft and Van Herle reported a malignancy risk of 4% in hot nodules [11, 12]. A recent study demonstrated higher than expected malignancy rates in hot nodules with an overall malignancy rate of 8.5% . The reported malignancy rates of hot nodules ranges broadly from 0.34 to 44% among patients undergoing thyroid surgery [14, 15]. In comparison, the reported malignancy rate of non-toxic nodules ranges from 8 to 16% [7, 11,12,13, 16, 17].
Given the current recommendation against cytologic evaluation of hot nodules, and the widely variable malignancy rate reported in these lesions, there is a need to critically appraise the current literature in this area. Therefore, this systematic review aims to address the question: among those individuals undergoing thyroidectomy for benign indication, are hot nodules diagnosed by scintigraphy associated with a lower risk of thyroid malignancy compared with non-toxic thyroid nodules? Secondary objectives include comparison of malignancy risk in single compared with multiple hot nodules, assessment of reported carcinomas within compared to outside the hot nodule, association of hyperfunctioning on scintigraphy compared with biochemical hyperfunctioning (as determined by TSH levels) and its impact on malignancy, and the impact of inclusion of microcarcinomas on malignancy rates of hot nodules.
Protocol and registration
This systematic review was registered with a pre-published protocol on PROSPERO (CRD42019119204). Reporting was in accordance with the preferred reporting items for systematic review and meta-analyses (PRISMA) .
Search strategy and databases
Two investigators (LL & RP) created a preliminary search strategy that was subsequently refined by a medical librarian (HLR). In brief, a search strategy aimed to include all articles from human studies published up to November 12, 2020 that utilized scintigraphy to assess functional status of thyroid nodules and subsequently included histopathologic data on these nodules. Complete search terms are available in Supplemental Fig. 1. Citations were found by searching the following databases from the first date available to November 12, 2020: Epub Ahead of Print, In-Process & Other Non-Indexed Citations, Ovid MEDLINE Daily and Ovid MEDLINE, EMBASE, Scopus, and Web of Science. Combinations of subject headings, keywords and synonyms used included all three key terms: 1) thyroid nodule, 2) hyperthyroidism, thyrotoxicosis, and hot nodule and 3) thyroid neoplasm, thyroid carcinoma, medullary carcinoma, follicular carcinoma, papillary carcinoma, and anaplastic carcinoma. The formalized search strategy is summarized in the Supplementary information.
After duplicates were removed, two reviewers (LL & AS) independently screened 1464 articles. Initial screen of the title & abstract for full text assessment was determined based on mention of thyroid nodule functional status and inclusion of surgical pathology. An additional 5 articles were added from other sources. These sources include review of references in published reviews and included articles, and additional articles recommended by expert researchers and clinicians in the field. Case reports, review articles, and small series (n ≤ 10) studies were excluded. Studies that included nodules noted outside the thyroid gland were also excluded. Inclusion criteria included studies that used thyroid scintigraphy (131I/123I or T99m) for nodule assessment, inclusion of both hyperfunctioning and normo−/hypo-functioning nodules based on scintigraphy, available postoperative histopathologic nodule results, and no age restriction. The reviewers (LL & AS) independently determined if studies met inclusion and exclusion criteria. Discrepancies were settled by a third reviewer (RP).
Among the articles that met inclusion and exclusion criteria for analysis, the data extracted is summarized in Supplemental Table 1. In brief, quantitative measures included sample size, gender distribution, number of hot nodules and non-hot nodules and distribution of thyroid carcinomas. Binary measures included clear description of the thyroid carcinoma within the nodule, inclusion of microcarcinomas, and presence of genetic mutations. Data management was performed with Microsoft Excel. Furthermore, incidence of malignancy was calculated for all hot nodules and non-toxic nodules.
Analyses were performed exploring the pooled odds ratio (OR) and 95% confidence interval (CI) of malignancy in: 1) single hot thyroid nodules compared with non-toxic nodules based on scintigraphy; 2) toxic multinodular goiters containing a hot nodule compared with non-toxic multinodular goiters; and 3) all hot nodules. Heterogeneity across studies was determined using Cochran’s Q and I2 statistic . Due to the presence of significant heterogeneity, Mantel-Haenszel-weighted DerSimonian and Laird random-effects model were utilized . Meta-regressions were not performed due to limited sample size. All analyses were performed using Stata 14.2 with an alpha of 0.1 and Review Manager 5.3 (Version 5.3.5, The Cochrane Collaboration, Copenhagen, Denmark).
The methodological assessment of included cohort studies was assessed by two independent reviewers (LL, RP) using the Newcastle-Ottawa Scale . The role of this tool is to assess for patient selection bias, and for comparability of study groups and study outcomes.
Our search results are summarized in Fig. 1. Among 2487 citations identified for review, there were 1644 remaining after removal of duplicates. Upon review of title and abstract, 83 full text articles were reviewed. Based on our exclusion criteria, 76 articles were excluded (reasons summarized in Supplementary Tables 2 and 3) with 7 studies included for qualitative and quantitative synthesis.
Characteristics of included studies
A summary of the 7 observational studies included in our synthesis is presented in Table 1 [9, 22,23,24,25,26,27]. Publication dates ranged from 1994 to 2019. Studies originated predominantly from Europe, with 2 of 7 from Italy and 2 of 7 from Turkey. Total number of thyroid nodules across all studies was 7726, which ranged from 120 to 2870 nodules per study. Mean age ranged from 11.5 to 54 years old. Overall, most studies were surgical cohort studies that retrospectively examined predictors of malignancy. Thyroid carcinomas were diagnosed by fine needle aspiration biopsy (FNAB) and/or surgical histology. Scintigraphy was conducted with Tc99m in 5 of 7 studies. In these five studies, scintigraphy was routinely performed in all the patient cohorts. Microcarcinomas were reported in 5 of 7 studies. Microcarcinomas comprised between 9.5 to 100% of the carcinomas reported in the studies. Among the 7 studies, only two study provided clear localization of the thyroid carcinoma within the hot nodule as these pediatric patients only had one nodule [23, 27]. In the other 4 studies, it is unclear if the carcinoma was confirmed within the hot nodule or in adjacent thyroid tissue.
TSH level was measured in all studies. However, only two studies reported the TSH levels and correlated these levels with scintigraphy results [9, 23]. The three other studies did not directly report TSH levels for hot nodules [22, 24,25,26,27].
Malignancy rate in hot nodules
Hot nodules were differentiated into single hot nodules and TMNG. Similarly, non-toxic nodules were differentiated into single non-toxic nodules (NTN) and non-toxic multinodular goiters (MNG). Study outcomes for the odds ratio of single hot nodules versus single NTN are shown in Fig. 2. Pooled odds ratio in 5 studies involving 6778 nodules demonstrated a lower odd of malignancy in single hot nodules (OR = 0.38; 95% CI 0.25, 0.59; I2 = < 0.0002) compared to single NTN. Mon et al. represented a distinct outlier with an OR of 5.50 (95% CI 0.23, 128.97) . Malignancy rates are reported malignancy per rates per nodule. Both Baser et al. and Tam et al. were excluded as it was unclear whether nodules were solitary or MNG [22, 27].
The pooled odds ratio of 4 studies involving 6658 individuals demonstrated a lower odd of malignancy in TMNG compared to non-toxic MNG (OR = 0.51; 95% CI 0.34, 0.75; I2 = 48.3%). These outcomes are summarized in Fig. 3. Mon et al. was a clear outlier in comparison with the three other studies with an OR of 23 (95% CI = 0.61, 862.86) . Corrias et al. was excluded from this analysis as MNGs were absent in their study .
The overall pooled OR for all hot nodules, including both single and multiple nodules, was lower in comparison to all non-hot nodules (OR = 0.45; 95% CI 0.31, 0.65; I2 = 57%). These outcomes are summarized in Fig. 4.
Incidence of malignancy was calculated for all nodules and is summarized in Table 2. Among the 7 studies, the overall incidence of malignancy in all hot nodules ranged from 5 to 100% in comparison with non-toxic nodules, ranging from 3.8–46%. The FNA cytology and surgical histology results are also summarized in Table 2.
Assessment of bias and quality of evidence
Risk of bias was assessed using the Newcastle-Ottawa assessment scale for cohort studies, which evaluated the quality of the evidence based on selection, comparability, and outcome (Table 3) . Only one study was assessed as low risk with 6 stars; however, this study evaluated only pediatric patients . All other studies were assessed as having high risk of bias as they were all surgical cohorts without a non-surgical (ie. medically managed) cohort for comparison, thus awarded 5 stars or less. Furthermore, Mon et al. was assessed with high risk of bias in comparability as this study selected specifically for patients with TSH receptor mutation without a mutation negative study control. Follow up duration and adequacy were not applicable to the assessment.
Post-hoc assessment of malignancy outcomes in studies reporting hot nodules only
Given the higher than expected incidence of malignancy in the included studies, studies that were excluded due to lack of non-toxic nodules were re-examined. Specifically, the incidence of malignancy in hot nodules was evaluated in single hot nodules and TMNG. These findings are reported in Supplementary Table 4. Quantitative assessment was not performed as the comparability of the studies was not appropriate. Incidence of malignancy ranged from 0 to 44% in single hot nodules, 0–26% in TMNG, and 0–29% in all hot nodules (single hot nodules and TMNG).
Furthermore, post hoc analysis of odds of malignancy in only adult patients without a prior knowledge of TSHR mutations is summarized in Supplemental Fig. 1. Pooled ORs of all hot nodules was lower than all non-toxic nodules (ORs 0.43, 95% CI 0.32, 0.58, I2 = 46%).
Case reports identified through the search strategy
Based on our search strategy, 62 case reports of thyroid carcinoma within a hot nodule were identified with publication dates from 1972 to present. Demographic information was extracted from these case reports and are seen in Table 4. Patient age varied from 2 months to 74 years of age. Most hot nodules were single hot nodules, though some TMNGs were also included. Papillary thyroid carcinomas (PTCs) and follicular thyroid carcinomas (FTCs) were the most commonly reported malignancies. However, follicular variant of papillary thyroid carcinomas (fvPTC), Hurthle cell, anaplastic (with a concomitant hot nodule) and medullary thyroid carcinomas (described as a cold area of the HN) were also identified [28, 29].
Among these 62 case reports, only two (4%) reported microcarcinomas within the hot nodules [30, 31]. In all 9 pediatric studies, there was sufficient evidence to support the presence of the thyroid carcinoma within the hot nodule [31,32,33,34,35,36,37,38,39]. In the 53 adult studies, 49% of studies had sufficient evidence to demonstrate thyroid carcinoma presence within the hot nodule [8, 29, 35, 40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63].
This systematic review and meta-analysis of observational studies comparing the malignancy rate of hot nodules compared with non-toxic thyroid nodules demonstrated a reduced malignancy rate in hot nodules; however, the rate was not as low as previously expected. Therefore, the findings of this review prompt us to question the widely adopted recommendation to avoid cytologic evaluation of hot nodules, based on the belief that hot nodules harbour a significantly lower malignancy rate than non-toxic nodules. Our findings cannot definitively support or refute this recommendation; however, this review gives us important insight into the methodological and evidence limitations in this area of the literature, including the need for meticulous cytologic-histologic and imaging correlation of nodules, and the need to explicitly report malignancy rates with and without inclusion of incidental papillary microcarcinomas. Each of these issues will be discussed in detail below.
Location of the thyroid carcinoma within the hot nodule
A major challenge in the assessment of thyroid malignancy, particularly in multinodular goiters, is the location of the malignancy. It is not uncommon for a malignant nodule to co-exist with a benign nodule within the same thyroid lobe. This challenge can also be applied to hot nodules. Schroder and Marthaler evaluated 63 publications describing the presence of hot nodules with concurrent follicular or papillary thyroid cancer . Out of the 63 publications, only 10 provided unequivocal confirmation of the carcinoma within the hot nodules, whereas in the other studies, it was uncertain whether the malignancy was found within the hot nodule or an adjacent non-toxic nodule. Interestingly, this study together with Pazaitou-Panaylotou et al described increased mortality in patients with carcinomas detected within the hot nodule [64, 65].
The identification of the carcinoma within the hot nodule can be technically difficult and requires close interdisciplinary collaboration. Localisation of the thyroid carcinoma in a specific nodule is particularly difficult in multi-nodular thyroid glands. However, accurate cytologic-histologic correlation of carcinomas is critical to understanding the true malignant potential of hot nodules . Among the five studies included in this systematic review, Corrias et al identified the location of the carcinoma . This study differed from the other four studies in that only pediatric patients were included. Given the increased malignancy risk reported in pediatric thyroid nodules compared to the adult population, malignancy rates found in pediatric populations cannot be extrapolated to the adult population . In all 9 pediatric case reports there was sufficient evidence to support the presence of the thyroid carcinoma within the hot nodule as there was a single hot nodule being investigated, which correlated to location of the carcinoma on pathology [31,32,33,34,35,36,37,38,39]. In the 53 adult studies, nearly half (49%) of the studies demonstrated sufficient evidence of the thyroid carcinoma within the hot nodule based on the presence of a single hot nodule on scintigraphy with the location of the carcinoma on pathology [8, 29, 35, 40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63, 67,68,69,70]. The other case reports were confounded by the presence of multiple thyroid nodules, and did not clearly delineate the location of the hot nodule on scintigraphy with pathology.
Inclusion of microcarcinomas
The percentage of carcinomas that were microcarcinomas in the seven included studies ranged from 9.5 to 100%. The increased detection of papillary thyroid microcarcinomas (defined as tumours less than or equal to 10 mm) has contributed significantly to the rise in incidence of thyroid cancer over the last few decades . Microcarcinomas can be found in up to 35% of post-mortem studies ; most of these lesions are believed to be clinically insignificant. This has led to the current American Thyroid Association (ATA) recommendation to monitor sonographically suspicious or biopsy-proven papillary microcarcinomas, in an effort to prevent over-diagnosis and over-treatment of asymptomatic disease. In future studies, these low-risk microcarcinomas should either be analyzed separately, or excluded from the analysis of malignancy rate, to reflect the true risk of clinically significant malignancy in the study population.
Mon et al. as the study outlier
The use of molecular diagnostics is gaining increasing recognition in the assessment of indeterminate thyroid nodules . A clear outlier in this review is a study that deliberately selected indeterminate nodules with TSHR mutations identified by molecular diagnostic testing of indeterminate thyroid nodules . Among the 16 TSHR mutation positive patients with available histology, 3 patients had evidence of thyroid cancer. This study represents a highly selected group with an unusual way of diagnosing hot nodules that is very distinct from the other study populations. A major deficiency in this study is the lack of appropriate clinical diagnosis of hot nodules prior to FNA and molecular diagnostics. TSH was only measured in 27 of the 703 thyroid samples tested for mutations and rearrangements and scintigraphy was used in only 4 of the 6 patients with suppressed TSH. Thus, the OR for this group cannot be generalized for hot nodules.
The notion that hot nodules rarely harbour malignancy is based on studies conducted in the 1960s to 1980s that examined scintigraphy in an undifferentiated patient population with thyroid nodules [12, 74]. At that time, the prevalence of thyroid nodules was estimated at 4 to 7% in the general adult population, with the risk of malignancy ranging from 10 to 20% [75, 76]. Since then, the prevalence of thyroid nodules has increased to 19–67% of the adult population based on increased use of and advances in ultrasonography, with similar malignancy rates of 8–16% [17, 77].
A wide variation of incidence rate of malignancy was reported in both hot nodules and non-toxic nodules in our study. A major confounder in all studies was the inclusion of only patients undergoing partial or total thyroidectomy. Given that these patients were selected for thyroidectomy instead of treatment with antithyroid medication or radioactive iodine therapy, there exists the potential for a selection bias influencing our primary outcome of the true rate of malignancy in hot nodules. For example, in the cohort of patients selected for thyroidectomy, as opposed to monitoring or radioactive iodine therapy, one reason for surgical intervention could be a high-risk sonographic pattern in the index hot nodule or other concurrent non-index lesions. In this cohort, it would be logical to see a higher rate of malignancy than expected. Furthermore, rate of malignancy may also vary based on geographical location, and local clinical practices (predominance of surgical resection versus treatment with radioactive iodine).
Current guidelines for the differential diagnosis and treatment of thyroid nodules recommend clinical assessment and measurement of serum TSH levels [5, 78]. In patients with low TSH levels, the next recommendation involves thyroid scintigraphy with further malignancy risk stratification applied only to non-toxic nodules. The AACE/AME guideline recognise that in geographic regions with past or present iodine deficiency scintigraphy is used as part of the evaluation of patients with MNG and that TSH may remain unsuppressed even when autonomy is present .
Based on this systematic review, we were unable to identify a prospective study that directly compared the malignancy risk of hot nodules with non-toxic nodules in adults. Also, each included study contained one or more limitations that negatively impacted its ability to answer our primary question (see Table 1). The lack of a well conducted prospective study assessing the malignancy risk in all patients with hot nodules, together with the identification of 62 case reports identifying thyroid carcinomas within hot nodules, challenges the hypothesis that hot nodules are rarely malignant.
With limitations in mind, this systematic review demonstrates that the odds of malignancy in hot nodules are reduced by 49–62% compared to non-toxic nodules. However, the overall rate of malignancy observed in hot nodules is higher than expected. Traditionally, hot thyroid nodules were thought to rarely harbour malignancy with rates reported as low as 0.34% . Higher incidence of malignancy in hot nodules was observed in the seven included studies ranging from 10 to 34% (Table 1) [9, 23,24,25,26]. FNA biopsy results available for 4 studies demonstrate a low diagnostic yield of FNA cytology for the diagnosis of malignancy (Table 2). A large number of studies were excluded from analysis for the inclusion of only hot nodules without a comparison with non-toxic nodules (Supplemental Table 3) [7, 10, 13,14,15, 65, 72, 79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98]. Furthermore, the search strategy identified 62 case reports that described the presence of thyroid malignancy within a hot nodule (Table 4).
In summary, this systematic review highlights the need for further research into the malignancy risk assessment of hot nodules. There is sufficient evidence to question the notion that hot nodules rarely harbour thyroid cancer. To adequately address this question, a study of adult patients would need to incorporate both scintigraphically hot and non-toxic nodules, resected for any indication, with histologic correlation of the location of the nodule by pre-operative imaging (ultrasound and scintigraphy) and histologic examination, and exclusion of low-risk papillary microcarcinomas. Furthermore, if hot nodules were to be subjected to further assessment, the ultrasonographic malignancy risk stratification would need to be assessed for this specific population.
Availability of data and materials
All data generated or analysed during this study are included in this published article and its supplementary information files.
Toxic multinodular goiters
Preferred reporting items for systematic review and meta-analyses
Fine needle aspiration biopsy
Papillary thyroid carcinomas
Follicular variant of papillary thyroid carcinomas
American Thyroid Association
Amercian Association of Clinical Endocrinologist (AACE), American College of Endocrinology (ACE) and Associazione Medici Endocrinologi (AME)
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Additional file 1: Supplemental Table 1.
Summary of data points extracted. Supplemental Table 2. Summary of excluded full text articles. Supplemental Table 3. Reasons for article exclusion. Supplemental Table 4. Incidence of malignancy in hot nodules reported in studies examining only hot nodules. Supplemental Figure 1. Pooled odds ratio of combined hot nodules compared with non-toxic nodules excluding pediatric patients and those with known TSHR mutations.
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Lau, L.W., Ghaznavi, S., Frolkis, A.D. et al. Malignancy risk of hyperfunctioning thyroid nodules compared with non-toxic nodules: systematic review and a meta-analysis. Thyroid Res 14, 3 (2021). https://doi.org/10.1186/s13044-021-00094-1
- Thyroid nodules
- Hot nodule
- Thyroid cancer