- Research article
- Open Access
Longer-term recurrence rate after low versus high dose radioiodine ablation for differentiated thyroid Cancer in low and intermediate risk patients: a meta-analysis
BMC Cancer volume 20, Article number: 550 (2020)
Regarding the longer-term recurrence rate the optimal activity for the remnant thyroid ablation in patients with differentiated thyroid cancer (DTC) is discussed controversially. For the short-term ablation success rate up to 12 months there are already several meta-analyses. In this study we performed the first meta-analysis regarding the longer-term recurrence rate after radioactive 131-I administration.
We conducted an electronic search using PubMed/MEDLINE, EMBASE and the Cochrane Library. All randomized controlled trials (RCTs) assessed the recurrence rate after radioactive iodine ablation in patients with DTC, with a follow-up of at least two years were selected. Statistics were performed by using Review Manager version 5.3 and Stata software.
Four RCTs were included in the study, involving 1501 patients. There was no indication for heterogeneity (I2 = 0%) and publication bias. The recurrence rate among patients who had a low dose 131-iodine ablation was not higher than for a high dose activity (odds ratio (OR) 0.93 [95% confidence interval (CI) 0.53–1.63]; P = 0.79). The mean follow-up time was between 4.25 and 10 years. The subgroup analysis regarding the TSH stimulated thyroglobulin values (< 10 ng/mL versus < 2 ng/mL versus ≤1 ng/mL) showed no influence on recurrence rate.
For the first time we showed that the longer-term, at least 2-year follow-up, recurrence rate among patients who had 131-iodine ablation with 1.1 GBq was not higher than with 3.7 GBq.
Most cases of thyroid cancer are differentiated, with a high five-year survival rate of 90–95% [1, 2]. These patients commonly have total or near-total thyroidectomy followed by radioactive iodine (RAI) ablation and thyroid-stimulation hormone suppression therapy with levothyroxine . In spite of lack of meta-analyses with longer-term follow-up data from RCTs in relation to recurrence rates, US and UK guidelines [4, 5] recommend a low radioactive iodine activity (1.1 GBq) in selected low-risk patients with DTC .
For the ablation success rate up to 12 months follow-up (comparing 1.1 GBq vs 3.7 GBq) in patients with DTC there are various meta-analyses with controversial results [7,8,9,10,11,12,13]. Three of these meta-analyses recommend low dose activity [7, 8, 10]: Cheng et al. analyzed 6 RCTs involving 1809 patients. There was no statistically difference in successful ablation (1.1 GBq vs 3.7 GBq radioiodine) (OR 0.91 [95% CI 0.79–1.04]; P = 0.15), and they found with 1.1 GBq significant benefits in reducing adverse effects . Ma et al. included three RCTs (637 patients with DTC). On the basis of diagnostic scans they found no statistically significant differences between 1.1 GBq and 3.7 GBq radioiodine ablation (OR 0.85 [95% CI 0.49–1.47]; P = 0.56) with significant reduction in adverse events . Valachis et al. analyzed eight randomized trials with 1772 patients. They reported no statistically difference between 1.1 GBq and 3.7 GBq (risk ratio (RR) 0.94 [95% CI 0.85–1.04]; P = 0.21) . Two of the meta-analyses recommend high dose activity [11, 12]: Song et al. included seventeen RCTs, involving 3737 patients. They showed that ablation with 3.7 GBq had statistically significant higher (11%) successful ablation rate than 1.1 GBq (RR 0.89 [95% CI 0.81–0.97]; P = 0.008) . Shengguang et al. analyzed nine RCTs (with 1769 patients). They found that the ablation success was 5% lower using 1.1 GBq compared with 3.7 GBq (OR 0.95 [95% CI 0.91–0.99]) . Two remaining meta-analyses showed that it cannot be determined whether 1.1 GBq or 3.7 GBq should be used [9, 13]: Hackshaw included three RCTs with 148 patients. The ablation success was not significantly different when using 1.1 GBq compared with 3.7 GBq. They recommend large randomized trials to guide this issue . Fang et al. included seven RCTs; they found no significant differences between 3.7 GBq and 1.1 GBq (RR 0.83 [95% CI 0.68–1.01]) .
Regarding the longer-term recurrence rate the optimal activity for the remnant thyroid ablation in patients with differentiated thyroid cancer (DTC) is discussed controversially.
To the best of our knowledge, in this study we performed the first meta-analysis regarding the longer-term recurrence rate after radioactive 131-I administration.
The meta-analysis was performed according to the PRISMA guidelines . The PRISMA check list is provided as Supplemental material [see Additional file 1].
Data search and study selection
The electronic databases of PubMed/MEDLINE, EMBASE and Cochrane Library were systematically searched with the following search strategies (updated on January 11, 2020): PubMed/MEDLINE (http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed): ((“Thyroid Neoplasms/radiotherapy”[Majr] AND ablat*) OR (thyroid AND (cancer OR carcinoma))) AND (radioiodine OR radiotherapy) AND ablat* AND (long-term OR recurrence); EMBASE (http://ovidsp.dc2.ovid.com/sp-4.02.0b/ovidweb.cgi): (((Thyroid and neoplasm* and radiotherapy and ablat*) or (thyroid and (cancer or carcinoma))) and (radioiodine or radiotherapy) and ablat* and (long-term or recurrence)).mp. [mp = title, abstract, heading word, drug trade name, original title, device manufacturer, drug manufacturer, device trade name, keyword, floating subheading word, candidate term word]; The Cochrane Library (https://www.cochranelibrary.com/advanced-search): (Thyroid neoplasms or thyroid) and (cancer or carcinoma) and (radioiodine or radiotherapy) and ablat* and long-term and recurrence; without language and time restriction in any of these databases. Furthermore, references of retrieved studies were searched for eligible studies. Electronic archives of medical societies (Deutsche Gesellschaft für Nuklearmedizin e.V. (https://www.nuklearmedizin.de/jahrestagungen/abstr_online2019/abstract_search.php?navId=227) and Endocrine Society (https://www.endocrine.org/meetings/endo-annual-meetings) were also searched. Studies were included if they met the following inclusion criteria: randomized controlled trial (RTC); patients with differentiated thyroid carcinoma; comparison of low versus high radioiodine ablation activity; longer-term follow-up (at least 2 years after randomization); patients after thyroidectomy, near-total-thyroidectomy or subtotal thyroidectomy as initial ablation therapy; patients with ablative radioiodine therapy, post-operatively; initial assessment of the ablation success within three to 12 months post radioiodine ablation. Exclusion criteria were: Patients with local or regional metastases at inclusion in the study; patients with hemithyroidectomy; patients with medullary or anaplastic carcinomas; no data corning the endpoints; no comparison group available; no randomization performed; duplication of a study (in this case, inclusion of the study with the longest follow-up); only congress communication, not published as full-text paper; animal study.
Data extraction and quality assessment
Two authors (IV and IB) independently reviewed all eligible articles and extracted the relevant data. In case of disagreement, after consultation with a third author (FW) regarding the eligibility, consensus was found. We used the Cochrane risk of bias tool to assess the risk of bias of each trial; following aspects were checked by two independent authors: random sequence generation (selection bias), allocation concealment (selection bias), blinding (performance bias), incomplete outcome data (attrition bias), selective reporting (reporting bias), and other source of bias. The two independent authors evaluated each item as unclear, high or low risk of bias .
After the data extraction a meta-analysis was performed. Heterogeneity and publication bias of the included studies were checked; odds ratio for the primary endpoint was calculated.
The primary endpoint was defined as the recurrence rate between the low and high radioiodine activity, as defined by each eligible study. Recurrence was defined as pathologic findings, as defined by each study (e.g., fine needle aspiration (FNA), serum thyroglobulin (Tg), ultrasonography, diagnostic radioactive iodine scan, PET-Scan or MRI scan) during the follow-up; histologic findings were not defined as conditio sine qua non. Predefined secondary endpoints were: Successful ablation rate at first evaluation between low and high radioidine activity, as defined by each eligible study; definition of successful ablation at first evaluation: No uptake in WBS and/or Tg level < 2.0 ng/mL or < 10.0 ng/mL, as defined by each eligible study; early adverse effects (within 1 week after ablation) related to radioiodine ablation (including salivary dysfunction, neck pain, lacrimal dysfunction, nausea and any serious adverse events). Following subgroup analyses for the primary endpoint were predefined: method of TSH-stimulation (withdrawal versus rhTSH versus both); surgery method (total thyroidectomy vs near-total thyroidectomy vs subtotal thyroidectomy); preablation (131-I ablation) Tg measurements; preablation scan (e.g. Tc99m, 131-I < 2.0 mCi, 131-I ≥ 2.0 mCi); definition of successful ablation (e.g., Tg < 2.0 ng/mL & WBS, Tg < 10.0 ng/mL &WBS, WBS only); sample size, as applicable; patients with lymph node metastases included versus not included; country of origin (europe, asia, others); early adverse effects, if applicable.
In case of heterogeneity a meta-regression analysis (using Stata, Stata Corp, College Station, Texas) with following predefined covariates (potential confounders) was intended: method for TSH-stimulation (withdrawal vs rhTSH); surgery method (total thyroidectomy versus near-total thyroidectomy vs subtotal thyroidectomy); preablation (131-I ablation) Tg measurement; preablation scan; definition of successful ablation; sample size, as applicable; country of origin (europe, asia, others).
The meta-analysis was performed using Review Manager (RevMan) version 5.3. (Nordic Cochrane Center). For the calculation of effect size (odds ratio, 95% CI) we used the random effects model . For the evaluation of heterogeneity Cochran‘s Q statistics  and the I2-statistic  were used; P > 0.1 and I2-statistic values less than 50% were considered as an indication of the lack of heterogeneity. For the assessment of publication bias we used funnel plot (using RevMan (Nordic Cochrane Center)).
Study selection and characteristics
The literature search identified 1709 records with potentially relevant studies. As shown in Fig. 1 four RCTs met the inclusion and exclusion criteria which were included in the meta-analysis [3, 19,20,21]. The included studies had a total of 1501 patients. All of these studies were conducted prospectively. The detailed characteristics of the included studies are given in Table 1.
Risk of bias and publication bias
The risk of bias and quality of included studies are outlined in Fig. 2. Overall, the included studies were carried out well and had a relatively low risk of bias.
The funnel plot suggested no evidence for obvious publication bias [see Additional file 2]. Due to the small number of included studies, the Egger’s regression test was not performed.
Even though there was no indication for heterogeneity (I2 = 0%) between the included studies, for the calculation of the effect size we used the random-effects model, as the test for heterogeneity often has a low power. Moreover, the effect sizes of the included trials can be seen having sampled from a distribution of effect sizes . In our meta-analysis Tau2 is zero, reducing the random-effects analysis to the fixed effect analysis . The included trials showed that the longer-term recurrence rate among patients who had low activity radioactive iodine ablation was not higher than for high dose (OR 0.93 [95% CI 0.53–1.63]; P = 0.79) (Fig. 3).
Mäenpää et al. showed in a randomized, open-label, single center study with 160 patients with papillary or follicular thyroid cancer after total thyroidectomy, comparing 1.1 GBq versus 3.7 GBq radioactive iodine activity, with a follow-up of 51 months (range18–77) that there is no conclusive evidence that 3.7 GBq activity is more effective for ablation of the thyroid remnant than 1.1 GBq activity. The 3.7 GBq activity was associated with more adverse effects .
Kukulska et al. showed in a randomized clinical trial with 309 patients with DTC (265 with papillary and 44 with follicular carcinoma) after total thyroidectomy and appropriate extent of neck lymph node dissection, comparing 30 mCi (1.1 GBq), 60 mCi (2.2 GBq) and 100 mCi (3.7 GBq) radioactive iodine activity, with a medial follow-up of 10 years [2,3,4,5,6,7,8,9,10,11,12] that no significant differences in the 5 year efficacy of thyroid remnant radioiodine ablation using 30, 60 and 100 mCi were observed .
Schlumberger et al. showed in a multicenter, randomized, open-label equivalence trial with 726 patients with low-risk differentiated thyroid cancer who had undergone total thyroidectomy, and a median follow-up since randomization of 5.4 years, comparing 1.1 GBq versus 3.7 GBq iodine-131-activity, that disease recurrence was not related to the strategy used for ablation, and stated that the data valid the use of 1.1 GBq radiodine-131 after rhTSH for postoperative ablation in patients with low-risk thyroid cancer .
Dehbi et al. showed in a non-inferiority, parallel, open-label, randomized controlled study with 438 patients with differentiated thyroid cancer after total or near-total thyroidectomy, comparing 1.1 versus 3.7 GBq radioactive iodine activity, that the recurrence rate among patients who had 1.1 GBq radioactive iodine ablation was not higher than that for 3.7 GBq; as providing further evidence in favor using low-dose radioactive iodine for treatment of patients with low-risk differentiated thyroid cancer. They found that the data indicate that recurrence risk was not affected by use of rhTSH .
The median follow-up time in the included studies in our meta-analysis was between 4.3 and 10 years (range 2–12). The ablation success was defined as Tg < 2 ng/mL or ≤ 1 ng/mL, respectively, in three trials [3, 19, 21] and as Tg < 10 ng/mL in one trial . The subgroup analysis regarding the TSH stimulated thyroglobulin values (< 10 ng/mL versus < 2 ng/mL versus ≤1 ng/mL) showed no influence on longer-term recurrence rate (Fig. 4a).
The subgroup analyses regarding the type of surgery (total thyroidectomy versus total or near-total thyroidectomy) (Fig. 4b) and the stimulation method (rhTSH versus levothyroxine withdrawal) showed no influence on the longer-term recurrence rate (Fig. 4c).
All included trials were conducted with the possibility of patients with lymph node metastases in the included patients; two studies [19, 20] described the status as Nx, whereas in two other studies [3, 21] the possibility was clear described. All included studies were performed in Europe. Adverse effects were not adequately reported in each of the included studies. Thus, subgroup analyses regarding these parameters could not be performed.
Several meta-analyses with a short follow-up (no longer than 2 years) showed conflicting results. Some of these meta-analyses recommend the low-dose RAI ablation [7, 8, 10], other meta-analyses recommend higher ablation activities [11, 12], or failed to conclude which activity is the best in successful ablation rates [9, 13]. This is the first meta-analysis evaluating the longer-term recurrence rate after RAI ablation in patients with DTC. In our meta-analysis the follow-up time was between 2 and 12 years in range. Our results indicate that the longer-term recurrence rate among patients who had low radioiodine ablation activity (1.1 GBq 131-I) was not higher than those who had a higher activity (3.7 GBq 131-I).
The treatment decision for RAI ablation must be individualized based on the individual risk profile of the patient, balancing the risk and benefits . A personalized postoperative approach for the management of DTC with low-risk status should be considered.
The feasibility of a randomized controlled trial investigating potential benefit of adjuvant radioiodine ablation in differentiated thyroid cancer has been frequently discussed; the sample size required to determine whether a mortality benefit exits with this intervention may not be feasible, especially given the rarity of thyroid cancer-related mortality in low-risk papillary cancer patients [23, 24]. However, a randomized controlled trial including a carefully stratified randomization strategy, with the outcome of recurrence may be feasible . Large randomized controlled trials comparing any particular postoperative strategy, especially using recommended response criteria by American Thyroid Association (ATA), with the intention of modulating decision making on RAI remnant ablation or RAI treatment are needed .
According to the nine Martinique principles , the goals of 131-I therapy must be defined, as remnant ablation, adjuvant treatment, or treatment of known disease; the importance of evaluating postoperative disease status and multiple other factors beyond clinicopathologic staging assessments in 131-I, including serum Tg measurement, neck ultrasonography and diagnostic radioactive iodine scanning , therapy decision making should be described; it should be recognized that the optimal administered activity of 131-I adjuvant treatment cannot be definitely determined from the published literature. Until definitive data are available, selection of the administered 131-I activity for individual adjuvant treatment should be preferably based on multidisciplinary team management recommendations .
Various definitions of ablation success concerning stimulated Tg has been used in studies investigating the longer-term recurrence of DTC. According to the 2015 ATA management guidelines for differentiated thyroid cancer, after total thyroidectomy and radioiodine ablation, an excellent response was defined as TSH-stimulated Tg of < 1 μg/mL [4, 28]. Biochemical incomplete response was defined as TSH- stimulated Tg of ≥10 ng/mL; 20% of which develop structural disease, and less than 1% disease specific death . In the primary studies, which we included in our meta-analysis, the ablation success was defined as TSH-stimulated Tg < 2 ng/mL or ≤ 1 ng/mL, respectively, in three trials [3, 19, 21] and as Tg < 10 ng/mL in one trial ; which is concurring with the 2015 ATA guidelines .
Kukulsa et al.  defined TSH-stimulated Tg of < 10 ng/ml (a gray zone) as successful ablation, in agreement with the ATA management guidelines, not as excellence response, but at least not as suspicious of biochemical incomplete response. Our subgroup analysis regarding the TSH-stimulated thyroglobulin values (< 10 ng/mL versus < 2 ng/mL versus ≤1 ng/mL) showed no influence on longer-term recurrence rate (Fig. 4). The 2015 ATA guideline recommend in low-risk and intermediate-risk patients (recommendation No. 63) who have had remnant ablation, measurement of Tg at 16–18 months after TSH stimulation to verify absence of disease (defined as excellence response) . Hence, in further primary studies investigating the long-term recurrence of DTC, for TSH stimulated Tg a cut-off of < 1 ng/mL should be used.
In our study there are some limitations. First one is the small number of included trials. However, currently in the literature there exists only four trials, which meets our inclusion criteria. Second, we cannot exclude publication bias; the visual interpretation of funnel plots may be too subjective, and even in absence of asymmetry in funnel plot, bias cannot be excluded. We did not performed the Egger’s regression test, as it has a low power when the number of studies included is small . Third, due to the small number of trials, the information given by the subgroup analyses is limited.
Our results indicate that the longer-term (median follow-up period 4.3–10 years) recurrence rate among patients who had low radioactive iodine ablation was not higher than for high dose. However, because of the small number of published trials on this issue, further appropriate RCTs analyzing the long-term recurrence after DTC are necessary.
Availability of data and materials
American thyroid association
Differentiated thyroid cancer
Fine needle aspiration cytology
Preferred reporting items for systematic reviews and meta-analyses
Randomized controlled trial
Recombinant human TSH
thyroid stimulating hormone
American Cancer Society. Key statistics for thyroid cancer. 2020. https://www.cancer.org/cancer/thyroid-cancer/detection-diagnosis-staging/survival-rates.html. Accessed 18 Jan 2020.
Cancer Research UK. Thyroid cancer statstics. 2020. https://www.cancerresearchuk.org/about-cancer/thyroid-cancer/survival. Accessed 18 Jan 2020.
Dehbi HM, Mallick U, Wadsley J, Newbold K, Harmer C, Hackshaw A. Recurrence after low-dose radioiodine ablation and recombinant human thyroid-stimulating hormone for differentiated thyroid cancer (HiLo): long-term results of an open-label, non-inferiority randomised controlled trial. Lancet Diabetes Endocrinol. 2019;7(1):44–51.
Haugen BR, Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, et al. 2015 American Thyroid Association management guidelines for adult patients with thyroid nodules and differentiated thyroid Cancer: the American Thyroid Association guidelines task force on thyroid nodules and differentiated thyroid Cancer. Thyroid. 2016;26(1):1–133.
Perros P, Boelaert K, Colley S, Evans C, Evans RM, Gerrard Ba G, et al. Guidelines for the management of thyroid cancer. Clin Endocrinol. 2014;81:1–122.
Blumhardt R, Wolin EA, Phillips WT, Salman UA, Walker RC, Stack BC Jr, et al. Current controversies in the initial post-surgical radioactive iodine therapy for thyroid cancer: a narrative review. Endocr Relat Cancer. 2014;21(6):R473–84.
Cheng W, Ma C, Fu H, Li J, Chen S, Wu S, et al. Low- or high-dose radioiodine remnant ablation for differentiated thyroid carcinoma: a meta-analysis. J Clin Endocrinol Metab. 2013;98(4):1353–60.
Ma C, Tang L, Fu H, Li J, Wang H. rhTSH-aided low-activity versus high-activity regimens of radioiodine in residual ablation for differentiated thyroid cancer: a meta-analysis. Nucl Med Commun. 2013;34(12):1150–6.
Fang Y, Ding Y, Guo Q, Xing J, Long Y, Zong Z. Radioiodine therapy for patients with differentiated thyroid cancer after thyroidectomy: direct comparison and network meta-analyses. J Endocrinol Investig. 2013;36(10):896–902.
Valachis A, Nearchou A. High versus low radioiodine activity in patients with differentiated thyroid cancer: a meta-analysis. Acta Oncol. 2013;52(6):1055–61.
Song X, Meng Z, Jia Q, Zhang L, Xu K, Tan J, et al. Different radioiodine dose for remnant thyroid ablation in patients with differentiated thyroid Cancer: a meta-analysis. Clin Nucl Med. 2015;40(10):774–9.
Shengguang Y, Ji-Eun C, Lijuan HL. I-131 for remnant ablation in differentiated thyroid Cancer after thyroidectomy: a meta-analysis of randomized controlled evidence. Med Sci Monit. 2016;22:2439–50.
Hackshaw A, Harmer C, Mallick U, Haq M, Franklyn JA. 131I activity for remnant ablation in patients with differentiated thyroid cancer: a systematic review. J Clin Endocrinol Metab. 2007;92(1):28–38.
Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7):e1000097.
Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch VA (editors). Cochrane Handbook for Systematic Reviews of Interventions. 2nd ed. Chichester: Wiley; 2019.
DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–88.
Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ. 2003;327(7414):557–60.
Higgins JP, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002;21(11):1539–58.
Maenpaa HO, Heikkonen J, Vaalavirta L, Tenhunen M, Joensuu H. Low vs. high radioiodine activity to ablate the thyroid after thyroidectomy for cancer: a randomized study. PLoS One. 2008;3(4):e1885.
Kukulska A, Krajewska J, Gawkowska-Suwinska M, Puch Z, Paliczka-Cieslik E, Roskosz J, et al. Radioiodine thyroid remnant ablation in patients with differentiated thyroid carcinoma (DTC): prospective comparison of long-term outcomes of treatment with 30, 60 and 100 mCi. Thyroid Res. 2010;3(1):9.
Schlumberger M, Leboulleux S, Catargi B, Deandreis D, Zerdoud S, Bardet S, et al. Outcome after ablation in patients with low-risk thyroid cancer (ESTIMABL1): 5-year follow-up results of a randomised, phase 3, equivalence trial. Lancet Diabetes Endocrinol. 2018;6(8):618–26.
Borenstein M, Hedges LV, Higgins JPT, Rothstein HR. Introduction to meta-analysis. Chisester, UK: John Wiley & Sons, Ltd; 2010.
Sawka AM, Thephamongkhol K, Brouwers M, Thabane L, Browman G, Gerstein HC. Clinical review 170: a systematic review and metaanalysis of the effectiveness of radioactive iodine remnant ablation for well-differentiated thyroid cancer. J Clin Endocrinol Metab. 2004;89(8):3668–76.
Wong JB, Kaplan MM, Meyer KB, Pauker SG. Ablative radioactive iodine therapy for apparently localized thyroid carcinoma. A decision analytic perspective. Endocrinol Metab Clin N Am. 1990;19(3):741–60.
Dragoiescu C, Hoekstra OS, Kuik DJ, Lips P, Plaizier MA, Rodrigus PT, et al. Feasibility of a randomized trial on adjuvant radio-iodine therapy in differentiated thyroid cancer. Clin Endocrinol. 2003;58(4):451–5.
Zakavi SR. Meta-analysis on successful ablation after low- versus high-dose radioiodine therapy in patients with differentiated thyroid carcinoma. Clin Nucl Med. 2016;41(8):674.
Tuttle RM, Ahuja S, Avram AM, Bernet VJ, Bourguet P, Daniels GH, et al. Controversies, consensus, and collaboration in the use of (131)I therapy in differentiated thyroid Cancer: a joint statement from the American thyroid association, the European association of nuclear medicine, the society of nuclear medicine and molecular imaging, and the European thyroid association. Thyroid. 2019;29(4):461–70.
Tuttle RM, Tala H, Shah J, Leboeuf R, Ghossein R, Gonen M, et al. Estimating risk of recurrence in differentiated thyroid cancer after total thyroidectomy and radioactive iodine remnant ablation: using response to therapy variables to modify the initial risk estimates predicted by the new American Thyroid Association staging system. Thyroid. 2010;20(12):1341–9.
Not applicable. No funding was received.
Ethics approval and consent to participate
Consent for publication
KH is a member of the editorial board (Section Editor) of this journal. The authors declare that they have no other competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1 Table S1.
The PRISMA check list.
Additional file 2 Figure S1.
Funnel plot of all included studies evaluating the longer-term recurrence in the low-activity versus high-activity 131-I group in patients with DTC, showing no indication for publication bias.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
About this article
Cite this article
Vardarli, I., Weidemann, F., Aboukoura, M. et al. Longer-term recurrence rate after low versus high dose radioiodine ablation for differentiated thyroid Cancer in low and intermediate risk patients: a meta-analysis. BMC Cancer 20, 550 (2020). https://doi.org/10.1186/s12885-020-07029-3
- Radioactive iodine ablation
- Differentiated thyroid carcinoma