Low versus high 131I therapeutic effectiveness for differentiated thyroid cancer with intermediate risk of recurrence
Main Article Content
Abstract
High 131I is recommended for the treatment of differentiated thyroid cancer (DTC) with the intermediate-to-high risk of recurrence. Since the lower 131I gives the lower side effects, the lower chance of secondary cancer and the lower radiation hazard, reduction of 131I doses with similar clinical outcomes is challenging. The aim of this study was to compare and assess the clinical outcome of low (30 mCi) and high (150 mCi) 131I treatment for DTC with the intermediate risk of recurrence. All DTC with the intermediate risk of recurrence between 2012 and 2019 were consecutively included. They were excluded if they had the blood tests of Thyroid-stimulating hormone (TSH) of ≤ 25 µIU/L on the day before 131I oral administration or during the first diagnostic total body study or having received an injection of thyrotropin alfa, having previous treatment for thyroid cancer except for surgery, and having incomplete medical records. Six hundred sixty-six patients with DTC with the intermediate risk of recurrence were included, 50 were in the low 131I and 616 were in the high 131I. Patients in the high 131I showed a higher odd of remission with an adjusted odds ratio of 1.96 (95% CI: 1.01 to 3.81; p = 0.048), compared to the low 131I. Therapeutic effectiveness of the low 131I for DTC with the intermediate risk of recurrence was lower than that of the high131I. Therefore, use of low 131I in patients who were in the misclassification of risk stratification of low-risk changing to intermediate-risk tended to be uncured.
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
References
National Cancer Institute Surveillance E and End Results Program. Cancer stat facts: Thyroid cancer [Internet]. 2019 [cited 2019 Mar 11]. Available from: https://seer.cancer.gov/statfacts/html/thyro.html.
Tuttle RM, Haugen B, Perrier ND. Updated American joint committee on cancer/tumor-node-metastasis staging system for differentiated and anaplastic thyroid cancer (eighth edition): what changed and why?. Thyroid. 2017;27(6):751-756.
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.
Ylli D, Nostrand VD, Wartofsky L. Conventional radioiodine therapy for differentiated thyroid cancer. Endocrinol Metab Clin North Am. 2019;48(1):181-197.
Asa SL. The current histologic classification of thyroid cancer. Endocrinol Metab Clin North Am. 2019;48(1):1-22.
Vaisman F, Tuttle RM. Clinical assessment and risk stratification in differentiated thyroid cancer. Endocrinol Metab Clin North Am. 2019;48(1):99-108.
Lamartina L, Durante C, Filetti S, Cooper DS. Low-risk differentiated thyroid cancer and radioiodine remnant ablation: a systematic review of the literature. J Clin Endocrinol Metab. 2015;100(5):1748-1761.
Ha S, Oh SW, Kim YK, Koo do H, Jung YH, Yi KH, et al. Clinical outcome of remnant thyroid ablation with low dose radioiodine in Korean patients with low to intermediate-risk thyroid cancer. J Korean Med Sci. 2015;30(7):876-881.
Du P, Jiao X, Zhou Y, Li Y, Kang S, Zhang D, et al. Low versus high radioiodine activity to ablate the thyroid after thyroidectomy for cancer: A meta-analysis of randomized controlled trials. Endocrine. 2015;48(1):96-105.
Ain KB. Radioiodine-remnant ablation in low-risk differentiated thyroid cancer: pros. Endocrine. 2015;50(1):61-66.
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.
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):1353-1360.
Valachis A, Nearchou A. High versus low radioiodine activity in patients with differentiated thyroid cancer: a meta-analysis. Acta Oncol. 2013;52(6):1055-1061.
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):774-779.
Shengguang Y, Eun JC, Lijuan HL. I-131 for remnant ablation in differentiated thyroid cancer after thyroidectomy: a meta-analysis of randomized controlled evidence. Med Sci Monit. 2016;22:2439-2450.
Schmidt D, Szikszai A, Linke R, Bautz W, Kuwert T. Impact of 131I SPECT/SPIRAL CT on nodal staging of differentiated thyroid carcinoma at the first radioablation. J Nucl Med. 2009;50(1):18-23.
Grewal RK, Tuttle RM, Fox J, Borkar S, Chou JF, Gonen M, et al. The effect of posttherapy 131I SPECT/CT on risk classification and management of patients with differentiated thyroid cancer. J Nucl Med. 2010;51(9):1361-1367.
Mizokami D, Kosuda S, Shiotani A, Kinoshita F, Saotome K, Morozumi K. Impact of 131I SPECT/CT on the management of differentiated thyroid carcinoma outpatients with radioablation. J Otolaryngol Jpn. 2014;117(5):673-680.
Hassan FU, Mohan HK. Clinical utility of SPECT/CT imaging post-radioiodine therapy: does it enhance patient management in thyroid cancer?. Eur Thyroid J. 2015;4(4):239-245.
Szujo S, Sira L, Bajnok L, Bodis B, Gyory F, Nemes O, et al. The impact of post-radioiodine therapy SPECT/CT on early risk stratification in differentiated thyroid cancer; a bi-institutional study. Oncotarget. 2017;8(45):79825-29834.
Zilioli V, Peli A, Panarotto MB, Magri G, Alkraisheh A, Wiefels C, et al. Differentiated thyroid carcinoma: incremental diagnostic value of (131)I SPECT/CT over planar whole body scan after radioiodine therapy. Endocrine. 2017;56(3):551-559.
Tuttle RM, Haugen B, Perrier ND. Updated American joint committee on cancer/tumor-node-metastasis staging system for differentiated and anaplastic thyroid cancer (eighth edition): what changed and why?. Thyroid. 2017;27(6):751-756.
Kay FU, Kandathil A, Batra K, Saboo SS, Abbara S, Rajiah P. Revisions to the tumor, node, metastasis staging of lung cancer (8th edition): rationale, radiologic findings and clinical implications. World J Radiol. 2017;9(6):269-279.
Reiners C, Hänscheid H, Verburg FA, Mäder U. Long-term survival in differentiated thyroid cancer is worse after low-activity initial post-surgical 131I therapy in both high- and low-risk patients. J Clin Endocrinol Metab. 2014;99(12):4487-4496.
Jeon MJ, Kim WG, Park WR, Han JM, Kim TY, Song DE, et al. Modified dynamic risk stratification for predicting recurrence using the response to initial therapy in patients with differentiated thyroid carcinoma. Eur J Endocrinol. 2014;170(1):23-30.
Cheng F, Chen Y, Zhu L, Zhou B, Xu Y, Chen Y, et al. Risk factors for cervical lymph node metastasis of papillary thyroid microcarcinoma: a single-center retrospective study. Int J Endocrinol. 2019;2019:8579828.
Verburg FA, Aktolun C, Chiti A, Frangos S, Giovanella L, Hoffmann M, et al. Why the European association of nuclear medicine has declined to endorse the 2015 American thyroid association management guidelines for adult patients with thyroid nodules and differentiated thyroid cancer. Eur J Nucl Med Mol Imaging. 2016;43(6):1001-1005.
Verburg FA, Mader U, Reiners C, Hanscheid H. Long-term survival in differentiated thyroid cancer is worse after low-activity initial post-surgical 131I therapy in both high- and low-risk patients. J Clin Endocrinol Metab. 2014;99(12):4487-4496.
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):1150-1156.
Trimboli P, Crescenzi A, Giovanella L. Performance of Italian consensus for the classification and reporting of thyroid cytology (ICCRTC) in discriminating indeterminate lesions at low and high risk of malignancy. A systematic review and meta-analysis. Endocrine. 2018;60(1):31-35.
Jeong JH, Kong EJ, Jeong SY, Lee SW, Cho IH, Chun AK, et al. Clinical outcomes of low-dose and high-dose postoperative radioiodine therapy in patients with intermediate-risk differentiated thyroid cancer. Nucl Med Commun. 2017;38(3):228-233.
Súss SKA, Mesa CO, Carvalho GAD, Miasaki FY, Chaves CP, Fuser DC, et al. Clinical outcomes of low and intermediate risk differentiated thyroid cancer patients treated with 30 mCi for ablation or without radioactive iodine therapy. Arch Endocrinol Metab. 2018;62(2):149-156.
Qu Y, Huang R, Li L. Low-and high-dose radioiodine therapy for low-/intermediate-risk differentiated thyroid cancer: a preliminary clinical trial. Ann Nucl Med. 2017;31(1):71-83.
Seo M, Kim YS, Lee JC, Han MW, Kim ES, Kim KB, et al. Low-dose radioactive iodine ablation is sufficient in patients with small papillary thyroid cancer having minor extrathyroidal extension and central lymph node metastasis (T3N1a). Clin Nucl Med. 2017;42(11):842-846.