2016
DOI: 10.1016/j.ejca.2015.12.006
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Ultrasound surveillance for radiation-induced thyroid carcinoma in adult survivors of childhood cancer

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Cited by 20 publications
(20 citation statements)
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“…Thyroid dysfunction can manifest as primary hyperthyroidism, primary hypothyroidism (either compensated or overt), central hypothyroidism, or a combination of the latter two [22, 23]. Ionizing radiation also increases the risk of both benign and malignant thyroid neoplasms [3, 8, 9, 13, 14, 16, 17, 21, 24-33]. In general, the risk of developing radiation-induced thyroid disease depends on numerous factors, including the age of the child at the time of treatment, the radiation dose delivered to the HPT axis, and the time elapsed since irradiation (Fig.…”
Section: Radiation-induced Thyroid Diseasementioning
confidence: 99%
“…Thyroid dysfunction can manifest as primary hyperthyroidism, primary hypothyroidism (either compensated or overt), central hypothyroidism, or a combination of the latter two [22, 23]. Ionizing radiation also increases the risk of both benign and malignant thyroid neoplasms [3, 8, 9, 13, 14, 16, 17, 21, 24-33]. In general, the risk of developing radiation-induced thyroid disease depends on numerous factors, including the age of the child at the time of treatment, the radiation dose delivered to the HPT axis, and the time elapsed since irradiation (Fig.…”
Section: Radiation-induced Thyroid Diseasementioning
confidence: 99%
“…Currently there is no consensus on the optimal surveillance strategy for thyroid cancer after radiotherapy in CCS. The use of ultrasound for early diagnosis of radiation-induced thyroid cancer may be suitable, nevertheless, routine ultrasound screening in irradiated CCS can actually not be recommended [20].…”
Section: Discussionmentioning
confidence: 99%
“…Follow-up durations since childhood cancer are generally too short to assess the risk for secondary malignant neoplasms in aging childhood cancer survivors. Average follow-up durations since childhood cancer vary between 6.3 and 27.3 years in studies assessing secondary breast cancer risk (Hancock et al 1993, Metayer et al 2000, Ng et al 2002, Bhatia et al 2003, Gold et al 2003, Guibout et al 2005, Inskip & Curtis 2007, Constine et al 2008, Friedman et al 2008, Marees et al 2008, Alm El-Din et al 2009, De Bruin et al 2009, Maule et al 2011, Reulen et al 2011, Cooke et al 2013, Danner-Koptik et al 2013, Little et al 2014, Dorffel et al 2015, Schaapveld et al 2015, and 5.1-27 years in studies investigating secondary thyroid carcinoma risk (Crom et al 1997, Bhatia et al 2002, Cohen et al 2007, Inskip & Curtis 2007, Constine et al 2008, Taylor et al 2009, van Beek et al 2009, Friedman et al 2010, Maule et al 2011, Vivanco et al 2012, Danner-Koptik et al 2013, Caglar et al 2014, Clement et al 2015, de Vathaire et al 2015, Dorffel et al 2015, Brignardello et al 2016. Specific subtypes of secondary malignant neoplasms and potential risk-modifying factors yet unknown may become apparent at an adv...…”
Section: Limitations Of Currently Available Literature and Recommendmentioning
confidence: 99%
“…Besides increasing the risk for differentiated thyroid carcinoma, radiotherapy involving the thyroid gland is also known to promote the occurrence of benign thyroid nodules in childhood cancer survivors (Table 11). Clinically, it may be difficult to distinguish malignant from benign thyroid nodules (Healy et al 1996, Crom et al 1997, Somerville et al 2002, Acharya et al 2003, Haddy et al 2012, Vivanco et al 2012, Kelly et al 2013, Caglar et al 2014, Agrawal et al 2016, Brignardello et al 2016. Studies investigating radiation-related thyroid carcinoma risk after childhood cancer treatment have predominantly assessed older radiotherapeutic modalities.…”
Section: :6mentioning
confidence: 99%
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