Anaplastic Thyroid Carcinoma
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Anaplastic carcinoma of the thyroid (ATC) is the most aggressive thyroid gland malignancy. Although ATC accounts for less than 2% of all thyroid cancers, it causes up to 40% of deaths from thyroid cancer. The aggressive nature of ATC makes treatment studies difficult to perform. The overall 5-year survival rate is reportedly less than 10%, and most patients do not live longer than a few months after diagnosis.
See the figure below.
Patients with ATC typically present with a rapidly growing neck mass. Metastases, particularly in the lung, are likely to be present at diagnosis more than 50% of the time. Treatment is mostly palliative. Surgical resection with adjuvant radiation therapy and chemotherapy may prolong survival somewhat and improve quality of life.
For patient education resources, see the Endocrine System Center, as well as Thyroid Problems.
Anaplastic carcinoma of the thyroid (ATC) generally occurs in people in iodine-deficient areas and in a setting of previous thyroid pathology (eg, preexisting goiter, follicular thyroid cancer, papillary thyroid cancer). Local invasion of adjacent structures (eg, trachea, esophagus) commonly occurs.
ATC is believed to occur from a terminal dedifferentiation of previously undetected long-standing thyroid carcinoma (eg, papillary, follicular).
ATC has a genetic association with oncogenes C-myc, H-ras, and Nm23. Mutations in genes that code for BRAF, RAS, catenin (cadherin-associated protein), beta 1, PIK3CA, TP53, AXIN1, PTEN, and APC have been found in ATC, and chromosomal abnormalities are common. [1, 2]
Jonker and collegues performed functional genomic RNA profiling on 25 anaplastic thyroid carcinoma and 80 normal thyroid samples and identified 301 significantly upregulated genes, of which the following were seen as potential therapeutic targets [3] :
Anaplastic carcinoma of the thyroid (ATC) constitutes less than 2% of all thyroid malignancies in the United States, whcih equates to slightly more than 1000 new cases annually. [4] Fortunately, the incidence appears to be declining. Worldwide frequency likely approximates that in the United States.
The female-to-male ratio is approximately 3:1. Peak incidence occurs during the sixth to seventh decades of life. The age range of affected patients reportedly is 15-90 years.
ATC has a rapidly progressive course and early dissemination. The most common sites of distant spread include, in descending order, the lung, bone, and brain. Metastases, particularly in the lung, are likely to be present at diagnosis in more than 50% of cases. The overall 5-year survival rate is reportedly less than 10%, and most patients do not live longer than a few months after diagnosis. [5]
One study has shown that patients younger than 60 years who have ATC confined to the thyroid have a better prognosis than patients who are older and have distant metastases. [6] A retrospective study from Korea found that age less than 60 years, tumor size less than 7 cm, and lesser extent of disease were independent predictors of lower disease-specific mortality. [7]
While some studies have suggested that postoperative radiotherapy may be of benefit in terms of survival, definitive prospective trials are lacking.
Akaishi et al conducted a review of 100 patients with ATC in a single hospital (Ito Hospital) from 1993-2009. [8] The 1-year survival rates were as follows:
Multivariate analysis demonstrated worse prognosis with age older than 70 years, white blood cell count of 10,000/μL or more, extrathyroidal invasion, and distant metastases at the time of diagnosis. Survival was significantly better if the patient received complete resection, external radiation at doses of 40 Gy or more, or both. [8]
Orita et al developed a prognostic index that can predict prognosis and assist in the early treatment of ATC. [9]
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Wong DD, Spagnolo DV, Bisceglia M, et al. Oncocytic adrenocortical neoplasms–a clinicopathologic study of 13 new cases emphasizing the importance of their recognition. Hum Pathol. 2011 Apr. 42(4):489-99. [Medline].
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Godbert Y, Henriques de Figueiredo B, Bonichon F, Chibon F, Hostein I, Pérot G, et al. Remarkable Response to Crizotinib in Woman With Anaplastic Lymphoma Kinase-Rearranged Anaplastic Thyroid Carcinoma. J Clin Oncol. 2015 Jul 10. 33 (20):e84-7. [Medline].
Hahn SY, Shin JH. Description and Comparison of the Sonographic Characteristics of Poorly Differentiated Thyroid Carcinoma and Anaplastic Thyroid Carcinoma. J Ultrasound Med. 2016 Sep. 35 (9):1873-9. [Medline]. [Full Text].
Bogsrud TV, Karantanis D, Nathan MA, Mullan BP, Wiseman GA, Kasperbauer JL, et al. 18F-FDG PET in the management of patients with anaplastic thyroid carcinoma. Thyroid. 2008 Jul. 18(7):713-9. [Medline].
Bhatia A, Rao A, Ang KK, Garden AS, Morrison WH, Rosenthal DI, et al. Anaplastic thyroid cancer: Clinical outcomes with conformal radiotherapy. Head Neck. 2009 Nov 2. [Medline].
Noguchi H, Yamashita H, Murakami T, Hirai K, Noguchi Y, Maruta J, et al. Successful treatment of anaplastic thyroid carcinoma with a combination of oral valproic acid, chemotherapy, radiation and surgery. Endocr J. 2009 Apr. 56(2):245-9. [Medline].
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Wiseman SM, Masoudi H, Niblock P, Turbin D, Rajput A, Hay J, et al. Anaplastic thyroid carcinoma: expression profile of targets for therapy offers new insights for disease treatment. Ann Surg Oncol. 2007 Feb. 14(2):719-29. [Medline].
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[Guideline] 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 Jan. 26 (1):1-133. [Medline]. [Full Text].
[Guideline] Smallridge RC, Ain KB, Asa SL, Bible KC, Brierley JD, Burman KD, et al. American Thyroid Association guidelines for management of patients with anaplastic thyroid cancer. Thyroid. 2012 Nov. 22 (11):1104-39. [Medline]. [Full Text].
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Anastasios K Konstantakos, MD Clinical Associate Surgeon, Department of Cardiovascular Surgery, Billings Clinic
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference
Disclosure: Received salary from Medscape for employment. for: Medscape.
Neetu Radhakrishnan, MD Associate Professor (Adjunct) of Medicine, Division of Hematology/Oncology, University of Cincinnati Medical Center; Hematology/Oncology Medical Director, West Chester Outpatient Clinics
Neetu Radhakrishnan, MD is a member of the following medical societies: American College of Physicians, American Society of Clinical Oncology, American Society of Hematology
Disclosure: Nothing to disclose.
Lodovico Balducci, MD Professor, Oncology Fellowship Director, Department of Internal Medicine, Division of Adult Oncology, H Lee Moffitt Cancer Center and Research Institute, University of South Florida Morsani College of Medicine
Lodovico Balducci, MD is a member of the following medical societies: American Association for the Advancement of Science, American Association for Cancer Research, American College of Physicians, American Geriatrics Society, American Society of Hematology, New York Academy of Sciences, American Society of Clinical Oncology, Southern Society for Clinical Investigation, International Society for Experimental Hematology, American Federation for Clinical Research, American Society of Breast Disease
Disclosure: Nothing to disclose.
Debra J Graham, MD, is gratefully acknowledged for the contributions made to this topic.
Anaplastic Thyroid Carcinoma
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