Cancer, Medullary Thyroid


Article Author:
Samip Master


Article Editor:
Bracken Burns


Editors In Chief:
Neha Amin
Manuj Agarwal


Managing Editors:
Avais Raja
Orawan Chaigasame
Carrie Smith
Abdul Waheed
Khalid Alsayouri
Frank Smeeks
Kristina Soman-Faulkner
Trevor Nezwek
Radia Jamil
Patrick Le
Sobhan Daneshfar
Anoosh Zafar Gondal
Saad Nazir
William Gossman
Pritesh Sheth
Hassam Zulfiqar
Navid Mahabadi
Steve Bhimji
John Shell
Matthew Varacallo
Heba Mahdy
Ahmad Malik
Mark Pellegrini
James Hughes
Beata Beatty
Nazia Sadiq
Hajira Basit
Phillip Hynes
Tehmina Warsi


Updated:
3/15/2019 9:45:18 AM

Introduction

Medullary thyroid cancer is a tumor arising from the parafollicular cells, or C cells, of the thyroid gland. Medullary thyroid cancer produces calcitonin, and elevated calcitonin levels are an essential feature of this tumor. Recent advances in molecular pathogenesis and genetic testing have led to risk stratification of the patients and identification of molecular targets for therapy. [1][2]Prophylactic thyroidectomy is recommended for patients with mutations that put them at high risk. Various tyrosine kinase inhibitors are approved for use in progressive, metastatic medullary thyroid cancer.[3]

Etiology

Seventy-five percent to 80% of medullary thyroid cancers are sporadic, and the remainder are familial as part of multiple endocrine neoplasia (MEN) 2A, MEN 2B, and familial medullary thyroid cancer (FMTC). RET mutations in neural crest tissue in thyroid gland can lead to medullary thyroid cancer development. Germline mutations are associated with MEN2 and FMTC medullary thyroid cancers. Forty percent to 50% of sporadic medullary thyroid cancers have acquired RET mutations.

Epidemiology

Medullary carcinoma of the thyroid constitutes approximately 4% to 10% of all thyroid cancers in the United States. Sporadic medullary thyroid cancer has a peak incidence in the fifth or sixth decade of life; whereas, those cancers associated with MEN 2A or MEN 2B peak around the second or third decade.[4]

Pathophysiology

As opposed to the sporadic medullary thyroid cancer which is usually unilateral, the medullary thyroid cancer associated with multiple MEN syndromes are usually multicentric and bilateral. Often these tumors involve the upper portions of both lobes because the C cells reside in the upper poles of the thyroid gland. Paraneoplastic syndromes like Cushing syndrome and carcinoid can occur as medullary thyroid cancer, and can also produce hormones like corticotropin, serotonin, prostaglandins, and melanin.

Histopathology

Medullary thyroid cancer is characterized by nests of round or ovoid cells with fibrovascular stroma. There is no follicle development as the tumor is developed from parafollicular C cell of the thyroid.

History and Physical

Approximately 75% to 95% of patients with medullary thyroid cancer present as a thyroid nodule in the upper portion of gland where C cells are located. About 70% will have cervical lymphadenopathy, and a few patients have compression symptoms like dysphagia, hoarseness, or respiratory difficulty. Metastatic spread can be present in less than 10% of patients at presentation. Liver, bone, lung, and brain are common sites for metastases in medullary thyroid cancer. High calcitonin levels can cause diarrhea in few patients.[5][6]

The index case in FMTC and MEN syndrome presents similarly to sporadic medullary thyroid cancer, except that presentation is often at an earlier age compared to sporadic medullary thyroid cancer.

Evaluation

Fine needle aspiration (FNA) of the solitary thyroid nodule or dominant nodule for multinodular thyroid is necessary for the diagnosis. If the FNA is nondiagnostic, sometimes the diagnosis is made after thyroid lobectomy. As the tumor cells originate from the parafollicular C cells, the pathology shows spindle-shaped cells without follicle development. Measuring serum calcitonin before FNA diagnosis is not recommended due to high false positive results. Once the diagnosis of medullary thyroid cancer is made based on histology, serum calcitonin, and carcinoembryonic antigen (CEA) should be measured. These tests help with discovery if the tumor is hypersecreting, and pre-operative levels can be compared to postoperative levels to confirm the biochemical response. The postoperative calcitonin and CEA doubling time provide a sensitive marker for disease progression.

Ultrasonography of the neck and thyroid is indicated once the histological diagnosis is made to evaluate for cervical lymph node involvement. The evaluation for systemic disease using CT neck and imaging of the liver by CT or MRI can be done in patients suspected of having metastatic disease like those with nodal disease and calcitonin level greater than 400 pg/ml. The sensitivity of PET and the nuclear scan is variable and is not recommended for evaluation for metastatic disease.[7][8][9]

It is recommended to discuss the risks and benefits of genetic testing with the patient. Genetic testing for RET protooncogene sequencing of exons 10, 11, and 13 through 16 is necessary to for all patients with parafollicular C cell hyperplasia or sporadic medullary thyroid cancer.

Since the results of genetic testing are rarely available before surgery in sporadic cases, it is recommended to do a biochemical evaluation of possible co-existing tumors associated with MEN2 syndromes before surgery. Screening for hyperparathyroidism and pheochromocytoma by using serum calcium and plasma metanephrines respectively is recommended for a patient with unknown RET mutational status and confirmed germline RET status.

The American Joint Committee on Cancer (AJCC) Staging

Five-year survival for stage I, II, and III MTC is 93% compared to 28% for stage IV.

Treatment / Management

Surgical resection is the primary treatment modality for medullary thyroid cancer. Medullary thyroid cancer does not respond to RAI or conventional chemotherapy. Thyroid-stimulating hormone (TSH) suppression is not required for medullary thyroid cancer as C cells do not have the thyroid-stimulating hormone receptor. As mentioned previously all patients should be evaluated for hyperparathyroidism and pheochromocytoma. If pheochromocytoma is found, it should be removed before thyroid surgery.[10]

Total thyroidectomy is indicated for all patients with medullary thyroid cancer. Bilateral neck dissection (level IV LN) is indicated for tumors more than one cm and bilateral disease while it should also be considered for unilateral tumosr and tumors less than one cm.

In cases of inherited disease, it is recommended to perform total prophylactic thyroidectomy by age five or when the mutation is found, especially with RET mutation codon 609, 611, 618, 630, 634. In multiple endocrine neoplasia 2B with RET codon 883, 918, or compound heterozygotes, prophylactic total thyroidectomy is recommended by age one. In patients with a less high-risk mutation in codon 768, 790, 791, 804, and 891 prophylactic surgery can be deferred if there is no family history for aggressive medullary thyroid cancer, the family agrees to postpone surgery, and annual basal calcitonin and ultrasounds are performed. Adjuvant radiotherapy has not been adequately studied but can be considered in extrathyroid extension and extensive nodal disease.

Two to three months after surgery, CEA and calcitonin levels should be checked. If CEA is within normal limits and calcitonin is not detectable, then the patient is considered cured and has the best prognosis. This group needs to be monitored by annual CEA, calcitonin, and probably ultrasound based on symptoms and physical exam. For multiple endocrine neoplasia 2A and 2b, also perform annual exams for hyperparathyroidism and pheochromocytoma.

Detectable calcitonin or elevated CEA two to three months after surgery raises suspicion for residual disease. These patients should have a neck ultrasound and in cases of calcitonin greater than 150 pg/ml perform further imaging in the form of CT neck, chest and abdomen liver protocol evaluating for metastatic disease. If the imaging is negative and the patient is asymptomatic, continue close surveillance with the physical exam and calcitonin/CEA measurements. If levels remain stable, no further imaging is needed. There is no indication to treat asymptomatic elevated calcitonin. If the imaging is positive and the patient is symptomatic, then consider surgical resection of residual lesions. In case of unresectable disease, consider radiotherapy. Also in cases of unresectable and symptomatic disease, tyrosine-kinase inhibitors (TKI) like vandetanib and cabozantinib are indicated. Vandetanib is an oral receptor kinase inhibitor that inhibits RET, EGFR, and VEGFR. In a phase III study, which included 331 patients with advanced, unresectable or metastatic medullary thyroid cancer, patients showed improved PFS compared to placebo [10]. Cabozantinib is also an oral multikinase inhibitor that inhibits MET, RET, and VEGFR2. In a phase III EXAM study, it showed improvement in PFS in advanced or metastatic medullary thyroid cancer.

Enhancing Healthcare Team Outcomes

Neck masses are commonly seen by primary care givers, nurse practitioners and internists. In most cases, the diagnosis of the neck mass is made by fine needle aspiration. When medullary thyroid cancer is diagnosed, the patient should be referred to a surgeon and an oncologist. In about 25% of cases, MTC is associated with the MEN syndrome.

Surgical resection is the primary treatment modality for medullary thyroid cancer. Medullary thyroid cancer does not respond to RAI or conventional chemotherapy. Thyroid-stimulating hormone (TSH) suppression is not required for medullary thyroid cancer as C cells do not have the thyroid-stimulating hormone receptor. As mentioned previously all patients should be evaluated for hyperparathyroidism and pheochromocytoma. If pheochromocytoma is found, it should be removed before thyroid surgery.[11][12]

Total thyroidectomy is indicated for all patients with medullary thyroid cancer.  Following surgery, patients need life long thyroxine and require monitoring for recurrence, which is rare. Most patients have a good progmosis after surgery.[13] (Level V)


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Cancer, Medullary Thyroid - Questions

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Which condition is associated with amyloid?



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A 33-year-old female who is diagnosed with medullary carcinoma of the thyroid has also been found to be borderline hypertensive. What is the next step in her investigation?



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A 39-year-old female undergoes a thyroidectomy for a mass. Pathology exam reveals a solid mass that stains positive for calcitonin and amyloid. She mentions that one of her brothers also had a similar neck problem. After surgery, the patient should be worked up for which of the following conditions?



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A patient presents with a neck mass which has been confirmed as a medullary thyroid carcinoma (MTC) with a needle aspiration biopsy. What is the next step in the management of this patient?



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C cells (parafollicular cells) are involved with which of the following?



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After a thyroid biopsy, the pathologist reports indicate that amyloid is present in the mass. What is the most likely diagnosis?



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A 55-year-old female has been diagnosed with medullary cancer of the thyroid. Which of the following is the best treatment for this patient?



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Elevated levels of calcitonin are most likely to be seen in patients with which condition?



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A 34-year-old patient has been found to have medullary cancer of the thyroid. What is the next step in the management of this patient?



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Which type of thyroid cancer secretes calcitonin?



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A female with a neck mass undergoes a fine needle aspiration biopsy. The pathologist reports that there is amyloid in the specimen. She may have which of the following conditions?



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A 48-year-old man develops a 2.5-cm, firm thyroid nodule. His neck is supple. Fine-needle aspiration biopsy (FNAB) yields indeterminate results, and he undergoes thyroid lobectomy for histopathologic diagnosis. The final pathology report states medullary thyroid carcinoma. What is the most appropriate next step in managing this nodule?



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Fine needle aspiration of a thyroid mass shows amyloid. What is the most likely diagnosis?



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Which of the following statements about medullary cancer of the thyroid is false?



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Fine needle aspiration of a thyroid mass in a 52-year-old female shows medullary carcinoma. Which of the following is most likely to be elevated in her serum?



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A patient has medullary carcinoma of the thyroid. What lab values are most likely in the initial phase of the disease?



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A 46-year-old man with a thyroid enlargement and family history of thyroid malignancy is informed that the histopathology report of biopsy samples from his thyroid gland reveals medullary thyroid carcinoma. Which of the following is a feature of this tumor?



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A middle age female presents with a lump on the left side of her neck. She noticed it a few weeks ago and thought it would go away, but it has persisted. She denies any symptoms of dysphagia, dyspnea, or pain. She does not have any significant medical history. Since she was adopted, she can't even provide her family history. On physical examination, a 3 x 3 cm irregular hard mass was palpated which also moves with swallowing. There is no cervical adenopathy. While blood work is pending, a fine needle biopsy is performed, and the image is shown. The patient is referred to a surgeon who feels that prior to surgery the patient should undergo testing for which of the following?

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  • Image 6141 Not availableImage 6141 Not available
    Image courtesy S.bhimji MD
Attributed To: Image courtesy S.bhimji MD



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Cancer, Medullary Thyroid - References

References

Hassan A,Siddique M,Riaz S,Khan AI,Nawaz MK,Bashir H, Medullary Thyroid Carcinoma: Prognostic Variables And Tumour Markers Affecting Survival. Journal of Ayub Medical College, Abbottabad : JAMC. 2018 Oct-Dec;     [PubMed]
Guo QQ,Zhang SH,Niu LJ,Zhang YK,Li ZJ,Chang Q, Comprehensive evaluation of medullary thyroid carcinoma before surgery. Chinese medical journal. 2019 Feb 26;     [PubMed]
Opsahl EM,Akslen LA,Schlichting E,Aas T,Brauckhoff K,Hagen AI,Rosenlund AF,Sigstad E,Grøholt KK,Mæhle L,Engebretsen LF,Jørgensen LH,Varhaug JE,Bjøro T, Trends in Diagnostics, Surgical Treatment, and Prognostic Factors for Outcomes in Medullary Thyroid Carcinoma in Norway: A Nationwide Population-Based Study. European thyroid journal. 2019 Jan;     [PubMed]
Hirsch D,Twito O,Levy S,Bachar G,Robenshtok E,Gross DJ,Mazeh H,Benbassat C,Grozinsky-Glasberg S, Temporal Trends in the Presentation, Treatment, and Outcome of Medullary Thyroid Carcinoma: An Israeli Multicenter Study. Thyroid : official journal of the American Thyroid Association. 2018 Mar;     [PubMed]
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Rodríguez-Bel L,Sabaté-Llobera A,Rossi-Seoane S,Reynés-Llompart G,Vercher Conejero JL,Cos-Domingo M,Moreno-Llorente P,Pérez-Maraver M,Cortés-Romera M,Gámez Cenzano C, Diagnostic Accuracy of 18F-FDG PET/CT in Patients With Biochemical Evidence of Recurrent, Residual, or Metastatic Medullary Thyroid Carcinoma. Clinical nuclear medicine. 2019 Mar;     [PubMed]
Viola D,Elisei R, Management of Medullary Thyroid Cancer. Endocrinology and metabolism clinics of North America. 2019 Mar;     [PubMed]
Barletta Carrillo CF,Poterico Rojas JA,Barrionuevo Cornejo C,Casavilca Zambrano S,Pinedo Cárdenas A,Quispe Santibañez I,Castro Mujica MDC, [Familial medullary thyroid carcinoma: case report and literature review.] Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina). 2018 Dec 12;     [PubMed]
Fuchs TL,Bell SE,Chou A,Gill AJ, Revisiting the Significance of Prominent C Cells in the Thyroid. Endocrine pathology. 2019 Jan 29;     [PubMed]
Weber T, Medullary Thyroid Carcinoma: Why Is Specialization Mandatory? Visceral medicine. 2018 Dec;     [PubMed]
Rao SN,Cabanillas ME, Navigating Systemic Therapy in Advanced Thyroid Carcinoma: From Standard of Care to Personalized Therapy and Beyond. Journal of the Endocrine Society. 2018 Oct 1;     [PubMed]
Raue F,Frank-Raue K, Update on Multiple Endocrine Neoplasia Type 2: Focus on Medullary Thyroid Carcinoma. Journal of the Endocrine Society. 2018 Aug 1;     [PubMed]
Saltiki K,Simeakis G,Anagnostou E,Zapanti E,Anastasiou E,Alevizaki M, Different outcomes in sporadic versus familial medullary thyroid cancer. Head     [PubMed]

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