Thyroid Cancer
The most common endocrine cancer — most types are highly treatable with excellent survival.
Survival Rate
5-year survival: Papillary: >98% | Follicular: ~92% | Anaplastic: ~7%
Incidence
~44,000 new US cases per year
What it is
Overview
Thyroid cancer is the most common endocrine malignancy. It encompasses several distinct types — papillary (most common, ~85%), follicular, medullary, and anaplastic (least common but most lethal). Incidence has risen dramatically over the past decades, largely due to increased detection of small nodules through neck ultrasound. Most thyroid cancers have excellent prognoses; anaplastic thyroid cancer is one of the most lethal cancers known.
Biology
How It Develops
Papillary thyroid cancer is driven by BRAF V600E mutation (~45%) or RET/PTC rearrangements. These activate the MAPK signaling pathway. Medullary thyroid cancer arises from C-cells (parafollicular cells) and is associated with RET proto-oncogene mutations — germline in MEN2 syndrome. Anaplastic thyroid cancer evolves from dedifferentiated papillary or follicular cancer with catastrophic genomic instability.
Warning signs
Symptoms
- Lump or nodule in the neck (most common presentation)
- Hoarseness or voice changes
- Difficulty swallowing
- Neck pain or pressure
- Swollen lymph nodes in the neck
- Anaplastic: rapidly growing neck mass with airway compromise
Detection
Diagnosis Methods
- Neck ultrasound
- Fine-needle aspiration (FNA) biopsy
- Thyroid function tests
- CT or MRI for locally advanced disease
- Thyroglobulin (tumor marker for differentiated thyroid cancer)
- Calcitonin (for medullary thyroid cancer)
- Genetic testing (RET, BRAF, RAS)
Medical care
Treatment Options
- Surgery (thyroidectomy with or without neck dissection)
- Radioactive iodine (RAI/I-131) ablation for differentiated cancer
- TSH suppression therapy (levothyroxine)
- External beam radiation (for invasive or unresectable disease)
- Targeted therapy (lenvatinib, sorafenib for RAI-refractory; vandetanib, cabozantinib for medullary)
- BRAF/MEK inhibitors + pembrolizumab for anaplastic thyroid cancer
Data
Statistics
Survival Rate
5-year survival: Papillary: >98% | Follicular: ~92% | Anaplastic: ~7%
Incidence (US)
~44,000 new US cases per year
Prevention
Risk Factors
- Radiation exposure to the neck or head (especially in childhood)
- Family history of thyroid cancer
- MEN2 syndrome (medullary thyroid cancer)
- Female sex (3x higher risk)
- Age 25–65
Further reading
Resources
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