I-131 Radioiodine Therapy is a targeted nuclear medicine treatment primarily used in the management of differentiated thyroid cancer, such as papillary and follicular carcinoma, especially after surgical removal of the thyroid gland (thyroidectomy). The thyroid gland has a natural tendency to absorb iodine for the production of thyroid hormones. Leveraging this physiological function, radioactive iodine (I-131) is selectively absorbed by any remaining thyroid cells, including normal remnant tissue and potentially malignant or metastatic thyroid cancer cells. The standard therapeutic dose varies depending on the clinical objective—ablation of remnant tissue, adjuvant treatment for possible microscopic disease, or treatment of known metastases. A dose of 150 mCi (millicurie) is typically recommended for ablation or treatment of intermediate-risk thyroid cancer, or in cases of suspected residual or minimal metastatic disease. This therapeutic intervention is designed to reduce recurrence and assist in long-term disease monitoring and control.
How I-131 Works
Radioiodine therapy uses Iodine-131, a radioactive isotope that emits beta radiation, which destroys thyroid tissue and cancer cells by causing DNA damage. When administered orally in capsule or liquid form, I-131 enters the bloodstream and is actively taken up by thyroid cells through the sodium-iodide symporter. Because healthy tissues in the body do not absorb iodine in significant quantities, I-131 provides a highly selective and localized form of radiation therapy, minimizing exposure to other organs.
Indications for I-131 Radioiodine Therapy – 150 mCi
This therapeutic dose of I-131 is commonly indicated in the following clinical scenarios:
Post-thyroidectomy ablation of remnant thyroid tissue
Treatment of regional lymph node involvement
Minimal distant metastasis (e.g., lungs)
Intermediate-risk thyroid carcinoma
Elevated thyroglobulin levels with no evident disease on imaging
Adjuvant therapy to eliminate microscopic residual disease
By eliminating any residual functioning thyroid tissue, the therapy not only lowers recurrence risk but also improves the effectiveness of future thyroglobulin monitoring and whole-body radioiodine scans.
Preparation for I-131 Radioiodine Therapy
Before undergoing radioiodine therapy, certain preparations are essential to ensure the treatment is effective:
1. Elevation of Thyroid Stimulating Hormone (TSH) Levels
To enhance uptake of radioactive iodine by thyroid cells, the TSH level must be elevated above 30 mIU/L. This can be achieved in two ways:
Thyroid Hormone Withdrawal
Discontinuation of thyroid hormone replacement (e.g., Thyronorm or Eltroxin) for 3–6 weeks
Induces hypothyroidism, which naturally increases TSH
May cause temporary symptoms: fatigue, depression, cold intolerance, constipation, and weight gain
Recombinant Human TSH (rhTSH or Thyrogen®) Injection
Synthetic TSH injection administered over two consecutive days
Allows patients to continue their thyroid hormone therapy
Avoids hypothyroid symptoms
May have limited accessibility or be costlier
Both approaches are effective; the choice depends on clinical judgment, patient preferences, and resource availability.
2. Low-Iodine Diet
Patients are advised to follow a low-iodine diet for 1–2 weeks prior to the therapy
This enhances I-131 uptake by depleting the body's iodine reserves
Avoid iodized salt, dairy products, seafood, eggs, soy products, and certain food colorings
3. Baseline Tests and Imaging
Before therapy, your physician may request:
Serum thyroglobulin and anti-thyroglobulin antibody levels
TSH and Free T4 levels
Neck ultrasound
Whole-body iodine scan (pre-therapy diagnostic scan, if required)
These assessments help evaluate the extent of disease and establish a baseline for post-therapy monitoring.
Procedure: What to Expect on the Day of Therapy
The I-131 dose (150 mCi) is administered orally, either as a capsule or liquid
Patients are required to fast for 2 hours before and after the ingestion
Minimal contact with family members, especially children and pregnant women, is recommended for 3–7 days following therapy due to radiation safety
Post-Therapy Instructions and Isolation Guidelines
Since I-131 is excreted through urine, sweat, saliva, and feces, patients are advised to follow radiation safety precautions:
Maintain distance from others, especially vulnerable individuals
Use separate bathrooms if possible
Wash hands frequently and flush toilets twice
Sleep in a separate room for a few days
Avoid public places or workplaces temporarily
Avoid conception (pregnancy) for at least 6 months post-therapy
These measures help protect others from unnecessary radiation exposure.
Possible Side Effects
Though generally well-tolerated, some patients may experience:
Neck pain or swelling due to inflammation of remnant tissue
Dry mouth or altered taste (from salivary gland involvement)
Nausea or fatigue for a few days
Temporary changes in menstrual cycles
Rarely, low blood cell counts or infertility with repeated high doses
Most of these effects are transient and resolve without medical intervention.
Follow-Up After Therapy
About 5–7 days after therapy, a post-therapy whole-body scan may be performed to assess:
Extent of I-131 uptake in residual thyroid tissue or metastasis
Efficacy of ablation or therapy
Guidance for further monitoring or treatment planning
Adjustments in thyroid hormone dosage for optimal suppression of TSH (to reduce cancer recurrence)
Conclusion
I-131 Radioiodine Therapy – 150 mCi plays a critical role in the comprehensive management of differentiated thyroid cancers, particularly after thyroidectomy. It allows for selective destruction of residual thyroid or cancerous tissues, reducing recurrence and enabling more effective long-term surveillance. This therapy is tailored based on individual patient risk factors, staging, and thyroglobulin levels. The 150 mCi dose is considered optimal for intermediate-risk patients or those with suspected minimal residual disease. With appropriate preparation, radiation safety protocols, and follow-up care, I-131 therapy is a safe and effective modality offering long-term disease control and peace of mind to thyroid cancer patients.
Reporting: Not applicable
Some medications interfere with the therapy and may need to be stopped for 03-04 weeks before radioiodine administration. You are advised to call on 7042928881/82 to check for medicine availability and appointment. Depending upon the availability of Medicine, you can stop medications as advised.
Serum TSH level should be measured 1–3 days before radioiodine administration and greater than about 30 mIU/L.
Fasting for 04 hours is needed.
Please carry all medical documents, including doctor referral, surgical discharge summary, histopathological report, previous radioiodine whole body scan reports, image, blood reports, etc.
Female patients are to inform the status of their pregnancy and breastfeeding and take advice from Radiation Safety Officer if any.
The procedure takes 01-02 days.
कुछ दवाएं हैं जो चिकित्सा में बाधा डालती हैं और रेडियोआयोडीन प्रशासन से पहले 03-04 सप्ताह के लिए बंद करने की आवश्यकता होती है। आपको सलाह दी जाती है कि दवा की उपलब्धता और अपॉइंटमेंट की जांच के लिए 7042928881/82 पर कॉल करें। अपॉइंटमेंट शेड्यूल के आधार पर ही सलाह के अनुसार दवा बंद करें।
सीरम टीएसएच स्तर रेडियोआयोडीन चिकित्सा से 1-3 दिन पहले मापा जाना चाहिए और लगभग 30 एमआईयू / एल से अधिक होना चाहिए।
04 घंटे के उपवास की जरूरत है।
कृपया डॉक्टर के रेफरल, सर्जिकल डिस्चार्ज सारांश, हिस्टोपैथोलॉजिकल रिपोर्ट, पिछली रेडियोआयोडीन स्कैन की रिपोर्ट सहित छवि, रक्त रिपोर्ट आदि सहित सभी चिकित्सा दस्तावेज ले आए।
महिला रोगियों को अपनी गर्भावस्था, स्तनपान की स्थिति के बारे में सूचित करना चाहिए और विकिरण सुरक्षा अधिकारी, यदि कोई हो, से सलाह लेनी चाहिए।
प्रक्रिया में 01-02 दिन लगते हैं।
Overnight stay is compulsory for this therapy. Once the radiation level falls below the regulatory authority's permissible limit, the patient is discharged.
On the day of therapy, the patient's medical history is taken after registration and payment, including checking referral, surgical and treatment details, investigation records, history of last meal, etc. Informed consent is also obtained at the same time.
Radioiodine is administered orally, and the patient is detained in an isolation ward.
The next day, they are surveyed to check the radiation level. If it falls below the permissible limit, they are discharged else retained further. If the radiation level is below the limit on the next survey, the patient is released and allowed to go home.
The patient is called again on day 5 for the post-therapy scan.
On the scan day, whole body and static images are obtained. • The duration of the scan may be up to 1.5 hours.
* For details, please see service-related policies
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