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NCT06820554Not yet recruiting

Thyroid Dysfunction Induced by Radiotherapy Treatment in Patients with Breast Cancer

Source: ClinicalTrials.gov · Last updated 11 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Breast cancer is the most common cancer and second most common cause of cancer death among US women,. External beam radiation therapy (RT) that involves the breast and regional lymph nodes, including axillary and supraclavicular (SCV) lymph nodes, has been demonstrated to decrease the risk of local recurrence and improve long-term survival in high-risk breast cancer patients . However, RT-induced toxicities to adjacent normal tissues can lead to serious morbidity in cancer survivors . The thyroid regulates the body's metabolism via producing thyroxine (T4) and triiodothyronine (T3) hormones. As the thyroid is sensitive to RT, radiation-induced thyroid disorders have been reported in cancer patients who received radiation in the cervical or SCV regions . In breast cancer patients, RT to the SCV area has been associated with a higher incidence of Hypothyriodism, particularly in younger patients This complication may be associated with radiation-induced thyroid volume reduction . Recent studies,have reported a significant decrease in thyroid volume (14-30 %) in patients with laryngeal or nasopharyngeal carcinoma (NPC), suggesting an association between HT and post-RT thyroid atrophy . Little is known about the changes of thyroid gland volume based on local thyroid gland radiation dose and its correlations with incidence of HT. Our study aim the changes in thyroid volume of breast cancer patients who received RT to the SCV nodal area, to evaluate RT-induced thyroid gland evolution based on local radiation dose. We then assessed the association between thyroid volume changes and the incidence of post-RT Hypothyrodism in breast cancer patients. the aim of the study to diagnose subclinical hypothyroidism and biochemical changes in thyroid function after radiotherapy for breast cancer

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
97 (estimated)
First submitted
6 Feb 2025
Start date
1 Mar 2025
Primary completion date
1 Mar 2026
Lead sponsor
Assiut University
NCT number
NCT06820554

What you commit to

  • Study type: Observational
  • Planned participants: 97
  • From 1 Mar 2025 to the primary completion date, 1 Mar 2026
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Thyriod dysfunction of any othe cause( no known pretreatment primary thyroid disease or dysfunction; no prior thyroid surgery; and no prior RT that involved the hypothalamic-pituitary axis or thyroid

Who the study is looking for

  • \>18 yrs old breast cancer ( pathological proved )
  • Stage II/III breast cancer
  • High risk local recurrence ( LVI/ G3/ LN positive)
  • Non metastatic breast cancer

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.