Study of External Beam Radiotherapy to Thyroid Carcinoma

Thyroid Cancer Clinical Trial

Official title:

A Phase II Study of External Beam Radiotherapy for Locoregionally Advanced or Recurrent Differentiated Thyroid Carcinoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01173289
• Other study ID #: NCCCTS-09-436
• Status: Completed
• Phase: Phase 2
• First received: July 22, 2010
• Last updated: October 5, 2015
• Start date: December 2009
• Est. completion date: August 2015

Study information

• Verified date: October 2015
• Source: National Cancer Center, Korea
• Contact: n/a
• Is FDA regulated: No
• Health authority: Korea: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The primary objective of this study is to estimate the 5 year locoregional control rate after External Beam Radiotherapy (EBRT) in the patient with locally advanced differentiated thyroid cancer. In a prior retrospective trial for this same group of patients, the 5 year locoregional control rate was 85% in EBRT group and 70% in no EBRT group. For the total number of patients to detect a minimum of 20% improvement in 5 year locoregional control rate with 80% of statistical power and the 5% significance level, the table for sample size planning given by Makuch and Simon was chosen. Forty-three patients are required for this regimen to regard as worthy of further investigation. Considering 15% follow up loss, 50 eligible patients will be enrolled.

Description:

The standard approaches to the treatment of differentiated thyroid cancer include surgical resection, radioactive iodine treatment, and thyroid-stimulating hormone suppression. The role of external beam radiotherapy (EBRT), however, remains controversial.

The purpose of this phase II study is to evaluate the impact of EBRT on the locoregional control in locoregionally advanced or recurrent differentiated thyroid cancer patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 62
• Est. completion date: August 2015
• Est. primary completion date: August 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Pathologically confirmed differentiated thyroid cancer

• Patient with locally advanced tumor (T4a, tumor of any size extending beyond the thyroid capsule to invade subcutaneous soft tissues, larynx, trachea, esophagus, or recurrent laryngeal nerve or T4b, tumor invades prevertebral fascia or encases carotid artery or mediastinal vessels or N1b, unilateral, bilateral, or contralateral cervical or mediastinal lymph node positive), or locoregionally recurrent tumor

• All patients must have radiographically assessable disease

• No previous irradiation to the planned field

• Age of = 18 years

• Performance status of 0 to 2 on the Eastern Cooperative Oncology Group (ECOG) score

• Required Entry Laboratory Parameters WBC count = 1,000/mm3; hemoglobin level = 7.5 g/dL; platelet count = 100,000/mm3; creatinine = 3.0 mg/dL

• Oral intake (including J-tube feeding) of = 1,500 calories/day should be maintained.

• Signed informed consent form prior to study entry

Exclusion Criteria:

• Patient with anaplastic carcinoma (focal anaplastic change associate with differentiated thyroid cancer is not excluded)

• Age of <18 years

• Previous history of RT adjacent to planned field

• Poor performance status of 3 to 4 on the Eastern Cooperative Oncology Group (ECOG) score

• Pregnant or breast feeding status

• Previous history of uncontrolled other malignancies within 2 years

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Thyroid Cancer
• Thyroid Diseases
• Thyroid Neoplasms

Intervention

Radiation:
• External Beam Radiotherapy
Definition of target volume: Gross tumor volume (GTV) = gross tumor defined with intravenous bolus contrast administration given CT scan Clinical target volume (CTV) = GTV + included volumes of clinical and suspected subclinical involvement (draining lymph nodes) Planning target volume (PTV) = CTV + 5-10 mm of lateral, craniocaudal, and anteroposterior margins. Radiation dose and planning Total dose 65 Gy for gross tumor, 62.4 Gy for microscopic involved area, 58.5 Gy for high risk lymph node area and 52 Gy for elective lymph node area in 26 fractions during 6 weeks Dose prescription: 90% isodose volume of prescribed dose encompassed PTV The dose-volume histogram (DVH) of targets, such as GTV, CTV, and PTV, and the normal tissues, such as the esophagus, lung, contralateral normal thyroid, arytenoids, vocal cord and spinal cord, etc., was calculated.

Locations

Country	Name	City	State
Korea, Republic of	National Cancer Center, Korea	Goyang-si	Gyeonggi-do

Sponsors (1)

Lead Sponsor	Collaborator
National Cancer Center, Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	All cause mortality		Two Years	No