To Study the Impact of Radiation Treatment After Surgery in Patient With Locally Advanced Thyroid Cancer. (THYRO-RT)
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| ClinicalTrials.gov Identifier: NCT03669432 |
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Recruitment Status : Unknown
Verified March 2020 by Dr. Gouri Pantvaidya, Tata Memorial Hospital.
Recruitment status was: Recruiting
First Posted : September 13, 2018
Last Update Posted : March 16, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Thyroid Cancer Stage IV Radiation Toxicity | Radiation: Intensity Modulated Radiotherapy Procedure: Surgery alone | Not Applicable |
Surgery, when possible offers the best chance of cure for cancer of the thyroid gland. Surgery for thyroid cancer involves removal of the thyroid gland along with removal of the lymph nodes which drain the gland. After surgery most patients will receive radio-iodine treatment to diagnose and treat any spread of the cancer in the body. Most thyroid cancers will have good outcomes with the above mentioned treatment. However, in advanced thyroid cancer there is a higher chance of recurrence even with surgery and radio iodine. Surgery for recurrence of these cancers is very morbid This may entail surgeries which may also involve removing portions of the voice box and food pipe. You may therefore develop and discomfort or inability to eat or speak.
Radiation therapy can be given to the neck along with radio-iodine therapy to decrease these re occurrences of the cancer. A number of studies have shown a benefit with the use of radiation therapy in advanced cases of thyroid cancer. However, the side effects of radiation, if any, have not been well documented. This study is being done to assess the impact of radiation on the outcome of cancer and the exact side effects of radiation therapy. If the side effects are not too many, then radiation therapy can be used to decrease the chances of recurrence in the neck after thyroid.
In this study, patients undergoing total thyroidectomy for thyroid cancer will be assessed for high risk features on the histopathology report and the intra operative findings. Those with advanced thyroid cancer as per the eligibility criteria will be counselled and consented for the study. Those patients willing to participate in the study will be randomised to either receive only surgery and radio-iodine or surgery, radio-iodine and external beam radiation.
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 72 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | Phase II Randomized Controlled Trial Of Postoperative Intensity Modulated Radiotherapy (IMRT) in Locally Advanced Thyroid Cancers. |
| Study Start Date : | July 2013 |
| Estimated Primary Completion Date : | July 2021 |
| Estimated Study Completion Date : | July 2021 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Intensity Modulated radiotherapy
In this Arm, after surgery, patient will receive radio-iodine treatment as per guidelines, 6-8 weeks after surgery. The patient will receive adjuvant radiation therapy about 8-10 weeks after completion of initial surgery. The duration of this radiation therapy will be approximately 45 days. : The goal of the treatment plan would be to encompass the PTV subclinical disease with a dose of 54-60 Gy and the PTV of the gross disease with 70-74 Gy while sparing as much of the aforesaid critical structures as possible. The maximum permissible point doses to the spinal cord will be limited to 46 Gy. IMRT planning and delivery will be carried out on the Tomotherapy Hi Art System. |
Radiation: Intensity Modulated Radiotherapy
The patient will receive adjuvant radiation therapy about 8-10 weeks after completion of initial surgery. The duration of this radiation therapy will be approximately 45 days. : The goal of the treatment plan would be to encompass the PTV subclinical disease with a dose of 54-60 Gy and the planned target volume (PTV) of the gross disease with 70-74 Gy while sparing as much of the aforesaid critical structures as possible. The maximum permissible point doses to the spinal cord will be limited to 46 Gy. IMRT planning and delivery will be carried out on the Tomotherapy Hi Art System. Procedure: Surgery alone This intervention is of no interest |
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Surgery alone
In this Arm, after surgery patient will receive radio-iodine treatment as per guidelines, 6-8 weeks after surgery. Patient under surgery arm will receive no further treatment after surgery and radio-iodine therapy and will be kept on a routine follow up
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Procedure: Surgery alone
This intervention is of no interest |
- locoregional recurrence [ Time Frame: after completion of treatment- till 5 years ]locoregional recurrence is defined as occurrence of pathology proven recurrence in the neck
- acute toxicity [ Time Frame: during treatment- till 23 months ]Acute toxicity will be measured during and after completion of radiation (3 months).
- late toxicity [ Time Frame: at 2 years after treatment completion ]Late toxicity will be measured using the LENT-SOMA scale
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years to 70 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
A) All patients of differentiated thyroid cancer (papillary/follicular/poorly differentiated/) who have undergone total/completion thyroidectomy at our institute and having at least two of the following features (listed below) intra-operatively and/or on histopathology
- Gross extrathyroidal spread into soft tissues of the neck, trachea, esophagus, recurrent laryngeal nerve (constituting stage T4a)
- R1/ shave resections (minimal residual disease)
- R2 resections (gross residual disease)
- Multiple lymph nodes positive(>2) with perinodal extension at level VI B) Normal baseline haematological and biochemical parameters.
Exclusion Criteria:
- Anaplastic or medullary thyroid cancer
- Previous history of radiation
- Pregnancy
- < 18 years Patient unwilling to participate in the study.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03669432
| Contact: Gouri H Pantvaidya, MS | +919833971155 | docgouri@gmail.com | |
| Contact: Sarbani Ghosh-Laskar, MD | 9820834386 | sarbanilaskar@gmail.com |
| India | |
| Gouri Pantvaidya | Recruiting |
| Mumbai, Maharashtra, India, 400012 | |
| Contact: Gouri Pantvaidya, MS +919833971155 docgouri@gmail.com | |
| Principal Investigator: Gouri Pantvaidya, MS | |
| Principal Investigator: Sarbani GhoshLaskar, MD | |
| Sub-Investigator: Sandeep Basu, MD | |
| Sub-Investigator: Anil D'Cruz, MS | |
Documents provided by Dr. Gouri Pantvaidya, Tata Memorial Hospital:
| Responsible Party: | Dr. Gouri Pantvaidya, Associate Professor & Assistant surgeon E, Tata Memorial Hospital |
| ClinicalTrials.gov Identifier: | NCT03669432 |
| Other Study ID Numbers: |
1076 |
| First Posted: | September 13, 2018 Key Record Dates |
| Last Update Posted: | March 16, 2020 |
| Last Verified: | March 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
| Product Manufactured in and Exported from the U.S.: | No |
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locally advanced thyroid cancers, IMRT, toxicity |
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Thyroid Neoplasms Thyroid Diseases Endocrine System Diseases Endocrine Gland Neoplasms |
Neoplasms by Site Neoplasms Head and Neck Neoplasms |

