Total Thyroidectomy With and Without Prophylactic Central Neck Lymph Node Dissection in People With Low-risk Papillary Thyroid Cancer

Phase 2

Terminated

Conditions: Endocrine Malignancy
Thyroid Cancer
Low-risk Papillary Thyroid Cancer

Interventions: Procedure: Total Thyroidectomy (TT)
Procedure: Prophylactic central neck lymph node dissection (pCND)

Registration Number: NCT02408887

Lead Sponsor: National Cancer Institute (NCI)

Brief Summary: Background:

- Papillary thyroid cancer (PTC) often spreads to lymph nodes in the neck. This can be hard to detect. People often have lymph nodes removed anyway, and researchers want to study if this is a good idea.

Objective:

- To compare the effectiveness of removing lymph nodes in the neck that show no evidence of cancer along with the thyroid, or removing only the thyroid.

Eligibility:

- Adults age 18 and older with PTC or thyroid nodules suspicious for PTC, with no evidence that the disease has spread in the body.

Design:

* Participants will be screened with medical history, physical exam, blood tests, scans, and x-rays.

* Participants will:

* Answer questions. They may have a tumor biopsy.

* Have a flexible laryngoscopy. A small tube will pass through the nose to the vocal cords.

* Group 1: have surgery to remove the thyroid gland only. Lymph nodes in the neck will be removed if the cancer has spread.

* Group 2: have surgery to remove the thyroid and lymph nodes in the neck.

* At all post-surgery visits, participants will answer questions and have blood drawn. In addition:

* 1 day: laryngoscopy.

* 2 weeks: possible laryngoscopy.

* 3 months: ultrasound of the thyroid and neck.

* Discuss whether to try hormone treatment and/or radioactive iodine.

* Possible diagnostic whole body radioiodine scan (WBS). Participants will swallow a capsule or liquid and lie under a camera.

* 6 months: ultrasound and maybe laryngoscopy.

* 1 year: diagnostic WBS and ultrasound. Participants may get thyroid stimulating hormone.

* Participants will have annual follow-up visits for 10 years. They will have a physical exam, blood drawn, scans, and may complete a questionnaire.

Detailed Description: Background:

* Thyroid cancer is the most common endocrine malignancy and papillary thyroid cancer (PTC) accounts for more than 80% of thyroid cancer.

* The incidence of thyroid cancer has risen over the past decades.

* Central neck lymph node metastasis (LNM) is common in PTC and preoperative imaging studies do not identify all involved lymph nodes in the central neck.

* It remains controversial if prophylactic central neck lymph node dissection (pCND) in patients with low-risk PTC results in lower rates of persistent/recurrent disease and higher complication rates as there has been no randomized controlled trial addressing these issues to date.

* Serum thyroglobulin (Tg), especially when thyroid stimulating hormone (TSH)-stimulated, is a very sensitive and specific marker for persistent/recurrent PTC, in the absence of interfering anti-Tg antibodies.

* Retrospective studies have compared the postoperative TSH-stimulated Tg levels between those who underwent prophylactic central neck dissection (pCND) and those who did not with conflicting results. A randomized trial is needed.

* Health-related quality of life (QOL) is a well-accepted tool to measure the outcome of cancer treatments. Short-form 36 (SF-36) version 2 (v2) questionnaire has been frequently used to evaluate the QOL in patients with thyroid cancer. There is no study evaluating the difference in QOL in patients with low-risk PTC undergoing total thyroidectomy (TT) with and without pCND.

Objectives:

-To determine and compare biochemical cure rates in patients with low-risk PTCs undergoing total thyroidectomy (TT) with and without pCND as measured by postoperative TSH-stimulated serum thyroglobulin (stim-Tg) at 3 months (prior to radioactive iodine treatment (RAI) treatment).

Eligibility:

* Patients greater than or equal to 18 years who have thyroid nodule(s) greater than or equal to 1 cm. but less than or equal to 4 cm. in size with either:

* inconclusive thyroid cytology positive for B-Raf Proto-oncogene Serine/Threonine Kinase (BRAF) Valine 600 Glutamic Acid (V600E) mutation or rearranged in transformation/papillary thyroid carcinomas (RET/PTC) rearrangement or

* cytologically suspicious for or consistent with PTC

* Absence of extrathyroidal extension or lymphadenopathy suggesting metastatic PTC on physical examination and neck ultrasound.

Design:

* Prospective, single-blinded, randomized controlled clinical trial.

* Cytology will be reviewed by Laboratory of Pathology, National Cancer Institute (NCI) or a pathology laboratory at the enrolling institution. Once patients provide written informed consent, they will receive routine history, physical, radiographic (neck ultrasonography (USG), and/or other indicated tests) examinations as well as blood tests. Preoperative fine needle aspiration for cytology and BRAFV600E mutation will be performed if participant has not had either test performed.

* Preoperative assessment of QOL using standardized questionnaire (SF-36 v2) will be obtained within 30 days prior to surgery

* Preoperative vocal cord assessment will be done by flexible laryngoscopy.

* Participants will be randomized after clinical staging, including ultrasonography, to receive TT and pCND or TT alone and will be blinded from the result of randomization and treatment. Patients will remain blinded from treatment assignment for the duration of the study except for patients assigned to TT alone but found to have lymph node metastases as described below.

* If participants in TT alone group are found to have lymph node metastasis at the time of the operation by frozen section analysis, a therapeutic central neck dissection (CND) will be performed. Participants will remain in the intention to treat (TT alone) group. TT patients will be informed if a therapeutic CND is indicated and as such the blind will be broken for these patients prior to study completion.

* All participants will have intact parathyroid hormone (PTH), calcium and electrolytes checked preoperatively, in the morning after surgery, 2 weeks, and 6 months postoperatively.

* Postoperative flexible laryngoscopy will be performed on postoperative day 1 (or postoperative day 2, if it cannot be performed on the first postoperative day) and 6 months postoperatively if vocal cord abnormality is found on postoperative day 1

* Postoperative assessment of QOL will be done on day 1, 2 weeks, 3 months and 6 months, 1, 5 and 10 years postoperatively.

* Participants with postoperative hypoparathyroidism (low PTH and hypocalcemia) will be treated with calcium replacement with or without vitamin D analogue. Serum PTH and electrolytes will be monitored until resolved.

* Stim-Tg will be checked at 3 months postoperatively (prior to RAI scan/ablation, if indicated) and at 1 year postoperatively or 1 year post-remnant ablation. 1 year stim-Tg evaluation will be performed in patients enrolled at the NIH but is optional in patients enrolled at non-NIH site(s) Unstimulated Tg, thyroid function tests, and anti-thyroglobulin antibodies will be checked annually for 10 years.

* Soft tissue neck ultrasonography will be performed in all patients preoperatively and every year postoperatively for the first 10 years.

* If biochemical evidence of tumor recurrence occurs, patients will undergo appropriate radiographic studies and/or nuclear scintigraphy. Tissue biopsy of suspicious lesion(s) will be performed if clinically indicated.

Recruitment & Eligibility

Status: TERMINATED

Sex: All

Target Recruitment: 14

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Arm 1/Total Thyroidectomy (TT) alone	Total Thyroidectomy (TT)	TT alone
Arm 2/Total Thyroidectomy (TT) Plus Prophylactic Central Neck Dissection (pCND)	Total Thyroidectomy (TT)	TT plus pCND
Arm 2/Total Thyroidectomy (TT) Plus Prophylactic Central Neck Dissection (pCND)	Prophylactic central neck lymph node dissection (pCND)	TT plus pCND

Primary Outcome Measures

Name	Time	Method
Number of Participants That Have Biochemical Cure After Total Thyroidectomy (TT) With and Without Prophylactic Central Neck Lymph Node Dissection (pCND)	At 3 months (prior to radioactive iodine (RAI) treatment)	number of participants that have biochemical cure after total thyroidectomy (TT) with and without pCND as measured by postoperative thyroid stimulating hormone (TSH)-stimulated serum thyroglobulin (stim-Tg). Per protocol, Biochemical cure is defined as "stim-Tg \< 2 ng/ml or unstimulated Tg ≤ 0.2 ng/ml" post-surgery. Biochemical persistent or recurrent disease is suspected when stim-Tg ≥5 ng/ml or unstimulated Tg \>0.3 ng/ml or a conversion or a rise in anti-Tg antibodies.

Secondary Outcome Measures

Name	Time	Method
B-Raf Proto-oncogene Serine/Threonine Kinase (BRAF) Valine 600 Glutamic Acid (V600E) Mutation Status on Lymph Node Metastasis	At progression	Correlation between BRAF V600E of tumor
Number of Participants That Have Biochemical Cure After Total Thyroidectomy (TT) With and Without Prophylactic Central Neck Lymph Node Dissection (pCND)	Up to 1 year postoperatively or 1 year post remnant ablation.	Participants that have biochemical cure after TT with and without pCND by postoperative thyroid-stimulating hormone (TSH)-stimulated serum thyroglobulin (stim-Tg) at 1 year postoperatively in participants who will not receive radioactive iodine (RAI) or 1 year post remnant ablation. Per protocol, Biochemical cure is defined as "stim-Tg \< 2 ng/ml or unstimulated Tg ≤ 0.2 ng/ml" post-surgery. Biochemical persistent or recurrent disease is suspected when stim-Tg ≥5 ng/ml or unstimulated Tg \>0.3 ng/ml or a conversion or a rise in anti-Tg antibodies.
Voice Quality After Total Thyroidectomy (TT) With and Without Prophylactic Central Neck Lymph Node Dissection (pCND) at 6 Months	baseline - pre-op and 6 months post-op	Participants that have improvement in voice quality after TT with and without pCND assessed by the Voice Handicap Index-10 questionnaire. The Voice Handicap Index-10 (VHI-10) is a self-administered questionnaire that assesses participant's subjective voice quality. The average voice scores/indices at 6 months post-operation was measured for all participants per group. Minimum score is 0 and maximum score is 40.The higher the score the worse voice quality.
Improvement in Swallowing Impairment After Total Thyroidectomy (TT) With and Without Prophylactic Central Neck Lymph Node Dissection (pCND) at 6 Months	baseline - pre-op and 6 months post-op	Participants that have improvement in swallowing impairment after Total Thyroidectomy (TT) with and without Prophylactic Central Neck Lymph Node Dissection (pCND) assessed by the Swallowing Impairment Score (SIS-6) questionnaire. The average swallowing scores/indices at 6 months post-operation was measured for all participants per group. Minimum score is 0 and maximum score is 24. The higher the score indicates worse swallowing symptoms.
Number of Participants Who Developed Disease Progression or Recurrence After Surgery	Completed at pre-operation (op), 3 months, 6 months, 1 year, 2 years and 3 years post-op.	Disease progression is defined as a clinically detectable evidence of disease recurrence after surgery. Disease recurrence is the progression since participants were deemed to have no evidence of disease after surgery. Post-op ultrasounds were assessed for findings that are indicative/suspicious of disease recurrence. No specific response criteria (i.e. RECIST) was used. Ultrasound of neck soft tissue findings indicate progression/recurrence.
Number of Participants With Hypoparathyroidism	6 months	Number of participants with hypoparathyroidism 6 months post total thyroidectomy with and without prophylactic central neck lymph node dissection. Hypoparathyroidism occurs when one or more of your parathyroid glands are underactive and can lead to low parathyroid hormone and hypocalcemia.
Number of Participants Who Completed Quality of Life (QOL) Survey at Following Timepoints: Quality of Life After Total Thyroidectomy (TT) With and Without Prophylactic Central Neck Lymph Node Dissection (pCND)	pre-operation(op), post-op day 1 and 2, 2 and 3 weeks post-op, 3, 6 and 9 months post-op, 1 and 2 years post-op. Approximately 4 years.	Number of participants that completed the Quality-of-Life SF-36 questionnaire after TT with and without pCND.
Number of Participants That Have Cervical Wound Complications	3 months	number of participants that have cervical wound complications such as a hematoma, seroma, and/or surgical site infection.
Proportion of Participants That Have Less Neck Pain.	6 months	Proportion of participants that have less neck pain assessed by the Neck Pain Scale (0 = no pain, and 10 = unimaginable, unspeakable pain).