MedPath

FDG-PET/CT in Evaluation of Cytological Indeterminate Thyroid Nodules to Prevent Unnecessary Surgery (EfFECTS)

Not Applicable
Completed
Conditions
Thyroid Nodule
Thyroid Neoplasms
Interventions
Procedure: Diagnostic Thyroid Surgery
Radiation: FDG-PET/CT
Device: Ultrasound of the head and neck
Registration Number
NCT02208544
Lead Sponsor
Radboud University Medical Center
Brief Summary

The purpose of this study is to determine whether the use of molecular imaging using FDG-PET/CT could prevent unnecessary diagnostic thyroid surgery in case of indeterminate cytology during fine-needle aspiration biopsy.

Detailed Description

Rationale: Only about ¼ of patients with thyroid nodules with indeterminate cytology are proven to suffer from a malignancy at diagnostic hemithyroidectomy. Therefore \~¾ is operated upon unbeneficially. Recent studies using FDG-PET/CT have suggested that it can decrease the fraction of unbeneficial procedures from \~73% to \~40%. Thereby the direct costs per patient, the number of hospitalization and average sick leave days might decrease and the experienced HRQoL might increase. A study will be undertaken to show the additional value of FDG-PET/CT after indeterminate cytology with respect to unbeneficial procedures, costs and utilities.

Main objective: To determine the impact of FDG-PET/CT on decreasing the fraction of patients with cytologically indeterminate thyroid nodules undergoing unbeneficial patient management.

Study design: A prospective, multicentre, randomized, stratified controlled blinded trial with an experimental study-arm (FDG-PET/CT-driven) and a control study-arm (diagnostic hemithyroidectomy, independent of FDG-PET/CT-result).

Study population: Adult patients with a cytologically indeterminate thyroid nodule, without exclusion criteria, in 15 (university and regional) hospitals distributed over the Netherlands.

Intervention: One single FDG-PET/low-dose non-contrast enhanced CT of the head and neck is performed in all patients. Patient management depends on allocation and results of this FDG-PET/CT.

Main study parameters/endpoints: The number of unbeneficial interventions, i.e. surgery for benign disease or watchful-waiting for malignancy.

Secondary objectives: complication rate, consequences of incidental PET-findings, number of hospitalisation and sick leave days, volumes of healthcare consumed, experienced health-related quality-of-life (HRQoL), genetic, cytological and (immuno)histopathological features of the nodules.

Sample size calculation/data analysis: Based on above-mentioned estimated reduction in unbeneficial interventions from \~73% to \~40%, at least 90 patients with nodules\>10 mm need to be analyzed (2:1 allocation, α=0.05, power=0.90, single-sided Fisher's exact test). After correction for nodule size and data-attrition, 132 patients need to be included in total. Intention-to-treat analysis will be performed. Incremental Net Monetary Benefit based on the total direct costs per patients and the gain in HRQoL-adjusted survival years are computed. Cytological, histological and genetic parameters for FDG-avidity will be described.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: All patients undergo one FDG-PET/CT scan of head/neck (effective dose: \<3.5 mSv) and are asked to fill in 6 questionnaires at 4 timepoints. FDG-PET/CT negative patients in the experimental arm will undergo a single confirmatory US (±FNAC). An interim/posterior analysis of the control subjects is performed to ensure oncological safety. In case of an unexpected high false-negative ratio in this control arm, all patients will be advised to undergo surgery.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
132
Inclusion Criteria
  1. Documented history of a solitary thyroid nodule or a dominant nodule within multinodular disease, with (US-guided) FNAC performed by a dedicated radiologist or experienced endocrinologist or pathologist, demonstrating an indeterminate cytological examination (i.e. Bethesda category III or IV) according to the local pathologist and confirmed after central review;
  2. Scheduled for surgical excision (preferably) within 2 months of the inclusion date;
  3. Age ≥ 18 years;
  4. Euthyroid state with a serum thyrotropin (TSH) or a free T4 level within the institutional upper and lower limits of normal, measured within 2 months of registration. In case of a suppressed TSH: a negative 123I, 131I or 99mTcO4- scintigraphy must be available ("cold nodule");
  5. In patients with multinodular disease and a dominant nodule, the nuclear medicine physician responsible for FDG-PET/CT scan interpretation must determine whether the nodule is likely to be discriminated on FDG-PET/CT imaging prior to enrolment;
  6. Willing to participate in all aspects of the study;
Read More
Exclusion Criteria

  1. High a priori probability of malignancy:

    • FNAC Bethesda category V or VI during local reading or central review;

    • Prior radiation exposure / radiotherapy to the thyroid;

    • Prior neck surgery or radiation that in the opinion of the PI has disrupted tissue architecture of the thyroid;

    • New unexplained hoarseness, change of voice, stridor or paralysis of a vocal cord;

      • In case a benign reason has been found (e.g. vocal cord edema), the patient is eligible;

    • Thyroid nodule discovered as a FDG-PET positive incidentaloma

    • New cervical lymphadenopathy highly suspicious for malignancy;

      • In case malignancy is excluded, patient is eligible;

    • Previous treatment for thyroid carcinoma or current diagnosis of any other malignancy that is known to metastasize to the thyroid;

    • Known metastases of thyroid carcinoma;

    • Known genetic predisposition for thyroid carcinoma:

      • Familiar Non-Medullary Thyroid Cancer (NMTC)
      • Familiar Papillary Thyroid Cancer (FPTC)
      • Familiar Adenomatoid Polyposis Coli syndrome (FAP, Gardner syndrome, APC-gene mutations on chromosome 5q21)
      • Morbus Cowden (PTEN mutation on chromosome 10q23.3)
      • PTC / nodular thyroid hyperplasia / papillary renal tumours. Linked to locus 1q21.

  2. Proven benign disease or insufficient material for a cytological diagnosis:

    • FNAC Bethesda category I or II during local reading or central review

  3. Performance of non-routine additional diagnostic tests that alter the patients treatment policy (e.g. mutation analysis on cytology)

  4. Inability to undergo randomization:

    • Any patient that will receive thyroid surgery for other reasons (e.g. mechanical or cosmetic complaints).

  5. Inability to undergo treatment:

    • Inability to undergo surgery in the opinion of the surgeon / anaesthetist.

  6. Contra-indications for FDG-PET/CT:

    • Patient has evidence of infection localized to the neck in the 14 days prior to the FDG-PET/CT scan;

    • Inability to tolerate lying supine for the duration of an FDG-PET/CT examination (~10-15min);

    • Poorly regulated diabetes mellitus (see next item);

    • Hyperglycaemia at time of FDG injection prior to PET/CT (fasting serum glucose >200mg/dL [>11.1 mmol/L]);

      • The use of short-acting insulins within 4 hours of the PET scan is not allowed

    • If female and fertile: signs and symptoms of pregnancy or a positive pregnancy test / breast-feeding;

      • A formal negative pregnancy test is not obligatory

    • (severe) claustrophobia;

      • Low dose benzodiazepines are allowed

  7. General contra-indications:

    • Inability to give informed consent;
    • Severe psychiatric disorder;
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Current PracticeDiagnostic Thyroid Surgerydiagnostic thyroid surgery despite results of FDG-PET/CT
Current PracticeFDG-PET/CTdiagnostic thyroid surgery despite results of FDG-PET/CT
FDG-PET/CT-drivenFDG-PET/CTFollowing treatment based on FDG-PET/CT: * negative: watchful waiting including confirmatory ultrasound * positive: diagnostic thyroid surgery as planned
FDG-PET/CT-drivenDiagnostic Thyroid SurgeryFollowing treatment based on FDG-PET/CT: * negative: watchful waiting including confirmatory ultrasound * positive: diagnostic thyroid surgery as planned
FDG-PET/CT-drivenUltrasound of the head and neckFollowing treatment based on FDG-PET/CT: * negative: watchful waiting including confirmatory ultrasound * positive: diagnostic thyroid surgery as planned
Primary Outcome Measures
NameTimeMethod
Fraction of unbeneficial treatment12 months after inclusion

Unbeneficial treatment is defined as either:

* surgery in benign disease

* watchful waiting in malignant disease

benign or malignant disease is defined on final histology (after surgery) or 12 month follow-up including confirmatory neck ultrasonography.

This parameter is compared between both study arms based on intention-to-treat.

Secondary Outcome Measures
NameTimeMethod
Lesion and Patient Characteristics12 months after inclusion

SO1d: To determine the influence of lesion size, pathological classification and patient characteristics on the diagnostic accuracy of FDG-PET/CT.

Fraction Incidental FDG-PET/CT Findings12 months after inclusion

SO1e: To determine whether incorporation of FDG-PET/CT of the head and neck lead to overdiagnosis in non-thyroidal incidental findings.

Fraction of Patients being operated despite negative FDG-PET/CT12 months after inclusion

SO1h: To determine the fraction of patients that cannot be reassured by a negative PET-scan (experimental arm only) despite careful selection of patients (implementability).

Fraction False-Negative FDG-PET/CT's12 months after inclusion

SO1c: To determine the false-negative fraction of FDG-PET/CT in this population.

incremental Net Monetary Benefit12 months after inclusion

SO3d: To determine the incremental Net Monetary Benefit of incorporation of FDG-PET/CT with respect to quality-adjusted life-years (QALYs, based on EQ-5D-5L index and overall survival) saved including sensitivity analysis.

SO3e: To determine the incremental Net Monetary Benefit of incorporation of FDG-PET/CT with respect to decrease in unbeneficial treatment.

Sensitivity analysis will be performed. A mere description will be given as there is no "accepted" value for this kind of analysis.

Fraction Complications12 months after inclusion

SO1b: To determine the effect of incorporation of FDG-PET/CT on the complication-ratio.

HRQoL-scores according to SF36-II, EQ-5D-5L, SF-HLQ and ThyPRO including changesBaseline, 2 months, 6 months and 12 months after inclusion

SO2a: To determine the impact on the experienced HRQoL between the group with and without FDG-PET/CT according to 4 different questionnaires at 4 timepoints during the first 12 months after FDG-PET/CT.

SO2b: To determine whether patients in the experimental arm with negative PET-findings have a different HRQoL than those who receive surgery independent of the FDG-PET/CT results.

Direct Costs12 months after inclusion

SO3a: To determine the effect of incorporation of FDG-PET/CT on the mean direct costs (=volume of care multiplied by activity based costs) per patient during the first 12 months after FDG-PET/CT.

Overall and Disease Free Survival12 months after inclusion

SO1f: To determine the short-term overall and disease free survival in both study arms.

FDG-PET/CT Implementation-hampering Factors12 months after inclusion

SO1g: To determine which factors hamper implementation of this modality for this indication (structured interviews).

Number of Sick Leave Days3 months after inclusions

SO3c: To determine the total number of sick leave days for the first three months in the patients? Do these differ between both study arms?

Tissue Protein- and Gene-expression profile12 months after inclusion of last patient

SO4a: Are there potential protein- or gene-expression profiles, capable of determining the nature of the FNAC-indeterminate nodes (cytology) SO4b: What is the interaction/correlation between the parameters mentioned in SO4a and the results of the FDG-PET/CT scan and the final diagnosis?

Number of Hospitalisation Days12 months after inclusion

SO3b: To determine the effect of incorporation of FDG-PET/CT on the average length of hospital stay for treatment of (complications of) thyroid lesions?

Molecular biomarkers in relation to FDG-PET/CT12 months after inclusion of last patient

SO4b: What is the interaction/correlation between the parameters mentioned in SO4a and the results of the FDG-PET/CT scan and the final diagnosis?

* Can these tissue molecular biomarkers help in selecting the patients that benefit most from FDG-PET, or vice versa?

* Can higher pre-operative diagnostic accuracy be achieved by combining FDG-PET and molecular biomarkers?

* Are molecular biomarkers related to false-positive or false-negative FDG-PET/CT results?

Trial Locations

Locations (15)

Radboudumc

🇳🇱

Nijmegen, Gelderland, Netherlands

MUMC

🇳🇱

Maastricht, Limburg, Netherlands

VUmc

🇳🇱

Amsterdam, Noord-Holland, Netherlands

MeanderMC

🇳🇱

Amersfoort, Utrecht, Netherlands

ErasmusMC

🇳🇱

Rotterdam, Zuid-Holland, Netherlands

Onze Lieve Vrouwe Gasthuis

🇳🇱

Amsterdam, Netherlands

Rijnstate

🇳🇱

Arnhem, Netherlands

Reinier de Graaf Ziekenhuis

🇳🇱

Delft, Netherlands

UMCG

🇳🇱

Groningen, Netherlands

HagaZiekenhuis

🇳🇱

The Hague, Netherlands

UMCU

🇳🇱

Utrecht, Netherlands

Isala Klinieken

🇳🇱

Zwolle, Netherlands

AMC

🇳🇱

Amsterdam, Noord-Holland, Netherlands

St. Antonius

🇳🇱

Nieuwegein, Netherlands

LUMC

🇳🇱

Leiden, Zuid-Holland, Netherlands

© Copyright 2025. All Rights Reserved by MedPath
HomeTerms & ConditionsPrivacy Policy