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Research ArticleStandard of Care

Management of Differentiated Thyroid Cancer: The Standard of Care

Anca M. Avram, Katherine Zukotynski, Helen Ruth Nadel and Luca Giovanella
Journal of Nuclear Medicine February 2022, 63 (2) 189-195; DOI: https://doi.org/10.2967/jnumed.121.262402
Anca M. Avram
1Division of Nuclear Medicine, Department of Radiology, University of Michigan, Ann Arbor, Michigan;
2Division of Endocrinology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan;
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Katherine Zukotynski
3Departments of Medicine and Radiology, McMaster University, Hamilton, Ontario, Canada;
4Department of Medical Imaging, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada;
5Department of Radiology, University of British Columbia, Vancouver, British Columbia, Canada;
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Helen Ruth Nadel
6Lucile Packard Children’s Hospital at Stanford, Stanford University School of Medicine, Stanford, California;
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Luca Giovanella
7Clinic for Nuclear Medicine and Competence Center for Thyroid Diseases, Imaging Institute of Southern Switzerland, Bellinzona, Switzerland; and
8Clinic for Nuclear Medicine, University Hospital and University of Zurich, Zurich, Switzerland
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  • FIGURE 1.
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    FIGURE 1.

    Radioiodine theranostics for 63-y-old man with 2.2-cm regionally advanced papillary thyroid carcinoma and of 11 lymph nodes dissected, all 11 were positive for metastasis, in surgical specimen of total thyroidectomy. (A) Diagnostic 37-MBq (1 mCi) 131I WBS, anterior projection, depicts multifocal neck activity and diffuse lung activity. (B and C, different anatomic levels within the neck, depicting lymph nodal metastases located in different cervical compartments) Neck SPECT/CT demonstrates iodine-avid soft-tissue nodules consistent with cervical nodal metastases. (D) Chest SPECT/CT demonstrates diffuse lung activity and branching pulmonary vasculature without definite lung nodules identified. Patient received dosimetry-guided 12.6-GBq (340 mCi) 131I treatment. (E) On posttherapy WBS at 3 d, anterior projection demonstrates therapeutic 131I localization to cervical lymph nodal metastases and diffuse miliary pulmonary metastatic disease.

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    FIGURE 2.

    Radioiodine theranostics for 66-y-old woman with 2.5-cm widely invasive follicular thyroid carcinoma with osseous metastatic disease. (A–F) Diagnostic 37-MBq (1 mCi) 131I WBS, anterior projection (A), depicts multifocal skeletal activity, which is further characterized on SPECT/CT as iodine-avid lytic osseous metastases involving right humerus (B), vertebrae (C), pelvis (D) left femoral neck (E), and left femoral diaphysis (F). Patient received dosimetry-guided 12-GBq (325 mCi) 131I treatment. (G) Posttherapy WBS, anterior projection, obtained at 2 d demonstrates therapeutic 131I targeting of extensive iodine-avid multifocal osseous metastatic disease involving axial and proximal appendicular skeleton, with increased lesion conspicuity and numerous new foci detected as compared with diagnostic scan.

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    TABLE 1

    Suggested Framework for 131I Therapy for DTC (28)

    StrategyPrescribed 131I activityClinical context
    Risk-adapted 131I therapy1.11–1.85 GBq (30–50 mCi)Remnant ablation
    1.85–3.7 GBq (50–100 mCi)Adjuvant treatment
    3.7–5.6 GBq (100–150 mCi)Treatment of small-volume locoregional disease
    5.6–7.4 GBq (150–200 mCi)Treatment of advanced locoregional disease or small-volume distant metastatic disease
    Whole-body/blood dosimetry≥7.4 GBq (≥200 mCi), maximum tolerable safe activityTreatment of diffuse distant metastatic disease
    • All pediatric therapeutic 131I activities are adjusted as multiplier based on 70-kg adult body weight.

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    TABLE 2

    Response to Treatment in DTC Patients: Assessment Criteria (4)

    ResponseCriteria
    Excellent (complete)No clinical, biochemical, or structural evidence of disease; definition: negative imaging and either suppressed thyroglobulin < 0.2 ng/mL or stimulated thyroglobulin < 1 ng/mL
    Biochemically incompleteAbnormal thyroglobulin (suppressed thyroglobulin > 1 ng/mL or stimulated thyroglobulin > 10 ng/mL or rising anti–thyroglobulin antibody levels in absence of localizable disease [i.e., negative imaging])
    Structurally incompletePersistent or new locoregional or distant metastases (any thyroglobulin)
    IndeterminateNonspecific biochemical findings (suppressed thyroglobulin = 0.2–1 ng/mL or stimulated thyroglobulin = 1–10 ng/mL or stable/declining anti–thyroglobulin antibody levels) or structural findings that cannot be confidently classified as benign or malignant

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Journal of Nuclear Medicine: 63 (2)
Journal of Nuclear Medicine
Vol. 63, Issue 2
February 1, 2022
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Management of Differentiated Thyroid Cancer: The Standard of Care
Anca M. Avram, Katherine Zukotynski, Helen Ruth Nadel, Luca Giovanella
Journal of Nuclear Medicine Feb 2022, 63 (2) 189-195; DOI: 10.2967/jnumed.121.262402

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Management of Differentiated Thyroid Cancer: The Standard of Care
Anca M. Avram, Katherine Zukotynski, Helen Ruth Nadel, Luca Giovanella
Journal of Nuclear Medicine Feb 2022, 63 (2) 189-195; DOI: 10.2967/jnumed.121.262402
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  • Article
    • Abstract
    • EPIDEMIOLOGY AND CLASSIFICATION
    • DIAGNOSIS
    • SURGICAL TREATMENT
    • POSTOPERATIVE MANAGEMENT
    • 131I THERAPY
    • THYROID HORMONE REPLACEMENT THERAPY
    • DTC MANAGEMENT IN CHILDREN
    • RESPONSE ASSESSMENT AFTER PRIMARY TREATMENT AND FOLLOW-UP
    • TREATMENT OF ADVANCED DISEASE
    • CONCLUSION
    • DISCLOSURE
    • ACKNOWLEDGMENT
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