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Papillary thyroid cancer medical therapy

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2] Ammu Susheela, M.D. [3]

Overview

Overview

Treatment options for papillary thyroid cancer differes according to the stage and invasion of the tumor and include surgery, external beam radiation therapy ( EBRT), Thyroid suppression therapy, and targeted therapy.

Medical Therapy

Medical Therapy

  • Treatment options for papillary thyroid cancer include:[1]
 
 
 
 
 
 
 
 
Papillary thyroid cnacer treatment
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Localized or regional tumor
 
 
 
 
Metastatic
 
 
 
 
Recurrent
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Surgery
Total thyroidectomy
Lobectomy
RAI therapy
Thyroid suppression therapy
EBRT
 
 
 
 
 
 
 
 
 
 
 
 
Surgery ± postoperative RAI therapy
Targeted therapy
EBRT
Chemotherapy
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Iodine sensitive
 
 
 
Iodine resistent
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
RAI therapy
Thyroid suppression therapy
 
 
 
Thyroid suppression therapy
Targeted therapy
Surgery
EBRT
 
Papillary Thyroid Cancer Treatment Options
  • Pharmacologic medical therapies for papillary thyroid cancer include thyroid-suppression therapy, and/or targeted therapy.

Thyroid-suppression therapy

Targeted therapy

  • This type of treatment is done using:[2][3]
    • Sorafenib, an Sorafenib is an orally active, multityrosine kinase inhibitor.
    • Lenvatinib, an orally active, multitargeted tyrosine kinase inhibitor.[4]
      • Adult
        • Preferred regimen: Lenvatinib 24 mg PO daily until disease progression or unacceptable toxicity.
        • Alternative regimen: Sorefenib 400 mg PO q12h until disease progression or unacceptable toxicity.
        • Alternative regimen: Larotrectinib 100 mg PO q12h until disease progression or unacceptable toxicity.
        • Alternative regimen: Entrectinib 600 mg PO daily until disease progression or unacceptable toxicity.
References

References

  1. “Thyroid Cancer Treatment (Adult) (PDQ®)–Health Professional Version – National Cancer Institute”.
  2. Carhill AA, Cabanillas ME, Jimenez C, Waguespack SG, Habra MA, Hu M, Ying A, Vassilopoulou-Sellin R, Gagel RF, Sherman SI, Busaidy NL (January 2013). “The noninvestigational use of tyrosine kinase inhibitors in thyroid cancer: establishing a standard for patient safety and monitoring”. J. Clin. Endocrinol. Metab. 98 (1): 31–42. doi:10.1210/jc.2012-2909. PMC 3537108. PMID 23185034.
  3. Cabanillas ME, Hu MI, Durand JB, Busaidy NL (2011). “Challenges associated with tyrosine kinase inhibitor therapy for metastatic thyroid cancer”. J Thyroid Res. 2011: 985780. doi:10.4061/2011/985780. PMC 3189619. PMID 22007339.
  4. Schlumberger M, Tahara M, Wirth LJ, Robinson B, Brose MS, Elisei R, Habra MA, Newbold K, Shah MH, Hoff AO, Gianoukakis AG, Kiyota N, Taylor MH, Kim SB, Krzyzanowska MK, Dutcus CE, de las Heras B, Zhu J, Sherman SI (February 2015). “Lenvatinib versus placebo in radioiodine-refractory thyroid cancer”. N. Engl. J. Med. 372 (7): 621–30. doi:10.1056/NEJMoa1406470. PMID 25671254.

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