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Establishment and Characterization of Patient-Derived Xenograft Models of Anaplastic Thyroid Carcinoma and Head and Neck Squamous Cell Carcinoma
Published on: June 2, 2023
Sunitinib in the Treatment of Thyroid Cancer
Silvia Martina Ferrari1, Marco Centanni2, Camilla Virili2
1Department of Clinical and Experimental Medicine, University of Pisa, Via Savi, 10, I-56126, Pisa, Italy.
Background:
Sunitinib (SU11248) is an oral multi-target tyrosine kinase inhibitor (TKI) with low molecular weight, that inhibits platelet-derived growth factor receptors (PDGF-Rs) and vascular endothelial growth factor receptors (VEGFRs), c-KIT, fms-related tyrosine kinase 3 (FLT3) and RET. The concurrent inhibition of these pathways reduces tumor vascularization and causes cancer cell apoptosis, inducing a tumor shrinkage. Sunitinib is approved for the treatment of imatinib-resistant gastrointestinal stromal tumor (GIST), renal carcinoma, and pancreatic neuroendocrine tumors.
Methods:
We searched the literature on PubMed library.
Results:
In vitro studies showed that sunitinib targeted the cytosolic MEK/ERK and SAPK/JNK pathways in the RET/PTC1 cell inhibiting cell proliferation and causing stimulation of sodium/iodide symporter (NIS) gene expression in RET/PTC1 cells. Furthermore sunitinib is active in vitro and in vivo against anaplastic thyroid cancer (ATC) cells. Most of the clinical studies report that sunitinib is effective as first- and second-line TKI therapy in patients with advanced dedifferentiated thyroid cancer (DeTC), or medullary thyroid cancer (MTC). Sunitinib 37.5 mg/day is well tolerated, and effective. The most common adverse events include: reduction in blood cell counts (in particular leukocytes), hand-foot skin reaction, diarrhea, fatigue, nausea, hypertension, and musculoskeletal pain.
Conclusion:
Even if sunitinib is promising in the therapy of differentiated thyroid carcinoma (DTC), until now no phase III studies have been published, and additional prospective researches are necessary in order to evaluate the real efficacy of sunitinib in aggressive thyroid cancer.
Insights
Sunitinib, a multi-target tyrosine kinase inhibitor, shows promise in treating advanced thyroid cancers by inhibiting tumor growth and vascularization. Further phase III studies are needed to confirm its efficacy in aggressive thyroid cancer.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Sunitinib is an oral multi-target tyrosine kinase inhibitor (TKI) targeting PDGF-Rs, VEGFRs, c-KIT, FLT3, and RET.
- It reduces tumor vascularization and induces apoptosis, leading to tumor shrinkage.
- Approved for imatinib-resistant GIST, renal carcinoma, and pancreatic neuroendocrine tumors.
Purpose of the Study:
- To review the efficacy and safety of sunitinib in treating various thyroid cancers.
- To evaluate sunitinib's potential in advanced dedifferentiated thyroid cancer (DeTC) and medullary thyroid cancer (MTC).
Main Methods:
- Literature search conducted on the PubMed database.
- In vitro and in vivo studies were reviewed.
- Clinical studies on sunitinib in thyroid cancer patients were analyzed.
Main Results:
- Sunitinib inhibits proliferation and stimulates sodium/iodide symporter (NIS) gene expression in RET/PTC1 cells.
- It is active against anaplastic thyroid cancer (ATC) cells in vitro and in vivo.
- Sunitinib is effective as first- and second-line TKI therapy in advanced DeTC and MTC, and is well-tolerated.
Conclusions:
- Sunitinib demonstrates promise for differentiated thyroid carcinoma (DTC) therapy.
- No phase III studies have been published to date.
- Further prospective research is required to ascertain sunitinib's true efficacy in aggressive thyroid cancer.
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