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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 for the treatment of thyroid cancer
1a Researcher of CIBERDEM (Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas), Endocrinology Service , Hospital Universitario de Bellvitge , Barcelona , Spain.
Introduction:
Sunitinib is an oral oxindol derivative and a potent inhibitor of vascular endothelial growth factor receptor and platelet-derived growth factor receptor and a multitargeted tyrosine-kinase inhibitor, which has antitumor and antiangiogenic activity due to the selective inhibition that can stabilize progressive metastatic disease. The aim of this review is to expose whether the drug could be considered as a new promising therapy compared with other tyrosine-kinase inhibitors. Areas covered: In seven open-label studies carried out with sunitinb, the drug showed its anti-tumoral activity in advanced differentiated thyroid carcinoma and in medullary thyroid carcinoma. The reported objectives in advanced differentiated thyroid carcinoma, partial response ranges 13% to 55.5%, stable disease ranges 44.4% to 68%, progressive disease ranges 10% to 21% of patients, progression free survival ranges 3 to 13.3% months. In medullary thyroid carcinoma, PR ranges 0% to 55%, SD ranges 44.4% to 87.5%, PD ranges 7% to 18.8% and progression free survivalranges seven to 21 months. Expert opinion: Sunitinib has demonstrated a potent anti-tumoral activity in differentiated thyroid carcinoma and in medullary thyroid carcinoma, but the results of the open-label trials single arm are limited. Further investigations with this agent with randomized trials are warranted.
Insights
Sunitinib shows anti-tumoral effects in advanced differentiated and medullary thyroid cancers. Further randomized trials are needed to confirm its efficacy compared to other tyrosine-kinase inhibitors.
Area of Science:
- Oncology
- Pharmacology
Background:
- Sunitinib is an oral oxindol derivative and a multitargeted tyrosine-kinase inhibitor.
- It exhibits antitumor and antiangiogenic activity by inhibiting vascular endothelial growth factor receptor and platelet-derived growth factor receptor.
Purpose of the Study:
- To evaluate sunitinib as a promising therapy for thyroid cancer compared to other tyrosine-kinase inhibitors.
- To review the efficacy of sunitinib in advanced differentiated and medullary thyroid carcinoma.
Main Methods:
- Review of seven open-label studies on sunitinib treatment.
- Analysis of objective response rates (partial response, stable disease, progressive disease) and progression-free survival.
Main Results:
- In advanced differentiated thyroid carcinoma, partial response ranged from 13% to 55.5%, and progression-free survival was 3 to 13.3 months.
- In medullary thyroid carcinoma, partial response ranged from 0% to 55%, and progression-free survival was 7 to 21 months.
Conclusions:
- Sunitinib demonstrates potent anti-tumoral activity in both differentiated and medullary thyroid carcinomas.
- Results from single-arm, open-label trials are limited; further randomized trials are warranted to validate these findings.
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