The Evolving Treatment Landscape of Medullary Thyroid Cancer

被引:2
|
作者
Lagana, Marta [1 ]
Cremaschi, Valentina [1 ]
Alberti, Andrea [1 ]
Vodopivec Kuri, Danica M. [2 ]
Cosentini, Deborah [1 ]
Berruti, Alfredo [1 ]
机构
[1] Univ Brescia, ASST Spedali Civili, Med Oncol Unit, Dept Med & Surg Specialties Radiol Sci & Publ Hlt, I-25123 Brescia, Italy
[2] Univ Alabama Birmingham, Dept Endocrinol Diabet & Metab, 619 19Th St S, Birmingham, AL 35249 USA
关键词
Medullary thyroid; Cancer; RET mutations; MultiTKI; RET inhibitors; Metastatic MTC; Future options; Pretreated MTC; QUALITY-OF-LIFE; RET PROTOONCOGENE; PHASE-II; CARCINOMA; TRIAL; VANDETANIB; HEREDITARY; METASTASES; MANAGEMENT; MUTATIONS;
D O I
10.1007/s11864-023-01145-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genetic assessment is crucial to address the correct treatment for advanced medullary thyroid cancer (MTC). Multi tyrosine kinase inhibitors (mTKIs) cabozantinib and vandetanib are good first line options, even vandetanib prescription is currently limited to RET mutated patients. Selective RET inhibitors such as pralsetinib could be a preferred upfront treatment in case of RET mutated MTC presenting common or gatekeeper RET mutations (e.g. M918T; V804L/M). Selpercatinib, otherwise, can be prescribed as the second line after disease progression to mTKIs. The best option for subsequent lines is to consider inclusion in clinical trials or alternatively other mTKIs such as sunitinib, sorafenib, lenvatinib, or pazopanib could be evaluated. New perspectives include next-generation RET inhibitors able to overcome resistance mechanisms responsible for disease progression to standard mTKIs and RET inhibitors, and immunotherapy for MTC presenting with high tumor mutational burden.
引用
收藏
页码:1815 / 1832
页数:18
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