Kinase-inhibitors for iodine-refractory differentiated thyroid cancer: still far from a structured therapeutic algorithm

Crit Rev Oncol Hematol. 2021 Jun:162:103353. doi: 10.1016/j.critrevonc.2021.103353. Epub 2021 May 14.

Abstract

The kinase-inhibitors (KIs) sorafenib and lenvatinib demonstrated efficacy in iodine-refractory DTC upon phase III studies. However, evidence allowing a punctual balance of benefits and risks is poor. Furthermore, the lack of a direct comparison hampers to establish the proper sequence of administration. However, some insights may provided: a) indirect comparison between phase III trials showed milder toxicity for sorafenib, which should be preferred in case of cardiovascular comorbidities; b) prospective evidence of efficacy in KIs pre-treated patients is available only for lenvatinib, which should be used as second-line. Promising activity was found for the majority of other tested KIs, but no placebo-controlled trials are available. Emerging, but still early, frontiers include the restoration of iodine-sensitivity and the selective activity on pathogenic mutations. In conclusion, the use of KIs in iodine-refractory DTC is far from a structured therapeutic algorithm.

Keywords: Iodine-refractory; Kinase-inhibitors; Targeted therapies; Thyroid cancer; Thyroid diseases; Thyroid nodules.

Publication types

  • Review

MeSH terms

  • Algorithms
  • Antineoplastic Agents* / therapeutic use
  • Humans
  • Iodine* / therapeutic use
  • Phenylurea Compounds / therapeutic use
  • Prospective Studies
  • Protein Kinase Inhibitors / therapeutic use
  • Quinolines* / therapeutic use
  • Thyroid Neoplasms* / drug therapy

Substances

  • Antineoplastic Agents
  • Phenylurea Compounds
  • Protein Kinase Inhibitors
  • Quinolines
  • Iodine