The majority of deaths due to thyroid cancer occur in patients with advanced DTC refractory to radioactive iodine. The spectacular advances in molecular medicine of recent years have opened new therapeutic possibilities. Currently, there is general agreement that treatment with Tyrosine Kinase Inhibitors (TKI) should only be considered in patients with differentiated thyroid carcinoma refractory to radioactive iodine, with progressive and / or symptomatic metastatic disease that can not otherwise be treated locally. Most of these "new molecules" are multichannel inhibitors with varied action, which interact on different proteins such as RET, BRAF, cKIT, MET, EGFR, MAPK, PDGFR, etc. In addition, they have the additional advantage that they markedly prevent angiogenesis by acting on VEGFR 1, 2, and 3. TKI are associated with progression-free survival but not curative. Also, causes adverse effects that can affect the quality of life.The prolongation of progression-free survival has been demonstrated with sorafenib and lenvatinib compared with placebo in two phase III trials. These two drugs have been approved by the FDA and the European Medicines Agency for use in patients refractory to radioactive iodine with metastatic disease. Based on the Phase II Trials there are other Tyrosine Kinase Inhibitors (TKI) available such as sunitinib, axitinib or pazopanib that can produce some kind of clinical benefit and therefore need further investigation.
Published in | Cancer Research Journal (Volume 7, Issue 2) |
DOI | 10.11648/j.crj.20190702.12 |
Page(s) | 39-44 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2019. Published by Science Publishing Group |
Target, Cancer, Thyroid
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APA Style
Lynda Marianela Vásconez Proaño. (2019). New Targets in Advanced Thyroid Cancer Refractory Iodine. Cancer Research Journal, 7(2), 39-44. https://doi.org/10.11648/j.crj.20190702.12
ACS Style
Lynda Marianela Vásconez Proaño. New Targets in Advanced Thyroid Cancer Refractory Iodine. Cancer Res. J. 2019, 7(2), 39-44. doi: 10.11648/j.crj.20190702.12
AMA Style
Lynda Marianela Vásconez Proaño. New Targets in Advanced Thyroid Cancer Refractory Iodine. Cancer Res J. 2019;7(2):39-44. doi: 10.11648/j.crj.20190702.12
@article{10.11648/j.crj.20190702.12, author = {Lynda Marianela Vásconez Proaño}, title = {New Targets in Advanced Thyroid Cancer Refractory Iodine}, journal = {Cancer Research Journal}, volume = {7}, number = {2}, pages = {39-44}, doi = {10.11648/j.crj.20190702.12}, url = {https://doi.org/10.11648/j.crj.20190702.12}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.crj.20190702.12}, abstract = {The majority of deaths due to thyroid cancer occur in patients with advanced DTC refractory to radioactive iodine. The spectacular advances in molecular medicine of recent years have opened new therapeutic possibilities. Currently, there is general agreement that treatment with Tyrosine Kinase Inhibitors (TKI) should only be considered in patients with differentiated thyroid carcinoma refractory to radioactive iodine, with progressive and / or symptomatic metastatic disease that can not otherwise be treated locally. Most of these "new molecules" are multichannel inhibitors with varied action, which interact on different proteins such as RET, BRAF, cKIT, MET, EGFR, MAPK, PDGFR, etc. In addition, they have the additional advantage that they markedly prevent angiogenesis by acting on VEGFR 1, 2, and 3. TKI are associated with progression-free survival but not curative. Also, causes adverse effects that can affect the quality of life.The prolongation of progression-free survival has been demonstrated with sorafenib and lenvatinib compared with placebo in two phase III trials. These two drugs have been approved by the FDA and the European Medicines Agency for use in patients refractory to radioactive iodine with metastatic disease. Based on the Phase II Trials there are other Tyrosine Kinase Inhibitors (TKI) available such as sunitinib, axitinib or pazopanib that can produce some kind of clinical benefit and therefore need further investigation.}, year = {2019} }
TY - JOUR T1 - New Targets in Advanced Thyroid Cancer Refractory Iodine AU - Lynda Marianela Vásconez Proaño Y1 - 2019/04/22 PY - 2019 N1 - https://doi.org/10.11648/j.crj.20190702.12 DO - 10.11648/j.crj.20190702.12 T2 - Cancer Research Journal JF - Cancer Research Journal JO - Cancer Research Journal SP - 39 EP - 44 PB - Science Publishing Group SN - 2330-8214 UR - https://doi.org/10.11648/j.crj.20190702.12 AB - The majority of deaths due to thyroid cancer occur in patients with advanced DTC refractory to radioactive iodine. The spectacular advances in molecular medicine of recent years have opened new therapeutic possibilities. Currently, there is general agreement that treatment with Tyrosine Kinase Inhibitors (TKI) should only be considered in patients with differentiated thyroid carcinoma refractory to radioactive iodine, with progressive and / or symptomatic metastatic disease that can not otherwise be treated locally. Most of these "new molecules" are multichannel inhibitors with varied action, which interact on different proteins such as RET, BRAF, cKIT, MET, EGFR, MAPK, PDGFR, etc. In addition, they have the additional advantage that they markedly prevent angiogenesis by acting on VEGFR 1, 2, and 3. TKI are associated with progression-free survival but not curative. Also, causes adverse effects that can affect the quality of life.The prolongation of progression-free survival has been demonstrated with sorafenib and lenvatinib compared with placebo in two phase III trials. These two drugs have been approved by the FDA and the European Medicines Agency for use in patients refractory to radioactive iodine with metastatic disease. Based on the Phase II Trials there are other Tyrosine Kinase Inhibitors (TKI) available such as sunitinib, axitinib or pazopanib that can produce some kind of clinical benefit and therefore need further investigation. VL - 7 IS - 2 ER -