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Antitumour effects of apatinib in progressive, metastatic differentiated thyroid cancer (DTC)

PURPOSE: Management of progressive, metastatic radioactive iodine refractory differentiated thyroid cancer (RAIR-DTC) has been a great challenge due to its poor prognosis and limited treatment options. Recently, apatinib, an orally anti-angiogenic tyrosine kinase inhibitor (TKI) is reported to be us...

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Autores principales: Shi, Liang, You, Qinqin, Wang, Jun, Wang, Hanjin, Li, Shaohua, Tian, Rui, Yao, Xiaocheng, Wu, Wenyu, Zhang, Lele, Wang, Feng, Lin, Yansong, Li, Shuren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474580/
https://www.ncbi.nlm.nih.gov/pubmed/35767182
http://dx.doi.org/10.1007/s12020-022-03113-9
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author Shi, Liang
You, Qinqin
Wang, Jun
Wang, Hanjin
Li, Shaohua
Tian, Rui
Yao, Xiaocheng
Wu, Wenyu
Zhang, Lele
Wang, Feng
Lin, Yansong
Li, Shuren
author_facet Shi, Liang
You, Qinqin
Wang, Jun
Wang, Hanjin
Li, Shaohua
Tian, Rui
Yao, Xiaocheng
Wu, Wenyu
Zhang, Lele
Wang, Feng
Lin, Yansong
Li, Shuren
author_sort Shi, Liang
collection PubMed
description PURPOSE: Management of progressive, metastatic radioactive iodine refractory differentiated thyroid cancer (RAIR-DTC) has been a great challenge due to its poor prognosis and limited treatment options. Recently, apatinib, an orally anti-angiogenic tyrosine kinase inhibitor (TKI) is reported to be useful for treatment of progressive RAIR-DIC. The aim of this study was to evaluate the antitumour effect of apatinib and the combination therapy with radioactive iodine (RAI) in patients with progressive metastatic DTC. METHODS: Five patients (all female, mean age 62 ± 8 years, ranged from 51 to 69 years) with distant metastatic DTC (dmDTC) after total thyroidectomy (TTE) and neck lymph node dissection were treated with apatinib at a dose 500 mg per day after (18)F-Fluorodeoxyglucose ((18)F-FDG) PET/CT. The effects of apatinib on DTC were evaluated at 4 ± 1 months after treatment with apatinib. RAI therapy was then initiated. The response to apatinib and the combination therapy with RAI treatment was evaluated by Response Evaluation Criteria in Solid Tumours (RECIST, version 1.1) and metabolic activity using serum thyroglobulin (Tg) and (18)F-FDG PET/CT. RESULTS: Positive (18)F-FDG PET/CT results were found in all patients before apatinib therapy. The immunohistochemical analysis of primary tumour tissues showed high expression of vascular endothelial growth factor receptor-2 (VEGFR-2). Four patients with follicular thyroid carcinoma (FTC) showed partial response (PR) with significant decrease in tumour size and maximum standardized uptake value (SUVmax) after 4 ± 1 month’s treatment with apatinib. Further significant reduction of tumour size and SUVmax were observed in three patients after combination therapy with apatinib and RAI. Only one patient with both FTC and papillary thyroid cancer (PTC) demonstrated progressive disease (PD) after treatment with apatinib alone, however, a decrease in tumour size and SUVmax as well as serum Tg levels was achieved after the combination with RAI therapy and apatinib. CONCLUSIONS: Apatinib had significant antitumour effects on progressive distant metastatic DTC. Moreover, beneficial synergistic and complementary effects were shown when apatinib combined with RAI therapy. CLINICAL TRIAL REGISTRATION: NCT 04180007, Registered November 26, 2019.
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spelling pubmed-94745802022-09-16 Antitumour effects of apatinib in progressive, metastatic differentiated thyroid cancer (DTC) Shi, Liang You, Qinqin Wang, Jun Wang, Hanjin Li, Shaohua Tian, Rui Yao, Xiaocheng Wu, Wenyu Zhang, Lele Wang, Feng Lin, Yansong Li, Shuren Endocrine Original Article PURPOSE: Management of progressive, metastatic radioactive iodine refractory differentiated thyroid cancer (RAIR-DTC) has been a great challenge due to its poor prognosis and limited treatment options. Recently, apatinib, an orally anti-angiogenic tyrosine kinase inhibitor (TKI) is reported to be useful for treatment of progressive RAIR-DIC. The aim of this study was to evaluate the antitumour effect of apatinib and the combination therapy with radioactive iodine (RAI) in patients with progressive metastatic DTC. METHODS: Five patients (all female, mean age 62 ± 8 years, ranged from 51 to 69 years) with distant metastatic DTC (dmDTC) after total thyroidectomy (TTE) and neck lymph node dissection were treated with apatinib at a dose 500 mg per day after (18)F-Fluorodeoxyglucose ((18)F-FDG) PET/CT. The effects of apatinib on DTC were evaluated at 4 ± 1 months after treatment with apatinib. RAI therapy was then initiated. The response to apatinib and the combination therapy with RAI treatment was evaluated by Response Evaluation Criteria in Solid Tumours (RECIST, version 1.1) and metabolic activity using serum thyroglobulin (Tg) and (18)F-FDG PET/CT. RESULTS: Positive (18)F-FDG PET/CT results were found in all patients before apatinib therapy. The immunohistochemical analysis of primary tumour tissues showed high expression of vascular endothelial growth factor receptor-2 (VEGFR-2). Four patients with follicular thyroid carcinoma (FTC) showed partial response (PR) with significant decrease in tumour size and maximum standardized uptake value (SUVmax) after 4 ± 1 month’s treatment with apatinib. Further significant reduction of tumour size and SUVmax were observed in three patients after combination therapy with apatinib and RAI. Only one patient with both FTC and papillary thyroid cancer (PTC) demonstrated progressive disease (PD) after treatment with apatinib alone, however, a decrease in tumour size and SUVmax as well as serum Tg levels was achieved after the combination with RAI therapy and apatinib. CONCLUSIONS: Apatinib had significant antitumour effects on progressive distant metastatic DTC. Moreover, beneficial synergistic and complementary effects were shown when apatinib combined with RAI therapy. CLINICAL TRIAL REGISTRATION: NCT 04180007, Registered November 26, 2019. Springer US 2022-06-29 2022 /pmc/articles/PMC9474580/ /pubmed/35767182 http://dx.doi.org/10.1007/s12020-022-03113-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Shi, Liang
You, Qinqin
Wang, Jun
Wang, Hanjin
Li, Shaohua
Tian, Rui
Yao, Xiaocheng
Wu, Wenyu
Zhang, Lele
Wang, Feng
Lin, Yansong
Li, Shuren
Antitumour effects of apatinib in progressive, metastatic differentiated thyroid cancer (DTC)
title Antitumour effects of apatinib in progressive, metastatic differentiated thyroid cancer (DTC)
title_full Antitumour effects of apatinib in progressive, metastatic differentiated thyroid cancer (DTC)
title_fullStr Antitumour effects of apatinib in progressive, metastatic differentiated thyroid cancer (DTC)
title_full_unstemmed Antitumour effects of apatinib in progressive, metastatic differentiated thyroid cancer (DTC)
title_short Antitumour effects of apatinib in progressive, metastatic differentiated thyroid cancer (DTC)
title_sort antitumour effects of apatinib in progressive, metastatic differentiated thyroid cancer (dtc)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474580/
https://www.ncbi.nlm.nih.gov/pubmed/35767182
http://dx.doi.org/10.1007/s12020-022-03113-9
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