Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma

ObjectiveTreatment options for patients with radioactive iodine (RaI) refractory metastases of differentiated thyroid carcinoma (DTC) are limited. We studied the effects of the multitarget tyrosine kinase inhibitor sorafenib on the reinduction of RaI uptake and tumor progression.DesignOpen, single c...

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Veröffentlicht in:European journal of endocrinology 2009-12, Vol.161 (6), p.923-931
Hauptverfasser: Hoftijzer, Hendrieke, Heemstra, Karen A, Morreau, Hans, Stokkel, Marcel P, Corssmit, Eleonora P, Gelderblom, Hans, Weijers, Karin, Pereira, Alberto M, Huijberts, Maya, Kapiteijn, Ellen, Romijn, Johannes A, Smit, Johannes W
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container_end_page 931
container_issue 6
container_start_page 923
container_title European journal of endocrinology
container_volume 161
creator Hoftijzer, Hendrieke
Heemstra, Karen A
Morreau, Hans
Stokkel, Marcel P
Corssmit, Eleonora P
Gelderblom, Hans
Weijers, Karin
Pereira, Alberto M
Huijberts, Maya
Kapiteijn, Ellen
Romijn, Johannes A
Smit, Johannes W
description ObjectiveTreatment options for patients with radioactive iodine (RaI) refractory metastases of differentiated thyroid carcinoma (DTC) are limited. We studied the effects of the multitarget tyrosine kinase inhibitor sorafenib on the reinduction of RaI uptake and tumor progression.DesignOpen, single center, single arm 26-week prospective phase II study with open-ended extension.MethodsWe treated 31 patients with progressive metastatic or locally advanced RaI refractory DTC with sorafenib 400 mg b.i.d. The primary endpoint was reinduction of RaI uptake at 26 weeks. Additional endpoints were the radiological response and the influence of bone metastases.ResultsAt 26 weeks of sorafenib therapy, no reinduction of RaI uptake at metastatic sites was observed, but 19 patients (59%) had a clinical beneficial response, eight of whom had a partial response (25%) and 11 had stable disease (34%). Seven patients had progressive disease (22%). Sorafenib was significantly less effective in patients with bone metastases. The estimated median progression free survival was 58 weeks (95% confidence interval, CI, 47–68). In general, thyroglobulin (Tg) response (both unstimulated and TSH stimulated) reflected radiological responses. The median time of the nadir of Tg levels was 3 months. Responses were not influenced by histological subtype, mutational status or other variables. No unusual side effects were observed.ConclusionsSorafenib has a beneficial effect on tumor progression in patients with metastatic DTC, but was less effective in patients with bone metastases. Diagnostic whole body scintigraphy did not reveal an effect of sorafenib on the reinduction of RaI uptake.
doi_str_mv 10.1530/EJE-09-0702
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We studied the effects of the multitarget tyrosine kinase inhibitor sorafenib on the reinduction of RaI uptake and tumor progression.DesignOpen, single center, single arm 26-week prospective phase II study with open-ended extension.MethodsWe treated 31 patients with progressive metastatic or locally advanced RaI refractory DTC with sorafenib 400 mg b.i.d. The primary endpoint was reinduction of RaI uptake at 26 weeks. Additional endpoints were the radiological response and the influence of bone metastases.ResultsAt 26 weeks of sorafenib therapy, no reinduction of RaI uptake at metastatic sites was observed, but 19 patients (59%) had a clinical beneficial response, eight of whom had a partial response (25%) and 11 had stable disease (34%). Seven patients had progressive disease (22%). Sorafenib was significantly less effective in patients with bone metastases. The estimated median progression free survival was 58 weeks (95% confidence interval, CI, 47–68). In general, thyroglobulin (Tg) response (both unstimulated and TSH stimulated) reflected radiological responses. The median time of the nadir of Tg levels was 3 months. Responses were not influenced by histological subtype, mutational status or other variables. No unusual side effects were observed.ConclusionsSorafenib has a beneficial effect on tumor progression in patients with metastatic DTC, but was less effective in patients with bone metastases. Diagnostic whole body scintigraphy did not reveal an effect of sorafenib on the reinduction of RaI uptake.</description><identifier>ISSN: 0804-4643</identifier><identifier>EISSN: 1479-683X</identifier><identifier>DOI: 10.1530/EJE-09-0702</identifier><identifier>PMID: 19773371</identifier><language>eng</language><publisher>Bristol: BioScientifica</publisher><subject>Adenocarcinoma, Follicular - drug therapy ; Adenocarcinoma, Follicular - radiotherapy ; Aged ; Aged, 80 and over ; Benzenesulfonates - adverse effects ; Benzenesulfonates - therapeutic use ; Biological and medical sciences ; Bone Neoplasms - drug therapy ; Bone Neoplasms - radiotherapy ; Bone Neoplasms - secondary ; Clinical Study ; Disease-Free Survival ; Endocrinopathies ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Iodine Radioisotopes - therapeutic use ; Male ; Malignant tumors ; Medical sciences ; Middle Aged ; Niacinamide - analogs &amp; derivatives ; Non tumoral diseases. Target tissue resistance. Benign neoplasms ; Phenylurea Compounds ; Protein-Tyrosine Kinases - antagonists &amp; inhibitors ; Pyridines - adverse effects ; Pyridines - therapeutic use ; Thyroglobulin - metabolism ; Thyroid Neoplasms - drug therapy ; Thyroid Neoplasms - pathology ; Thyroid Neoplasms - radiotherapy ; Thyroid. 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We studied the effects of the multitarget tyrosine kinase inhibitor sorafenib on the reinduction of RaI uptake and tumor progression.DesignOpen, single center, single arm 26-week prospective phase II study with open-ended extension.MethodsWe treated 31 patients with progressive metastatic or locally advanced RaI refractory DTC with sorafenib 400 mg b.i.d. The primary endpoint was reinduction of RaI uptake at 26 weeks. Additional endpoints were the radiological response and the influence of bone metastases.ResultsAt 26 weeks of sorafenib therapy, no reinduction of RaI uptake at metastatic sites was observed, but 19 patients (59%) had a clinical beneficial response, eight of whom had a partial response (25%) and 11 had stable disease (34%). Seven patients had progressive disease (22%). Sorafenib was significantly less effective in patients with bone metastases. The estimated median progression free survival was 58 weeks (95% confidence interval, CI, 47–68). In general, thyroglobulin (Tg) response (both unstimulated and TSH stimulated) reflected radiological responses. The median time of the nadir of Tg levels was 3 months. Responses were not influenced by histological subtype, mutational status or other variables. No unusual side effects were observed.ConclusionsSorafenib has a beneficial effect on tumor progression in patients with metastatic DTC, but was less effective in patients with bone metastases. Diagnostic whole body scintigraphy did not reveal an effect of sorafenib on the reinduction of RaI uptake.</description><subject>Adenocarcinoma, Follicular - drug therapy</subject><subject>Adenocarcinoma, Follicular - radiotherapy</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Benzenesulfonates - adverse effects</subject><subject>Benzenesulfonates - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bone Neoplasms - drug therapy</subject><subject>Bone Neoplasms - radiotherapy</subject><subject>Bone Neoplasms - secondary</subject><subject>Clinical Study</subject><subject>Disease-Free Survival</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Iodine Radioisotopes - therapeutic use</subject><subject>Male</subject><subject>Malignant tumors</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Niacinamide - analogs &amp; derivatives</subject><subject>Non tumoral diseases. Target tissue resistance. Benign neoplasms</subject><subject>Phenylurea Compounds</subject><subject>Protein-Tyrosine Kinases - antagonists &amp; inhibitors</subject><subject>Pyridines - adverse effects</subject><subject>Pyridines - therapeutic use</subject><subject>Thyroglobulin - metabolism</subject><subject>Thyroid Neoplasms - drug therapy</subject><subject>Thyroid Neoplasms - pathology</subject><subject>Thyroid Neoplasms - radiotherapy</subject><subject>Thyroid. Thyroid axis (diseases)</subject><subject>Vertebrates: endocrinology</subject><issn>0804-4643</issn><issn>1479-683X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1vVCEUhomxsdPqyr1h48reChcG7l1qM9aaJm40cXfDx6FzdAZugEnTP-DvlsmMH3HRFZDznBfOAyEvObvkS8Herj6tOjZ2TLP-CVlwqcdODeLbU7JgA5OdVFKckrNSvjPG2549I6d81FoIzRfk53uIENCh2VAIAVwtNAVaUjYBIlqaIq27bcp0zukuQymY4gW1u0pjqvtqNh4TJo8R6G6u5gdcUIx0NhUhtrR7rGvqsWXndkZTwdO6fsgJPXUmO4xpa56Tk2A2BV4c13Py9cPqy9XH7vbz9c3Vu9vOStHXTgyj8Fr4AMKNalyOXFnfK2VBgxTCe2WdHvwSgmqjWG2YDEsxCAXCK6mtOCdvDrkup1IyhGnOuDX5YeJs2tucms2JjdPeZqNfHeh5Z7fg_7JHfQ14fQRMcWYTsokOyx-u73sm1aAb1x-4Nd6t7zHDZDEVtxeETb759_bff9ma-KHpP_axF_8CcqqgTQ</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Hoftijzer, Hendrieke</creator><creator>Heemstra, Karen A</creator><creator>Morreau, Hans</creator><creator>Stokkel, Marcel P</creator><creator>Corssmit, Eleonora P</creator><creator>Gelderblom, Hans</creator><creator>Weijers, Karin</creator><creator>Pereira, Alberto M</creator><creator>Huijberts, Maya</creator><creator>Kapiteijn, Ellen</creator><creator>Romijn, Johannes A</creator><creator>Smit, Johannes W</creator><general>BioScientifica</general><general>European Society of Endocrinology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20091201</creationdate><title>Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma</title><author>Hoftijzer, Hendrieke ; Heemstra, Karen A ; Morreau, Hans ; Stokkel, Marcel P ; Corssmit, Eleonora P ; Gelderblom, Hans ; Weijers, Karin ; Pereira, Alberto M ; Huijberts, Maya ; Kapiteijn, Ellen ; Romijn, Johannes A ; Smit, Johannes W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b432t-3893d73dfe3c9695916bd266be7e433dd6bc78d5ef6fecb7a04f53836e3d647b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adenocarcinoma, Follicular - drug therapy</topic><topic>Adenocarcinoma, Follicular - radiotherapy</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Benzenesulfonates - adverse effects</topic><topic>Benzenesulfonates - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Bone Neoplasms - drug therapy</topic><topic>Bone Neoplasms - radiotherapy</topic><topic>Bone Neoplasms - secondary</topic><topic>Clinical Study</topic><topic>Disease-Free Survival</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Iodine Radioisotopes - therapeutic use</topic><topic>Male</topic><topic>Malignant tumors</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Niacinamide - analogs &amp; derivatives</topic><topic>Non tumoral diseases. Target tissue resistance. Benign neoplasms</topic><topic>Phenylurea Compounds</topic><topic>Protein-Tyrosine Kinases - antagonists &amp; inhibitors</topic><topic>Pyridines - adverse effects</topic><topic>Pyridines - therapeutic use</topic><topic>Thyroglobulin - metabolism</topic><topic>Thyroid Neoplasms - drug therapy</topic><topic>Thyroid Neoplasms - pathology</topic><topic>Thyroid Neoplasms - radiotherapy</topic><topic>Thyroid. Thyroid axis (diseases)</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoftijzer, Hendrieke</creatorcontrib><creatorcontrib>Heemstra, Karen A</creatorcontrib><creatorcontrib>Morreau, Hans</creatorcontrib><creatorcontrib>Stokkel, Marcel P</creatorcontrib><creatorcontrib>Corssmit, Eleonora P</creatorcontrib><creatorcontrib>Gelderblom, Hans</creatorcontrib><creatorcontrib>Weijers, Karin</creatorcontrib><creatorcontrib>Pereira, Alberto M</creatorcontrib><creatorcontrib>Huijberts, Maya</creatorcontrib><creatorcontrib>Kapiteijn, Ellen</creatorcontrib><creatorcontrib>Romijn, Johannes A</creatorcontrib><creatorcontrib>Smit, Johannes W</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>European journal of endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoftijzer, Hendrieke</au><au>Heemstra, Karen A</au><au>Morreau, Hans</au><au>Stokkel, Marcel P</au><au>Corssmit, Eleonora P</au><au>Gelderblom, Hans</au><au>Weijers, Karin</au><au>Pereira, Alberto M</au><au>Huijberts, Maya</au><au>Kapiteijn, Ellen</au><au>Romijn, Johannes A</au><au>Smit, Johannes W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma</atitle><jtitle>European journal of endocrinology</jtitle><addtitle>Eur J Endocrinol</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>161</volume><issue>6</issue><spage>923</spage><epage>931</epage><pages>923-931</pages><issn>0804-4643</issn><eissn>1479-683X</eissn><abstract>ObjectiveTreatment options for patients with radioactive iodine (RaI) refractory metastases of differentiated thyroid carcinoma (DTC) are limited. We studied the effects of the multitarget tyrosine kinase inhibitor sorafenib on the reinduction of RaI uptake and tumor progression.DesignOpen, single center, single arm 26-week prospective phase II study with open-ended extension.MethodsWe treated 31 patients with progressive metastatic or locally advanced RaI refractory DTC with sorafenib 400 mg b.i.d. The primary endpoint was reinduction of RaI uptake at 26 weeks. Additional endpoints were the radiological response and the influence of bone metastases.ResultsAt 26 weeks of sorafenib therapy, no reinduction of RaI uptake at metastatic sites was observed, but 19 patients (59%) had a clinical beneficial response, eight of whom had a partial response (25%) and 11 had stable disease (34%). Seven patients had progressive disease (22%). Sorafenib was significantly less effective in patients with bone metastases. The estimated median progression free survival was 58 weeks (95% confidence interval, CI, 47–68). In general, thyroglobulin (Tg) response (both unstimulated and TSH stimulated) reflected radiological responses. The median time of the nadir of Tg levels was 3 months. Responses were not influenced by histological subtype, mutational status or other variables. No unusual side effects were observed.ConclusionsSorafenib has a beneficial effect on tumor progression in patients with metastatic DTC, but was less effective in patients with bone metastases. Diagnostic whole body scintigraphy did not reveal an effect of sorafenib on the reinduction of RaI uptake.</abstract><cop>Bristol</cop><pub>BioScientifica</pub><pmid>19773371</pmid><doi>10.1530/EJE-09-0702</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current)
subjects Adenocarcinoma, Follicular - drug therapy
Adenocarcinoma, Follicular - radiotherapy
Aged
Aged, 80 and over
Benzenesulfonates - adverse effects
Benzenesulfonates - therapeutic use
Biological and medical sciences
Bone Neoplasms - drug therapy
Bone Neoplasms - radiotherapy
Bone Neoplasms - secondary
Clinical Study
Disease-Free Survival
Endocrinopathies
Female
Fundamental and applied biological sciences. Psychology
Humans
Iodine Radioisotopes - therapeutic use
Male
Malignant tumors
Medical sciences
Middle Aged
Niacinamide - analogs & derivatives
Non tumoral diseases. Target tissue resistance. Benign neoplasms
Phenylurea Compounds
Protein-Tyrosine Kinases - antagonists & inhibitors
Pyridines - adverse effects
Pyridines - therapeutic use
Thyroglobulin - metabolism
Thyroid Neoplasms - drug therapy
Thyroid Neoplasms - pathology
Thyroid Neoplasms - radiotherapy
Thyroid. Thyroid axis (diseases)
Vertebrates: endocrinology
title Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma
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