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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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 & 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</subject><ispartof>European journal of endocrinology, 2009-12, Vol.161 (6), p.923-931</ispartof><rights>2009 European Society of Endocrinology</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b432t-3893d73dfe3c9695916bd266be7e433dd6bc78d5ef6fecb7a04f53836e3d647b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22204687$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19773371$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma</title><title>European journal of endocrinology</title><addtitle>Eur J Endocrinol</addtitle><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.</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 & derivatives</subject><subject>Non tumoral diseases. Target tissue resistance. Benign neoplasms</subject><subject>Phenylurea Compounds</subject><subject>Protein-Tyrosine Kinases - antagonists & 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 & derivatives</topic><topic>Non tumoral diseases. Target tissue resistance. Benign neoplasms</topic><topic>Phenylurea Compounds</topic><topic>Protein-Tyrosine Kinases - antagonists & 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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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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