Efficacy of pazopanib in progressive, radioiodine-refractory, metastatic differentiated thyroid cancers: results of a phase 2 consortium study
Summary Background Chemotherapy has historically proven ineffective in advanced differentiated thyroid cancers, but the realisation that various tyrosine kinases are activated in the disease suggested a potential therapeutic role for tyrosine-kinase inhibitors. We investigated the safety and efficac...
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creator | Bible, Keith C, Dr Suman, Vera J, Prof Molina, Julian R, MD Smallridge, Robert C, Prof Maples, William J, MD Menefee, Michael E, MD Rubin, Joseph, Prof Sideras, Kostandinos, MD Morris, John C, MD McIver, Bryan, MB Burton, Jill K Webster, Kevin P Bieber, Carolyn Traynor, Anne M, MD Flynn, Patrick J, MD Goh, Boon Cher, MBBS Tang, Hui, PhD Ivy, Susan Percy, MD Erlichman, Charles, Prof |
description | Summary Background Chemotherapy has historically proven ineffective in advanced differentiated thyroid cancers, but the realisation that various tyrosine kinases are activated in the disease suggested a potential therapeutic role for tyrosine-kinase inhibitors. We investigated the safety and efficacy of pazopanib. Methods This phase 2 trial was done from Feb 22, 2008, to Jan 31, 2009, in patients with metastatic, rapidly progressive, radioiodine-refractory differentiated thyroid cancers. Each patient received 800 mg continuous pazopanib daily in 4-week cycles until disease progression, drug intolerance, or both occurred. Up to two previous therapies were allowed, and measurable disease with radiographic progression in the 6-month period before enrolment was a requirement for inclusion. The primary endpoint was any tumour response, according to the Response Evaluation Criteria in Solid Tumors 1.0. This study is registered with ClinicalTrials.gov , number NCT00625846. Findings 39 patients were enrolled. One patient had received no previous radioiodine therapy and another withdrew consent before treatment. Clinical outcomes could, therefore, be assessed in 37 patients (19 [51%] men, median age 63 years). The study is closed to accrual of new patients, but several enrolled patients are still being treated. Patients received a median of 12 cycles (range 1 to >23, total >383). Confirmed partial responses were recorded in 18 patients (response rate 49%, 95% CI 35–68), with likelihood of response lasting longer than 1 year calculated to be 66%. Maximum concentration of pazopanib in plasma during cycle one was significantly correlated with radiographic response ( r =−0·40, p=0·021). 16 (43%) patients required dose reductions owing to adverse events, the most frequent of which (any grade) were fatigue (29 patients), skin and hair hypopigmentation (28), diarrhoea (27), and nausea (27). Two patients who died during treatment had pre-existing contributory disorders. Interpretation Pazopanib seems to represent a promising therapeutic option for patients with advanced differentiated thyroid cancers. The correlation of the patient's response and pazopanib concentration during the first cycle might indicate that treatment can be individualised to achieve optimum outcomes. Assessment of pazopanib in an expanded cohort of patients with differentiated thyroid cancer, as well as in cohorts of patients with medullary and anaplastic thyroid cancers, is presently being done. Fund |
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We investigated the safety and efficacy of pazopanib. Methods This phase 2 trial was done from Feb 22, 2008, to Jan 31, 2009, in patients with metastatic, rapidly progressive, radioiodine-refractory differentiated thyroid cancers. Each patient received 800 mg continuous pazopanib daily in 4-week cycles until disease progression, drug intolerance, or both occurred. Up to two previous therapies were allowed, and measurable disease with radiographic progression in the 6-month period before enrolment was a requirement for inclusion. The primary endpoint was any tumour response, according to the Response Evaluation Criteria in Solid Tumors 1.0. This study is registered with ClinicalTrials.gov , number NCT00625846. Findings 39 patients were enrolled. One patient had received no previous radioiodine therapy and another withdrew consent before treatment. Clinical outcomes could, therefore, be assessed in 37 patients (19 [51%] men, median age 63 years). The study is closed to accrual of new patients, but several enrolled patients are still being treated. Patients received a median of 12 cycles (range 1 to >23, total >383). Confirmed partial responses were recorded in 18 patients (response rate 49%, 95% CI 35–68), with likelihood of response lasting longer than 1 year calculated to be 66%. Maximum concentration of pazopanib in plasma during cycle one was significantly correlated with radiographic response ( r =−0·40, p=0·021). 16 (43%) patients required dose reductions owing to adverse events, the most frequent of which (any grade) were fatigue (29 patients), skin and hair hypopigmentation (28), diarrhoea (27), and nausea (27). Two patients who died during treatment had pre-existing contributory disorders. Interpretation Pazopanib seems to represent a promising therapeutic option for patients with advanced differentiated thyroid cancers. The correlation of the patient's response and pazopanib concentration during the first cycle might indicate that treatment can be individualised to achieve optimum outcomes. Assessment of pazopanib in an expanded cohort of patients with differentiated thyroid cancer, as well as in cohorts of patients with medullary and anaplastic thyroid cancers, is presently being done. Funding National Cancer Institute , supported in part by NCI CA15083 and CM62205.</description><identifier>ISSN: 1470-2045</identifier><identifier>ISSN: 1474-5488</identifier><identifier>EISSN: 1474-5488</identifier><identifier>DOI: 10.1016/S1470-2045(10)70203-5</identifier><identifier>PMID: 20851682</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Aged ; Antineoplastic Agents - adverse effects ; Antineoplastic Agents - therapeutic use ; Cell Differentiation ; Disease Progression ; Disease-Free Survival ; Female ; Hematology, Oncology and Palliative Medicine ; Humans ; Indazoles ; Iodine Radioisotopes - therapeutic use ; Male ; Middle Aged ; Protein Kinase Inhibitors - adverse effects ; Protein Kinase Inhibitors - therapeutic use ; Pyrimidines - adverse effects ; Pyrimidines - therapeutic use ; Radiography ; Radiopharmaceuticals - therapeutic use ; Sulfonamides - adverse effects ; Sulfonamides - therapeutic use ; Thyroid Neoplasms - diagnostic imaging ; Thyroid Neoplasms - drug therapy ; Thyroid Neoplasms - mortality ; Thyroid Neoplasms - radiotherapy ; Thyroid Neoplasms - secondary ; Time Factors ; Treatment Failure ; United States ; Young Adult</subject><ispartof>The lancet oncology, 2010-10, Vol.11 (10), p.962-972</ispartof><rights>Elsevier Ltd</rights><rights>2010 Elsevier Ltd</rights><rights>Copyright © 2010 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited Oct 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c666t-acfa0360881b0fd818938e603ebbd44fcabbbe0f95544598de05e2188cb55fc83</citedby><cites>FETCH-LOGICAL-c666t-acfa0360881b0fd818938e603ebbd44fcabbbe0f95544598de05e2188cb55fc83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1470204510702035$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20851682$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bible, Keith C, Dr</creatorcontrib><creatorcontrib>Suman, Vera J, Prof</creatorcontrib><creatorcontrib>Molina, Julian R, MD</creatorcontrib><creatorcontrib>Smallridge, Robert C, Prof</creatorcontrib><creatorcontrib>Maples, William J, MD</creatorcontrib><creatorcontrib>Menefee, Michael E, MD</creatorcontrib><creatorcontrib>Rubin, Joseph, Prof</creatorcontrib><creatorcontrib>Sideras, Kostandinos, MD</creatorcontrib><creatorcontrib>Morris, John C, MD</creatorcontrib><creatorcontrib>McIver, Bryan, MB</creatorcontrib><creatorcontrib>Burton, Jill K</creatorcontrib><creatorcontrib>Webster, Kevin P</creatorcontrib><creatorcontrib>Bieber, Carolyn</creatorcontrib><creatorcontrib>Traynor, Anne M, MD</creatorcontrib><creatorcontrib>Flynn, Patrick J, MD</creatorcontrib><creatorcontrib>Goh, Boon Cher, MBBS</creatorcontrib><creatorcontrib>Tang, Hui, PhD</creatorcontrib><creatorcontrib>Ivy, Susan Percy, MD</creatorcontrib><creatorcontrib>Erlichman, Charles, Prof</creatorcontrib><creatorcontrib>the Mayo Phase 2 Consortium</creatorcontrib><creatorcontrib>for the Endocrine Malignancies Disease Oriented Group</creatorcontrib><creatorcontrib>Mayo Clinic Cancer Center</creatorcontrib><creatorcontrib>Endocrine Malignancies Disease Oriented Group</creatorcontrib><creatorcontrib>Mayo Phase 2 Consortium</creatorcontrib><title>Efficacy of pazopanib in progressive, radioiodine-refractory, metastatic differentiated thyroid cancers: results of a phase 2 consortium study</title><title>The lancet oncology</title><addtitle>Lancet Oncol</addtitle><description>Summary Background Chemotherapy has historically proven ineffective in advanced differentiated thyroid cancers, but the realisation that various tyrosine kinases are activated in the disease suggested a potential therapeutic role for tyrosine-kinase inhibitors. We investigated the safety and efficacy of pazopanib. Methods This phase 2 trial was done from Feb 22, 2008, to Jan 31, 2009, in patients with metastatic, rapidly progressive, radioiodine-refractory differentiated thyroid cancers. Each patient received 800 mg continuous pazopanib daily in 4-week cycles until disease progression, drug intolerance, or both occurred. Up to two previous therapies were allowed, and measurable disease with radiographic progression in the 6-month period before enrolment was a requirement for inclusion. The primary endpoint was any tumour response, according to the Response Evaluation Criteria in Solid Tumors 1.0. This study is registered with ClinicalTrials.gov , number NCT00625846. Findings 39 patients were enrolled. One patient had received no previous radioiodine therapy and another withdrew consent before treatment. Clinical outcomes could, therefore, be assessed in 37 patients (19 [51%] men, median age 63 years). The study is closed to accrual of new patients, but several enrolled patients are still being treated. Patients received a median of 12 cycles (range 1 to >23, total >383). Confirmed partial responses were recorded in 18 patients (response rate 49%, 95% CI 35–68), with likelihood of response lasting longer than 1 year calculated to be 66%. Maximum concentration of pazopanib in plasma during cycle one was significantly correlated with radiographic response ( r =−0·40, p=0·021). 16 (43%) patients required dose reductions owing to adverse events, the most frequent of which (any grade) were fatigue (29 patients), skin and hair hypopigmentation (28), diarrhoea (27), and nausea (27). Two patients who died during treatment had pre-existing contributory disorders. Interpretation Pazopanib seems to represent a promising therapeutic option for patients with advanced differentiated thyroid cancers. The correlation of the patient's response and pazopanib concentration during the first cycle might indicate that treatment can be individualised to achieve optimum outcomes. Assessment of pazopanib in an expanded cohort of patients with differentiated thyroid cancer, as well as in cohorts of patients with medullary and anaplastic thyroid cancers, is presently being done. Funding National Cancer Institute , supported in part by NCI CA15083 and CM62205.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Cell Differentiation</subject><subject>Disease Progression</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Indazoles</subject><subject>Iodine Radioisotopes - therapeutic use</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Protein Kinase Inhibitors - adverse effects</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Pyrimidines - adverse effects</subject><subject>Pyrimidines - therapeutic use</subject><subject>Radiography</subject><subject>Radiopharmaceuticals - therapeutic use</subject><subject>Sulfonamides - adverse effects</subject><subject>Sulfonamides - therapeutic use</subject><subject>Thyroid Neoplasms - diagnostic imaging</subject><subject>Thyroid Neoplasms - drug therapy</subject><subject>Thyroid Neoplasms - mortality</subject><subject>Thyroid Neoplasms - radiotherapy</subject><subject>Thyroid Neoplasms - secondary</subject><subject>Time Factors</subject><subject>Treatment Failure</subject><subject>United States</subject><subject>Young Adult</subject><issn>1470-2045</issn><issn>1474-5488</issn><issn>1474-5488</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkstu1TAQhiMEoqXwCCCLDSA1ME7ixIdFEarKRarEAlhbjj3ucUni1HaOFB6CZ8Y5KUfQDStb43--ufzOsqcUXlOg9ZuvtGogL6BiLym8aqCAMmf3suMUrnJWcX5_f18lR9mjEK4BaEOBPcyOCuCM1rw4zn5dGGOVVDNxhozypxvlYFtiBzJ6d-UxBLvDU-Klts46bQfMPRovVXR-PiU9RhmijFYRbY1Bj0O0MqImcTt7ZzVRclDow1uSWFMXw1JHknErA5KCKDcE56OdehLipOfH2QMju4BPbs-T7PuHi2_nn_LLLx8_n7-_zFVd1zGXykgoa-CctmA0p3xTcqyhxLbVVWWUbNsWwWwYqyq24RqBYUE5Vy1jRvHyJDtbuePU9qhVatvLToze9tLPwkkr_n0Z7FZcuZ0oKTRNSRPgxS3Au5sJQxS9DQq7Tg7opiAaxnnJYQNJ-fyO8tpNfkjT7UUFp6xIIraKlHchpA0fWqEgFr_F3m-xmLmE9n4LlvKe_T3HIeuPwUnwbhVg2ubOohdBWUyWaOtRRaGd_W-JszsE1dkh_ZnuB84YDsNQEQoBK2RhpEUtBFb-BkN801w</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Bible, Keith C, Dr</creator><creator>Suman, Vera J, Prof</creator><creator>Molina, Julian R, MD</creator><creator>Smallridge, Robert C, Prof</creator><creator>Maples, William J, MD</creator><creator>Menefee, Michael E, MD</creator><creator>Rubin, Joseph, Prof</creator><creator>Sideras, Kostandinos, MD</creator><creator>Morris, John C, MD</creator><creator>McIver, Bryan, MB</creator><creator>Burton, Jill K</creator><creator>Webster, Kevin P</creator><creator>Bieber, Carolyn</creator><creator>Traynor, Anne M, MD</creator><creator>Flynn, Patrick J, MD</creator><creator>Goh, Boon Cher, MBBS</creator><creator>Tang, Hui, PhD</creator><creator>Ivy, Susan Percy, MD</creator><creator>Erlichman, Charles, Prof</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0TZ</scope><scope>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20101001</creationdate><title>Efficacy of pazopanib in progressive, radioiodine-refractory, metastatic differentiated thyroid cancers: results of a phase 2 consortium study</title><author>Bible, Keith C, Dr ; Suman, Vera J, Prof ; Molina, Julian R, MD ; Smallridge, Robert C, Prof ; Maples, William J, MD ; Menefee, Michael E, MD ; Rubin, Joseph, Prof ; Sideras, Kostandinos, MD ; Morris, John C, MD ; McIver, Bryan, MB ; Burton, Jill K ; Webster, Kevin P ; Bieber, Carolyn ; Traynor, Anne M, MD ; Flynn, Patrick J, MD ; Goh, Boon Cher, MBBS ; Tang, Hui, PhD ; Ivy, Susan Percy, MD ; Erlichman, Charles, Prof</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c666t-acfa0360881b0fd818938e603ebbd44fcabbbe0f95544598de05e2188cb55fc83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Cell Differentiation</topic><topic>Disease Progression</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Indazoles</topic><topic>Iodine Radioisotopes - therapeutic use</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Protein Kinase Inhibitors - adverse effects</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Pyrimidines - adverse effects</topic><topic>Pyrimidines - therapeutic use</topic><topic>Radiography</topic><topic>Radiopharmaceuticals - therapeutic use</topic><topic>Sulfonamides - adverse effects</topic><topic>Sulfonamides - therapeutic use</topic><topic>Thyroid Neoplasms - diagnostic imaging</topic><topic>Thyroid Neoplasms - drug therapy</topic><topic>Thyroid Neoplasms - mortality</topic><topic>Thyroid Neoplasms - radiotherapy</topic><topic>Thyroid Neoplasms - secondary</topic><topic>Time Factors</topic><topic>Treatment Failure</topic><topic>United States</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bible, Keith C, Dr</creatorcontrib><creatorcontrib>Suman, Vera J, Prof</creatorcontrib><creatorcontrib>Molina, Julian R, MD</creatorcontrib><creatorcontrib>Smallridge, Robert C, Prof</creatorcontrib><creatorcontrib>Maples, William J, MD</creatorcontrib><creatorcontrib>Menefee, Michael E, MD</creatorcontrib><creatorcontrib>Rubin, Joseph, Prof</creatorcontrib><creatorcontrib>Sideras, Kostandinos, MD</creatorcontrib><creatorcontrib>Morris, John C, MD</creatorcontrib><creatorcontrib>McIver, Bryan, MB</creatorcontrib><creatorcontrib>Burton, Jill K</creatorcontrib><creatorcontrib>Webster, Kevin P</creatorcontrib><creatorcontrib>Bieber, Carolyn</creatorcontrib><creatorcontrib>Traynor, Anne M, MD</creatorcontrib><creatorcontrib>Flynn, Patrick J, MD</creatorcontrib><creatorcontrib>Goh, Boon Cher, MBBS</creatorcontrib><creatorcontrib>Tang, Hui, PhD</creatorcontrib><creatorcontrib>Ivy, Susan Percy, MD</creatorcontrib><creatorcontrib>Erlichman, Charles, Prof</creatorcontrib><creatorcontrib>the Mayo Phase 2 Consortium</creatorcontrib><creatorcontrib>for the Endocrine Malignancies Disease Oriented Group</creatorcontrib><creatorcontrib>Mayo Clinic Cancer Center</creatorcontrib><creatorcontrib>Endocrine Malignancies Disease Oriented Group</creatorcontrib><creatorcontrib>Mayo Phase 2 Consortium</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Lancet Titles</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The lancet oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bible, Keith C, Dr</au><au>Suman, Vera J, Prof</au><au>Molina, Julian R, MD</au><au>Smallridge, Robert C, Prof</au><au>Maples, William J, MD</au><au>Menefee, Michael E, MD</au><au>Rubin, Joseph, Prof</au><au>Sideras, Kostandinos, MD</au><au>Morris, John C, MD</au><au>McIver, Bryan, MB</au><au>Burton, Jill K</au><au>Webster, Kevin P</au><au>Bieber, Carolyn</au><au>Traynor, Anne M, MD</au><au>Flynn, Patrick J, MD</au><au>Goh, Boon Cher, MBBS</au><au>Tang, Hui, PhD</au><au>Ivy, Susan Percy, MD</au><au>Erlichman, Charles, Prof</au><aucorp>the Mayo Phase 2 Consortium</aucorp><aucorp>for the Endocrine Malignancies Disease Oriented Group</aucorp><aucorp>Mayo Clinic Cancer Center</aucorp><aucorp>Endocrine Malignancies Disease Oriented Group</aucorp><aucorp>Mayo Phase 2 Consortium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of pazopanib in progressive, radioiodine-refractory, metastatic differentiated thyroid cancers: results of a phase 2 consortium study</atitle><jtitle>The lancet oncology</jtitle><addtitle>Lancet Oncol</addtitle><date>2010-10-01</date><risdate>2010</risdate><volume>11</volume><issue>10</issue><spage>962</spage><epage>972</epage><pages>962-972</pages><issn>1470-2045</issn><issn>1474-5488</issn><eissn>1474-5488</eissn><coden>LANCAO</coden><abstract>Summary Background Chemotherapy has historically proven ineffective in advanced differentiated thyroid cancers, but the realisation that various tyrosine kinases are activated in the disease suggested a potential therapeutic role for tyrosine-kinase inhibitors. We investigated the safety and efficacy of pazopanib. Methods This phase 2 trial was done from Feb 22, 2008, to Jan 31, 2009, in patients with metastatic, rapidly progressive, radioiodine-refractory differentiated thyroid cancers. Each patient received 800 mg continuous pazopanib daily in 4-week cycles until disease progression, drug intolerance, or both occurred. Up to two previous therapies were allowed, and measurable disease with radiographic progression in the 6-month period before enrolment was a requirement for inclusion. The primary endpoint was any tumour response, according to the Response Evaluation Criteria in Solid Tumors 1.0. This study is registered with ClinicalTrials.gov , number NCT00625846. Findings 39 patients were enrolled. One patient had received no previous radioiodine therapy and another withdrew consent before treatment. Clinical outcomes could, therefore, be assessed in 37 patients (19 [51%] men, median age 63 years). The study is closed to accrual of new patients, but several enrolled patients are still being treated. Patients received a median of 12 cycles (range 1 to >23, total >383). Confirmed partial responses were recorded in 18 patients (response rate 49%, 95% CI 35–68), with likelihood of response lasting longer than 1 year calculated to be 66%. Maximum concentration of pazopanib in plasma during cycle one was significantly correlated with radiographic response ( r =−0·40, p=0·021). 16 (43%) patients required dose reductions owing to adverse events, the most frequent of which (any grade) were fatigue (29 patients), skin and hair hypopigmentation (28), diarrhoea (27), and nausea (27). Two patients who died during treatment had pre-existing contributory disorders. Interpretation Pazopanib seems to represent a promising therapeutic option for patients with advanced differentiated thyroid cancers. The correlation of the patient's response and pazopanib concentration during the first cycle might indicate that treatment can be individualised to achieve optimum outcomes. Assessment of pazopanib in an expanded cohort of patients with differentiated thyroid cancer, as well as in cohorts of patients with medullary and anaplastic thyroid cancers, is presently being done. Funding National Cancer Institute , supported in part by NCI CA15083 and CM62205.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>20851682</pmid><doi>10.1016/S1470-2045(10)70203-5</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1470-2045 |
ispartof | The lancet oncology, 2010-10, Vol.11 (10), p.962-972 |
issn | 1470-2045 1474-5488 1474-5488 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3107731 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Adult Aged Antineoplastic Agents - adverse effects Antineoplastic Agents - therapeutic use Cell Differentiation Disease Progression Disease-Free Survival Female Hematology, Oncology and Palliative Medicine Humans Indazoles Iodine Radioisotopes - therapeutic use Male Middle Aged Protein Kinase Inhibitors - adverse effects Protein Kinase Inhibitors - therapeutic use Pyrimidines - adverse effects Pyrimidines - therapeutic use Radiography Radiopharmaceuticals - therapeutic use Sulfonamides - adverse effects Sulfonamides - therapeutic use Thyroid Neoplasms - diagnostic imaging Thyroid Neoplasms - drug therapy Thyroid Neoplasms - mortality Thyroid Neoplasms - radiotherapy Thyroid Neoplasms - secondary Time Factors Treatment Failure United States Young Adult |
title | Efficacy of pazopanib in progressive, radioiodine-refractory, metastatic differentiated thyroid cancers: results of a phase 2 consortium study |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T15%3A25%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Efficacy%20of%20pazopanib%20in%20progressive,%20radioiodine-refractory,%20metastatic%20differentiated%20thyroid%20cancers:%20results%20of%20a%20phase%202%20consortium%20study&rft.jtitle=The%20lancet%20oncology&rft.au=Bible,%20Keith%20C,%20Dr&rft.aucorp=the%20Mayo%20Phase%202%20Consortium&rft.date=2010-10-01&rft.volume=11&rft.issue=10&rft.spage=962&rft.epage=972&rft.pages=962-972&rft.issn=1470-2045&rft.eissn=1474-5488&rft.coden=LANCAO&rft_id=info:doi/10.1016/S1470-2045(10)70203-5&rft_dat=%3Cproquest_pubme%3E2165025611%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=758828152&rft_id=info:pmid/20851682&rft_els_id=1_s2_0_S1470204510702035&rfr_iscdi=true |