Literature DB >> 20851682

Efficacy of pazopanib in progressive, radioiodine-refractory, metastatic differentiated thyroid cancers: results of a phase 2 consortium study.

Keith C Bible1, Vera J Suman, Julian R Molina, Robert C Smallridge, William J Maples, Michael E Menefee, Joseph Rubin, Kostandinos Sideras, John C Morris, Bryan McIver, Jill K Burton, Kevin P Webster, Carolyn Bieber, Anne M Traynor, Patrick J Flynn, Boon Cher Goh, Hui Tang, Susan Percy Ivy, Charles Erlichman.   

Abstract

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.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20851682      PMCID: PMC3107731          DOI: 10.1016/S1470-2045(10)70203-5

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  26 in total

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2.  Increased expression of vascular endothelial growth factor C in papillary thyroid carcinoma correlates with cervical lymph node metastases.

Authors:  Xiao-Min Yu; Chung-Yau Lo; Wai-Fan Chan; King-Yin Lam; Pauline Leung; John M Luk
Journal:  Clin Cancer Res       Date:  2005-11-15       Impact factor: 12.531

3.  Increased expression of the vascular endothelial growth factor is a pejorative prognosis marker in papillary thyroid carcinoma.

Authors:  M Klein; J M Vignaud; V Hennequin; B Toussaint; L Bresler; F Plénat; J Leclère; A Duprez; G Weryha
Journal:  J Clin Endocrinol Metab       Date:  2001-02       Impact factor: 5.958

4.  Influence of the BRAF V600E mutation on expression of vascular endothelial growth factor in papillary thyroid cancer.

Authors:  Young Suk Jo; Shengjin Li; Jung Hun Song; Ki Hyun Kwon; Jun Chul Lee; So Young Rha; Hyo Jin Lee; Ji Young Sul; Gi Ryang Kweon; Heung-Kyu Ro; Jin-Man Kim; Minho Shong
Journal:  J Clin Endocrinol Metab       Date:  2006-06-13       Impact factor: 5.958

5.  Treatment with tyrosine kinase inhibitors for patients with differentiated thyroid cancer: the M. D. Anderson experience.

Authors:  Maria E Cabanillas; Steven G Waguespack; Yulia Bronstein; Michelle D Williams; Lei Feng; Mike Hernandez; Adriana Lopez; Steven I Sherman; Naifa L Busaidy
Journal:  J Clin Endocrinol Metab       Date:  2010-04-14       Impact factor: 5.958

6.  Neutralizing vascular endothelial growth factor activity inhibits thyroid cancer growth in vivo.

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Authors:  C M Lennard; A Patel; J Wilson; B Reinhardt; C Tuman; C Fenton; E Blair; G L Francis; R M Tuttle
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9.  A phase II study of gefitinib in patients with advanced thyroid cancer.

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Journal:  Thyroid       Date:  2008-03       Impact factor: 6.568

10.  Phase II study of celecoxib in metastatic differentiated thyroid carcinoma.

Authors:  Ewa Mrozek; Richard T Kloos; Matthew D Ringel; Laura Kresty; Paulette Snider; Daria Arbogast; Merrill Kies; Reginald Munden; Naifa Busaidy; Mary Jean Klein; Steven I Sherman; Manisha H Shah
Journal:  J Clin Endocrinol Metab       Date:  2006-03-07       Impact factor: 5.958

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  146 in total

Review 1.  Treatment strategies for radioactive iodine-refractory differentiated thyroid cancer.

Authors:  Francis Worden
Journal:  Ther Adv Med Oncol       Date:  2014-11       Impact factor: 8.168

Review 2.  Pharmacotherapy options for advanced thyroid cancer: a systematic review.

Authors:  Christian Lerch; Bernd Richter
Journal:  Drugs       Date:  2012-01-01       Impact factor: 9.546

3.  Effect of dasatinib against thyroid cancer cell lines in vitro and a xenograft model in vivo.

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4.  Synergistic action of a RAF inhibitor and a dual PI3K/mTOR inhibitor in thyroid cancer.

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Journal:  Clin Cancer Res       Date:  2011-08-10       Impact factor: 12.531

5.  A multiinstitutional phase 2 trial of pazopanib monotherapy in advanced anaplastic thyroid cancer.

Authors:  Keith C Bible; Vera J Suman; Michael E Menefee; Robert C Smallridge; Julian R Molina; William J Maples; Nina J Karlin; Anne M Traynor; Priya Kumar; Boon Cher Goh; Wan-Teck Lim; Ayoko R Bossou; Crescent R Isham; Kevin P Webster; Andrea K Kukla; Carolyn Bieber; Jill K Burton; Pamela Harris; Charles Erlichman
Journal:  J Clin Endocrinol Metab       Date:  2012-07-06       Impact factor: 5.958

Review 6.  Preclinical rationale and clinical efficacy of antiangiogenic therapy and immune checkpoint blockade combination therapy in urogenital tumors.

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7.  A phase I pharmacokinetic and safety evaluation of oral pazopanib dosing administered as crushed tablet or oral suspension in patients with advanced solid tumors.

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Review 8.  Current status of novel agents in advanced gastroesophageal adenocarcinoma.

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Review 9.  Molecular pathogenesis and mechanisms of thyroid cancer.

Authors:  Mingzhao Xing
Journal:  Nat Rev Cancer       Date:  2013-03       Impact factor: 60.716

Review 10.  Biologic and Clinical Perspectives on Thyroid Cancer.

Authors:  James A Fagin; Samuel A Wells
Journal:  N Engl J Med       Date:  2016-09-15       Impact factor: 91.245

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