RAYMOND, Eric, Matthew H. KULKE, Shukui QIN, Xianjun YU, Mchael SCHENKER, Antonio CUBILLO, Wenhui LOU, Jiří TOMÁŠEK, Espen THIIS-EVENSEN, Jian-Ming XU, Adina E. CROITORU, Mustafa KHASRAW, Eva SEDLACKOVA, Ivan BORBATH, Paul RUFF, Paul E. OBERSTEIN, Tetsuhide ITO, Li Quin JIA, Pascal HAMMEL, Lin SHEN, Shailesh V. SHRIKHANDE, Yali SHEN, Jozef SUFLIARSKY, Gazala N. KHAN, Chigusa MORIZANE, Salvatore GALDY, Reza KHOSRAVAN, Kathrine C. FERNANDEZ, Brad ROSBROOK and Nicola FAZIO. Efficacy and Safety of Sunitinib in Patients with Well-Differentiated Pancreatic Neuroendocrine Tumours. NEUROENDOCRINOLOGY. BASEL: KARGER, 2018, vol. 107, No 3, p. 237-245. ISSN 0028-3835. Available from: https://dx.doi.org/10.1159/000491999.
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Basic information
Original name Efficacy and Safety of Sunitinib in Patients with Well-Differentiated Pancreatic Neuroendocrine Tumours
Authors RAYMOND, Eric (250 France), Matthew H. KULKE (840 United States of America), Shukui QIN (156 China), Xianjun YU (156 China), Mchael SCHENKER (642 Romania), Antonio CUBILLO (724 Spain), Wenhui LOU (156 China), Jiří TOMÁŠEK (203 Czech Republic, belonging to the institution), Espen THIIS-EVENSEN (578 Norway), Jian-Ming XU (156 China), Adina E. CROITORU (642 Romania), Mustafa KHASRAW (36 Australia), Eva SEDLACKOVA (203 Czech Republic), Ivan BORBATH (56 Belgium), Paul RUFF (710 South Africa), Paul E. OBERSTEIN (840 United States of America), Tetsuhide ITO (392 Japan), Li Quin JIA (156 China), Pascal HAMMEL (250 France), Lin SHEN (156 China), Shailesh V. SHRIKHANDE (356 India), Yali SHEN (156 China), Jozef SUFLIARSKY (703 Slovakia), Gazala N. KHAN (840 United States of America), Chigusa MORIZANE (392 Japan), Salvatore GALDY (380 Italy), Reza KHOSRAVAN (840 United States of America), Kathrine C. FERNANDEZ (840 United States of America), Brad ROSBROOK (840 United States of America) and Nicola FAZIO (380 Italy).
Edition NEUROENDOCRINOLOGY, BASEL, KARGER, 2018, 0028-3835.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30103 Neurosciences
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 6.804
RIV identification code RIV/00216224:14110/18:00106277
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1159/000491999
UT WoS 000456060200004
Keywords in English Pancreatic neuroendocrine tumour; Progression-free survival; Overall survival; Safety; Sunitinib
Tags 14110811, rivok
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 21/2/2019 13:52.
Abstract
Background: In a phase III study, sunitinib led to a significant increase in progression-free survival (PFS) versus placebo in patients with pancreatic neuroendocrine tumours (pan-NETs). This study was a post-marketing commitment to support the phase III data. Methods: In this ongoing, open-label, phase IV trial (NCT01525550), patients with progressive, advanced unresectable/metastatic, well-differentiated pan-NETs received continuous sunitinib 37.5 mg once daily. Eligibility criteria were similar to those of the phase III study. The primary endpoint was investigator-assessed PFS per Response Evaluation Criteria in Solid Tumours v1.0 (RECIST). Other endpoints included PFS per Choi criteria, overall survival (OS), objective response rate (ORR), and adverse events (AEs). Results: Sixty-one treatment-naive and 45 previously treated patients received sunitinib. By March 19, 2016, 82 (77%) patients had discontinued treatment, mainly due to disease progression. Median treatment duration was 11.7 months. Investigator-assessed median PFS per RECIST (95% confidence interval [CI]) was 13.2 months (10.9-16.7): 13.2 (7.4-16.8) and 13.0 (9.2-20.4) in treatment-naive and previously treated patients, respectively. ORR (95% CI) per RECIST was 24.5% (16.7-33.8) in the total population: 21.3% (11.9-33.7) in treatment-naive and 28.9% (16.4-44.3) in previously treated patients. Median OS, although not yet mature, was 37.8 months (95% CI, 33.0-not estimable). The most common treatment-related AEs were neutropenia (53.8%), diarrhoea (46.2%), and leukopenia (43.4%). Conclusions: This phase IV trial confirms sunitinib as an efficacious and safe treatment option in patients with advanced/metastatic, well-differentiated, unresectable panNETs, and supports the phase III study outcomes. AEs were consistent with the known safety profile of sunitinib. (C) 2018 S. Karger AG, Basel
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