Abstract |
Sunitinib inhibits several receptor tyrosine kinases involved in cancer growth, metastasis, and neoangiogenesis, with its active metabolite (SU012662) demonstrating similar potency. In a randomized, double-blind, multinational, phase III trial, continuous treatment with oral sunitinib 37.5 mg/day significantly prolonged median progression-free survival time (primary endpoint) ≈2-fold relative to placebo in adults with locally advanced and/or metastatic, well differentiated pancreatic neuroendocrine tumors ( pNETs). Sunitinib was also associated with a significantly greater objective tumor response rate than placebo, although limited data from an updated analysis demonstrated no significant difference between the treatments groups in terms of median overall survival. Continuous treatment with sunitinib generally had no detrimental effect on health-related quality of life and was generally well tolerated in patients with pNETs in this trial, with most adverse events being manageable and of grade 1 or 2 severity.
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Authors | Emma D Deeks, Eric Raymond |
Journal | BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy
(BioDrugs)
Vol. 25
Issue 5
Pg. 307-16
(Oct 01 2011)
ISSN: 1179-190X [Electronic] New Zealand |
PMID | 21942915
(Publication Type: Clinical Trial, Phase III, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Antineoplastic Agents
- Indoles
- Pyrroles
- Receptor Protein-Tyrosine Kinases
- Sunitinib
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Antineoplastic Agents
(adverse effects, pharmacokinetics, pharmacology, therapeutic use)
- Female
- Humans
- Indoles
(adverse effects, pharmacokinetics, pharmacology, therapeutic use)
- Male
- Middle Aged
- Neuroendocrine Tumors
(drug therapy)
- Pancreatic Neoplasms
(drug therapy)
- Pyrroles
(adverse effects, pharmacokinetics, pharmacology, therapeutic use)
- Receptor Protein-Tyrosine Kinases
(antagonists & inhibitors)
- Sunitinib
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