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Everolimus in Neuroendocrine Tumors of the Gastrointestinal Tract and Unknown Primary.
- Source :
- Neuroendocrinology; Apr2018, Vol. 106 Issue 3, p211-220, 10p, 3 Charts, 2 Graphs
- Publication Year :
- 2018
-
Abstract
- <bold><italic>Purpose:</italic></bold> The RADIANT-4 randomized phase 3 study demonstrated significant prolongation of median progression-free survival (PFS) with everolimus compared to placebo (11.0 [95% CI 9.2-13.3] vs. 3.9 [95% CI 3.6-7.4] months) in patients with advanced, progressive, nonfunctional gastrointestinal (GI) and lung neuroendocrine tumors (NET). This analysis specifically evaluated NET patients with GI and unknown primary origin. <bold><italic>Methods:</italic></bold> Patients in the RADIANT-4 trial were randomized 2:1 to everolimus 10 mg/day or placebo. The effect of everolimus on PFS was evaluated in patients with NET of the GI tract or unknown primary site. <bold><italic>Results:</italic></bold> Of the 302 patients enrolled, 175 had GI NET (everolimus, 118; placebo, 57) and 36 had unknown primary (everolimus, 23; placebo, 13). In the GI subset, the median PFS by central review was 13.1 months (95% CI 9.2-17.3) in the everolimus arm versus 5.4 months (95% CI 3.6-9.3) in the placebo arm; the hazard ratio (HR) was 0.56 (95% CI 0.37-0.84). In the unknown primary patients, the median PFS was 13.6 months (95% CI 4.1-not evaluable) for everolimus versus 7.5 months (95% CI 1.9-18.5) for placebo; the HR was 0.60 (95% CI 0.24-1.51). Everolimus efficacy was also demonstrated in both midgut and non-midgut populations; a 40-46% reduction in the risk of progression or death was reported for patients in the combined GI and unknown primary subgroup. Everolimus had a benefit regardless of prior somatostatin analog therapy. <bold><italic>Conclusions:</italic></bold> Everolimus showed a clinically meaningful PFS benefit in patients with advanced progressive nonfunctional NET of GI and unknown primary, consistent with the overall RADIANT-4 results, providing an effective new standard treatment option in this patient population and filling an unmet treatment need for these patients. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00283835
- Volume :
- 106
- Issue :
- 3
- Database :
- Complementary Index
- Journal :
- Neuroendocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 129070776
- Full Text :
- https://doi.org/10.1159/000477585