2024-11-0920151107-0625N/A2-s2.0-84953852698https://hdl.handle.net/20.500.14288/9367Purpose: Benefits of somatostatin analogues have been mostly studied in mixed samples of patients including both functional and non-functional neuroendocrine tumors. This study aimed to examine the response of patients with non-functional metastatic or inoperable gastroenteropancreatic neuroendocrine tumors (GEP-NETs) that received first-line treatment with the somatostatin analogue octreotide LAR. Methods: The medical records of 23 patients with locally inoperable or metastatic non-functional neuroendocrine tumors who received octreotide LAR (long acting release) treatment were retrospectively reviewed for clinical data and disease course. All patients had received first-line octreotide MR 30 mg for 4 weeks. Progression free survival (PFS) and overall survival (OS) were the primary and secondary endpoints, respectively. Results: All patients were followed for a median of 47 months. Mean PFS and OS were 25.0 +/- 3.4 months (95% Cl: 18.4-31.5) and 71.3 +/- 9.5 months (95% Cl: 52.7-89.9), respectively, with an estimated 5-year OS of 58%. Patients with <= 25% of hepatic tumor load had better PFS when compared to patients with >25% hepatic tumor load (32.2 +/- 6.2 vs 19.4 +/- 2.7 months, p=0.043). During treatment, the following adverse events developed: skin reaction (N=1, 4.3%), cholestasis (N=1, 4.3%), grade 1 diarrhea (N=1, 4.3%), and newly onset diabetes (N=3; 13.0%). Conclusion: Octreotide LAR seems to be an effective treatment option with acceptable tolerability for patients with well-differentiated non-functional GEP-NETs. Survival benefits warrant further testing in future large-scale prospective trials.OncologyJournal Article366872500004Q4959