Comparison of survival with somatostatin analog and chemotherapy and prognostic factors for treatment in 165 advanced neuroendocrine tumor patients with Ki-67 20% or less

dc.contributor.authorOzaslan, Ersin
dc.contributor.authorKaraca, Halit
dc.contributor.authorKoca, Sinan
dc.contributor.authorSevinc, Alper
dc.contributor.authorHacioglu, Bekir
dc.contributor.authorOzkan, Metin
dc.contributor.authorDane, Faysal
dc.date.accessioned2026-08-12T17:17:01Z
dc.date.issued2017
dc.departmentFırat Üniversitesi
dc.description.abstractThe objectives of this study were to compare progression-free survival (PFS) with somatostatin analog (SSA) versus chemotherapy (CTx) in first-line therapy and to determine the patient group in which these treatments were more effective in neuroendocrine tumors (NETs) with a Ki-67 index of 20% or less. Patients who received SSA or CTx and had unresectable locally advanced and metastatic NETs with a Ki-67 index of 20% or less were retrospectively selected from 13 centers in the Turkish database between 2000 and 2015. One hundred and sixty-five patients were enrolled. The median age was 56 years and the male-to-female ratio was 1.09. Seventy-four (45%) patients were of grade 1 NET and 91 (55%) were of grade 2. SSA was given to 104 patients, whereas 61 were treated with CTx. The objective response rate after SSA was 15.4%; another 73.1% had stable disease. The objective response rate after CTx was 36.1%, and 40.9% had stable disease (P = 0.008). The median PFS in SSA patients was 21 months (95% confidence interval: 12.4-29.6), and 8 months for CTx (95% confidence interval: 5.5-10.6) (P < 0.001). There was no significant difference between PFS of receiving SSA and CTx in pancreatic neuroendocrine tumor (PNET) patients; however, the PFS of receiving SSA was longer in non-PNET patients (P < 0.001). SSA was better treatment in advanced NET patients with a Ki-67 index of less than 5%, having a primary resected and a performance status of 0 (P < 0.05). SSA may be preferred over CTx in advanced NET patients with low-to-intermediate grade. Copyright (C) 2017 Wolters Kluwer Health, Inc. All rights reserved.
dc.identifier.doi10.1097/CAD.0000000000000445
dc.identifier.endpage229
dc.identifier.issn0959-4973
dc.identifier.issn1473-5741
dc.identifier.issue2
dc.identifier.orcid0000-0002-0598-7284
dc.identifier.orcid0000-0001-8490-3239
dc.identifier.orcid0000-0002-0499-8918
dc.identifier.orcid0000-0002-0333-7405
dc.identifier.orcid0000-0002-5609-9658
dc.identifier.pmid27768606
dc.identifier.scopus2-s2.0-84992092875
dc.identifier.scopusqualityQ2
dc.identifier.startpage222
dc.identifier.urihttps://doi.org/10.1097/CAD.0000000000000445
dc.identifier.urihttps://hdl.handle.net/11508/52511
dc.identifier.volume28
dc.identifier.wosWOS:000392824000012
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherLippincott Williams & Wilkins
dc.relation.ispartofAnti-Cancer Drugs
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectchemotherapy
dc.subjectKi-67 index
dc.subjectlanreotide
dc.subjectneuroendocrine tumor
dc.subjectoctreotide
dc.subjectpancreatic neuroendocrine tumor
dc.subjectsomatostatin analog
dc.titleComparison of survival with somatostatin analog and chemotherapy and prognostic factors for treatment in 165 advanced neuroendocrine tumor patients with Ki-67 20% or less
dc.typeArticle

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