Cargando…
Predictive factors of antiproliferative activity of octreotide LAR as first-line therapy for advanced neuroendocrine tumours
BACKGROUND: The antiproliferative activity of octreotide LAR in neuroendocrine tumours (NETs) has been demonstrated by small retrospective studies and confirmed by a prospective phase III trial (PROMID). However, there are limited data about the duration and predictors of response. The aim of our re...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129835/ https://www.ncbi.nlm.nih.gov/pubmed/27811856 http://dx.doi.org/10.1038/bjc.2016.349 |
_version_ | 1782470638734147584 |
---|---|
author | Laskaratos, Faidon-Marios Walker, Martin Naik, Keval Maragkoudakis, Emmanouil Oikonomopoulos, Nikolaos Grant, Lee Meyer, Tim Caplin, Martyn Toumpanakis, Christos |
author_facet | Laskaratos, Faidon-Marios Walker, Martin Naik, Keval Maragkoudakis, Emmanouil Oikonomopoulos, Nikolaos Grant, Lee Meyer, Tim Caplin, Martyn Toumpanakis, Christos |
author_sort | Laskaratos, Faidon-Marios |
collection | PubMed |
description | BACKGROUND: The antiproliferative activity of octreotide LAR in neuroendocrine tumours (NETs) has been demonstrated by small retrospective studies and confirmed by a prospective phase III trial (PROMID). However, there are limited data about the duration and predictors of response. The aim of our retrospective study was to determine the time to radiological progression (TTRP) of disease and the factors that were associated with better response. METHODS: A total of 254 treatment naïve patients with advanced NETs and positive somatostatin receptor scintigraphy were included. Mean follow-up period was 42 months. RESULTS: The location of primary was in the small bowel in 204, pancreas in 22, lungs in 14, rectum in 7 and unknown in 7 patients. Most tumours were well-differentiated, G1 (58%) and G2 (23%). The majority of patients commenced octreotide LAR due to functional symptoms (57%), radiological progression (10%) or in the presence of asymptomatic and stable disease on the basis of data from the PROMID trial (18.5%). Partial response occurred in 5%. For all patients, the median TTRP was 37 months (95% confidence interval, CI: 32–52 months). There was a statistically significant shorter TTRP in patients with pancreatic tumours, liver metastases and intermediate grade tumours. Extremely raised (>10 times the upper limit of normal) baseline chromogranin A levels were associated with an unfavourable outcome. In contrast, male sex, carcinoid heart disease and initiation of treatment in the presence of stable disease were predictive of a better response. Age, extra-hepatic metastases, presence of mesenteric desmoplasia, previous resection and functional status of the primary tumour did not affect response. CONCLUSIONS: The duration of the antiproliferative effect of octreotide LAR seems to be longer than previously reported. This study has identified several predictors of response in a large cohort of patients with NETs on somatostatin analogue therapy. |
format | Online Article Text |
id | pubmed-5129835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51298352017-11-22 Predictive factors of antiproliferative activity of octreotide LAR as first-line therapy for advanced neuroendocrine tumours Laskaratos, Faidon-Marios Walker, Martin Naik, Keval Maragkoudakis, Emmanouil Oikonomopoulos, Nikolaos Grant, Lee Meyer, Tim Caplin, Martyn Toumpanakis, Christos Br J Cancer Clinical Study BACKGROUND: The antiproliferative activity of octreotide LAR in neuroendocrine tumours (NETs) has been demonstrated by small retrospective studies and confirmed by a prospective phase III trial (PROMID). However, there are limited data about the duration and predictors of response. The aim of our retrospective study was to determine the time to radiological progression (TTRP) of disease and the factors that were associated with better response. METHODS: A total of 254 treatment naïve patients with advanced NETs and positive somatostatin receptor scintigraphy were included. Mean follow-up period was 42 months. RESULTS: The location of primary was in the small bowel in 204, pancreas in 22, lungs in 14, rectum in 7 and unknown in 7 patients. Most tumours were well-differentiated, G1 (58%) and G2 (23%). The majority of patients commenced octreotide LAR due to functional symptoms (57%), radiological progression (10%) or in the presence of asymptomatic and stable disease on the basis of data from the PROMID trial (18.5%). Partial response occurred in 5%. For all patients, the median TTRP was 37 months (95% confidence interval, CI: 32–52 months). There was a statistically significant shorter TTRP in patients with pancreatic tumours, liver metastases and intermediate grade tumours. Extremely raised (>10 times the upper limit of normal) baseline chromogranin A levels were associated with an unfavourable outcome. In contrast, male sex, carcinoid heart disease and initiation of treatment in the presence of stable disease were predictive of a better response. Age, extra-hepatic metastases, presence of mesenteric desmoplasia, previous resection and functional status of the primary tumour did not affect response. CONCLUSIONS: The duration of the antiproliferative effect of octreotide LAR seems to be longer than previously reported. This study has identified several predictors of response in a large cohort of patients with NETs on somatostatin analogue therapy. Nature Publishing Group 2016-11-22 2016-11-03 /pmc/articles/PMC5129835/ /pubmed/27811856 http://dx.doi.org/10.1038/bjc.2016.349 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Clinical Study Laskaratos, Faidon-Marios Walker, Martin Naik, Keval Maragkoudakis, Emmanouil Oikonomopoulos, Nikolaos Grant, Lee Meyer, Tim Caplin, Martyn Toumpanakis, Christos Predictive factors of antiproliferative activity of octreotide LAR as first-line therapy for advanced neuroendocrine tumours |
title | Predictive factors of antiproliferative activity of octreotide LAR as first-line therapy for advanced neuroendocrine tumours |
title_full | Predictive factors of antiproliferative activity of octreotide LAR as first-line therapy for advanced neuroendocrine tumours |
title_fullStr | Predictive factors of antiproliferative activity of octreotide LAR as first-line therapy for advanced neuroendocrine tumours |
title_full_unstemmed | Predictive factors of antiproliferative activity of octreotide LAR as first-line therapy for advanced neuroendocrine tumours |
title_short | Predictive factors of antiproliferative activity of octreotide LAR as first-line therapy for advanced neuroendocrine tumours |
title_sort | predictive factors of antiproliferative activity of octreotide lar as first-line therapy for advanced neuroendocrine tumours |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5129835/ https://www.ncbi.nlm.nih.gov/pubmed/27811856 http://dx.doi.org/10.1038/bjc.2016.349 |
work_keys_str_mv | AT laskaratosfaidonmarios predictivefactorsofantiproliferativeactivityofoctreotidelarasfirstlinetherapyforadvancedneuroendocrinetumours AT walkermartin predictivefactorsofantiproliferativeactivityofoctreotidelarasfirstlinetherapyforadvancedneuroendocrinetumours AT naikkeval predictivefactorsofantiproliferativeactivityofoctreotidelarasfirstlinetherapyforadvancedneuroendocrinetumours AT maragkoudakisemmanouil predictivefactorsofantiproliferativeactivityofoctreotidelarasfirstlinetherapyforadvancedneuroendocrinetumours AT oikonomopoulosnikolaos predictivefactorsofantiproliferativeactivityofoctreotidelarasfirstlinetherapyforadvancedneuroendocrinetumours AT grantlee predictivefactorsofantiproliferativeactivityofoctreotidelarasfirstlinetherapyforadvancedneuroendocrinetumours AT meyertim predictivefactorsofantiproliferativeactivityofoctreotidelarasfirstlinetherapyforadvancedneuroendocrinetumours AT caplinmartyn predictivefactorsofantiproliferativeactivityofoctreotidelarasfirstlinetherapyforadvancedneuroendocrinetumours AT toumpanakischristos predictivefactorsofantiproliferativeactivityofoctreotidelarasfirstlinetherapyforadvancedneuroendocrinetumours |