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Low dose DTIC is effective and safe in pretreated patients with well differentiated neuroendocrine tumors
BACKGROUND: Streptozocin (STZ) based chemotherapy is recommended for patients with metastatic pancreatic neuroendocrine tumors (pNET). Temozolomide as mono- or combination therapy has been suggested to be a promising alternative. However, the treatment is costly and not approved for the treatment of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989525/ https://www.ncbi.nlm.nih.gov/pubmed/27538897 http://dx.doi.org/10.1186/s12885-016-2642-1 |
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author | Mueller, Daniela Krug, Sebastian Majumder, Moushumee Rinke, Anja Gress, Thomas Matthias |
author_facet | Mueller, Daniela Krug, Sebastian Majumder, Moushumee Rinke, Anja Gress, Thomas Matthias |
author_sort | Mueller, Daniela |
collection | PubMed |
description | BACKGROUND: Streptozocin (STZ) based chemotherapy is recommended for patients with metastatic pancreatic neuroendocrine tumors (pNET). Temozolomide as mono- or combination therapy has been suggested to be a promising alternative. However, the treatment is costly and not approved for the treatment of pNETs. Dacarbazine (DTIC) shares the active metabolite with temozolomide and is broadly available at a low cost. The aim of this study was a retrospective evaluation of the efficacy and tolerability of a lower dose DTIC-regimen in patients with progressive advanced NETs. METHODS: We retrospectively analyzed 75 patients with NETs predominantly of pancreatic origin treated at our center between 1998 and 2013. 650 mg/m(2) of DTIC were administered intravenously over 60 min every 4 weeks. Morphological response was assessed according to RECIST1.1 criteria. The median progression free survival (PFS) was calculated using Kaplan-Meier and Cox regression methods, respectively. Univariate analyses of possible prognostic markers were performed. RESULTS: The objective response rate (ORR) was 27 % for the entire cohort and 32 % in 50 pNET patients, respectively. Stable disease (SD) was documented in 29 patients (39 %). Median PFS (mPFS) in patients receiving DTIC was 7 months (3.9–10; 95 % confidence interval). Radiological and biochemical response were the only significant prognostic markers for longer PFS in univariate analysis. Treatment was well tolerated. Nausea was the most common side effect (31 %), only one case (1.3 %) of grade 3 toxicity (vomiting) occurred. CONCLUSION: Low dose DTIC chemotherapy is an effective and well-tolerated treatment option in patients with progressive well differentiated neuroendocrine neoplasms, especially of pancreatic origin. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2642-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4989525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49895252016-08-19 Low dose DTIC is effective and safe in pretreated patients with well differentiated neuroendocrine tumors Mueller, Daniela Krug, Sebastian Majumder, Moushumee Rinke, Anja Gress, Thomas Matthias BMC Cancer Research Article BACKGROUND: Streptozocin (STZ) based chemotherapy is recommended for patients with metastatic pancreatic neuroendocrine tumors (pNET). Temozolomide as mono- or combination therapy has been suggested to be a promising alternative. However, the treatment is costly and not approved for the treatment of pNETs. Dacarbazine (DTIC) shares the active metabolite with temozolomide and is broadly available at a low cost. The aim of this study was a retrospective evaluation of the efficacy and tolerability of a lower dose DTIC-regimen in patients with progressive advanced NETs. METHODS: We retrospectively analyzed 75 patients with NETs predominantly of pancreatic origin treated at our center between 1998 and 2013. 650 mg/m(2) of DTIC were administered intravenously over 60 min every 4 weeks. Morphological response was assessed according to RECIST1.1 criteria. The median progression free survival (PFS) was calculated using Kaplan-Meier and Cox regression methods, respectively. Univariate analyses of possible prognostic markers were performed. RESULTS: The objective response rate (ORR) was 27 % for the entire cohort and 32 % in 50 pNET patients, respectively. Stable disease (SD) was documented in 29 patients (39 %). Median PFS (mPFS) in patients receiving DTIC was 7 months (3.9–10; 95 % confidence interval). Radiological and biochemical response were the only significant prognostic markers for longer PFS in univariate analysis. Treatment was well tolerated. Nausea was the most common side effect (31 %), only one case (1.3 %) of grade 3 toxicity (vomiting) occurred. CONCLUSION: Low dose DTIC chemotherapy is an effective and well-tolerated treatment option in patients with progressive well differentiated neuroendocrine neoplasms, especially of pancreatic origin. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2642-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-18 /pmc/articles/PMC4989525/ /pubmed/27538897 http://dx.doi.org/10.1186/s12885-016-2642-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Mueller, Daniela Krug, Sebastian Majumder, Moushumee Rinke, Anja Gress, Thomas Matthias Low dose DTIC is effective and safe in pretreated patients with well differentiated neuroendocrine tumors |
title | Low dose DTIC is effective and safe in pretreated patients with well differentiated neuroendocrine tumors |
title_full | Low dose DTIC is effective and safe in pretreated patients with well differentiated neuroendocrine tumors |
title_fullStr | Low dose DTIC is effective and safe in pretreated patients with well differentiated neuroendocrine tumors |
title_full_unstemmed | Low dose DTIC is effective and safe in pretreated patients with well differentiated neuroendocrine tumors |
title_short | Low dose DTIC is effective and safe in pretreated patients with well differentiated neuroendocrine tumors |
title_sort | low dose dtic is effective and safe in pretreated patients with well differentiated neuroendocrine tumors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989525/ https://www.ncbi.nlm.nih.gov/pubmed/27538897 http://dx.doi.org/10.1186/s12885-016-2642-1 |
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