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Chemotherapy for metastatic colon cancer: No effect on survival when the dose is reduced due to side effects

BACKGROUND: 5-Fluorouracil (5FU), Folinic acid (FA), and Oxaliplatin (FOLFOX) or 5FU, FA, and Irinotecan (FOLFIRI) are standard regimens for palliative chemotherapy of metastatic colon cancer. Since data showing the influence of dose reduction in palliative treatment are rare, the objective of this...

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Autores principales: Munker, Stefan, Gerken, Michael, Fest, Petra, Ott, Claudia, Schnoy, Elisabeth, Fichtner-Feigl, Stefan, Wiggermann, Philipp, Vogelhuber, Martin, Herr, Wolfgang, Stroszczynski, Christian, Schlitt, Hans Jürgen, Evert, Matthias, Reng, Michael, Klinkhammer-Schalke, Monika, Teufel, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913883/
https://www.ncbi.nlm.nih.gov/pubmed/29685155
http://dx.doi.org/10.1186/s12885-018-4380-z
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author Munker, Stefan
Gerken, Michael
Fest, Petra
Ott, Claudia
Schnoy, Elisabeth
Fichtner-Feigl, Stefan
Wiggermann, Philipp
Vogelhuber, Martin
Herr, Wolfgang
Stroszczynski, Christian
Schlitt, Hans Jürgen
Evert, Matthias
Reng, Michael
Klinkhammer-Schalke, Monika
Teufel, Andreas
author_facet Munker, Stefan
Gerken, Michael
Fest, Petra
Ott, Claudia
Schnoy, Elisabeth
Fichtner-Feigl, Stefan
Wiggermann, Philipp
Vogelhuber, Martin
Herr, Wolfgang
Stroszczynski, Christian
Schlitt, Hans Jürgen
Evert, Matthias
Reng, Michael
Klinkhammer-Schalke, Monika
Teufel, Andreas
author_sort Munker, Stefan
collection PubMed
description BACKGROUND: 5-Fluorouracil (5FU), Folinic acid (FA), and Oxaliplatin (FOLFOX) or 5FU, FA, and Irinotecan (FOLFIRI) are standard regimens for palliative chemotherapy of metastatic colon cancer. Since data showing the influence of dose reduction in palliative treatment are rare, the objective of this single center, retrospective study was to further characterize the influence of dose reduction on efficacy of these therapeutic regimens. METHODS: One hundred nine patients, diagnosed with stage IV colon cancer between 2004 and 2012 and receiving palliative first-line chemotherapy with either FOLFOX or FOLFIRI regimens in our outpatient clinic were analyzed for treatment efficacy. Patients who received dose reductions due to side effects usually received doses of 80% or lower of per protocol dose. Survival data were obtained from the Regensburg Tumor Registry. Survival analysis was performed using Kaplan-Meier statistical analysis and multivariable analysis. RESULTS: A dose reduction due to side effects was necessary in 46 (42%) patients. Dose reduction was independent of age. Major reasons for dose reduction were neutropenia (30%) followed by polyneuropathy (16%) and diarrhea (14%). Dosage was more often reduced in patients receiving FOLFOX based therapy. Comparison of patients with dose reduction versus patients with full dosage showed no significant difference on overall survival (p = 0.430). Subgroup analysis revealed dose reduction in patients with N2 stage disease was associated with improved survival. Patients who underwent dose reduction received more cycles of chemotherapy (13.7 vs. 10.8 cycles) and cumulative dosage was similar in both groups. CONCLUSION: Contrary to our expectations, the need to reduce chemotherapy dosage due to side effects does not indicate a worse prognosis in our retrospective analysis. We believe this can in part be explained by better adaption to interindividual pharmacokinetics and longer time of treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4380-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-59138832018-04-30 Chemotherapy for metastatic colon cancer: No effect on survival when the dose is reduced due to side effects Munker, Stefan Gerken, Michael Fest, Petra Ott, Claudia Schnoy, Elisabeth Fichtner-Feigl, Stefan Wiggermann, Philipp Vogelhuber, Martin Herr, Wolfgang Stroszczynski, Christian Schlitt, Hans Jürgen Evert, Matthias Reng, Michael Klinkhammer-Schalke, Monika Teufel, Andreas BMC Cancer Research Article BACKGROUND: 5-Fluorouracil (5FU), Folinic acid (FA), and Oxaliplatin (FOLFOX) or 5FU, FA, and Irinotecan (FOLFIRI) are standard regimens for palliative chemotherapy of metastatic colon cancer. Since data showing the influence of dose reduction in palliative treatment are rare, the objective of this single center, retrospective study was to further characterize the influence of dose reduction on efficacy of these therapeutic regimens. METHODS: One hundred nine patients, diagnosed with stage IV colon cancer between 2004 and 2012 and receiving palliative first-line chemotherapy with either FOLFOX or FOLFIRI regimens in our outpatient clinic were analyzed for treatment efficacy. Patients who received dose reductions due to side effects usually received doses of 80% or lower of per protocol dose. Survival data were obtained from the Regensburg Tumor Registry. Survival analysis was performed using Kaplan-Meier statistical analysis and multivariable analysis. RESULTS: A dose reduction due to side effects was necessary in 46 (42%) patients. Dose reduction was independent of age. Major reasons for dose reduction were neutropenia (30%) followed by polyneuropathy (16%) and diarrhea (14%). Dosage was more often reduced in patients receiving FOLFOX based therapy. Comparison of patients with dose reduction versus patients with full dosage showed no significant difference on overall survival (p = 0.430). Subgroup analysis revealed dose reduction in patients with N2 stage disease was associated with improved survival. Patients who underwent dose reduction received more cycles of chemotherapy (13.7 vs. 10.8 cycles) and cumulative dosage was similar in both groups. CONCLUSION: Contrary to our expectations, the need to reduce chemotherapy dosage due to side effects does not indicate a worse prognosis in our retrospective analysis. We believe this can in part be explained by better adaption to interindividual pharmacokinetics and longer time of treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4380-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-23 /pmc/articles/PMC5913883/ /pubmed/29685155 http://dx.doi.org/10.1186/s12885-018-4380-z Text en © The Author(s). 2018 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
Munker, Stefan
Gerken, Michael
Fest, Petra
Ott, Claudia
Schnoy, Elisabeth
Fichtner-Feigl, Stefan
Wiggermann, Philipp
Vogelhuber, Martin
Herr, Wolfgang
Stroszczynski, Christian
Schlitt, Hans Jürgen
Evert, Matthias
Reng, Michael
Klinkhammer-Schalke, Monika
Teufel, Andreas
Chemotherapy for metastatic colon cancer: No effect on survival when the dose is reduced due to side effects
title Chemotherapy for metastatic colon cancer: No effect on survival when the dose is reduced due to side effects
title_full Chemotherapy for metastatic colon cancer: No effect on survival when the dose is reduced due to side effects
title_fullStr Chemotherapy for metastatic colon cancer: No effect on survival when the dose is reduced due to side effects
title_full_unstemmed Chemotherapy for metastatic colon cancer: No effect on survival when the dose is reduced due to side effects
title_short Chemotherapy for metastatic colon cancer: No effect on survival when the dose is reduced due to side effects
title_sort chemotherapy for metastatic colon cancer: no effect on survival when the dose is reduced due to side effects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913883/
https://www.ncbi.nlm.nih.gov/pubmed/29685155
http://dx.doi.org/10.1186/s12885-018-4380-z
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