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Importance of response to neoadjuvant chemotherapy in potentially curable colorectal cancer liver metastases

BACKGROUND: Surgical resection of liver metastases arising from colorectal cancer is considered the only curative treatment option. However, many patients subsequently experience disease recurrence. We prospectively investigated whether neoadjuvant chemotherapy reduces the risk of recurrence followi...

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Autores principales: Gruenberger, Birgit, Scheithauer, Werner, Punzengruber, Robert, Zielinski, Christoph, Tamandl, Dietmar, Gruenberger, Thomas
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386791/
https://www.ncbi.nlm.nih.gov/pubmed/18439246
http://dx.doi.org/10.1186/1471-2407-8-120
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author Gruenberger, Birgit
Scheithauer, Werner
Punzengruber, Robert
Zielinski, Christoph
Tamandl, Dietmar
Gruenberger, Thomas
author_facet Gruenberger, Birgit
Scheithauer, Werner
Punzengruber, Robert
Zielinski, Christoph
Tamandl, Dietmar
Gruenberger, Thomas
author_sort Gruenberger, Birgit
collection PubMed
description BACKGROUND: Surgical resection of liver metastases arising from colorectal cancer is considered the only curative treatment option. However, many patients subsequently experience disease recurrence. We prospectively investigated whether neoadjuvant chemotherapy reduces the risk of recurrence following potentially curative liver resection. Special emphasis was directed to the importance of response. METHODS: 50 patients with resectable liver metastases received neoadjuvant XELOX or FOLFOX4 for six cycles (3 months). Complete resection of liver metastases was intended thereafter. Assessments included response rate, postoperative morbidity and recurrence-free survival. RESULTS: An objective response was observed in 72% of all patients, including two complete responses. Chemotherapy was well tolerated and the majority of adverse events were mild to moderate (grade 1/2). Potentially curative R0 resection was performed in all patients and postoperative complications were observed in only 12%. The median recurrence-free survival was significantly influenced by tumor response with 24.7 months (95% CI: 4.50 to 44.97) in responding patients, 8.2 months (95% CI: 3.09 to 13.31) in patients with stable disease and 3.0 months (95% CI: 0 to 8.91) in patients with progressive disease. CONCLUSION: These data suggest that neoadjuvant Oxaliplatin based chemotherapy provides high response rates without increased risk of perioperative morbidity. Response to chemotherapy can lead to long-term recurrence-free survival. Neoadjuvant chemotherapy may identify best candidates for a potentially curative treatment approach.
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spelling pubmed-23867912008-05-17 Importance of response to neoadjuvant chemotherapy in potentially curable colorectal cancer liver metastases Gruenberger, Birgit Scheithauer, Werner Punzengruber, Robert Zielinski, Christoph Tamandl, Dietmar Gruenberger, Thomas BMC Cancer Research Article BACKGROUND: Surgical resection of liver metastases arising from colorectal cancer is considered the only curative treatment option. However, many patients subsequently experience disease recurrence. We prospectively investigated whether neoadjuvant chemotherapy reduces the risk of recurrence following potentially curative liver resection. Special emphasis was directed to the importance of response. METHODS: 50 patients with resectable liver metastases received neoadjuvant XELOX or FOLFOX4 for six cycles (3 months). Complete resection of liver metastases was intended thereafter. Assessments included response rate, postoperative morbidity and recurrence-free survival. RESULTS: An objective response was observed in 72% of all patients, including two complete responses. Chemotherapy was well tolerated and the majority of adverse events were mild to moderate (grade 1/2). Potentially curative R0 resection was performed in all patients and postoperative complications were observed in only 12%. The median recurrence-free survival was significantly influenced by tumor response with 24.7 months (95% CI: 4.50 to 44.97) in responding patients, 8.2 months (95% CI: 3.09 to 13.31) in patients with stable disease and 3.0 months (95% CI: 0 to 8.91) in patients with progressive disease. CONCLUSION: These data suggest that neoadjuvant Oxaliplatin based chemotherapy provides high response rates without increased risk of perioperative morbidity. Response to chemotherapy can lead to long-term recurrence-free survival. Neoadjuvant chemotherapy may identify best candidates for a potentially curative treatment approach. BioMed Central 2008-04-25 /pmc/articles/PMC2386791/ /pubmed/18439246 http://dx.doi.org/10.1186/1471-2407-8-120 Text en Copyright © 2008 Gruenberger et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gruenberger, Birgit
Scheithauer, Werner
Punzengruber, Robert
Zielinski, Christoph
Tamandl, Dietmar
Gruenberger, Thomas
Importance of response to neoadjuvant chemotherapy in potentially curable colorectal cancer liver metastases
title Importance of response to neoadjuvant chemotherapy in potentially curable colorectal cancer liver metastases
title_full Importance of response to neoadjuvant chemotherapy in potentially curable colorectal cancer liver metastases
title_fullStr Importance of response to neoadjuvant chemotherapy in potentially curable colorectal cancer liver metastases
title_full_unstemmed Importance of response to neoadjuvant chemotherapy in potentially curable colorectal cancer liver metastases
title_short Importance of response to neoadjuvant chemotherapy in potentially curable colorectal cancer liver metastases
title_sort importance of response to neoadjuvant chemotherapy in potentially curable colorectal cancer liver metastases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386791/
https://www.ncbi.nlm.nih.gov/pubmed/18439246
http://dx.doi.org/10.1186/1471-2407-8-120
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