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FOLFOX6 and bevacizumab in non-optimally resectable liver metastases from colorectal cancer

BACKGROUND: In patients with colorectal liver metastases (CLM) R0 resection significantly improves overall survival (OS). METHODS: In this report, we present the results of a phase II trial of FOLFOX6+bevacizumab in patients with non-optimally resectable CLM. Patients received six cycles of FOLFOX6+...

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Autores principales: Bertolini, F, Malavasi, N, Scarabelli, L, Fiocchi, F, Bagni, B, Giovane, C Del, Colucci, G, Gerunda, G E, Depenni, R, Zironi, S, Fontana, A, Pettorelli, E, Luppi, G, Conte, P F
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068493/
https://www.ncbi.nlm.nih.gov/pubmed/21386839
http://dx.doi.org/10.1038/bjc.2011.43
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author Bertolini, F
Malavasi, N
Scarabelli, L
Fiocchi, F
Bagni, B
Giovane, C Del
Colucci, G
Gerunda, G E
Depenni, R
Zironi, S
Fontana, A
Pettorelli, E
Luppi, G
Conte, P F
author_facet Bertolini, F
Malavasi, N
Scarabelli, L
Fiocchi, F
Bagni, B
Giovane, C Del
Colucci, G
Gerunda, G E
Depenni, R
Zironi, S
Fontana, A
Pettorelli, E
Luppi, G
Conte, P F
author_sort Bertolini, F
collection PubMed
description BACKGROUND: In patients with colorectal liver metastases (CLM) R0 resection significantly improves overall survival (OS). METHODS: In this report, we present the results of a phase II trial of FOLFOX6+bevacizumab in patients with non-optimally resectable CLM. Patients received six cycles of FOLFOX6+ five of bevacizumab. Patients not achieving resectability received six additional cycles of each. A PET-CT was performed at baseline and again within 1 month after initiating treatment. RESULTS: From September 2005 to July 2009, 21 patients were enrolled (Male/Female: 15/6; median age: 65 years). An objective response (OR) was documented in 12 cases (57.1% complete responses (CRs): 3, partial response (PR): 9); one patient died from toxicity before surgery. Thirteen patients underwent radical surgery (61.9%). Three (23%) had a pathological CR (pCR). Six patients (46.1%) experienced minor postsurgical complications. After a median 38.8-month follow-up, the median OS was 22.5 months. Patients achieving at least 1 unit reduction in Standard uptake value (SUV)max on PET-CT had longer progression-free survival (PFS) (median PFS: 22 vs 14 months, P=0.001). CONCLUSIONS: FOLFOX6+bevacizumab does not increase postsurgical complications, yields high rates of resectability and pCR. Early changes in PET-CT seem to be predictive of longer PFS.
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spelling pubmed-30684932012-03-29 FOLFOX6 and bevacizumab in non-optimally resectable liver metastases from colorectal cancer Bertolini, F Malavasi, N Scarabelli, L Fiocchi, F Bagni, B Giovane, C Del Colucci, G Gerunda, G E Depenni, R Zironi, S Fontana, A Pettorelli, E Luppi, G Conte, P F Br J Cancer Clinical Study BACKGROUND: In patients with colorectal liver metastases (CLM) R0 resection significantly improves overall survival (OS). METHODS: In this report, we present the results of a phase II trial of FOLFOX6+bevacizumab in patients with non-optimally resectable CLM. Patients received six cycles of FOLFOX6+ five of bevacizumab. Patients not achieving resectability received six additional cycles of each. A PET-CT was performed at baseline and again within 1 month after initiating treatment. RESULTS: From September 2005 to July 2009, 21 patients were enrolled (Male/Female: 15/6; median age: 65 years). An objective response (OR) was documented in 12 cases (57.1% complete responses (CRs): 3, partial response (PR): 9); one patient died from toxicity before surgery. Thirteen patients underwent radical surgery (61.9%). Three (23%) had a pathological CR (pCR). Six patients (46.1%) experienced minor postsurgical complications. After a median 38.8-month follow-up, the median OS was 22.5 months. Patients achieving at least 1 unit reduction in Standard uptake value (SUV)max on PET-CT had longer progression-free survival (PFS) (median PFS: 22 vs 14 months, P=0.001). CONCLUSIONS: FOLFOX6+bevacizumab does not increase postsurgical complications, yields high rates of resectability and pCR. Early changes in PET-CT seem to be predictive of longer PFS. Nature Publishing Group 2011-03-29 2011-03-08 /pmc/articles/PMC3068493/ /pubmed/21386839 http://dx.doi.org/10.1038/bjc.2011.43 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Study
Bertolini, F
Malavasi, N
Scarabelli, L
Fiocchi, F
Bagni, B
Giovane, C Del
Colucci, G
Gerunda, G E
Depenni, R
Zironi, S
Fontana, A
Pettorelli, E
Luppi, G
Conte, P F
FOLFOX6 and bevacizumab in non-optimally resectable liver metastases from colorectal cancer
title FOLFOX6 and bevacizumab in non-optimally resectable liver metastases from colorectal cancer
title_full FOLFOX6 and bevacizumab in non-optimally resectable liver metastases from colorectal cancer
title_fullStr FOLFOX6 and bevacizumab in non-optimally resectable liver metastases from colorectal cancer
title_full_unstemmed FOLFOX6 and bevacizumab in non-optimally resectable liver metastases from colorectal cancer
title_short FOLFOX6 and bevacizumab in non-optimally resectable liver metastases from colorectal cancer
title_sort folfox6 and bevacizumab in non-optimally resectable liver metastases from colorectal cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068493/
https://www.ncbi.nlm.nih.gov/pubmed/21386839
http://dx.doi.org/10.1038/bjc.2011.43
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