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A single-institution experience with bevacizumab in the treatment of metastatic colorectal cancer and in conjunction with liver resection
BACKGROUND: Bevacizumab is active in the treatment of metastatic colorectal cancer (mCRC). However, efficacy of bevacizumab has predominantly been evaluated on selected patients with relatively good performance status and minor comorbidities. We evaluated the efficacy and safety of bevacizumab in un...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085307/ https://www.ncbi.nlm.nih.gov/pubmed/25061319 http://dx.doi.org/10.2147/OTT.S63739 |
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author | Osterlund, Pia Peltonen, Reetta Alanko, Tuomo Bono, Petri Isoniemi, Helena |
author_facet | Osterlund, Pia Peltonen, Reetta Alanko, Tuomo Bono, Petri Isoniemi, Helena |
author_sort | Osterlund, Pia |
collection | PubMed |
description | BACKGROUND: Bevacizumab is active in the treatment of metastatic colorectal cancer (mCRC). However, efficacy of bevacizumab has predominantly been evaluated on selected patients with relatively good performance status and minor comorbidities. We evaluated the efficacy and safety of bevacizumab in unselected patients with mCRC, some of whom underwent liver resection. MATERIAL AND METHODS: All patients with inoperable mCRC, fit for combination chemotherapy (n=180), who were initially not resectable, not included into studies and without contraindications to bevacizumab, and initiated on bevacizumab at the Helsinki University Central Hospital between April 2004 and December 2005 were included (n=114). Most (n=70) received 5-fluorouracil/leucovorin/irinotecan plus bevacizumab as first-line therapy. The remainder (n=44) of the patients received bevacizumab in combination with oxaliplatin or irinotecan with or without 5-fluorouracil or capecitabine. Minimum follow-up was 7 years. Treatment response was evaluated every 8–10 weeks according to RECIST criteria. RESULTS: Median age was 59.6 years (range 35–79); male/female ratio was 54%/46%; World Health Organization performance status 0/1/2–3 was 33%/55%/11%, respectively; and the number of metastatic sites, one/two/three or more, was 31%/21%/48%, respectively. Median duration of bevacizumab therapy was 7.8 months (range 0.5–70.5 with pauses). In first-line (n=40), response rate (RR) was 62%, progression-free survival (PFS) 11.7 months, and overall survival (OS) 22.1 months. In second-line (n=43), RR was 44%, PFS 8.7 months, and OS 18.7 months. In later lines (n=31), RR was 14%, PFS 6.7 months, and OS 14.2 months. Ten patients with initially unresectable liver metastases became operable and R0 resection was achieved in 90% (9/10 resections). In 23% (7/31) of operated metastases, no vital tumor cells were found in histologic examination. Operative morbidity was low: two mild infections, no increased bleeding tendency was noticed, and no impaired wound healing occurred. DISCUSSION: Bevacizumab-containing combination therapy was effective with acceptable tolerability in an unselected mCRC patient population in which liver resections could be safely performed. |
format | Online Article Text |
id | pubmed-4085307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40853072014-07-24 A single-institution experience with bevacizumab in the treatment of metastatic colorectal cancer and in conjunction with liver resection Osterlund, Pia Peltonen, Reetta Alanko, Tuomo Bono, Petri Isoniemi, Helena Onco Targets Ther Original Research BACKGROUND: Bevacizumab is active in the treatment of metastatic colorectal cancer (mCRC). However, efficacy of bevacizumab has predominantly been evaluated on selected patients with relatively good performance status and minor comorbidities. We evaluated the efficacy and safety of bevacizumab in unselected patients with mCRC, some of whom underwent liver resection. MATERIAL AND METHODS: All patients with inoperable mCRC, fit for combination chemotherapy (n=180), who were initially not resectable, not included into studies and without contraindications to bevacizumab, and initiated on bevacizumab at the Helsinki University Central Hospital between April 2004 and December 2005 were included (n=114). Most (n=70) received 5-fluorouracil/leucovorin/irinotecan plus bevacizumab as first-line therapy. The remainder (n=44) of the patients received bevacizumab in combination with oxaliplatin or irinotecan with or without 5-fluorouracil or capecitabine. Minimum follow-up was 7 years. Treatment response was evaluated every 8–10 weeks according to RECIST criteria. RESULTS: Median age was 59.6 years (range 35–79); male/female ratio was 54%/46%; World Health Organization performance status 0/1/2–3 was 33%/55%/11%, respectively; and the number of metastatic sites, one/two/three or more, was 31%/21%/48%, respectively. Median duration of bevacizumab therapy was 7.8 months (range 0.5–70.5 with pauses). In first-line (n=40), response rate (RR) was 62%, progression-free survival (PFS) 11.7 months, and overall survival (OS) 22.1 months. In second-line (n=43), RR was 44%, PFS 8.7 months, and OS 18.7 months. In later lines (n=31), RR was 14%, PFS 6.7 months, and OS 14.2 months. Ten patients with initially unresectable liver metastases became operable and R0 resection was achieved in 90% (9/10 resections). In 23% (7/31) of operated metastases, no vital tumor cells were found in histologic examination. Operative morbidity was low: two mild infections, no increased bleeding tendency was noticed, and no impaired wound healing occurred. DISCUSSION: Bevacizumab-containing combination therapy was effective with acceptable tolerability in an unselected mCRC patient population in which liver resections could be safely performed. Dove Medical Press 2014-07-01 /pmc/articles/PMC4085307/ /pubmed/25061319 http://dx.doi.org/10.2147/OTT.S63739 Text en © 2014 Osterlund et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Osterlund, Pia Peltonen, Reetta Alanko, Tuomo Bono, Petri Isoniemi, Helena A single-institution experience with bevacizumab in the treatment of metastatic colorectal cancer and in conjunction with liver resection |
title | A single-institution experience with bevacizumab in the treatment of metastatic colorectal cancer and in conjunction with liver resection |
title_full | A single-institution experience with bevacizumab in the treatment of metastatic colorectal cancer and in conjunction with liver resection |
title_fullStr | A single-institution experience with bevacizumab in the treatment of metastatic colorectal cancer and in conjunction with liver resection |
title_full_unstemmed | A single-institution experience with bevacizumab in the treatment of metastatic colorectal cancer and in conjunction with liver resection |
title_short | A single-institution experience with bevacizumab in the treatment of metastatic colorectal cancer and in conjunction with liver resection |
title_sort | single-institution experience with bevacizumab in the treatment of metastatic colorectal cancer and in conjunction with liver resection |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085307/ https://www.ncbi.nlm.nih.gov/pubmed/25061319 http://dx.doi.org/10.2147/OTT.S63739 |
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