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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...

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Autores principales: Osterlund, Pia, Peltonen, Reetta, Alanko, Tuomo, Bono, Petri, Isoniemi, Helena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
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.
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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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