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Increased incidence of chemoport-related thrombosis in patients with colorectal cancer receiving bevacizumab: A single-institutional experience

OBJECTIVE: Chemoport-related thrombosis (CRT) is a serious complication that causes morbidities and interrupts administration of intravenous cancer therapy. We investigated the incidence and risk of CRT in colorectal cancer (CRC) patients treated with bevacizumab (BEV). METHODS: We retrospectively r...

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Autores principales: Kim, Jwa Hoon, Kim, Jeong Eun, Hong, Yong Sang, Kim, Sun Young, Kim, Kyu-pyo, Choi, Ki Eun, Shin, Ji Hoon, Kim, Tae Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129570/
https://www.ncbi.nlm.nih.gov/pubmed/30210226
http://dx.doi.org/10.21147/j.issn.1000-9604.2018.04.09
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author Kim, Jwa Hoon
Kim, Jeong Eun
Hong, Yong Sang
Kim, Sun Young
Kim, Kyu-pyo
Choi, Ki Eun
Shin, Ji Hoon
Kim, Tae Won
author_facet Kim, Jwa Hoon
Kim, Jeong Eun
Hong, Yong Sang
Kim, Sun Young
Kim, Kyu-pyo
Choi, Ki Eun
Shin, Ji Hoon
Kim, Tae Won
author_sort Kim, Jwa Hoon
collection PubMed
description OBJECTIVE: Chemoport-related thrombosis (CRT) is a serious complication that causes morbidities and interrupts administration of intravenous cancer therapy. We investigated the incidence and risk of CRT in colorectal cancer (CRC) patients treated with bevacizumab (BEV). METHODS: We retrospectively reviewed 1,534 CRC patients who received chemotherapy with or without BEV using a chemoport between 2014 and 2016. RESULTS: The participants had a median age of 58 (18−85) years, and 60.3% were male. All participants were stratified into three groups: adjuvant chemotherapy (AC) (n=670), palliative chemotherapy (PC) without BEV (n=356), and PC with BEV (n=508). The median follow-up was 20.19 (interquartile range, 14.07−27.19) months. CRT occurred in 3.8% of all patients; incidence of symptomatic and asymptomatic CRT was 2.9% and 0.9%, respectively. CRT occurred more in patients with BEV (5.7%) than in patients without BEV (2.9%, P=0.008). The cumulative incidence of CRT in patients administered PC with BEV was significantly higher than that in those administered AC (P=0.011) and there was a trend toward increased CRT in patients administered PC with BEV compared with those administered PC without BEV (P=0.044). Multivariate analysis found that BEV treatment was the only variable that was significantly associated with CRT (hazard ratio, 2.06; 95% confidence interval, 1.24−3.43; P=0.006). CONCLUSIONS: BEV treatment was significantly associated with increased incidence of CRT in CRC patients.
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spelling pubmed-61295702018-09-12 Increased incidence of chemoport-related thrombosis in patients with colorectal cancer receiving bevacizumab: A single-institutional experience Kim, Jwa Hoon Kim, Jeong Eun Hong, Yong Sang Kim, Sun Young Kim, Kyu-pyo Choi, Ki Eun Shin, Ji Hoon Kim, Tae Won Chin J Cancer Res Original Article OBJECTIVE: Chemoport-related thrombosis (CRT) is a serious complication that causes morbidities and interrupts administration of intravenous cancer therapy. We investigated the incidence and risk of CRT in colorectal cancer (CRC) patients treated with bevacizumab (BEV). METHODS: We retrospectively reviewed 1,534 CRC patients who received chemotherapy with or without BEV using a chemoport between 2014 and 2016. RESULTS: The participants had a median age of 58 (18−85) years, and 60.3% were male. All participants were stratified into three groups: adjuvant chemotherapy (AC) (n=670), palliative chemotherapy (PC) without BEV (n=356), and PC with BEV (n=508). The median follow-up was 20.19 (interquartile range, 14.07−27.19) months. CRT occurred in 3.8% of all patients; incidence of symptomatic and asymptomatic CRT was 2.9% and 0.9%, respectively. CRT occurred more in patients with BEV (5.7%) than in patients without BEV (2.9%, P=0.008). The cumulative incidence of CRT in patients administered PC with BEV was significantly higher than that in those administered AC (P=0.011) and there was a trend toward increased CRT in patients administered PC with BEV compared with those administered PC without BEV (P=0.044). Multivariate analysis found that BEV treatment was the only variable that was significantly associated with CRT (hazard ratio, 2.06; 95% confidence interval, 1.24−3.43; P=0.006). CONCLUSIONS: BEV treatment was significantly associated with increased incidence of CRT in CRC patients. AME Publishing Company 2018-08 /pmc/articles/PMC6129570/ /pubmed/30210226 http://dx.doi.org/10.21147/j.issn.1000-9604.2018.04.09 Text en Copyright © 2018 Chinese Journal of Cancer Research. All rights reserved. http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-Non Commercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Kim, Jwa Hoon
Kim, Jeong Eun
Hong, Yong Sang
Kim, Sun Young
Kim, Kyu-pyo
Choi, Ki Eun
Shin, Ji Hoon
Kim, Tae Won
Increased incidence of chemoport-related thrombosis in patients with colorectal cancer receiving bevacizumab: A single-institutional experience
title Increased incidence of chemoport-related thrombosis in patients with colorectal cancer receiving bevacizumab: A single-institutional experience
title_full Increased incidence of chemoport-related thrombosis in patients with colorectal cancer receiving bevacizumab: A single-institutional experience
title_fullStr Increased incidence of chemoport-related thrombosis in patients with colorectal cancer receiving bevacizumab: A single-institutional experience
title_full_unstemmed Increased incidence of chemoport-related thrombosis in patients with colorectal cancer receiving bevacizumab: A single-institutional experience
title_short Increased incidence of chemoport-related thrombosis in patients with colorectal cancer receiving bevacizumab: A single-institutional experience
title_sort increased incidence of chemoport-related thrombosis in patients with colorectal cancer receiving bevacizumab: a single-institutional experience
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129570/
https://www.ncbi.nlm.nih.gov/pubmed/30210226
http://dx.doi.org/10.21147/j.issn.1000-9604.2018.04.09
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