Volume 15 Supplement 1
Factors in the success of the subcutaneous central venous port catheter in 626 colorectal carcinoma patients: long-term follow-up results according to the treatment groups
© Aribas et al. 2015
Published: 2 October 2015
Our purpose is retrospectively to investigate the effect of factors on the patency of subcutaneous central venous port catheters inserted to 626 colorectal carcinoma patients.
Patients and methods
Subcutaneous central venous port catheters were inserted to 1,408 patients. 241 were female, 383 were male. Patients were given chemotherapy agents as bevacizumab in 106, cetuximab in 30, and outside of these target-directed agents in 488. The groups to chemotherapy time were divided by 3 days cut-off. Age, gender, jugular-subclavian access, the chemotherapy to be given in 3 days as bevacizumab, cetuximab, other chemotherapy agents were also investigated.
The average age was 57.7 ± 11.3. The average follow-up period was 445.2 ± 387.8 days (1-1787 days). The catheters were removed depending on the port complications in 6 patients of bevacizumab group, 3 patients of cetuximab, and 11 patients of other chemotherapy group. A significant difference was observed in 3 days chemotherapy between cetuximab and out-of bevacizumab-cetuximab groups (p=0.013), also between bevacizumab and out-of bevacizumab-cetuximab the groups (p=0.007). No significant difference was observed out of 3 days chemotherapy (p>0.05). There was no difference between groups in Cox regression test. Significant difference was observed in catheter patency of bevacizumab-cetuximab group, due to the skin necrosis and thrombosis (p=0.011).
Significant effect was found by reducing the duration time in patients with the target-directed chemotherapy agent as bevacizumab-cetuximab.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.