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Multicenter, randomized single-port versus multiport laparoscopic surgery (SIMPLE) trial in colon cancer: an interim analysis

Authors
Kang, Byung MoKim,Hyung JinKye,Bong-HyeonLee, Sang ChulLee, Kil YeonPark, Sun JinLee, Suk-HwanLim, Sang WooLee, Yoon SukKim, Ji HoonLee,JinkwonKim, Min KiKim,Jun-Gi
Issue Date
Mar-2018
Publisher
SPRINGER
Keywords
Colon cancer; Laparoscopy; Randomized controlled trial; Short-term outcomes; Single-port
Citation
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES, v.32, no.3, pp.1540 - 1549
Indexed
SCIE
SCOPUS
Journal Title
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES
Volume
32
Number
3
Start Page
1540
End Page
1549
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/150361
DOI
10.1007/s00464-017-5842-0
ISSN
0930-2794
Abstract
Background: Single-port laparoscopic surgery (SPLS) was recently introduced as an innovative minimally invasive surgery method. Retrospective studies have revealed the safety and feasibility of SPLS for colon cancer treatment. However, no prospective randomized trials have been performed. The multicenter, randomized SIMPLE (single-port versus multiport laparoscopic surgery) trial aimed to investigate short-term perioperative outcomes of SPLS for colon cancer treatment, compared with multiport laparoscopic surgery (MPLS). Methods: Between August 2011 and April 2014, a total of 194 patients with colon cancer were recruited from seven hospitals in Korea. Patients were randomly allocated into the SPLS group (n = 99) or MPLS group (n = 95). The primary endpoint was postoperative complications. Operative, postoperative, and pathologic outcomes were analyzed after 50% of the patient study population had been recruited. Results: The patients’ demographic characteristics, operative times, estimated blood volume losses, numbers of harvested lymph nodes, and lengths of both resection margins were not significantly different between groups. In the SPLS group, the rates of conversion to MPLS and open surgery were 12.9 and 2.2%, respectively. Postoperative complications occurred in 10.8% of the SPLS, and 12.5% of the MPLS patients (p = 0.714). Times to functional recovery, pain scores, and amounts of analgesia were similar between groups. Conclusion: The results of this interim analysis suggested that SPLS is technically safe and appropriate when used for radical resection of colon cancer. (ClinicalTrials.gov Identifier: NCT01480128).
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