Open versus laparoscopic surgery for mid or low rectal cancer after neoadjuvant chemoradiotherapy (COREAN trial): short-term outcomes of an open-label randomised controlled trial

• Published in: The lancet oncology 2010-07, Vol.11 (7), p.637-645
• Main Authors: Kang, Sung-Bum, MD, Park, Ji Won, MD, Jeong, Seung-Yong, MD, Nam, Byung Ho, PhD, Choi, Hyo Seong, MD, Kim, Duck-Woo, MD, Lim, Seok-Byung, MD, Lee, Taek-Gu, MD, Kim, Dae Yong, MD, Kim, Jae-Sung, Prof, Chang, Hee Jin, MD, Lee, Hye-Seung, MD, Kim, Sun Young, MD, Jung, Kyung Hae, MD, Hong, Yong Sang, MD, Kim, Jee Hyun, MD, Sohn, Dae Kyung, MD, Kim, Dae-Hyun, MD, Oh, Jae Hwan, Dr
• Format: Article
• Language: English
• Subjects: Female; Hematology, Oncology and Palliative Medicine; Humans; Laparoscopy; Male; Middle Aged; Neoadjuvant Therapy; Postoperative Complications; Quality of Life; Rectal Neoplasms - pathology; Rectal Neoplasms - surgery; Safety; Survival Analysis
• ISSN: 1470-2045; 1474-5488
• DOI: 10.1016/S1470-2045(10)70131-5

Summary Background The safety and short-term efficacy of laparoscopic surgery for rectal cancer after preoperative chemoradiotherapy has not been demonstrated. The aim of the randomised Comparison of Open versus laparoscopic surgery for mid and low REctal cancer After Neoadjuvant chemoradiotherapy (COREAN) trial was to compare open surgery with laparoscopic surgery for mid or low rectal cancer after neoadjuvant chemoradiotherapy. Methods Between April 4, 2006, and Aug 26, 2009, patients with cT3N0–2 mid or low rectal cancer without distant metastasis after preoperative chemoradiotherapy were enrolled at three tertiary-referral hospitals. Patients were randomised 1:1 to receive either open surgery (n=170) or laparoscopic surgery (n=170), stratified according to sex and preoperative chemotherapy regimen. Short-term outcomes assessed were involvement of the circumferential resection margin, macroscopic quality of the total mesorectal excision specimen, number of harvested lymph nodes, recovery of bowel function, perioperative morbidity, postoperative pain, and quality of life. Analyses were based on the intention-to-treat population. Patients continue to be followed up for the primary outcome (3-year disease-free survival). This study is registered with ClinicalTrials.gov , number NCT00470951. Findings Two patients (1·2%) in the laparoscopic group were converted to open surgery, but were included in the laparoscopic group for analyses. Estimated blood loss was less in the laparoscopic group than in the open group (median 217·5 mL [150·0–400·0] in the open group vs 200·0 mL [100·0–300·0] in the laparoscopic group, p=0·006), although surgery time was longer in the laparoscopic group (mean 244·9 min [SD 75·4] vs 197·0 min [62·9], p