Outcomes of neoadjuvant chemoradiotherapy followed by total mesorectal excision surgery for locally advanced rectal cancer: a single-institution experience

被引:6
作者
Tseng, Michelle Shu Fen [1 ]
Zheng, Huili [2 ]
Ng, Ivy Wei Shan [1 ]
Leong, Yiat Horng [1 ]
Leong, Cheng Nang [1 ]
Yong, Wei Peng [3 ]
Cheong, Wai Kit [4 ]
Tey, Jeremy Chee Seong [1 ]
机构
[1] Natl Univ Hlth Syst, Natl Univ Canc Inst, Dept Radiat Oncol, Tower Block,Level 7,5 Lower Kent Ridge Rd, Singapore 119074, Singapore
[2] Hth Promot Board, Singapore, Singapore
[3] Natl Univ Canc Inst, Dept Haematol Oncol, Singapore, Singapore
[4] Natl Univ Hlth Syst, Univ Surg Cluster, Div Colorectal Surg, Singapore, Singapore
关键词
chemotherapy; neoadjuvant therapy; radiotherapy; rectal cancer; surgery; DISEASE-FREE SURVIVAL; PATHOLOGICAL COMPLETE RESPONSE; PREOPERATIVE CHEMORADIATION; POSTOPERATIVE CHEMORADIOTHERAPY; MANAGEMENT; TRIAL;
D O I
10.11622/smedj.2017105
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
INTRODUCTION Neoadjuvant chemoradiotherapy (CRT) followed by total mesorectal excision (TME) surgery for locally advanced rectal cancer has been shown to improve local control and reduce toxicity, as compared to adjuvant CRT. We reported the outcomes of our patients with locally advanced rectal cancer treated at National University Hospital, Singapore. METHODS From April 2002 to December 2014, 117 patients with T3/4, NO/+, M0 rectal cancer received neoadjuvant CRT followed by TME surgery. The treatment regimen comprised a total radiotherapy dose of 50.4 Gy in 28 daily fractions delivered concurrently with 5-fluorouracil or capecitabine chemotherapy over 5.5 weeks. All patients were planned for TME surgery. Local control, disease-free survival, overall survival and treatment toxicities were analysed. RESULTS Median follow-up was 34 (range 2-122) months. 11.5% (13/113) of patients achieved a pathological complete response (pCR) and 72.6% (85/117) had either tumour or nodal downstaging following neoadjuvant CRT. 5.2% (5/96) of patients had Grade 3 acute toxicities (dermatitis and diarrhoea) and 3.1% (3/96) had Grade 3 late toxicities (fistula and stricture). There was no Grade 4 toxicity noted. The five-year local recurrence, disease-free survival and overall survival rates were 4.5%, 65.7% and 80.6%, respectively. Multivariate analysis showed that nodal positivity was a predictor of poor disease-free survival and poor overall survival. Tumour downstaging and pCR did not improve outcomes. CONCLUSION Our outcomes were comparable to internationally published data, and this treatment regimen remains the standard of care for locally advanced rectal cancer in our local population.
引用
收藏
页码:305 / 310
页数:6
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