Delaying surgery after neoadjuvant chemoradiotherapy for rectal cancer may reduce postoperative morbidity without compromising prognosis
✍ Scribed by S. F. Kerr; S. Norton; R. Glynne-Jones
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 117 KB
- Volume
- 95
- Category
- Article
- ISSN
- 0007-1323
- DOI
- 10.1002/bjs.6377
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Background
This retrospective study investigated whether the interval between neoadjuvant chemoradiotherapy and surgery for rectal cancer influences postoperative morbidity or prognosis.
Methods
Data from 189 patients receiving neoadjuvant 5-fluorouracil-based chemoradiotherapy were examined. Associations between interval length and clinicopathological characteristics were analysed.
Results
The median interval was 73 (range 6–215) days. Operations performed were abdominoperineal resection (60·3 per cent), anterior resection (37·6 per cent) and Hartmann's procedure (2·1 per cent). Forty-six patients (24·3 per cent) received postoperative chemotherapy. Interval was not significantly associated with pathological tumour (P = 0·648) or node (P = 0·964) category after chemoradiotherapy, or pathological complete response (P = 0·499). Logistic regression showed that shorter intervals (by 1 week) independently predicted anastomotic leakage (odds ratio (OR) 0·97 (95 per cent confidence interval (c.i.) 0·94 to 1·00)) and perineal wound complications (OR 0·97 (0·95 to 0·99)). Interval was not related to local recurrence (hazard ratio (HR) 1·01 (95 per cent c.i. 1·00 to 1·02)), metastasis (HR 1·00 (0·99 to 1·01)) or death (HR 1·00 (0·99 to 1·01)). Only circumferential resection margin and nodal involvement were independent predictors of survival.
Conclusion
Delaying surgery beyond 8 weeks after neoadjuvant chemoradiotherapy may reduce postoperative morbidity, without compromising prognosis.