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pubmed-article:17118843pubmed:abstractTextDetermine feasibility and toxicity of preoperative short course pelvic CHART (25 Gy in 15 fractions over 5 days) for treatment of clinically resectable primary rectal tumours. Between 1998 and 2004, 20 patients with clinically staged T3 resectable rectal carcinoma were treated in this prospective pilot study with preoperative short course CHART to their pelvis. The aim was for total mesorectal excision within 7 days. Radiation toxicity, surgical morbidity, locoregional control (LRC), overall (OS), cause specific (CSS) and disease free survival (DFS) outcomes were documented. Nineteen of the 20 patients completed planned radiotherapy. One discontinued radiotherapy due to toxicity. All patients underwent potentially curative radical surgery. One patient developed grade 3, and three patients grade 2 gastrointestinal toxicity. With a median follow-up of 31 months (range 0.9-88), there is no grade 3, 4 or 5 late toxicity. Two patients experienced grade 2, and three patients grade 1 late bowel toxicity. Two patients died from postoperative complications, and two developed grade 2 abdominal wound infections. At 3 years LRC is 95% (95% CI 83-100), OS 72% (95% CI 51-94), CSS 86% (95% CI 68-100) and DFS 80% (95% CI 60-100). Two patients died from metastatic disease, one patient from a second primary and one patient is alive after successful resection of hepatic metastases. This small study suggests preoperative short course CHART for clinically resectable rectal carcinoma is feasible with acceptable compliance and tolerable side effects.lld:pubmed
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pubmed-article:17118843pubmed:pagination1079-85lld:pubmed
pubmed-article:17118843pubmed:dateRevised2009-5-12lld:pubmed
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pubmed-article:17118843pubmed:articleTitleShort course continuous, hyperfractionated, accelerated radiation therapy (CHART) as preoperative treatment for rectal cancer.lld:pubmed
pubmed-article:17118843pubmed:affiliationMount Vernon Cancer Center, Northwood, Middlesex, HA6 2RN, London, United Kingdom.lld:pubmed
pubmed-article:17118843pubmed:publicationTypeJournal Articlelld:pubmed
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