Abstract

BackgroundThe aim of this study was to evaluate the survival outcomes and toxicity of postoperative chemoradiotherapy with capecitabine and concurrent intensity-modulated radiotherapy (IMRT) or three-dimensional conformal radiotherapy (3D-CRT) in patients with stage II and III rectal cancer.PatientsWe recruited 184 patients with pathologically proven, stage II or III rectal cancer. Following total mesorectal excision (TME), the patients were treated with capecitabine and concurrent IMRT/3D-CRT. The treatment regimen consisted of two cycles of oral capecitabine (1600 mg/m2/day), administered twice daily from day 1–14 of radiotherapy, followed by a 7-day rest. The median pelvic dose was 50 Gy in 25 fractions. Oxaliplatin-based adjuvant chemotherapy was administered after the chemoradiotherapy.ResultsThe 5-year overall survival, disease-free survival and locoregional control (LRC) rates were 85.1%, 80% and 95.4%, respectively. Grade 3 and 4 toxicities were observed in 28.3% of patients during treatment. Grade 3 or 4 late toxicity, including neurotoxicity or gastrointestinal toxicity, was only observed in nine patients (4.9%).ConclusionsThis study demonstrated that capecitabine chemotherapy with concurrent IMRT/3D-CRT following TME is safe, is well tolerated and achieves superior LRC and favorable survival rates, with acceptable toxicity.

Highlights

  • Rectal cancer is a common malignancy worldwide [1]

  • This study demonstrated that capecitabine chemotherapy with concurrent intensity-modulated radiotherapy (IMRT)/three-dimensional conformal radiotherapy. doi (3D-CRT) following total mesorectal excision (TME) is safe, is well tolerated and achieves superior locoregional control (LRC) and favorable survival rates, with acceptable toxicity

  • Preoperative chemoradiotherapy is considered the standard treatment for patients with locally advanced rectal cancer, postoperative chemoradiotherapy remains the choice of treatment for such patients [10, 11]

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Summary

Introduction

Rectal cancer is a common malignancy worldwide [1]. Several randomized trials have demonstrated improved locoregional control (LRC) and survival rates with preoperative or postoperative chemoradiotherapy in patients with stage II and III rectal cancer [2,3,4,5,6,7]. Preliminary trials in patients with metastatic colorectal cancer have indicated that capecitabine may be as effective as standard 5-FU-based chemotherapy in terms of progression-free survival (PFS) and overall survival (OS) rates, while offering a better tolerability profile and a lower incidence of stomatitis [12,13,14,15,16,17,18]. Based on these reports, we carried out a phase I trial to evaluate the maximum tolerated dose (MTD) of capecitabine with concurrent postoperative radiotherapy for stage II and III rectal cancer.

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