AI Article Synopsis

  • The study evaluated postoperative chemoradiotherapy combining capecitabine with either intensity-modulated radiotherapy (IMRT) or three-dimensional conformal radiotherapy (3D-CRT) in patients with stage II and III rectal cancer.
  • A total of 184 patients underwent treatment post-surgery, receiving two cycles of capecitabine and a pelvic radiation dose of 50 Gy, followed by adjuvant chemotherapy.
  • The results indicated high survival rates (85.1% overall survival, 80% disease-free survival) and minimal severe toxicity, suggesting this treatment approach is safe and effective.

Article Abstract

Background: The 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.

Patients: We 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.

Results: The 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%).

Conclusions: This 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411062PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0124601PLOS

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