Aim: To evaluate the activity, safety and long-term survival of patients after preoperative oxaliplatin and 5- fluorouracil chemoradiation therapy in locally advanced rectal cancer (LARC). Patients and Methods: Patients with resectable, T3-4 and/or nodal involvement rectal adenocarcinoma were treated with oxaliplatin 60 mg/m2 weekly and 5-fluorouracil 200 mg/m 2/d infused continuously for five days, over a period of five weeks, and radiotherapy (45 Gy/25 fractions). The primary end-point was pathological complete response (ypCR). Safety, overall survival (OS) and relapse-free survival (RFS) were secondary end-points. Results: Sixty-six patients were treated. Grade 1-2 diarrhea was the most common adverse event. The ypCR rate was 16.7% (95% confidence interval=7.7-25.7%). After a median follow-up of 73.5 months, 23 patients (34.8%) had experienced relapse. Five-year actuarial RFS and OS rates were 64% and 73%, respectively. Five-year actuarial RFS was 91.7% in the ypCR group versus 57.8% in non-ypCR cases. Conclusion: Long-term local control and survival after this very well-tolerated regimen appear encouraging. © 2013 Anticancer Research.
Fontana, E., Pucci, F., Camisa, R., Bui, S., Galdy, S., Leonardi, F., et al. (2013). Long-term results of preoperative 5-fluorouracil-oxaliplatin chemoradiation therapy in locally advanced rectal cancer. ANTICANCER RESEARCH, 33(2), 725-730.
Long-term results of preoperative 5-fluorouracil-oxaliplatin chemoradiation therapy in locally advanced rectal cancer
ARDIZZONI, ANDREA
2013
Abstract
Aim: To evaluate the activity, safety and long-term survival of patients after preoperative oxaliplatin and 5- fluorouracil chemoradiation therapy in locally advanced rectal cancer (LARC). Patients and Methods: Patients with resectable, T3-4 and/or nodal involvement rectal adenocarcinoma were treated with oxaliplatin 60 mg/m2 weekly and 5-fluorouracil 200 mg/m 2/d infused continuously for five days, over a period of five weeks, and radiotherapy (45 Gy/25 fractions). The primary end-point was pathological complete response (ypCR). Safety, overall survival (OS) and relapse-free survival (RFS) were secondary end-points. Results: Sixty-six patients were treated. Grade 1-2 diarrhea was the most common adverse event. The ypCR rate was 16.7% (95% confidence interval=7.7-25.7%). After a median follow-up of 73.5 months, 23 patients (34.8%) had experienced relapse. Five-year actuarial RFS and OS rates were 64% and 73%, respectively. Five-year actuarial RFS was 91.7% in the ypCR group versus 57.8% in non-ypCR cases. Conclusion: Long-term local control and survival after this very well-tolerated regimen appear encouraging. © 2013 Anticancer Research.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


