A phase II study of oxaliplatin with 5-FU/folinic acid and concomitant radiotherapy as a preoperative treatment in patients with locally advanced rectal cancer
Objective: To evaluate the activity and safety of adding oxaliplatin to a standard chemoradiotherapy schema, including 5-fluorouracil (5-FU)/folinic acid (FA), in locally-advanced rectal cancer (LARC). Methods: Two cycles of oxaliplatin 130 mg/m 2 plus FA 20 mg/m 2 bolus for 5 days and 5-FU 350 mg/m...
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th-cmuir.6653943832-499262018-09-04T04:25:03Z A phase II study of oxaliplatin with 5-FU/folinic acid and concomitant radiotherapy as a preoperative treatment in patients with locally advanced rectal cancer I. Chitapanarux T. Chitapanarux E. Tharavichitkul S. Mayurasakorn P. Siriwittayakorn S. Yamada V. Lorvidhaya Engineering Health Professions Medicine Objective: To evaluate the activity and safety of adding oxaliplatin to a standard chemoradiotherapy schema, including 5-fluorouracil (5-FU)/folinic acid (FA), in locally-advanced rectal cancer (LARC). Methods: Two cycles of oxaliplatin 130 mg/m 2 plus FA 20 mg/m 2 bolus for 5 days and 5-FU 350 mg/m 2 continuous infusion for 5 days were given during week 1 and 4 of pelvic radiotherapy 46 Gy. Patients with a T3/4 and/or node-positive rectal tumour were eligible. Surgery was performed 4-6 weeks after radiotherapy. The primary endpoint was to determine the rate of pathological response. Secondary endpoints were to assess the rate of clinical response and the safety profile. Results: Between March 2005 and January 2009, a total of 35 patients were enrolled. The pathological downstaging rate was 79% with a pathological complete response rate of 17%. The overall clinical response rate (assessed by computed tomography or transrectal ultrasound) was 77%. Grade 3 diarrhoea and Grade 3 neutropaenia were reported in 14% and 11% of the patients, respectively. Eleven patients did not undergo surgery: four of them refused the operation, and seven patients were inoperable due to disease progression. In 24 patients who had surgery, a sphincter-preserving procedure could be performed in 29%. At the median follow-up time of 28.1 months, 25 patients (71%) survived with no evidence of disease. Conclusion: The promising results in terms of pathological response, and the associated good safety profile of a regimen of oxaliplatin plus 5-FU/FA with concomitant radiotherapy, suggest that the regimen could be used in LARC. © 2011 Biomedical Imaging and Intervention Journal. All rights reserved. 2018-09-04T04:20:26Z 2018-09-04T04:20:26Z 2011-12-20 Journal 18235530 2-s2.0-83455220049 10.2349/biij.7.4.e25 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=83455220049&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/49926 |
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Engineering Health Professions Medicine I. Chitapanarux T. Chitapanarux E. Tharavichitkul S. Mayurasakorn P. Siriwittayakorn S. Yamada V. Lorvidhaya A phase II study of oxaliplatin with 5-FU/folinic acid and concomitant radiotherapy as a preoperative treatment in patients with locally advanced rectal cancer |
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Objective: To evaluate the activity and safety of adding oxaliplatin to a standard chemoradiotherapy schema, including 5-fluorouracil (5-FU)/folinic acid (FA), in locally-advanced rectal cancer (LARC). Methods: Two cycles of oxaliplatin 130 mg/m 2 plus FA 20 mg/m 2 bolus for 5 days and 5-FU 350 mg/m 2 continuous infusion for 5 days were given during week 1 and 4 of pelvic radiotherapy 46 Gy. Patients with a T3/4 and/or node-positive rectal tumour were eligible. Surgery was performed 4-6 weeks after radiotherapy. The primary endpoint was to determine the rate of pathological response. Secondary endpoints were to assess the rate of clinical response and the safety profile. Results: Between March 2005 and January 2009, a total of 35 patients were enrolled. The pathological downstaging rate was 79% with a pathological complete response rate of 17%. The overall clinical response rate (assessed by computed tomography or transrectal ultrasound) was 77%. Grade 3 diarrhoea and Grade 3 neutropaenia were reported in 14% and 11% of the patients, respectively. Eleven patients did not undergo surgery: four of them refused the operation, and seven patients were inoperable due to disease progression. In 24 patients who had surgery, a sphincter-preserving procedure could be performed in 29%. At the median follow-up time of 28.1 months, 25 patients (71%) survived with no evidence of disease. Conclusion: The promising results in terms of pathological response, and the associated good safety profile of a regimen of oxaliplatin plus 5-FU/FA with concomitant radiotherapy, suggest that the regimen could be used in LARC. © 2011 Biomedical Imaging and Intervention Journal. All rights reserved. |
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I. Chitapanarux T. Chitapanarux E. Tharavichitkul S. Mayurasakorn P. Siriwittayakorn S. Yamada V. Lorvidhaya |
author_facet |
I. Chitapanarux T. Chitapanarux E. Tharavichitkul S. Mayurasakorn P. Siriwittayakorn S. Yamada V. Lorvidhaya |
author_sort |
I. Chitapanarux |
title |
A phase II study of oxaliplatin with 5-FU/folinic acid and concomitant radiotherapy as a preoperative treatment in patients with locally advanced rectal cancer |
title_short |
A phase II study of oxaliplatin with 5-FU/folinic acid and concomitant radiotherapy as a preoperative treatment in patients with locally advanced rectal cancer |
title_full |
A phase II study of oxaliplatin with 5-FU/folinic acid and concomitant radiotherapy as a preoperative treatment in patients with locally advanced rectal cancer |
title_fullStr |
A phase II study of oxaliplatin with 5-FU/folinic acid and concomitant radiotherapy as a preoperative treatment in patients with locally advanced rectal cancer |
title_full_unstemmed |
A phase II study of oxaliplatin with 5-FU/folinic acid and concomitant radiotherapy as a preoperative treatment in patients with locally advanced rectal cancer |
title_sort |
phase ii study of oxaliplatin with 5-fu/folinic acid and concomitant radiotherapy as a preoperative treatment in patients with locally advanced rectal cancer |
publishDate |
2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=83455220049&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/49926 |
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