Clinical Trial

Prospectively Randomized Control Clinical Trial of FOLFOXIRI Preoperative Chemotherapy Alone on Rectal Cancer in Local Advance Comparing to Oral Capecitabine Combined With Long-term Radiation

Recruiting Phase 3
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Record status
This record was last updated January 23, 2019 (before its estimated September 25, 2025 completion). Its status may not reflect the trial's current state.
Summary
Preoperative radiation and chemotherapy is the standard treatment for local advanced rectal cancer. The addition of oxaliplatin to capecitabine combined with radiotherapy does not improve local control and long-term survival. Most importantly,chemoradiotherapy significantly increased surgical complication and poor long-term quality of life .In the absence of effective measures of predicting chemo-sensitivity, there is considerable risk of using any two-drug regimen for neoadjuvant therapy. Simultaneous use of the three chemotherapeutic drugs may be able to reduce the likelihood of resistance to both dual drug regimen and single drug regimen. The purpose of this study is to compare the efficacy and safety of three chemotherapeutic regimen known as FOLFOXIRI (the drug 5-fluorouracil, oxaliplatin, Irinotecan) with standard radiotherapy combined with capecitabine in neoadjuvant therapy for local advanced rectal cancer. The drugs in the FOLFOXIRI regimen are all FDA(Food and Drug Administration) approved and have been used routinely to treat patients with advanced colorectal cancer.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2018-09-12; most recent amendment 2019-01-20.
Status change: Not Yet Recruiting → Recruiting 2018-09-17
Trial Details
NCT Number NCT03671252
Lead Sponsor Sun Yat-sen University
Conditions Rectal Cancer
Enrollment 776 participants
Start Date 2018-11-16
Primary Completion 2025-09-25 (estimated)
Study Completion 2028-09-25 (estimated)
Updated on ClinicalTrials.gov 2019-01-23