National Cancer Center/Cancer Hospital, Chinese ACademy of Medical Sciences and Peking Union Medical College
Beijing, 100021, China
NCT Number: NCT03443661
This study aims to investigate the feasibility, safety and efficacy of triplet regimen of neoadjuvant chemotherapy in patients with locally advanced rectal cancer
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Notify Me18 year–70 year
All sexes
Interventional
Phase 2
Beijing, 100021, China
In this pilot phase II study, the investigators enrolled Chinese adults(age 18 to 70 years) with locally advanced stage II/III rectal cancer. The neuadjuvant chemotherapy regimen is : oxaliplatin 85 mg/m2 and irinotecan 150 mg/m2, combined with 5FU 2,400 mg/m2 by 46 h infusion, repeated at 2week intervals for 5 cycles. Total mesorectal excision was scheduled 4-5 weeks after completion of neoadjuvant treatment and followed by a further 7 cycles of mFOLFOX or 4 cycles of XELOX. Primary outcome measures of this phase II trial were feasibility, safety, tolerance and efficacy of neoadjuvant treatment.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
oxaliplatin 85 mg/m2 irinotecan 150 mg/m2, 5FU 2,400 mg/m2 by 46 h infusion repeated at 2week intervals
Time frame: 1 year
Pathological complete response according to Mandard tumor regression grading
Time frame: 1 year
R0 resection rate
Time frame: 1 year
locoregional recurrence rate
Time frame: 1 year
Including adverse events during neoadjuvant chemotherapy,surgery and perioperative complications
Aiping Zhou
Unknown
A Pilot Phase II Study of Neoadjuvant Triplet Chemotherapy Regimen (FOLFOXIRI) in Patients With Locally Advanced Rectal Cancer
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