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Completed

NCT Number: NCT03443661

Neoadjuvant Triplet Chemotherapy Regimen in Patients With Locally Advanced Rectal Cancer

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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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

National Cancer Center/Cancer Hospital, Chinese ACademy of Medical Sciences and Peking Union Medical College

Beijing, 100021, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically confirmed locally advanced rectal cancer;
  • 18-70 years ;
  • Clinicalstage:T3,4a,N0,M0;T1-4a,N+,M0;
  • Tumor from anus >5cm and ≤15cm;
  • ECOG=0-1;
  • Available organ function:ALT≤1.5xULN;AST≤1.5xULN;TBIL≤1.0xULN; NEUT≥2×109/L;PLT≥100×109/L;Hb≥90g/L;Creatinine≤1.0xULN;
  • Informed consent;
  • UGT1A1:UGT1A1*1/UGT1A1*1,UGT1A1*1/UGT1A1*28,UGT1A1*1/UGT1A1*6;

Exclusion criteria

  • Clinical stage T4b or unresectable disease;
  • History of pelvic radiotherapy;
  • History of chemotherapy within 5 years;
  • History of chronic diarrhea;
  • Tumor causes intestinal obstruction, intestinal perforation, and severe bleeding;
  • Hepatitis B surface antigen positive; Hepatitis C virus infection; Cirrhosis of the liver for any cause;
  • UGT1A1:UGT1A1*28/UGT1A1*28,UGT1A1*6/UGT1A1*6;
  • Other cancers in the past 5 years, except for cervical carcinoma in situ or non-melanoma skin cancer;
  • Myocardial infarction (in the last 6 months), severe instability angina, congestive heart failure; interstitial pneumonia,pulmonary fibrosis, uncontrolled diabetes, renal insufficiency;
  • Mental illness;Pregnant or lactating women;

Treatment and study plan

FOLFOXIRI

Drug

oxaliplatin 85 mg/m2 irinotecan 150 mg/m2, 5FU 2,400 mg/m2 by 46 h infusion repeated at 2week intervals

Primary outcomes

  1. pCR

    Time frame: 1 year

    Pathological complete response according to Mandard tumor regression grading

Secondary outcomes

  1. R0 resection rate

    Time frame: 1 year

    R0 resection rate

  2. locoregional recurrence rate

    Time frame: 1 year

    locoregional recurrence rate

  3. Safety

    Time frame: 1 year

    Including adverse events during neoadjuvant chemotherapy,surgery and perioperative complications

Sponsors and collaborators

Lead sponsor

Aiping Zhou

Unknown

Registry information

Official study title

A Pilot Phase II Study of Neoadjuvant Triplet Chemotherapy Regimen (FOLFOXIRI) in Patients With Locally Advanced Rectal Cancer

Important dates

Study start
2016
Primary completion
2019
Study completion
2020
First posted
Feb 23, 2018
Registry last updated
Feb 1, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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