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Irinotecan/Oxaliplatin/5-Fluorouracil/Leucovorin/Cetuximab As First Line Treatment In Colorectal Cancer

Primary Purpose

Metastatic Colorectal Cancer

Status
Completed
Phase
Phase 2
Locations
Greece
Study Type
Interventional
Intervention
Irinotecan
Leukovorin
Oxaliplatin
5-FLUOROURACIL
Cetuximab
Sponsored by
University Hospital of Crete
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Colorectal Cancer focused on measuring Colorectal Cancer, Cetuximab, FOLFOXIRI

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with histologically proven metastatic adenocarcinoma of the colon or rectum
  • Previous chemotherapy for metastatic disease not allowed. Patients who received prior adjuvant 5-FU-based chemotherapy are eligible if they have remained free of disease for at least 6 months after the completion of adjuvant therapy
  • Patients with operable metastatic disease are excluded from the study
  • Age 18-70 years
  • Performance status (ECOG) 0-1
  • At least one bidimensionally measurable lesion of >= 2cm
  • Life expectancy of at least 6 months
  • Adequate hematologic parameters (absolute neutrophil count >= 1.5x109/L and platelets >=100x109/L)
  • Creatinine and total bilirubin < 1.25 times the upper limit of normal
  • Aspartate and alanine aminotransferase < 3.0 times the upper limit of normal (<5 times in case of liver mets)

Exclusion Criteria:

  • Absence of active infection or malnutrition (loss of more than 20% of the body weight)
  • No history of a second primary tumor other than non-melanoma skin cancer or in situ cervical carcinoma. curatively treated
  • Patients treated with palliative radiotherapy had to have measurable metastatic disease outside the irradiation fields.
  • Patients with severe cardiac dysfunction, liver metastases involving more than 50% of the liver parenchyma, chronic diarrhea, or prior irradiation affecting more than 30% of the active bone marrow are excluded.
  • All patients will have to sign written informed consent in order to participate in the study

Sites / Locations

  • University Hospital of Crete

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

FOLFOXIRI+Erbitux

Outcomes

Primary Outcome Measures

Objective Response Rate

Secondary Outcome Measures

Resectability rates
Time to Tumor Progression
Overall Survival
Toxicity profile
Pharmacogenomic analysis
Q-Twist analysis of Quality of life

Full Information

First Posted
May 29, 2008
Last Updated
September 25, 2015
Sponsor
University Hospital of Crete
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1. Study Identification

Unique Protocol Identification Number
NCT00689624
Brief Title
Irinotecan/Oxaliplatin/5-Fluorouracil/Leucovorin/Cetuximab As First Line Treatment In Colorectal Cancer
Official Title
A Triplet Combination With Irinotecan Plus Oxaliplatin,Continuous Infusion 5-Fluorouracil And Leucovorin Plus Cetuximab As First Line Treatment In Metastatic Colorectal Cancer. A Pilot Phase II Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
July 2007 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital of Crete

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will evaluate the efficacy of FOLOFOXIRI plus Cetuximab combination in young patients with good performance status with unresectable metastatic colorectal cancer.
Detailed Description
The combination of FOLFOXIRI plus cetuximab is reasonable safe regimen especially for patients with good performance status. The estimated benefit from the combination is greater than the possible risk, especially for the patients who will become resectable after treatment. It will be extremely interesting to evaluate the resectability rate of this specific group of patient with good performance status and unresectable disease when they are treated with all active chemotherapeutic agents and cetuximab

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Colorectal Cancer
Keywords
Colorectal Cancer, Cetuximab, FOLFOXIRI

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
FOLFOXIRI+Erbitux
Intervention Type
Drug
Intervention Name(s)
Irinotecan
Other Intervention Name(s)
CPT-11, Campto
Intervention Description
Irinotecan will be administered at a dose of 150mg/m2 as a 30 min IV infusion on day 1
Intervention Type
Drug
Intervention Name(s)
Leukovorin
Other Intervention Name(s)
LV
Intervention Description
Leukovorin will be administered at a dose of 200mg/m2 as a 2-hour IV infusion on days 2 and 3
Intervention Type
Drug
Intervention Name(s)
Oxaliplatin
Other Intervention Name(s)
LoHP, Eloxatin
Intervention Description
Oxaliplatin will be administered on day 2 at the dose of 65mg/m2 as a 2-hours IV
Intervention Type
Drug
Intervention Name(s)
5-FLUOROURACIL
Other Intervention Name(s)
5-FU
Intervention Description
5-FLUOROURACIL at the dose of 400mg/m2 as IV bolus and then, 600mg/m2 as a 22-hour continuous IV infusion, on days 2 and 3
Intervention Type
Drug
Intervention Name(s)
Cetuximab
Other Intervention Name(s)
Erbitux
Intervention Description
Cetuximab will be administered at the dose of 500mg/m2 as a 2-hour infusion on day 1 at least one hour before chemotherapy
Primary Outcome Measure Information:
Title
Objective Response Rate
Time Frame
2 months
Secondary Outcome Measure Information:
Title
Resectability rates
Time Frame
Resectability at the end of treatment (4 or 6 months from the entry to the study)
Title
Time to Tumor Progression
Time Frame
1 year
Title
Overall Survival
Time Frame
1 year
Title
Toxicity profile
Time Frame
Toxicity assessment on each chemotherapy cycles (every 15 days)
Title
Pharmacogenomic analysis
Time Frame
During the treatment
Title
Q-Twist analysis of Quality of life
Time Frame
Quality of life assessment every 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with histologically proven metastatic adenocarcinoma of the colon or rectum Previous chemotherapy for metastatic disease not allowed. Patients who received prior adjuvant 5-FU-based chemotherapy are eligible if they have remained free of disease for at least 6 months after the completion of adjuvant therapy Patients with operable metastatic disease are excluded from the study Age 18-70 years Performance status (ECOG) 0-1 At least one bidimensionally measurable lesion of >= 2cm Life expectancy of at least 6 months Adequate hematologic parameters (absolute neutrophil count >= 1.5x109/L and platelets >=100x109/L) Creatinine and total bilirubin < 1.25 times the upper limit of normal Aspartate and alanine aminotransferase < 3.0 times the upper limit of normal (<5 times in case of liver mets) Exclusion Criteria: Absence of active infection or malnutrition (loss of more than 20% of the body weight) No history of a second primary tumor other than non-melanoma skin cancer or in situ cervical carcinoma. curatively treated Patients treated with palliative radiotherapy had to have measurable metastatic disease outside the irradiation fields. Patients with severe cardiac dysfunction, liver metastases involving more than 50% of the liver parenchyma, chronic diarrhea, or prior irradiation affecting more than 30% of the active bone marrow are excluded. All patients will have to sign written informed consent in order to participate in the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Souglakos, MD
Organizational Affiliation
University Hospital of Crete
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Crete
City
Heraklion
Country
Greece

12. IPD Sharing Statement

Learn more about this trial

Irinotecan/Oxaliplatin/5-Fluorouracil/Leucovorin/Cetuximab As First Line Treatment In Colorectal Cancer

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