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Combination Chemotherapy and Radiation Therapy in Treating Patients With Recurrent Metastatic Colorectal Cancer

Primary Purpose

Colorectal Cancer

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
fluorouracil
leucovorin calcium
oxaliplatin
neoadjuvant therapy
Sponsored by
GERCOR - Multidisciplinary Oncology Cooperative Group
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Cancer focused on measuring adenocarcinoma of the colon, adenocarcinoma of the rectum, stage IV colon cancer, stage III colon cancer, stage III rectal cancer, stage IV rectal cancer

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the colon or rectum Metastatic disease isolated to the following lymph nodes: Aortic Interaortic Celiomesenteric Retroperitoneal, including the following sites: Peri-uretal Liver Iliac Clavicle Mediastinum Inguinal Cervical Incompletely resected disease Recurrent disease, defined by 1 of the following criteria: Progression occurred within 6 months after prior oxaliplatin or after the patient received no prior oxaliplatin Progressive disease after cisplatin or fluorouracil Must be able to be encompassed in radiation field PATIENT CHARACTERISTICS: ECOG performance status (PS) 0-2 or Karnofsky PS 60-100% Life expectancy more than 12 weeks Absolute neutrophil count ≥ 1,500/mm^3 Platelet count ≥ 100,000 /mm^3 Alkaline phosphatase ≤ 5 times normal Bilirubin ≤ 2 times normal Creatinine < 2 times normal or creatinine clearance ≥ 40 mL/min No peripheral neuropathy > grade 1 Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception No weight loss > 15% since diagnosis of recurrent disease No uncontrolled heart disease No angina No symptomatic disease of the inferior artery No psychological, familial, sociological, or geographical condition that would preclude study treatment or compliance PRIOR CONCURRENT THERAPY: See Disease Characteristics No prior chemotherapy or radiotherapy No concurrent corticosteroids

Sites / Locations

  • Institut Sainte Catherine
  • Centre Hospitalier Regional de Besancon - Hopital Jean Minjoz
  • Hopital Drevon
  • Hopital Robert Boulin
  • Polyclinique des Quatre Pavillons
  • Hopital Europeen Georges Pompidou
  • Hopital Tenon
  • Polyclinique De Courlancy
  • C.H. Senlis

Outcomes

Primary Outcome Measures

Response rate

Secondary Outcome Measures

Overall survival
Disease-free survival
Primary site of recurrence
Time to recurrence
Quality of life

Full Information

First Posted
December 20, 2005
Last Updated
February 6, 2009
Sponsor
GERCOR - Multidisciplinary Oncology Cooperative Group
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1. Study Identification

Unique Protocol Identification Number
NCT00268333
Brief Title
Combination Chemotherapy and Radiation Therapy in Treating Patients With Recurrent Metastatic Colorectal Cancer
Official Title
Phase II Study of Recurrent Ganglionic Colorectal Cancer Not Accessible By Surgery Treated Using Chemotherapy With Simplified FOLFOX7 Followed By Radiotherapy Combined With 5FU and Oxaliplatin
Study Type
Interventional

2. Study Status

Record Verification Date
May 2007
Overall Recruitment Status
Completed
Study Start Date
August 2005 (undefined)
Primary Completion Date
January 2006 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
GERCOR - Multidisciplinary Oncology Cooperative Group

4. Oversight

5. Study Description

Brief Summary
RATIONALE: Drugs used in chemotherapy, such as oxaliplatin, fluorouracil, and leucovorin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving more than one drug (combination chemotherapy) together with radiation therapy may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving combination chemotherapy together with radiation therapy works in treating patients with recurrent metastatic colorectal cancer.
Detailed Description
OBJECTIVES: Primary Determine the response rate in patients with recurrent metastatic colorectal cancer treated with neoadjuvant oxaliplatin, fluorouracil, and leucovorin calcium followed by radiotherapy and concurrent fluorouracil and oxaliplatin. Secondary Determine the overall survival and disease-free survival of patients treated with this regimen. Determine the primary site of recurrence and time to recurrence in patients treated with this regimen. Determine quality of life of patients treated with this regimen. OUTLINE: This is a nonrandomized, open-label, multicenter study. Neoadjuvant chemotherapy: Patients receive oxaliplatin IV over 2 hours and leucovorin calcium IV over 2 hours on day 1. Patients also receive fluorouracil IV continuously over 46 hours beginning day 1. Treatment repeats every 14 days for 4 courses in the absence of disease progression or unacceptable toxicity. Two to 5 weeks later, patients with stable or responding disease proceed to chemoradiotherapy. Chemoradiotherapy: Patients receive fluorouracil IV continuously 5 days a week for 5 weeks and oxaliplatin IV over 1 hour on days 1, 8, 15, 22, and 29. Patients also undergo radiotherapy 5 days a week for 5 weeks beginning on day 1. Quality of life is assessed at baseline, 1 week after the completion of neoadjuvant chemotherapy, on days 15, 30, and 42 of chemoradiotherapy, and at 1 and 2 months after the completion of study treatment. After completion of study treatment, patients are followed periodically. PROJECTED ACCRUAL: A total of 39 patients will be accrued for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
adenocarcinoma of the colon, adenocarcinoma of the rectum, stage IV colon cancer, stage III colon cancer, stage III rectal cancer, stage IV rectal cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
39 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
fluorouracil
Intervention Type
Drug
Intervention Name(s)
leucovorin calcium
Intervention Type
Drug
Intervention Name(s)
oxaliplatin
Intervention Type
Procedure
Intervention Name(s)
neoadjuvant therapy
Primary Outcome Measure Information:
Title
Response rate
Secondary Outcome Measure Information:
Title
Overall survival
Title
Disease-free survival
Title
Primary site of recurrence
Title
Time to recurrence
Title
Quality of life

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the colon or rectum Metastatic disease isolated to the following lymph nodes: Aortic Interaortic Celiomesenteric Retroperitoneal, including the following sites: Peri-uretal Liver Iliac Clavicle Mediastinum Inguinal Cervical Incompletely resected disease Recurrent disease, defined by 1 of the following criteria: Progression occurred within 6 months after prior oxaliplatin or after the patient received no prior oxaliplatin Progressive disease after cisplatin or fluorouracil Must be able to be encompassed in radiation field PATIENT CHARACTERISTICS: ECOG performance status (PS) 0-2 or Karnofsky PS 60-100% Life expectancy more than 12 weeks Absolute neutrophil count ≥ 1,500/mm^3 Platelet count ≥ 100,000 /mm^3 Alkaline phosphatase ≤ 5 times normal Bilirubin ≤ 2 times normal Creatinine < 2 times normal or creatinine clearance ≥ 40 mL/min No peripheral neuropathy > grade 1 Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception No weight loss > 15% since diagnosis of recurrent disease No uncontrolled heart disease No angina No symptomatic disease of the inferior artery No psychological, familial, sociological, or geographical condition that would preclude study treatment or compliance PRIOR CONCURRENT THERAPY: See Disease Characteristics No prior chemotherapy or radiotherapy No concurrent corticosteroids
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Laurent Mineur, MD
Organizational Affiliation
Institut Sainte Catherine
Official's Role
Study Chair
Facility Information:
Facility Name
Institut Sainte Catherine
City
Avignon
ZIP/Postal Code
84082
Country
France
Facility Name
Centre Hospitalier Regional de Besancon - Hopital Jean Minjoz
City
Besancon
ZIP/Postal Code
25030
Country
France
Facility Name
Hopital Drevon
City
Dijon
ZIP/Postal Code
21000
Country
France
Facility Name
Hopital Robert Boulin
City
Libourne
ZIP/Postal Code
33500
Country
France
Facility Name
Polyclinique des Quatre Pavillons
City
Lormont
ZIP/Postal Code
33310
Country
France
Facility Name
Hopital Europeen Georges Pompidou
City
Paris
ZIP/Postal Code
75015
Country
France
Facility Name
Hopital Tenon
City
Paris
ZIP/Postal Code
75970
Country
France
Facility Name
Polyclinique De Courlancy
City
Reims
ZIP/Postal Code
F-51100
Country
France
Facility Name
C.H. Senlis
City
Senlis
ZIP/Postal Code
60309
Country
France

12. IPD Sharing Statement

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Combination Chemotherapy and Radiation Therapy in Treating Patients With Recurrent Metastatic Colorectal Cancer

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