search
Back to results

Treatment Outcomes of Hepatic Metastasis After FOLFOX-4 Therapy

Primary Purpose

Colorectal Cancer

Status
Unknown status
Phase
Phase 3
Locations
Taiwan
Study Type
Interventional
Intervention
Hepatic resection
Sponsored by
National Taiwan University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Cancer focused on measuring FOLFOX-4, neoadjuvant chemotherapy, colorectal cancer, liver metastasis, resectability

Eligibility Criteria

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

Inclusion Criteria:

  1. Secondary resectable hepatic metastasis converted by FOLFOX-4 regimen.
  2. age between 18-80 y/o.
  3. no extra-hepatic disease
  4. life expectancy ≥ 3 months
  5. Karnofsky performance status ≥ 50%.
  6. WBC count ≥ 4,000/μl, platelet count ≥ 100,000/μl, serum bilirubin ≤ 2.0 mg/dl and normal serum glucose and electrolyte levels.-

Exclusion Criteria:

  1. Secondary resectable hepatic metastasis with extra-hepatic disease
  2. poor liver function including: serum bilirubin > 2.0 mg/dl, GOT,GPT >100 U/L
  3. severe steatosis hepatitis or sinusoidal dilation
  4. Karnoofsky performance status <50%.-

Sites / Locations

  • Division of Colorectal Surgery, Department of Surgery , National Taiwan University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

The patients with secondary resectable colorectal hepatic metastasis undergoing surgery

The patients with secondary resectable colorectal hepatic metastasis who underwent continuous chemotherapy

Outcomes

Primary Outcome Measures

Both groups of patients were analyzed with intention-to-treat principle. The primary end-point was time-to-progression. The secondary points were overall survival and surgical morbidity.

Secondary Outcome Measures

Surgical morbidity, Chemotherapeutic complications

Full Information

First Posted
January 28, 2008
Last Updated
December 6, 2012
Sponsor
National Taiwan University Hospital
Collaborators
National Science Council, Taiwan
search

1. Study Identification

Unique Protocol Identification Number
NCT00610636
Brief Title
Treatment Outcomes of Hepatic Metastasis After FOLFOX-4 Therapy
Official Title
Oncologic Outcomes of Surgical Versus Non-surgical Methods for the Treatment of Resectable Colorectal Liver-confined Metastases Converted From Initially Non-resectable Metastases by FOLFOX-4 Neoadjuvant Chemotherapy: A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2012
Overall Recruitment Status
Unknown status
Study Start Date
January 2002 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital
Collaborators
National Science Council, Taiwan

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The role of surgical resection in the subset of patients with resectable hepatic metastases converted from initially non-resectable liver metastasis was still not clearly established. To further explore the oncologic results of surgical versus non-surgical methods for the treatment of this subset of patients, we designed and conducted the present randomized prospective study beginning in 2002. The present study was based on the following arguments against the predominant survival benefits of surgical resection in previous reported series: (1) The initially non-resectable liver metastasis was basically a disseminated disease, even though some metastases were highly responsive to chemotherapy and become resectable; (2) Since the evaluation of resectability was based on the imaging studies, it was difficult to consider the surgical resection as "curative" for the resectable hepatic metastases converted from non-resectable ones, given the limitation of the current imaging stools of high-technology; (3) The resectable hepatic metastases after neoadjuvant chemotherapy might represent a subset of hepatic metastases biologically highly responsive to chemotherapy and the time-to-progression for these metastases might be fairly long after a response. Additionally, these metastases might be also biologically responsive to other cytotoxic or targeted therapies that justified the patients' continuous adoption of non-surgical treatment.
Detailed Description
In 2000, de Gramont et al. and Giacchetti et al. reported that combination chemotherapy including modulated infusional 5-Fu plus irinotecan and oxaliplatin could achieve a response rate of approximately 50% and a median survival of in excess of 20 months. These encouraging results implied that chemotherapy is likely to play an increasingly important role in decreasing the size of metastasis to allow for liver resection. Interestingly, Adam and Bismuth et al. reported that the 5-year overall survival of 50% (95% confidence interval 33-68%), observed in patients with resection following neoadjuvant chemotherapy, was comparable to patients with primarily resectable hepatic metastasis as reported by Scheele et al. (39%, 469 patients), Fong et al. (37%, 1001 patients), Nordlinger et al.(28%, 1568 patients), and Fiqueras et al. (36%, 235 patients). Recently, Zelek et al. reported that intravenous and hepatic artery infusion of irinotecan/ 5-fluorouracil/ leucovorin could facilitate complete resection of initially non-resectable hepatic metastases. Pozzo et al. indicated that neoadjuvant treatment of unresectable liver disease with irinotecan/ 5-fluorouracil/ leucovorin enabled a significant portion of patients to undergo surgical resection. Alberts et al. showed that FOLFOX-4 therapy allowed for successful resection of disease in a portion of patients initially not judged to be optimally resectable but with a high recurrence rate after surgery. Masi et al. reported that neoadjuvant approach with irinotecan plus FOLFOX-4 had significant antitumor activity and provided a radical surgical resection of initially unresctable hepatic colorectal metastases with promising median survival of patients. However, most studies published till now are retrospective analyses without a control group or case series with limited patient number and/or short time of follow-up. Therefore, the role of surgical resection in the subset of patients with resectable hepatic metastases converted from initially non-resectable liver metastasis was still not clearly established. To further explore the oncologic results of surgical versus non-surgical methods for the treatment of this subset of patients, we designed and conducted the present randomized prospective study beginning in 2002. The present study was based on the following arguments against the predominant survival benefits of surgical resection in previous reported series: (1) The initially non-resectable liver metastasis was basically a disseminated disease, even though some metastases were highly responsive to chemotherapy and become resectable; (2) Since the evaluation of resectability was based on the imaging studies, it was difficult to consider the surgical resection as "curative" for the resectable hepatic metastases converted from non-resectable ones, given the limitation of the current imaging stools of high-technology; (3) The resectable hepatic metastases after neoadjuvant chemotherapy might represent a subset of hepatic metastases biologically highly responsive to chemotherapy and the time-to-progression for these metastases might be fairly long after a response. Additionally, these metastases might be also biologically responsive to other cytotoxic or targeted therapies that justified the patients' continuous adoption of non-surgical treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
FOLFOX-4, neoadjuvant chemotherapy, colorectal cancer, liver metastasis, resectability

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
The patients with secondary resectable colorectal hepatic metastasis undergoing surgery
Arm Title
2
Arm Type
Active Comparator
Arm Description
The patients with secondary resectable colorectal hepatic metastasis who underwent continuous chemotherapy
Intervention Type
Procedure
Intervention Name(s)
Hepatic resection
Intervention Description
Hepatic resection
Primary Outcome Measure Information:
Title
Both groups of patients were analyzed with intention-to-treat principle. The primary end-point was time-to-progression. The secondary points were overall survival and surgical morbidity.
Time Frame
evaluated every 6 months
Secondary Outcome Measure Information:
Title
Surgical morbidity, Chemotherapeutic complications
Time Frame
Evaluated every 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Secondary resectable hepatic metastasis converted by FOLFOX-4 regimen. age between 18-80 y/o. no extra-hepatic disease life expectancy ≥ 3 months Karnofsky performance status ≥ 50%. WBC count ≥ 4,000/μl, platelet count ≥ 100,000/μl, serum bilirubin ≤ 2.0 mg/dl and normal serum glucose and electrolyte levels.- Exclusion Criteria: Secondary resectable hepatic metastasis with extra-hepatic disease poor liver function including: serum bilirubin > 2.0 mg/dl, GOT,GPT >100 U/L severe steatosis hepatitis or sinusoidal dilation Karnoofsky performance status <50%.-
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jin-Tung Liang, PhD
Phone
886-2-23123456
Ext
5683
Email
jintung@ntu.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jin-Tung Liang, PhD
Organizational Affiliation
National Taiwan University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Division of Colorectal Surgery, Department of Surgery , National Taiwan University Hospital
City
Taipei
ZIP/Postal Code
100
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jin-Tung Liang, PhD
Phone
886-2-23123456
Ext
5683
Email
jintung@ntu.edu.tw

12. IPD Sharing Statement

Links:
URL
http://clinicaltrials.gov/ct2/show/NCT00172159
Description
Influence of Neoadjuvant Therapy on the Resectability of Hepatic Metastases From Colorectal Cancers
URL
http://clinicaltrials.gov/ct2/show/NCT00173472
Description
Association of MSI, TS, DPD, MVD and EGFR With Chemosensitivity in Stage IV in Colorectal Cancer

Learn more about this trial

Treatment Outcomes of Hepatic Metastasis After FOLFOX-4 Therapy

We'll reach out to this number within 24 hrs