A Phase II Study of Tegafur-Uracil as Maintenance Chemotherapy in Patients With Stage II of Colon Cancer

NCT ID: NCT02887365

Last Updated: 2016-09-07

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 300 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-09-30
• Study Completion Date: 2017-08-31

Brief Summary

Investigators would like to assess the efficacy and safety of tegafur-uracil in patients with stage II MSI-L or MSS colon cancer under metronomic setting for one year.

Detailed Description

Approximately 15% cases of colon cancer are associated a type of inherited susceptibility called defective DNA mismatch repair (MMR), which is frequently measured by either the presence of microsatellite instability (MSI) or by testing for loss of the protein products for genes involved in DNA MMR (MLH1, MSH2, MSH6 and PMS2). Tumors are classified according to the percentage of abnormal microsatellite regions present: >30-40% as high-level MSI (MSI-H), <30-40% as low-level MSI (MSI-L) and no abnormalities as microsatellite stable (MSS). In the condition of MSI presence, evidence shows that MSI is a marker of a more favorable survival outcome and a predictor of decreased benefit from adjuvant therapy with 5-FU in patients with stage II disease. MSI status can be used in the clinic as a prognostic tool to identify a subgroup of stage II patients with improved prognosis. Patients with MSI-H tumors are not suggested to have adjuvant chemotherapy while patients with MSI-L or MSS tumors can benefit from adjuvant chemotherapy. oral tegafur-uracil as an adjuvant chemotherapy in patients with Dukes' stage B2 and C2 colon cancer could be a good alternative to infusional 5-FU. Current evidences suggest adjuvant 5-FU-based therapy could improve survival outcome for patients with stage II MSI-L or MSS colon cancer, but not for patients with MSI-H colon cancer. Thus, oral tegafur-uracil is considered to have similar efficacy as 5-FU in this population.

Conditions

MSI-L/MSS; Stage II Colon Cancer

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Blinding Strategy: NONE

Study Groups

tegafur-uracil

tegafur-uracil treatment in patients with stage II MSI-L or MSS colon cancer

Group Type: EXPERIMENTAL

tegafur-uracil

Intervention Type: DRUG

Observation

Observation for one year

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

tegafur-uracil

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

To be eligible for inclusion, each subject must fulfill all of the following criteria:

1. pathologically confirmed adenocarcinoma of the colon with stage II disease;

2. complete resection of primary tumor;

3. detection of low level microsatellite instability (MSI-L) or microsatellite stable (MSS) in resected tumor sample;

4. no prior chemotherapy or radiotherapy for colon cancer;

5. ECOG performance status 0 to 1;

6. age of 20 years or older;

7. able to start the study treatment within 8 weeks after surgery;

8. able to understand and willingness to sign a written informed consent document.

Exclusion Criteria

Subjects who fulfill any of the following criteria will be excluded from the trial:

1. Severe postoperative complications;

2. inadequate hematopoietic function which is defined as below:

1. hemoglobin < 9 g/dL;

2. absolute neutrophil count (ANC) ≤ 1,500/mm3;

3. platelet count < 100,000/mm3;

3. inadequate hepatic function which is defined as below:

1. total bilirubin > 2 times upper limit of normal (ULN);

2. hepatic transaminases (ALT and AST) > 2.5 x ULN;

4. inadequate renal function which is defined as below:

a.creatinine > 1.5 x ULN;

5. significant medical conditions that is contraindicated to study medication or render patient at high risk from treatment complications based on investigator's discretion;

6. other malignancy within the past 5 years except for adequately treated basal or squamous cell skin cancer or cervical cancer in situ;

7. participation in another clinical trial with any investigational drug within 30 days prior to entry;

8. pregnant women or nursing mothers, or positive pregnancy test for women of childbearing potential. Patients with childbearing potential should have effective contraception for both the patient and his or her partner during the study.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Taiwan University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Been Ren Lin, Ph.D

Role: PRINCIPAL_INVESTIGATOR

National Taiwan University Hospital

Locations

National Taiwan University Hospital

Taipei, , Taiwan

Site Status: RECRUITING

Countries

Taiwan

Central Contacts

Been Ren Lin, Ph.D

Role: CONTACT

dtsurg92@yahoo.com.tw

886-972651798

Facility Contacts

Been Ren Lin

Role: primary

dtsurg92@yahoo.com.tw

886-972651798

Other Identifiers

201407054MINC

Identifier Type: -

Identifier Source: org_study_id