NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
JRCT ID: jRCT1051190106

Registered date:13/02/2020

LOFT trial

Basic Information

Recruitment status Complete
Health condition(s) or Problem(s) studiedColorectal liver metastasis
Date of first enrollment13/02/2020
Target sample size50
Countries of recruitment
Study typeInterventional
Intervention(s)Postoperative adjuvant chemotherapy with L-OHP base regimen (6courses of mFOLFOX6 or 4courses of CapeOX) followed by 3courses of UFT plus LV.

Outcome(s)

Primary Outcomethe completion rate
Secondary Outcomeoverall survival, relapse-free survival, 3-year relapse-free survival rate, adverse event, relative dose intensity, the correlation between the remnant liver ratio and the completion rate, change over time about sensory nerve disorder

Key inclusion & exclusion criteria

Age minimum>= 20age old
Age maximum<= 80age old
GenderBoth
Include criteria1. Histlogically proven colorectal carcinoma. 2. Curatively resected metastatic liver tumors of colorectal cancer. 3. No extrahepatic metastasis. 4. Within 4-8 weeks from the date of liver resection. 5. Age >= 20 years, Age <= 80 years 6. The Eastern Cooperative Oncology Group(ECOG) Performance Status of 0-1 7. Cases that meet all the following criteria (Check all items using the test values of the latest within 14 days prior to entry). i.Neutrophil count >=1500/mm3 ii.Platelets>=100,000/mm3 iii.Hemoglobin >=9.0g/dL iv. Total bilirubin <=1.5g/dL v. AST, ALT, ALP <=2.5ULN vi. Creatinine<=1.5mg/dL 8. Checked chest and abdominal CT within 30 days. 9. Promised of more than 3 months survival 10.Written informed consent.
Exclude criteria1. Neurologic symptom due to cerebrovascular diseases. 2. Cardiac diseases. 3. Uncontrollable hypertension, Uncontrollable diabetes. 4. Renal dysfunction. 5. Uncontrollable gastrointestinal ulcer 6. Prior hypersensitivity reaction to drugs used in this trial. 7. Suspected of DPD Deficiency. 8. Prior treatment with L-OHP within 6 months. 9. Treatment with MTX to RA. 10. Uncontrollable infectious diseases. 11. Uncontrollable diarrhea. 12. Neuropathy >= Grade2 according to the CTCAE. 13. Body fruid (ascites,pleural effusion.pericardiac effsion). 14. Multiple malignancies to be treated within 5 years. 15. Prior treatment with immunosuppressant and transplantation. 16. Pregnant. 17. Any other cases who are regarded as inadequate for study enrollment by investigators.

Related Information

Contact

Public contact
Name Rei Toda
Address 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto Kyoto Japan 606-8507
Telephone +81-75-751-4323
E-mail rtoda@kuhp.kyoto-u.ac.jp
Affiliation Department of Surgery, Graduate School of Medi cine, Kyoto University
Scientific contact
Name Etsuro Hatano
Address 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto Kyoto Japan 606-8507
Telephone +81-75-751-4323
E-mail rutosa@kuhp.kyoto-u.ac.jp
Affiliation Department of Surgery, Graduate School of Medi cine, Kyoto University