Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

FUDR/Oxaliplatin HAI Plus Irinotecan vs. FOLFOXIRI Chemotherapy in Treating Initially Unresectable CRCLM

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03678428
Recruitment Status : Not yet recruiting
First Posted : September 19, 2018
Last Update Posted : October 1, 2018
Sponsor:
Information provided by (Responsible Party):
Yuhong Li, Sun Yat-sen University

Brief Summary:
The aim of the trial is to compare the objective response rates of FUDR/Oxaliplatin HAI plus CPT-11 and FOLFOXIRI chemotherapy in patients with initially non-resectable metastatic colorectal cancer liver metastases. The patients will be treated with systemic FOLFOXIRI chemotherapy or FUDR/Oxaliplatin hepatic arterial infusion with CPT-11 systemic chemotherapy.

Condition or disease Intervention/treatment Phase
Metastatic Colorectal Cancer Liver Metastases Drug: Irinotecan Drug: Oxaliplatin HAI Drug: Floxuridine Drug: Leucovorin Drug: 5-FU Drug: Oxaliplatin Phase 3

Detailed Description:
Previous studies and our experience have proved the efficacy and safety of systemic chemotherapy combined with hepatic arterial infusion (HAI) with floxuridine and dexamethasone in patients with initially unresectable colorectal liver metastasis. Hepatic arterial infusion oxaliplatin trials have been done with oxaliplatin alone and in combination with irinotecan, 5-FU/LV, and mitomycin-C and have showed that Hepatic arterial infusion oxaliplatin and FUDR could increase response rate and resection rate for colorectal liver metastasis. Therefore, we designed this study to compare objective response rates of FUDR/Oxaliplatin HAI plus CPT-11 and FOLFOXIRI chemotherapy in patients with initially non-resectable metastatic colorectal cancer liver metastases.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 160 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: FUDR/Oxaliplatin HAI Plus Irinotecan Chemotherapy vs. FOLFOXIRI Chemotherapy in Treating Initially Unresectable CRCLM
Estimated Study Start Date : October 31, 2018
Estimated Primary Completion Date : October 31, 2021
Estimated Study Completion Date : December 31, 2022

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: FUDR/Oxaliplatin HAI plus irinotecan

Patients will receive Systemic CPT-11 + HAI (FUDR+L-OHP) every 28 days:

Irinotecan 150 mg/m2 IV over 90 minutes on Day 1; followed by Oxaliplatin 85 mg/m2 over 3 hours through the HAI pump on Day 1 and 0.12 mg/kg/day floxuridine (FUDR) and 25 mg dexamethasone in normal saline to a total volume of 300 ml will be administered through the HAI pump.

then Irinotecan 150 mg/m2 IV over 90 minutes on Day 15, followed by Oxaliplatin 85 mg/m2 IV over 3 hours on Day 15.

This will be repeated on Day 1 of each 28-day cycle. FUDR will be administered through a 14-day continuous infusion with the HAI pump.

Drug: Irinotecan
Irinotecan 150 mg/m2 IV over 90 minutes on Day 1 and 15.

Drug: Oxaliplatin HAI
Oxaliplatin 85 mg/m2 over 3 hours will be administered through the HAI pump on day 1. Oxaliplatin 85 mg/m2 IV over 3 hours on day 15.

Drug: Floxuridine
0.12 mg/kg/day floxuridine (FUDR) and 25 mg dexamethasone in normal saline to a total volume of 300 ml will be administered through the HAI pump.

Active Comparator: FOLFOXIRI

Patients will receive Systemic FOLFOXIRI every 28 days:

Irinotecan 150 mg/m2 IV over 90 minutes on Day 1 and Day 15; Oxaliplatin 85 mg/m2 IV in 3-6 hours on Day 1 and Day 15; Leucovorin 200mg/m2 and 5-FU 2400mg/m2 CIV in 46 hours on Day 1 and Day 15.

Drug: Irinotecan
Irinotecan 150 mg/m2 IV over 90 minutes on Day 1 and 15.

Drug: Leucovorin
Leucovorin 200mg/m2 IV on Day 1 and 15.

Drug: 5-FU
5-FU 2400mg/m2 CIV in 46h on Day 1 and 15.

Drug: Oxaliplatin
Oxaliplatin 85 mg/m2 IV over 3 hours on Day1 and 15.




Primary Outcome Measures :
  1. Overall Response Rate and bilateral 95% confidence interval [ Time Frame: Up to 2-4 months ]
    defined as complete remission rates and partial remission rates after treatment.


Secondary Outcome Measures :
  1. R0 resection rates [ Time Frame: Up to 2-4 months ]
    defined as no macroscopic or microscopic residual tumor

  2. Depth of tumor regression(DpR) [ Time Frame: Up to 2-4 months ]
    defined as the largest depth of tumor regression

  3. Progress-free Survival(PFS) [ Time Frame: Up to 2-4 months ]
    defined as the period from the date of receiving treatment to disease progress caused by any reason.

  4. Relapse-free Survival(RFS) of patients with resectable tumor [ Time Frame: Up to 2-4 months ]
    defined as the period from the date of resection to tumor relapse caused by any reason.

  5. Overall Survival(OS) [ Time Frame: Up to 2-4 months ]
    defined as the period from the date of receiving treatment to death caused by any reason.

  6. Adverse events, servere adverse events and surgery-related adverse events rates [ Time Frame: Up to 2-4 months ]
    defined as the incidence and severity of adverse events related to chemotherapy, HAI and surgery.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 70 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age ≥ 18 and ≤70.
  • Diagnosed as colorectal adenocarcinoma by histology.
  • Confirmed as liver metastases by medical imaging or pathology.
  • MDT determined as unresectable liver metastases, defined as:①more than 5 metastases; ②unable to conduct R0 resection; ③no sufficient residual liver volume after resection; ④none of 3 hepatic vein can be reserved after resection, no sufficient blood supply or bibliary duct can be reserved, none of 2 adjacent liver segment can be reserved. Whenever meets any of the criteria mentioned above would be defined as unresectable liver metastases.
  • No previous treatment aiming at treating liver metastases, including chemotherapy, surgery, radiotherapy, transcatheter hepatic arterial chemoembolization(TACE) or target therapy.
  • Confirmed by CT, MRI or PET/CT(if necessary) that there is no extrahepatic metastases or only oligos extrahepatic metastases(no more than 2 organs and 5 leisions, maximum diameters of single leision ≤ 1cm).
  • Unsuitable for cetuximab treatment(RAS mutation, unable to afford the cost).
  • No hematologic dysfunction(Platelets >90×10^9/L; WBC >3×10^9/L; Neutrophil >1.5×109/L).
  • Serum bilirubin ≤ 1.5 × ULN; aminotransferase ≤ 5 × ULN.
  • No ascites; no coagulation dysfunction; albumin ≥ 30g/L.
  • Hepatic function was classified as class A by Child-Pugh classification.
  • Serum creatinine < 1 × ULN, or creatinine clearance rate(CCR) > 50ml/min(calculated by Cockcroft-Gault formula).
  • ECOG scored as 0-1.
  • Life expectancy > 3 months.
  • Informed consent.
  • Willing and able to receive follow-up until death or trial is finished or trial is terminated.

Exclusion Criteria:

  • Presence of extensive extrahepatic metastases(more than 2 organs and 5 leisions, or maximum diameter of single leision > 10 cm).
  • Severe arterial embolism or ascites.
  • Presence of hemorrhagic tendency or coagulation dysfunction.
  • Presentive of hypertensive crisis or hypertensive encephalopathy.
  • Severe uncontrolled systemic complications, such as infection or diabetes.
  • Severe clinical CVD(cardiovascular disease), such as cerebrovascular accident(within 6 months before recruitment), myocardial infarction(within 6 months before recruitment), uncontrolled hypertension; unstable angina pectoris; congestive heart-failure(NYHA 2-4 grade); arrhythmia that needs medication treatment.
  • Previous diagnosed or physical examination showed presence of central nervous system(CNS) disease(i.e. primary brain tumor, epilepsy uncontrolled by standard treatment, any history of brain metastases or stroke).
  • Previous history of other malignancy within 5 years(except basal cell carcinoma after radical resection and/or cervical carcinoma in situ).
  • Received any medication under research within 28 days before the trial.
  • Any residual toxicity of previous chemotherapy(except hair loss), i.e. peripheral neuropathy ≥ NCI CTC v3.0 Grade 2, will be excluded from oxaliplatin-based chemotherapy regimen research pair.
  • Allergic to any medication involved in the trial.
  • Pregnant and lactating women.
  • Patient who does not use or refuses to take any appropriate contraceptive measures (intrauterine contraceptive ring, barrier contraception combined with spermicidal gel or sterilization operation), including women of childbearing age (within 2 years after the last menstrual period) and men who are with possible fertility.
  • Unable or unwilling to comply with the research plan.
  • The existence of any other disease, dysfunction caused by metastatic lesions, or suspicious disease found on the regular examination, which indicating contraindications to the use of study drugs or may bring high risks of treatment related complications

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03678428


Contacts
Layout table for location contacts
Contact: Yuhong Li, MD +86(20)87343135 liyh@sysucc.org.cn

Locations
Layout table for location information
China, Guangdong
Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, China, 510060
Sponsors and Collaborators
Sun Yat-sen University
Investigators
Layout table for investigator information
Study Director: Yuhong Li, MD Sun Yat-sen University

Layout table for additonal information
Responsible Party: Yuhong Li, Director, Department of Medical Oncology, Principal Investigator, Clinical Professor, Yuhong Li, Sun Yat-sen University
ClinicalTrials.gov Identifier: NCT03678428     History of Changes
Other Study ID Numbers: TRIUMPH
First Posted: September 19, 2018    Key Record Dates
Last Update Posted: October 1, 2018
Last Verified: September 2018

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
Layout table for MeSH terms
Colorectal Neoplasms
Intestinal Neoplasms
Gastrointestinal Neoplasms
Digestive System Neoplasms
Neoplasms by Site
Neoplasms
Digestive System Diseases
Gastrointestinal Diseases
Colonic Diseases
Intestinal Diseases
Rectal Diseases
Oxaliplatin
Irinotecan
Floxuridine
Antineoplastic Agents
Topoisomerase I Inhibitors
Topoisomerase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Antimetabolites, Antineoplastic
Antimetabolites