A Multicenter, Clinical Study of FOLFOXIRI With Bevacizumab As First-line Therapy in Patients With mCRC

Colorectal Neoplasms Clinical Trial

— QUATTRO  

Official title:

A Multicenter, Clinical Phase II Study of FOLFOXIRI With Bevacizumab As First-line Therapy in Patients With Metastatic Colorectal Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02246049
• Other study ID #: QUATTRO
• Status: Completed
• Phase: Phase 2
• First received: September 12, 2014
• Last updated: June 15, 2017
• Start date: May 2014
• Est. completion date: February 2017

Study information

• Verified date: June 2017
• Source: EPS Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study to assess efficacy and tolerability of combination therapy FOLFOXIRI with Bevacizumab (BV) as a first-line therapy in patients with metastatic colorectal cancer.

Description:

This is a single-arm, multicentre phase II study evaluating the efficacy and safety of Bevacizumab (BV) in combination with oxaliplatin, irinotecan hydrochloride, fluorouracil, and leucovorin calcium regimen ( FOLFOXIRI +BV ; Falcone et al. ASCO2013) as first-line treatment for Japanese metastatic colorectal cancer patients.

This study is composed two steps because of collecting safety issue in Japanese patient.

As First step (Step 1), It assess on the initial safety information in ten Japanese patients of the end of 2nd cycle. it is evaluated by DMC.

In parallel with the confirmation of the initial safety issue, register up to 65 cases in total and Step 1 patient, to evaluate the efficacy and safety (Step2).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 69
• Est. completion date: February 2017
• Est. primary completion date: February 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Written Informed consent.

2. Histopathologically proven diagnosis of colorectal cancer (adenocarcinoma) excluding vermiform appendix cancer and proctos cancer.

3. Not resectable metastatic colorectal cancer

4. Age at enrollment is >= 20 and <= 75 years

5. ECOG PS < 2 if age < 70 years, ECOG PS = 0 if age = 71-75 years

6. One or more measurable lesion in RECIST ver.1.1 criteria according to contrast enhanced CT chest / abdomen / pelvis diagnosis.

7. Not previously treated with chemotherapy. ( Previous adjuvant by fluoropyrimidine monotherapy is allowed if more than 24 weeks have elapsed between the end of adjuvant therapy and first relapse.)

8. Vital organ functions (listed below) are preserved within 2 weeks prior to entry. Data recorded nearest to the entry should be referred. Blood transfusion or erythropoiesis stimulating agents less than 2 weeks prior to the tests are not allowed.

Neu. >= 1,500/cubicmillimeter Pt. >= 100,000/cubicmillimeter Hb. >= 9.0 g/dL T-bil. <= upper limit of normal (ULN)*1.5 AST and ALT,ALP <= upper limit of normal (ULN)*2.5 (<= ULN*5 in case of liver metastasis) Serum creatinine <= upper limit of normal (ULN) *1.5 PT-INR < 1.5 Proteinuria <= 2+

9. UGT1A1 genotype tested. Categorized into Wild or single Hetero.

Exclusion Criteria:

1. Previously treated with irradiation to bone marrow constituting 20% or more of irradiation field.

2. Untreated brain metastases or spinal cord compression or primary brain tumors.

3. History of CNS disease.[except for asymptomatic Lacunar stroke]

4. Requiring chronic systemic corticosteroid treatment.

5. Current or recent ongoing treatment with anticoagulants.

6. Clinically significant cardiovascular disease for example cerebrovascular accidents, myocardial infarction, unstable angina, congestive heart failure, serious cardiac arrhythmia requiring medication.

7. Treatment with any investigational drug within 4 weeks.

8. Patient with Uncontrolled hypertension, Uncontrolled diabetes, Uncontrolled diarrhea, >=grade 1 peripheral neuropathy, Active peptic ulcer, Non-healing wound, Clinically important diseases.

9. Major surgical procedure within 28 days prior to study treatment start, open biopsy, or significant traumatic injury, or anticipation of the need for major surgical procedure.[except for implantation of central venous catheter and port system.]

10. Lack of physical integrity of the upper gastrointestinal tract.

11. Pregnant women, lactating woman , positive by pregnancy test , wishing to become pregnant, and Sexually active males.

12. Hepatitis B or hepatitis C. Evidence of HIV infection.

13. Previous Chemotherapy for other organs.

14. Other active co-existing malignancies.

15. History / Presence of thrombosis within 1 year requiring medication.

16. History / Presence of paralytic ileus, obstruction or gastrointestinal perforation.

17. Malignant coelomic fluid required drainage.

18. History of allergy to Chinese hamster ovary cell proteins, or any of the components of the study medications.

19. History of fluoropyrimidine severe side effects caused by DPD defect.

20. Interstitial pneumonitis or pulmonary fibrosis.

21. Evidence or requiring systemic treatment for Infectious disease.

22. Patient who is judged by the investigator to be inappropriate for study participation for any reason.

Related Conditions & MeSH terms

• Colorectal Neoplasms

Intervention

Biological:
• Bevacizumab
Given IV

Drug:
• 5-fluorouracil
Given IV
• Irinotecan hydrochloride
Given IV
• Leucovorin calcium
Given IV
• Oxaliplatin
Given IV

Locations

Country	Name	City	State
Japan	EPS Corporation	Shinjuku	Tokyo

Sponsors (1)

Lead Sponsor	Collaborator
EPS Corporation

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression-free survival (PFS) at 10 months	PFS by investigator-reported measurements according to CT image. PFS was calculated from the day of treatment start to the first observation of progression disease (PD) or death from any cause.; PD was defined as Overall Response by RECIST criteria v1.1 according to CT image.	PFS rate at 10 months from study entry
Secondary	Response rate (RR) by central review.	Response evaluation was performed according to RECIST criteria v1.1.	Up to 18 months
Secondary	Response rate (RR) by investigator-reported measurements.	Response evaluation was performed according to RECIST criteria v1.1.	Up to 30 months
Secondary	PFS by central review according to CT image.	PFS was calculated from the day of treatment start to the first observation of progression disease (PD) or death from any cause.	Up to 18 months
Secondary	Overall survival (OS)	OS was calculated from the day of registration in this study to death from any cause.	Up to 30 months
Secondary	Efficacy by RAS status ; RR,PFS,OS	RR,PFS,OS according to tumor RAS status.	Up to 30 months
Secondary	Incidence of adverse events	Adverse events were evaluated according to Common Terminology Criteria for Adverse Events (CTCAE) v4.0. All adverse events was collected in duration from starting treatment to whichever shorter "after 30 days from withdrawal treatment" or "later treatment was started".	Up to 30 months
Secondary	Time to treatment-failure		Up to 30 months
Secondary	Completion rate in Induction treatment		Up to 30 months
Secondary	Relative Dose Intensity		Up to 30 months
Secondary	Treatment duration		Up to 30 months