Metastatic Colorectal Cancer
Conditions
Keywords
colorectal cancer, metastatic, regorafenib, CHOI criteria, RECIST criteria
Brief summary
The purpose of the study is to evaluate the performance of various tumor response criteria (Choi and RECIST1.1 criteria) in the assessment of regorafenib activity. Moreover, an assessment of the tumor heterogeneity will be made using computed tomographic texture analysis (CTTA)
Detailed description
This is a phase II study in patients with metastatic colorectal cancer treated by regorafenib.
Interventions
DRUGregorafenib
160mg once daily during 3 weeks followed by 1 week off therapy. Regorafenib will be taken until disease progression according to the CHOI and RECIST1.1 criteria, death or inacceptable toxicity.
Sponsors
GERCOR - Multidisciplinary Oncology Cooperative Group
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Signed and dated informed consent. 2. Patients with histologically proven metastatic colorectal cancer 3. Patients previously treated with, or who are not considered candidates for available therapies, i.e., fluoropyrimidine-based chemotherapy, anti-VEGF therapy and anti-EGFR therapy (if patients were RAS wild-type). 4. ECOG PS = 0 or 1 5. Aged 18-years or older 6. Life expectancy of at least 3 months 7. Adequate renal, bone marrow, liver and pancreatic functions: * Estimated creatinine clearance ≥ 30 mL/min as calculated using the Cockcroft-Gault equation * Platelet count ≥ 100.000/mm3; hemoglobin ≥ 9 g/dL; absolute neutrophil count ≥ 1500/mm3. Transfusion to meet the inclusion criteria will not be allowed * Total bilirubin ≤ 1.5 the upper limit of normal value (ULN); alanine aminotransferase (ALAT) and aspartame aminotransferase (ASAT) ≤ 3.0 x ULN (≤ 5.0 x ULN for patients with liver involvement of their cancer); alkaline phosphatase (ALP) ≤ 2.5 x ULN (≤ 5.0 x ULN for patients with liver involvement of their cancer and/or have bone metastases) 8. International normalized ratio (INR) ≤ 1.5 x ULN and partial thromboplastin time (PTT) or activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless receiving treatment with therapeutic anticoagulation. Patients being treated with anticoagulant, e.g., heparin, will be allowed to participate provided no prior evidence of an underlying abnormality in these parameters exists. Close monitoring of at least weekly evaluation will be performed until INR and PTT are stable based on a pre-dose measurement as defined by the local standard of care 9. At least one target lesion on CT scan 10. No contraindication to Iodine contrast media injection during CT. 11. For women of childbearing potential, blood or urine pregnancy test performed a maximum of 7 days before start of study treatment and negative result documented before start of study treatment 12. When applicable, i.e., women of childbearing potential having sexual activity, men having sexual activity, must agree to use an adequate contraception before entering the study, until at least 8 weeks after the last study drug administration 13. Registration in a national health care system (CMU included).
Exclusion criteria
1. Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before inclusion in the trial ; planned surgical procedure within the first month of treatment or any procedure that might change the timing of regorafenib administration during the first month of treatment 2. Patients under judicial protection (curatorship, tutorship) and/or deprived of freedom 3. Major surgical procedure, open biopsy or significant traumatic injury within 28 days before start of study medication 4. Pregnancy or breastfeeding 5. Congestive heart failure ≥ New York Heart Association (NYHA) class 2 6. Unstable angina (angina symptoms at rest), new-onset angina (begun within the last 3 months) 7. Myocardial infarction less than 6 months before the start of study medication 8. Cardiac arrhythmias requiring anti-arrhythmic therapy (beta-blockers or digoxin are permitted) 9. Uncontrolled hypertension (systolic blood pressure \>140 mmHg or diastolic pressure \>90 mmHg despite optimal medical management) 10. Arterial or venous thrombotic or embolic events such as cerebrovascular accident (including transient ischemic attacks), deep vein thrombosis or pulmonary embolism within 6 months before the start of study medication (except for adequately treated catheter-related venous thrombosis occurring more than one month before the start of study medication 11. Pleural effusion or ascites that causes respiratory compromise (≥ CTCAE grade 2, NCI-CTCAE v 4.0 dyspnea) 12. Ongoing infection \>grade 2, NCI- CTCAE v 4.0 13. Previous or concurrent cancer that is distinct in primary site or histology from colorectal cancer within 5 years prior to inclusion, except for curatively treated cervical cancer in situ, non-melanoma skin cancer and superficial bladder tumors (Ta \[non-invasive tumor\], Tis \[carcinoma in situ\] and T1 \[tumor invades lamina propria\]) 14. Known history of human immunodeficiency virus (HIV) infection 15. Active hepatitis B or C or chronic hepatitis B or C requiring treatment with antiviral therapy 16. Patients with seizure disorder requiring medication 17. History of organ allograft 18. Patients with evidence or history of any bleeding diathesis, irrespective of severity 19. Any hemorrhage or bleeding event ≥ Grade 3, NCI-CTCAE v 4.0 within 4 weeks prior to the start of study medication 20. Non-healing wound, non-healing ulcer or non-healing bone fracture 21. Dehydration grade ≥1, NCI-CTCAE v 4.0 22. Known hypersensitivity to the study drug, study drug classes or excipient in the formulation 23. Interstitial lung disease with ongoing signs or symptoms at the time of inclusion 24. Persistent proteinuria \>3.5 g/24 hour measured by urine protein-creatinine ratio from a random urine sample (≥ Grade 3, NCI-CTCAE v 4.0) 25. Patients unable to swallow oral medication 26. Any malabsorption condition 27. Unresolved toxicity higher than Grade 1, NCI-CTCAE v 4.0, attributed to any prior therapy/procedure excluding alopecia and oxaliplatin induced neuropathy 28. Systemic anticancer therapy including cytotoxic therapy, signal transduction inhibitors, immunotherapy, and hormonal therapy during this trial or within 3 weeks 29. Treatment with any other investigational medicinal product within 28 days prior to study entry 30. Chronic treatment potentially interacting with the study medication, i.e. strong CYP3A4 inducers/inhibitors, strong UGT1A9 inhibitors
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tumor response rate at 2 months according Choi Criteria | 2 months after the beginning of treatment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Tumor response rate at 1 month according to Choi criteria | At 1 month after the beginning of treatment | — |
| Best overall response rate (BOR) according to Choi criteria and to RECIST 1.1 | BOR is the best response recorded from the strat of treatment until treatment failure up to 36 months | — |
| Disease control rate (DCR) | DCR is the proportion of patient with tumor response (CR or RP) or tumor stabilization as best response from the inclusion until treatment failure, up to 36 months | — |
| Overall Survival (OS) | Assessed from the date of study drug start to the date of patient death, due to any cause or to the last date the patient was known to be alive, up to 36 months | — |
| Progression free survival (PFS) | PFS is the time from the date of study drug start to the date of progressive disease or death due to any cause, up to 36 months | — |
| Tumor response rate at 1 and 2 months according to RECIST1.1 | At 1 month and 2 months after the beginning of treatment | — |
| Evaluation of tumor heterogeneity with TexRAD software | At baseline and 1 month after inclusion | Threshold of the CTTA parameters (Skewness, Kurtosis, Entropy, Uniformity) provided by the TexRAD software at baseline and optimal variations of these parameters on the CT performed at one month (compared to baseline). |
| Serious adverse events( SAE) and adverse event (AE) | Up to 36 months | assessed by NCI-CTCAE4.0 |
| Identify early prognostic biomarkers of regorafenib | at baseline, Cycle 1 Day 15, cycle 2 Day 15 and end of treatment | — |
| Correlation between Baseline cell free DNA and survival outcomes (PFS and OS) | at baseline, Cycle 1 Day 15, cycle 2 Day 15 and end of treatment | — |
| Specificity of Choi criteria at 1 month in identifying patients with long or short OS (using median OS as cut-off value). | At 1 month after inclusion | — |
Countries
France
Outcome results
None listed