Actively Recruiting
Study of Folfiri/Cetuximab in FcGammaRIIIa V/V Stage IV Colorectal Cancer Patients
Led by National Cancer Institute, Naples · Updated on 2024-11-07
34
Participants Needed
1
Research Sites
312 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Patients' selection thorough the identification of predictive factors still represent a challenge in metastatic colorectal cancer (mCRC). Cetuximab (Erbitux®), a chimeric monoclonal antibody binding to the Epidermal Growth Factor Receptor (EGFR), belongs to the Immunoglobulins (Ig) grade 1 subclass able to elicit both in vitro and in vivo the Antibody-Dependent Cell-mediated Cytotoxicity (ADCC). ADCC is the cytotoxic killing of antibody-coated target cells by immunologic effectors. The effector cells express a receptor for the Fc portion of these antibodies (FcγR); genetic polymorphisms of FcγR modify the binding affinity with the Fc of IgG1 (Immunoglobulins Gamma subclass 1). Interestingly, the high-affinity FcγRIIIa (FcγR type IIIa) V/V is associated with increased ADCC in vitro and in vivo. Thus, ADCC could partially account for cetuximab activity. CIFRA is a single arm, open-label, phase II study assessing the activity of cetuximab in combination with irinotecan and fluorouracile in FcγRIIIa V/V patients with KRAS (Kirsten RAt Sarcoma), NRAS (Neuroblastoma Rat Sarcoma), BRAF (B-Rapidly Accelerated Fibrosarcoma) wild type mCRC. The study is designed with a two-stage Simon model based on a hypothetical higher response rate (+10%) of FcγRIIIa V/V patients as compared to previous trials (about 60%) assuming ADCC as one of the mechanisms of cetuximab action. The test power is 95%, the alpha value of the I-type error is 5%. With these assumptions the sample for passing the first stage is 14 patients with \>6 responses and the final sample is 34 patients with \>18 responses to draw positive conclusions. Secondary objectives include toxicity, responses' duration, progression-free and overall survival. Furthermore, an associated translational study will assess the patients' cetuximab-mediated ADCC and characterize the tumor microenvironment. The CIFRA study will determine whether ADCC contributes to cetuximab activity in mCRC patients selected on an innovative immunological screening. Data from the translational study will support results'interpretation as well as provide new insights in host-tumor interactions and cetuximab activity.
CONDITIONS
Official Title
Study of Folfiri/Cetuximab in FcGammaRIIIa V/V Stage IV Colorectal Cancer Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Cytological or histological diagnosis of colorectal adenocarcinoma
- KRAS, NRAS, BRAF wild-type
- Fcb3RIIIa V/V genotype
- Stage IV colorectal cancer
- Age less than 75 years
- At least one measurable lesion
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0 or 1
- Life expectancy greater than 3 months
- Negative pregnancy test for all potentially childbearing women
- Written informed consent
You will not qualify if you...
- Previous systemic anti-tumor treatment (except capecitabine or fluorouracil and radiotherapy in neoadjuvant rectal tumor setting, completed at least 6 months before)
- Presence of untreated primary stenosing colorectal tumor
- Neutrophils less than 2000/mm, platelets less than 100,000/mm, or hemoglobin less than 9 g/dl
- Serum creatinine level more than 1.5 times the upper normal limit
- Liver enzymes (GOT and/or GPT) more than 5 times upper normal limit or bilirubin more than 3 times upper normal limit
- Previous malignant neoplasms (except basal or spinocellular cutaneous carcinoma or in situ carcinoma of the uterine cervix)
- Active or uncontrolled infections
- Other uncontrolled diseases or conditions contraindicating study drugs as judged by clinician
- Presence of brain metastases
- Refusal or inability to provide informed consent
- Inability to guarantee follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Istituto Nazionale dei Tumori,
Naples, Italy
Actively Recruiting
Research Team
A
Alessandro Ottaiano, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here