Actively Recruiting

Phase 2
Age: 18Years - 75Years
All Genders
NCT03874026

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

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Istituto Nazionale dei Tumori,

Naples, Italy

Actively Recruiting

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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

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