Dual Inhibition of EGFR Signalling Using the Combination of Cetuximab and Erlotinib

NCT00784667 | Unknown Phase 2 DMC

• 1 other identifier: H2008/03282
• Study Type: interventional
• Target: 50
• Locations: 1 country
• Sites: 4

Brief Summary

This is a clinical trial investigating the effectiveness and safety of the combination of the study drugs cetuximab and erlotinib in patients with advanced (metastatic) refractory colorectal (bowel) cancer. If bowel cancer has spread to other organs (metastatic colorectal cancer), it is usually incurable and life-expectancy without treatment is less then 6 months on average. Currently, chemotherapy has been shown to have a significant impact in advanced colorectal cancer in terms of maintenance of quality of life and extension of survival. However, ultimately tumours will develop resistance to chemotherapy. Treatment options and subsequent survival at that stage are very limited. Therefore, new therapeutic approaches are urgently needed. It is common for colorectal cancer cells to contain growth receptors, like antennae, on their surface which regulate their growth. The drugs used in this trial have been shown to be effective in targeting one of these growth receptors; the epidermal growth factor receptor (EGFR). Cetuximab is an antibody (protein produced by the immune system involved in the defense of the body against infections) against EGFR. Cetuximab has been shown to improve the survival of patients with chemotherapy refractory advanced colorectal cancer. Erlotinib is a protein that prevents activation and hence signaling by EGFR. Erlotinib improves survival in patients with advanced lung cancer. Although, each of these drugs are known to be effective at inhibiting EGFR when they are given alone, at least in some cases, it is hoped that using two drugs that target the same receptor pathway in different ways will provide a more effective treatment. 50 patients from four hospitals in Australia will participate in this trial, with approximately 25 patients being enrolled at Austin Health. All participants will receive the same treatment. Neither of the study drugs are chemotherapy, and hence it is expected that the treatment would be well tolerated. The most frequent side effect associated with EGFR inhibitors is skin rash. Other possible side effects are diarrhea and low magnesium levels.

Conditions

Metastatic Colorectal Cancer

Keywords

Colorectal neoplasm; Metastasis

Outcome Measures

Primary Outcomes (1)

• To determine the response rate (RECIST criteria). Responses will be evaluated for the whole patient group and separately for k-ras wild-type and k-ras mutant tumours

  6 weekly

Secondary Outcomes (3)

• Toxicity

  Weekly

• Progression free survival

  6 weekly

• Overall survival

  Weekly

Interventions

Cetuximab DRUG

400mg/m2 intravenously week 1, then 250 mg/m2 weekly intravenously

Also known as: Erbitux

Erlotinib DRUG

100mg orally daily continuously

Also known as: Tarceva

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age\>18 years
• Histological diagnosis of colorectal cancer
• Metastatic disease not amenable to resection
• Measurable disease as assessed by CT scan using RECIST criteria
• Received and failed fluoropyrimidine therapy, where failure is defined as radiological progression after therapy for metastatic disease, prior adjuvant therapy, or toxicity limiting further therapy
• Received and failed oxaliplatin therapy, where failure is defined as radiological progression after therapy for metastatic disease, prior adjuvant therapy ,or toxicity (including neuro-toxicity) limiting further therapy
• Received and failed irinotecan therapy, where failure is defined as radiological progression after therapy for metastatic disease or toxicity limiting further therapy
• ECOG PS 0-1
• Adequate bone marrow function with platelets \> 100 X 109/l; neutrophils \> 1.5 X 109/l
• Adequate renal function, with calculated creatinine clearance \>40 ml/min (Cockcroft and Gault).
• Adequate hepatic function with serum total bilirubin \< 1.25 X upper limit of normal range and ALT or AST\<2.5xULN (\<5xULN if liver metastases present)
• Life expectancy of at least 12 weeks
• No other concurrent uncontrolled medical conditions
• No other malignant disease apart from non-melanotic skin cancer or carcinoma in situ of the uterine cervix or any other cancer treated with curative intent \>2 years previously without evidence of relapse
• Women and partners of women of childbearing potential must agree to use adequate contraception

You may not qualify if:

• Medical or psychiatric conditions that compromise the patient's ability to give informed consent or to complete the protocol
• Prior treatment with drugs targeting EGFR such as cetuximab, panitumumab or erlotinib
• Participation in any investigational drug study within the previous 4 weeks
• Patients with uncontrolled clinically significant cardiac disease, arrhythmias or angina pectoris
• Untreated CNS metastases
• Pregnancy or lactation
• k-ras mutant tumours now excluded

Sponsors & Collaborators

• Austin Health: lead
• Ballarat Health Services: collaborator
• Queen Elizabeth Hospital, Adelaide: collaborator
• Royal North Shore Hospital: collaborator

Study Sites (4)

Royal North Shore Hospital

Sydney, New South Wales, Australia

Location

Queen Elizabeth Hospital

Adelaide, South Australia, Australia

Location

Ballarat Base Hospital

Ballarat, Victoria, Australia

Location

Austin Health

Melbourne, Victoria, 3084, Australia

Location

MeSH Terms

Conditions

Colorectal Neoplasms; Neoplasm Metastasis

Interventions

Cetuximab; Erlotinib Hydrochloride

Condition Hierarchy (Ancestors)

Intestinal Neoplasms; Gastrointestinal Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Neoplasms; Digestive System Diseases; Gastrointestinal Diseases; Colonic Diseases; Intestinal Diseases; Rectal Diseases; Neoplastic Processes; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal; Antibodies; Immunoglobulins; Immunoproteins; Blood Proteins; Proteins; Amino Acids, Peptides, and Proteins; Serum Globulins; Globulins; Quinazolines; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER GOV

Study Record Dates

• First Submitted: November 3, 2008
• First Posted: November 4, 2008
• Study Start: October 1, 2008
• Primary Completion: January 1, 2010
• Study Completion: February 1, 2011
• Last Updated: November 30, 2010

Record last verified: 2008-11

Locations

AU (4)