Toxicities Associated With Subcutaneous Administration of Ethyol (Amifostine) for the Prevention of Radiation-Induced Toxicities

Open-Label Prospective Trial Evaluating the Toxicities Associated With Subcutaneous Administration of Ethyol (Amifostine) for the Prevention of Radiation-Induced Toxicities

Dry mouth occurs very often in patients who receive radiation treatment. Amifostine is a drug approved to reduce the short and long-term occurrence of dry mouth when patients receive radiation treatment for head and neck cancer. Some studies have shown that Amifostine reduces the side effects of radiation treatment for lung cancer. The use of Amifostine is still being investigated in lung malignancies. Amifostine is found to be a protectant from radiation side effects of such normal tissues as bone marrow, skin, oral mucosal, esophagus, kidney and testes. Patients that receive radiation treatments for lung cancer may experience side effects involving the esophagus. It is hoped that patients will benefit from the protection of their esophagus and avoid delays in radiation treatment due to side effects of the radiation.

Study Overview

• Status: Completed
• Conditions: Head and Neck Cancer; Lung Cancer
• Intervention / Treatment: Drug: Ethyol (Amifostine)

Detailed Description

The protective capacity of thio-containing compounds against normal tissue damage from radiation have been recognized for over 40 years..

Although intravenous administration is the approved standard route, because of practical advantages there has been increasing interest in the subcutaneous administration of Ethyol, which presents multiple advantages when used for radioprotection.

Based on the data that has been presented, as well as the personal experience of this and other physicians/centers with subcutaneous administration of amifostine, the researchers are proposing an open-label study evaluating the rate and severity of toxicities associated with this route of administration. Toxicities to be assessed include nausea/vomiting, hypotension, and skin/fever reactions.

• Study Type: Interventional
• Enrollment: 20
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Pennsylvania
    • East Stroudsburg, Pennsylvania, United States, 18301
      • The Dale & Frances Hughes Cancer Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: N/A
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Patient is eligible to receive subcutaneous amifostine under site's current practice guidelines for radioprotection.
• Eastern Cooperative Oncology Group (ECOG) performance status < 2
• Age > 18
• Patient receiving radiation therapy or combined modality therapy to treat malignancy.
• No evidence of distant metastatic disease.
• Granulocyte count (segs & bands) > 2000/mm3 and platelet count > 100,000/mm3
• Serum creatinine <2.0mg/dL
• Total bilirubin <2.0mg%, SGOT < times the upper limit of normal.
• Patients may not be entered on investigational therapeutic trials.
• Patients or guardians must be informed of and understand the investigational nature of this study and give written informed consent prior to any study procedures.

Exclusion Criteria:

• Life expectancy of <6 months
• Patients receiving only chemotherapy to treat malignancy.
• Patients who have been treated with any investigational drugs <4 weeks prior to study entry.
• General medical or psychological conditions which would not permit the patient to complete the study or sign the informed consent.
• Pregnancy; Women of childbearing potential should use an effective (for them) method of birth control throughout their participation in this study.
• Patients who are currently receiving or have received amifostine for radioprotection within the prior 6 months are excluded.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Primary endpoint: To evaluate how amifostine is given subcutaneously at each institution
To determine treatment related toxicities and safety of subcutaneous administration of amifostine for the prevention of radiation-induced toxicities

Secondary Outcome Measures

Outcome Measure
Secondary endpoints: Evaluate efficacy of amifostine in reducing radiation induced toxicities in these patients

Collaborators and Investigators

• Sponsor: The Dale & Frances Hughes Cancer Center
• Collaborators: MedImmune LLC
• Investigators: Principal Investigator: Michael J. Greenberg, M.D., The Dale & Frances Hughes Cancer Center

Study record dates

Study Major Dates

• Study Start: June 1, 2003
• Study Completion: September 1, 2004

Study Registration Dates

• First Submitted: August 12, 2005
• First Submitted That Met QC Criteria: August 12, 2005
• First Posted (Estimate): August 15, 2005

Study Record Updates

• Last Update Posted (Estimate): September 27, 2005
• Last Update Submitted That Met QC Criteria: September 26, 2005
• Last Verified: August 1, 2005

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms; Neoplasms by Site; Head and Neck Neoplasms; Physiological Effects of Drugs; Protective Agents; Radiation-Protective Agents; Amifostine
• Other Study ID Numbers: Ethyol Study #ETH156-03D