Selenomethionine in Reducing Mucositis in Patients With Locally Advanced Head and Neck Cancer Receiving Cisplatin and Radiation Therapy



Status:Archived
Conditions:Cancer, Cancer, Other Indications
Therapuetic Areas:Oncology, Other
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:June 2009

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Randomized, Double-Blind, Placebo-Controlled, Multi-Center Phase II Trial of Selenomethionine as a Modulator of Efficacy and Toxicity of Chemoradiation in Locally-Advanced Squamous Cell Carcinoma of the Head and Neck


RATIONALE: Selenomethionine may prevent or reduce mucositis, or mouth sores, in patients
receiving chemotherapy and radiation therapy. It is not yet known whether selenomethionine
is more effective than a placebo in reducing mucositis.

PURPOSE: This randomized phase II trial is studying selenomethionine to see how well it
works in reducing mucositis in patients with locally advanced head and neck cancer receiving
cisplatin and radiation therapy.


OBJECTIVES:

Primary

- Assess whether selenomethionine (SLM) reduces the incidence of grade 3 or 4 mucositis
in patients with locally advanced squamous cell carcinoma of the head and neck treated
with concurrent cisplatin and radiotherapy over 7 weeks.

Secondary

- Assess the impact of SLM on tumor complete response rate, relapse-free survival,
overall survival, and quality of life of these patients.

- Assess whether SLM reduces the incidence and severity of treatment-related toxicities,
including xerostomia, renal impairment, and myelosuppression in these patients.

- Assess whether SLM improves chemoradiotherapy dose delivery in these patients.

- Determine the safety of SLM in these patients.

OUTLINE: This is a multicenter study. Patients are randomized to 1 of 2 treatment arms.

- Arm I: Patients receive oral placebo twice daily in week 1 and then once daily in weeks
2-11. Patients also receive cisplatin IV over 3 hours once in weeks 2, 5, and 8 and
undergo radiotherapy 5 days a week in weeks 2-8.

- Arm II: Patients receive oral selenomethionine twice daily in week 1 and then once
daily in weeks 2-11. Patients also receive cisplatin and radiotherapy as in arm I.

Patients complete quality-of-life questionnaires at baseline and then periodically
thereafter.

After completion of study therapy, patients are followed up periodically.


We found this trial at
1
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Elm St,
Buffalo, New York 14263
(716) 845-2300
Roswell Park Cancer Center Institute Welcome to Roswell Park Cancer Institute (RPCI), America's first cancer...
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