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Sargramostim to Prevent Mucositis in Patients Receiving Radiation Therapy for Laryngeal Cancer - Article


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Clinical Trial: Sargramostim to Prevent Mucositis in Patients Receiving Radiation Therapy for Laryngeal Cancer

This study has been completed.

Sponsored by: Royal Marsden NHS Trust
Information provided by: National Cancer Institute (NCI)

Purpose

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs such as sargramostim may protect normal cells from the side effects of radiation therapy. PURPOSE: Randomized phase II trial to determine the effectiveness of sargramostim in preventing mucositis in patients who are receiving radiation therapy for laryngeal cancer.

Condition Treatment or Intervention Phase
Laryngeal Cancer
 Procedure: supportive care
 Procedure: radiation therapy
 Procedure: radioprotection
 Procedure: complications of therapy assessment/management
 Behavior: supportive care/therapy
 Procedure: quality-of-life assessment
 Drug: sargramostim
Phase II

MedlinePlus related topics:  Head and Neck Cancer

Study Type: Interventional
Study Design: Educational/Counseling/Training

Official Title: Phase II Randomized Study of Sargramostim (GM-CSF) To Reduce Severity of Mucositis Resulting From Accelerated Radiotherapy in Patients With Laryngeal Cancer

Further Study Details: 

Study start: October 1997

OBJECTIVES: I. Determine the efficacy of sargramostim (GM-CSF) in reducing the duration and severity of mucositis resulting from accelerated radiotherapy in patients with laryngeal carcinoma. II. Determine the effect of GM-CSF on quality of life aspects of these patients as assessed by nutritional status, analgesic use, and days in the hospital.

PROTOCOL OUTLINE: This is a randomized study. Patients receive radiotherapy in 16 fractions over 21 days. Patients are randomly allocated to one of two treatment arms before scheduled radiotherapy begins. Arm I: Patients receive sargramostim (GM-CSF) SC daily for 14 days beginning on day 14 of the course of radiotherapy. Arm II: Patients do not receive GM-CSF. Patients are followed weekly until mucositis is healed, as well as at weeks 2 and 6 following the end of radiotherapy.

PROJECTED ACCRUAL: A total of 34 patients (17 per arm) will be accrued for this study.

Eligibility

Ages Eligible for Study:  20 Years   -   80 Years

Criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

--Prior/Concurrent Therapy--

  • Biologic therapy: No concurrent immunotherapy
  • Chemotherapy: No concurrent chemotherapy
  • Endocrine therapy: No prior or concurrent corticosteroids No concurrent hormonal therapy
  • Radiotherapy: See Disease Characteristics
  • Surgery: No major organ allografts
  • Other: No other concurrent investigational drugs

--Patient Characteristics--

  • Age: 20 to 80
  • Performance status: WHO 0-1
  • Life expectancy: Not specified
  • Hematopoietic: Not specified
  • Hepatic: Hepatic function normal
  • Renal: Renal function normal
  • Other: Not pregnant or nursing No serious active infection requiring antibiotic therapy No autoimmune disease No known seizures No psychosocial factors that would preclude study compliance No allergies to sargramostim (GM-CSF) Willingness to cooperate for regular mirror examination of the larynx

Location Information


United Kingdom, England
      Royal Marsden NHS Trust, London,  England,  SW3 6JJ,  United Kingdom

Study chairs or principal investigators

J.M. Henk,  Study Chair,  Royal Marsden NHS Trust   

More Information

Clinical trial summary from the National Cancer Institute's PDQ® database

Study ID Numbers:  CDR0000067503; RMNHS-GMCSF; EU-99041
Record last reviewed:  August 2003
Last Updated:  October 13, 2004
Record first received:  January 28, 2000
ClinicalTrials.gov Identifier:  NCT00004256
Health Authority: Unspecified
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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