Glutamine in Preventing Oral Mucositis in Patients Receiving Chemotherapy for Sarcoma

Sarcoma Clinical Trial

Official title:

Prevention of Mucositis in Children With AES-14 (IND#36978), a Glutamine Based Oral Care Regimen, for Patients Diagnosed With Solid Tumors: A Randomized Placebo-Controlled Clinical Study

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00334984
• Other study ID #: ANUR0532
• Secondary ID: COG-ANUR0532CDR0
• Status: Withdrawn
• Phase: N/A
• First received: June 7, 2006
• Last updated: July 9, 2013
• Start date: January 2007

Study information

• Verified date: July 2013
• Source: Children's Oncology Group
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Glutamine may help prevent mucositis, or mouth sores, in patients receiving chemotherapy for sarcoma. It is not yet known whether glutamine is more effective than a placebo in preventing mucositis in patients receiving chemotherapy for sarcoma.

PURPOSE: This randomized clinical trial is studying glutamine to see how well it works compared to a placebo in preventing oral mucositis in patients receiving chemotherapy for sarcoma.

Description:

OBJECTIVES:

Primary

• Compare the efficacy of a new preparation of glutamine (AES-14) vs placebo in reducing the incidence of grade 3 or 4 chemotherapy-induced oral mucositis during the first course of chemotherapy in patients with sarcomas.

Secondary

• Compare the rates of mucositis-related chemotherapy dose reductions for the subsequent course of anthracycline-based chemotherapy in patients treated with AES-14 vs placebo.

• Compare the rates of mucositis-related delays of chemotherapy administration for the next chemotherapy course in patients treated with AES-14 vs placebo.

• Compare the rates of systemic and oral infections during the first course of chemotherapy in patients treated with AES-14 vs placebo.

• Compare the number of days of narcotic use for mucositis-related pain during the first course of chemotherapy in patients treated with AES-14 vs placebo.

• Determine the inter-rater reliability between caregivers and nurses in the use of the modified Walsh scale.

OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to age (5-10 years vs 11-18 years vs 19-30 years) and diagnosis (Ewing's sarcoma vs osteogenic sarcoma vs rhabdomyosarcoma vs other sarcomas). Patients are randomized to 1 of 2 treatment arms.

• Arm I (glutamine [AES-14]): Patients rinse with oral AES-14 for at least 30 seconds and then swallow (swish and swallow) three times daily beginning on the day of or within 1 day before starting their first course of chemotherapy. Patients also undergo a standard oral care regimen comprising brushing their teeth at least twice daily, 30 minutes or more after taking AES-14, and rinsing with water at least twice daily. Treatment continues until blood counts recover and patient's total modified Walsh score ≤ 2 (mucositis score).

• Arm II (placebo): Patients swish and swallow oral placebo and undergo a standard oral care regimen as in arm I.

Caregivers assess the patient's mouth daily while the patient is receiving the study drug. Caregivers keep a daily diary rating the patient's oral mucosal areas and degree of pain, describing the patient's oral intake, and documenting that the study drug was used and standardized oral care was performed.

PROJECTED ACCRUAL: A total of 180 patients will be accrued for this study.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 5 Years to 30 Years

Eligibility

DISEASE CHARACTERISTICS:

• Diagnosed with any of the following:

• Ewing's sarcoma

• Osteogenic sarcoma

• Rhabdomyosarcoma

• Other sarcomas (i.e., fibrosarcoma or synovial sarcoma)

• Scheduled to receive first course of chemotherapy that includes = 75 mg/m² of anthracyclines

• Total modified Walsh score = 2 (mucositis score)

PATIENT CHARACTERISTICS:

• Must have a caregiver (parent, other relative, or friend) available to perform daily mucositis assessments

• Bilirubin = 1.5 times upper limit of normal (ULN)

• ALT = 5 times ULN

• Albumin = 2 g/dL

• No history of hypersensitivity to any known component of AES-14

PRIOR CONCURRENT THERAPY:

• No prior glutamine (AES-14)

• No prior or concurrent head and/or neck radiation therapy

• No concurrent supplementation with another glutamine product

• No other concurrent agents for mucositis prophylaxis

Study Design

Allocation: Randomized, Masking: Double-Blind, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Childhood Malignant Fibrous Histiocytoma of Bone
• Histiocytoma
• Histiocytoma, Malignant Fibrous
• Sarcoma

Intervention

Drug:
• glutamine

Procedure:
• chemoprotection

• management of therapy complications

• therapeutic nutritional supplementation

Locations

Country	Name	City	State
n/a

Sponsors (2)

Lead Sponsor	Collaborator
Children's Oncology Group	National Cancer Institute (NCI)