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Study Summary
No. ECOGE3F05:.......Brain; CNS......John DeGroot......Neuro Oncology
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Study Summary Title
Study Summary
Number:
ECOGE3F05
Study Title:Phase III Study of Radiation Therapy with or without Temozolomide for Symptomatic or Progressive Low-Grade Gliomas
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Physician New Patient Referral
Name:John DeGrootPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:Neuro OncologyReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-792-2883
Contact us about clinical trials
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General Information
Disease Group:Brain
CNS
Supported By:Eastern Cooperative Oncology Group/NCI Cancer Trials Support Unit (CTSU)
Phase of Study:Phase IIIReturn
Visit:
Treatment
Agents:
Radiation
Temozolomide
Home Care:
Treatment Loc:Both at MDACC & and Other Sites
Estimated
Length of Stay
in Houston:
Description/
Intervention:
The goal of this clinical research study is to learn if adding temozolomide to
radiation therapy can help to control low-grade glioma better than treatment
with standard radiation therapy alone. The safety of this treatment
combination will also be studied.

The radiation therapy in this study is designed to stop the reproduction and
repair of cancer cells by damaging the DNA (the genetic material of cells).
The damaged DNA may cause tumor cell death. Radiation therapy is the commonly
used standard of care for low-grade glioma.

Temozolomide is also designed to damage the DNA of cancer cells. The damaged
DNA may cause tumor cell death.
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Study Objectives / Outcomes
1. Primary Objectives
    • To determine whether the addition of temozolomide(TMZ) to fractionated radiotherapy(RT) improves the progression-free survival (PFS) of patients requiring treatment for low grade gliomas(LGG).
    • To determine whether the addition of temozolomide to fractionated radiotherapy improves the median overall survival (OS) of patients with low-grade gliomas requiring treatment.

2. Secondary Objectives
    • To determine whether combination therapy with temozolomide and radiotherapy improves or maintains cognition and quality of life (QOL) compared to radiotherapy alone.
    • To compare the severe or worse toxicities (>/= grade 3) of patients receiving radiation therapy alone or radiation therapy plus temozolomide chemotherapy.
    • To assess the impact of the presence or absence of 1p and 19q deletion on PFS and OS, and to determine the impact of 1p and 19q status on PFS and OS in patients receiving chemotherapy.
    • To create a tumor and tissue bank, including plasma and germ line DNA, within the Eastern Cooperative Oncology Group(ECOG) Pathology Coordinating Office (PCO).
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Study Status Information
Study Activation / Registration Date:
IRB Review and Approval Date:11/28/2011
Study Type:Phase Iii
Recruitment Status:Open
Projected Accrual:540
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Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) Age >/= 18 years.

2) Tumors must be supratentorially located.

3) Pathological diagnosis of astrocytoma grade 2, oligodendroglioma grade 2, or oligoastrocytoma grade 2 (mixed glioma containing astrocytoma and oligodendroglioma). Pilocytic astrocytoma, ganglioglioma, pleomorphic xanthastrocytoma, or dysembryoplastic neuroepithelial tumors are not eligible. NOTE: If the pathology from multiple procedures supports the diagnosis of a brain tumor, the qualifying pathology of grade 2 astrocytoma, oligodendroglioma, or oligoastrocytoma must be the most recent pathological diagnosis, and a pathological diagnosis of a grade 3 or grade 4 glioma must not have been made at any time.

4) Patients must have paraffin-embedded tumor specimen available for submission for pathological review and determination of 1p/19q deletion status. NOTE: It is recommended that patients not be Pre-registered until the required tumor specimens are on hand and ready for submission. If submission of tissue will be submitted more than 5 working days after pre-registration, immediately notify the Mayo Clinic Cytogenetics Laboratory.

5) The patient must currently have at least one of the following: 1) Uncontrolled symptoms, defined as any of the below: Headaches associated with mass effect; Uncontrolled seizures despite 2 different antiepileptic drug regimens (i.e., 2 antiepileptic drugs tested either sequentially or in combination); Focal neurological symptoms; Cognitive symptoms or deficits. OR 2) Tumor progression by serial MRIs, defined as any of the below: New or progressive enhancement; New or progressive T2 or FLAIR signal abnormality. OR 3) Age >/= 40 years. NOTE: Patients aged less than 40 whose only symptom of low-grade glioma is seizures that are well-controlled on antiepileptic drugs, and who have no evidence of radiographic progression, are ineligible.

6) Patient must be able to undergo MRI with and without contrast. Patients who are unable to undergo MRI are ineligible.

7) MRI and chest x-ray within 6 weeks prior to pre-registration. A postoperative MRI is required for all patients who underwent open biopsy, or resection, but is not mandatory following stereotactic biopsy.

8) Karnofsky performance status (KPS) >/= 60%.

9) Patients who have undergone gross total resection and have no detectable residual disease are eligible.

10) 1p/19q deletion status assessment as determined by the Mayo Cytogenetics Laboratory has been received.

11) Must be able to start treatment with RT within 2 weeks or 10 working days at a qualified center (to be defined by the Radiation Oncology chair) and to start TMZ prescribed at a participating center within 2 weeks or 10 working days of randomization.

12) CBC requirements within 14 days prior to randomization: White blood count (WBC) >/= 3,000 /mm3; Absolute neutrophil count (ANC) > 1,500 /mm3; Platelets >/= 100,000 /mm3; Hematocrit > 30%

13) Chemistry requirements within 14 days prior to randomization: Bilirubin </= 2 x upper limit of normal (ULN); AST </= 3 x ULN (SGOT); Creatinine </= 2.0 x ULN; ALT < 3 x ULN (SGPT)

14) Women must not be pregnant or breast-feeding due to known and potential teratogenic effects of radiotherapy and temozolomide and the uncertain safety of temozolomide in lactation. All females of childbearing potential must have a blood test or urine study within 2 weeks prior to randomization to rule out pregnancy.

15) Women of childbearing potential and sexually active males are strongly advised to use an accepted and effective method of contraception.

16) Patient must be at least two weeks post any brain surgery (whether stereotactic biopsy, open biopsy or resection) at the time of randomization.

Exclusion Criteria:1) No previous radiation, cytotoxic chemotherapy, radio surgery, or investigational treatment directed at the brain tumor at any time. No limit on number of previous surgical procedures of this tumor.

2) No previous radiation treatment to the head (unless the ports for that radiation entirely excluded the brain) for any condition.

3) No other diagnosed malignancy (except non-melanoma skin cancer or cervical carcinoma in situ, which are allowable), unless the patient has been disease-free for at least 5 years.

4) No medical disorder that increases risks of radiation or TMZ chemotherapy. No uncontrolled infection. No known positivity for human immunodeficiency virus (HIV), as temozolomide is known to cause immunosuppression and increase risk of opportunistic infection. No other disorder limiting expected survival to < 5 years.

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Links
Registration Number: NCT00978458
Study Information on Clinical Trials Registry (clinicaltrials.gov)

Other Links:
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Results


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