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Surgery, Radiation Therapy, and Chemotherapy With or Without Photodynamic Therapy in Treating Patients With Newly Diagnosed or Recurrent Malignant Supratentorial Gliomas

Primary Purpose

Brain and Central Nervous System Tumors

Status
Unknown status
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
carmustine
lomustine
porfimer sodium
procarbazine hydrochloride
neoadjuvant therapy
surgical procedure
radiation therapy
Sponsored by
Colorado Health Foundation
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain and Central Nervous System Tumors focused on measuring recurrent adult brain tumor, adult glioblastoma, adult anaplastic astrocytoma, adult giant cell glioblastoma, adult gliosarcoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS: Histologically confirmed newly diagnosed or recurrent supratentorial glioblastoma or malignant astrocytoma Grade 3 or 4 astrocytoma as defined by the Daumas-Duport classification Suitable for radical resection on the basis of imaging studies Patients with recurrent disease must have failed surgery and radiotherapy PATIENT CHARACTERISTICS: Age: 18 and over Performance status: Karnofsky 60-100% for newly diagnosed tumor Karnofsky 70-100% for recurrent tumor Life expectancy: At least 3 months Hematopoietic: Recurrent tumor: WBC at least 2,000/mm^3 Platelet count at least 80,000/mm^3 Hepatic: Recurrent tumor: PT/PTT no greater than 1.5 times upper limit of normal (ULN) Bilirubin and LFTs less than 2 times ULN Alkaline phosphatase no greater than 3 times ULN GGT no greater than 3 times ULN Renal: Creatinine no greater than 2 mg/dL Other: Not pregnant or nursing PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: Not specified Endocrine therapy: Not specified Radiotherapy: See Disease Characteristics No prior cranial radiotherapy for newly diagnosed tumor Surgery: See Disease Characteristics

Sites / Locations

  • Rocky Mountain Neurological Associates
  • Roswell Park Cancer Institute
  • Western Pennsylvania Hospital
  • St. Michael's Hospital-Annex

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 1, 1999
Last Updated
November 5, 2013
Sponsor
Colorado Health Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00003788
Brief Title
Surgery, Radiation Therapy, and Chemotherapy With or Without Photodynamic Therapy in Treating Patients With Newly Diagnosed or Recurrent Malignant Supratentorial Gliomas
Official Title
Prospective Clinical Trials in the Use of Photodynamic Therapy (PDT) for the Treatment of Malignant Supratentorial Brain Tumors
Study Type
Interventional

2. Study Status

Record Verification Date
September 2003
Overall Recruitment Status
Unknown status
Study Start Date
April 1998 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Colorado Health Foundation

4. Oversight

5. Study Description

Brief Summary
RATIONALE: Photodynamic therapy uses light and drugs that make cancer cells more sensitive to light to kill tumor cells. It is not yet known if the addition of photodynamic therapy to combined therapy with surgery, radiation therapy, and chemotherapy is more effective than combined therapy alone for supratentorial gliomas. PURPOSE: Randomized phase III trial to study the effectiveness of surgery, radiation therapy, and chemotherapy with or without photodynamic therapy in treating patients who have newly diagnosed or recurrent malignant supratentorial gliomas.
Detailed Description
OBJECTIVES: Determine whether the addition of photodynamic therapy to standard brain tumor care (surgical resection, postoperative radiotherapy, and chemotherapy) will result in a significant prolongation of time to recurrence and survival in newly diagnosed malignant supratentorial gliomas. Compare the effect of high or low light dose photodynamic therapy on survival of patients with recurrent malignant supratentorial gliomas. OUTLINE: This is a randomized, multicenter, two part study. Patients are stratified according to clinical center. Newly diagnosed patients (Study 1) Patients are randomized to receive either high light dose photodynamic therapy (arm I) or no photodynamic therapy (arm II): Arm I: Patients receive porfimer sodium (Photofrin) IV one day prior to surgery. Craniotomy and tumor resection are performed. Upon completion of resection, patients undergo intracavitary photoillumination with a high light dose. Arm II: Craniotomy and tumor resection are performed. Postoperatively, all patients receive external beam radiotherapy 5 days per week for 5-6 weeks. After completing radiotherapy, patients receive nitrosourea (carmustine or lomustine) chemotherapy. Recurrent tumor patients (Study 2) Patients receive Photofrin IV one day prior to surgery. Craniotomy and tumor resection are performed. Arm I: Patients receive high dose light therapy during surgery. Arm II: Patients receive low dose light therapy during surgery. Patients receive chemotherapy with procarbazine for 28 days beginning 2-4 weeks after surgery. Courses repeat every 56 days in the absence of disease progression or unacceptable toxicity. Patients are followed on both studies at 4 weeks postsurgery, then every 3 months until death or for 1 year after study closure. PROJECTED ACCRUAL: A minimum of 150 patients with newly diagnosed tumor will be accrued for this study within 4 years (Study 1). A maximum of 120 patients with recurrent disease will be accrued within 4.5 years (Study 2)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain and Central Nervous System Tumors
Keywords
recurrent adult brain tumor, adult glioblastoma, adult anaplastic astrocytoma, adult giant cell glioblastoma, adult gliosarcoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Allocation
Randomized
Enrollment
270 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
carmustine
Intervention Type
Drug
Intervention Name(s)
lomustine
Intervention Type
Drug
Intervention Name(s)
porfimer sodium
Intervention Type
Drug
Intervention Name(s)
procarbazine hydrochloride
Intervention Type
Procedure
Intervention Name(s)
neoadjuvant therapy
Intervention Type
Procedure
Intervention Name(s)
surgical procedure
Intervention Type
Radiation
Intervention Name(s)
radiation therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed newly diagnosed or recurrent supratentorial glioblastoma or malignant astrocytoma Grade 3 or 4 astrocytoma as defined by the Daumas-Duport classification Suitable for radical resection on the basis of imaging studies Patients with recurrent disease must have failed surgery and radiotherapy PATIENT CHARACTERISTICS: Age: 18 and over Performance status: Karnofsky 60-100% for newly diagnosed tumor Karnofsky 70-100% for recurrent tumor Life expectancy: At least 3 months Hematopoietic: Recurrent tumor: WBC at least 2,000/mm^3 Platelet count at least 80,000/mm^3 Hepatic: Recurrent tumor: PT/PTT no greater than 1.5 times upper limit of normal (ULN) Bilirubin and LFTs less than 2 times ULN Alkaline phosphatase no greater than 3 times ULN GGT no greater than 3 times ULN Renal: Creatinine no greater than 2 mg/dL Other: Not pregnant or nursing PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: Not specified Endocrine therapy: Not specified Radiotherapy: See Disease Characteristics No prior cranial radiotherapy for newly diagnosed tumor Surgery: See Disease Characteristics
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fred W. Hetzel, PhD, JD
Organizational Affiliation
Colorado Health Foundation
Official's Role
Study Chair
Facility Information:
Facility Name
Rocky Mountain Neurological Associates
City
Englewood
State/Province
Colorado
ZIP/Postal Code
80110
Country
United States
Facility Name
Roswell Park Cancer Institute
City
Buffalo
State/Province
New York
ZIP/Postal Code
14263-0001
Country
United States
Facility Name
Western Pennsylvania Hospital
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15224
Country
United States
Facility Name
St. Michael's Hospital-Annex
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B 1A6
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

Surgery, Radiation Therapy, and Chemotherapy With or Without Photodynamic Therapy in Treating Patients With Newly Diagnosed or Recurrent Malignant Supratentorial Gliomas

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