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Ph. I Temozolomide + O6-BG + Irinotecan in Treatment of Pts w Recurrent / Progressive Cerebral Anaplastic Gliomas

Primary Purpose

Glioblastoma, Gliosarcoma

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Temodar, O6-BG, and Irinotecan
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glioblastoma focused on measuring Temodar, Temozolomide, O6-Benzylguanine, O6-BG, NSC 637037, Irinotecan, CPT-11, Recurrent cerebral anaplastic glioma, Progressive cerebral anaplastic glioma, Malignant glioma

Eligibility Criteria

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

Inclusion Criteria:

  • Pts have histologically confirmed diagnosis of recurrent primary malignant glioma
  • Age >18yrs
  • Evidence of measurable recurrent/residual primary CNS neoplasm on contrast-enhanced MRI, unless medically contraindicated
  • An interval of >2 wks between prior surgical resection/6 wks between prior XRT/chemo, & enrollment on protocol, unless there is unequivocal evidence of tumor progression after surgery, XRT/chemo
  • KPS>60 percent
  • Adequate hematologic, renal & liver function as demonstrated by lab values performed within 14 days, inclusive, prior to administration of chemo:
  • ANC >1500/mm3
  • Platelet count > 00,000/mm3
  • Hemoglobin > 10gm/dL
  • BUN & serum creatinine <1.5 x ULN
  • Total serum bilirubin <1.5 x ULN
  • SGOT & SGPT < 2.5 x ULN
  • Alkaline phosphatase of< 2 x ULN
  • Pts must have recovered from any effects of major surgery.=
  • Pts must have life expectancy of >12wks
  • Pts/legal guardian must give written, informed consent

Exclusion Criteria:

  • Pts requiring immediate XRT
  • Pts have not recovered from surgery
  • Pts are not neurologically stable for 2wks prior to study entry
  • Pts are poor medical risks because of non-malignant systemic disease as well as those w acute infection treated w intravenous antibiotics
  • Frequent vomiting/medical condition that could interfere w oral medication intake
  • Previous active malignancy treated in past year except for localized in-situ carcinomas & basal/squamous cell carcinoma of skin
  • Known HIV positivity/AIDS-related illness
  • Pregnant/nursing women
  • Women of childbearing potential who are not using effective method of contraception. Women of childbearing potential must have negative serum pregnancy test 24 hrs prior to administration of study drug & be practicing medically approved contraceptive precautions
  • Men who are not advised to use effective method of contraception
  • Prior failure of CPT-11
  • Pts taking immuno-suppressive agents other than prescribed corticosteroids

Sites / Locations

  • Duke University Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

1

2

Arm Description

Pts receiving Dilantin, Tegretol or Phenobarbital

Pts on anti-convulsants other than Dilantin, Tegretol / Phenobarbital / pts not on any anti-convulsants

Outcomes

Primary Outcome Measures

Incidence of toxicities

Secondary Outcome Measures

Response rate & progression-free survival

Full Information

First Posted
January 29, 2008
Last Updated
June 18, 2013
Sponsor
Duke University
Collaborators
Keryx / AOI Pharmaceuticals, Inc., Pharmacia
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1. Study Identification

Unique Protocol Identification Number
NCT00612638
Brief Title
Ph. I Temozolomide + O6-BG + Irinotecan in Treatment of Pts w Recurrent / Progressive Cerebral Anaplastic Gliomas
Official Title
Phase I Trail of Temodar Plus O6-Benzylguanine (O6-BG) (NSC 637037) Plus Irinotecan (CPT-11) (NSC 616348) in the Treatment of Patients With Recurrent / Progressive Cerebral Anaplastic Gliomas
Study Type
Interventional

2. Study Status

Record Verification Date
January 2009
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
January 2007 (Actual)
Study Completion Date
July 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Duke University
Collaborators
Keryx / AOI Pharmaceuticals, Inc., Pharmacia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Objectives: To determine maximum tolerated dose of CPT-11 when administered following Temodar plus O6-benzylguanine To characterize any toxicity associated w combo of CPT-11 + Temodar plus O6-BG To observe pts for clinical antitumor response when treated w combo of CPT-11 + Temodar + O6-BG
Detailed Description
Objectives of study: to determine maximum tolerated dose of CPT-11 when administered following Temodar + O6-benzylguanine (O6-BG); to characterize any toxicity associated w combo of CPT-11 + Temodar + O6-BG; to observe pts for clinical antitumor response when treated w combo of CPT-11 + Temodar plus O6-BG. Pts have histologically confirmed diagnosis of recurrent primary malignant glioma. 2 separate strata accrued independently of each other: Stratum 1-pts receiving Dilantin, Tegretol/phenobarbital. Stratum 2-pts on anti-convulsants other than Dilantin, Tegretol/phenobarbital/pts not on any anti-convulsants. Each strata will be treated & escalated independent of each other. Pre-chemo, O6-BG administered intravenously at 120 mg/m2, over 1hr, prior to administration of Temodar on day 1 of 21-day cycle. Post-chemo, O6-BG administered intravenously at 30 mg/m2/day, over 48hrs, immediately after completion of the CPT-11 infusion on day 1 of 21-day cycle. Temodar administered orally at 355 mg/m2, in fasting state, within 60 minutes of the end of 1hr O6-BG infusion. Treatment cycles may be repeated every 3 weeks following dose of Temozolomide from previous cycle. CPT-11 will be administered intravenously in fasting state over 90min. CPT-11 infusion will begin 1hr after Temozolomide administration. Initial doses 60 mg/m2 for stratum 1 & 40 mg/m2 for stratum 2. Treatment cycles may be repeated every 3 wks following dose of CPT-11 from previous cycle. Major toxicities associated w CPT- 11 are myelosuppression & diarrhea. Temozolomide has been well tolerated by both adults & children w most common toxicity being mild myelosuppression. Other, less likely, potential toxicities include nausea & vomiting, constipation, headache, alopecia, rash, burning sensation of skin, esophagitis, pain, diarrhea, lethargy, & hepatotoxicity. Hypersensitivity reactions have not yet been noted w Temozolomide. As is case w many anti-cancer drugs, Temozolomide may be carcinogenic. O6-BG toxicities include transient lymphopenia has been seen w O6-BG as single agent. O6-BG in combo w other agents could cause exacerbation of any adverse event currently known to be caused by other agent,/ combo may result in events never previously associated w either agent. Animal studies indicated that agitation, lethargy, convulsions, nausea, vomiting, rapid heart rate, elevated liver functions, leukopenia, lymphopenia could be seen.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma, Gliosarcoma
Keywords
Temodar, Temozolomide, O6-Benzylguanine, O6-BG, NSC 637037, Irinotecan, CPT-11, Recurrent cerebral anaplastic glioma, Progressive cerebral anaplastic glioma, Malignant glioma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
96 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Pts receiving Dilantin, Tegretol or Phenobarbital
Arm Title
2
Arm Type
Experimental
Arm Description
Pts on anti-convulsants other than Dilantin, Tegretol / Phenobarbital / pts not on any anti-convulsants
Intervention Type
Drug
Intervention Name(s)
Temodar, O6-BG, and Irinotecan
Other Intervention Name(s)
Temodar-Temozolomide, O6-Benzylguanine-O6-BG, Irinotecan-Camptosar-CPT 11
Intervention Description
2 separate strata accrued independently: Stratum 1-pts receiving Dilantin, Tegretol or phenobarbital. Stratum 2-pts on anti-convulsants other than Dilantin, Tegretol/phenobarbital/pts not on any anti-convulsants. O6-BG administered intravenously 120mg/m2, over 1hr, prior to administration of Temozolomide on day 1 of 21day cycle. O6-BG administered intravenously 30mg/m2/day, over 48hrs, immediately after completion of CPT-11 infusion on day 1 of 21-day cycle. Temozolomide administered orally 355mg/m2 within 60 mins of end of 1hr O6-BG infusion. Treatment cycles may be repeated every 3wks following dose of Temozolomide from previous cycle. CPT-11 administered intravenously in fasting state over 90mins. CPT-11 infusion will begin 1hr after Temozolomide administration. Initial doses 60mg/m2 for stratum 1 & 40mg/m2 for stratum2. Treatment cycles repeated every 3 wks following dose of CPT-11 from previous cycle.
Primary Outcome Measure Information:
Title
Incidence of toxicities
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Response rate & progression-free survival
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pts have histologically confirmed diagnosis of recurrent primary malignant glioma Age >18yrs Evidence of measurable recurrent/residual primary CNS neoplasm on contrast-enhanced MRI, unless medically contraindicated An interval of >2 wks between prior surgical resection/6 wks between prior XRT/chemo, & enrollment on protocol, unless there is unequivocal evidence of tumor progression after surgery, XRT/chemo KPS>60 percent Adequate hematologic, renal & liver function as demonstrated by lab values performed within 14 days, inclusive, prior to administration of chemo: ANC >1500/mm3 Platelet count > 00,000/mm3 Hemoglobin > 10gm/dL BUN & serum creatinine <1.5 x ULN Total serum bilirubin <1.5 x ULN SGOT & SGPT < 2.5 x ULN Alkaline phosphatase of< 2 x ULN Pts must have recovered from any effects of major surgery.= Pts must have life expectancy of >12wks Pts/legal guardian must give written, informed consent Exclusion Criteria: Pts requiring immediate XRT Pts have not recovered from surgery Pts are not neurologically stable for 2wks prior to study entry Pts are poor medical risks because of non-malignant systemic disease as well as those w acute infection treated w intravenous antibiotics Frequent vomiting/medical condition that could interfere w oral medication intake Previous active malignancy treated in past year except for localized in-situ carcinomas & basal/squamous cell carcinoma of skin Known HIV positivity/AIDS-related illness Pregnant/nursing women Women of childbearing potential who are not using effective method of contraception. Women of childbearing potential must have negative serum pregnancy test 24 hrs prior to administration of study drug & be practicing medically approved contraceptive precautions Men who are not advised to use effective method of contraception Prior failure of CPT-11 Pts taking immuno-suppressive agents other than prescribed corticosteroids
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David A. Reardon, MD
Organizational Affiliation
Duke Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke University Health System
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.cancer.duke.edu/btc/
Description
The Preston Robert Tisch Brain Tumor Center at DUKE

Learn more about this trial

Ph. I Temozolomide + O6-BG + Irinotecan in Treatment of Pts w Recurrent / Progressive Cerebral Anaplastic Gliomas

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