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Temozolomide in Relapsed or Advanced Anaplastic Oligodendroglioma and Oligoastrocytoma: Single-arm, Phase II Trial

Primary Purpose

Anaplastic Oligodendroglioma, Anaplastic Oligoastrocytoma

Status
Completed
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Temozolomide
Sponsored by
Seoul National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anaplastic Oligodendroglioma focused on measuring Temozolomide

Eligibility Criteria

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

Inclusion Criteria:

  • Histologically proven anaplastic oligodendroglioma or oligoastrocytoma
  • Progressed or relapsed after surgery or radiation therapy
  • Female or male aged 20 years or over
  • At least 1 measurable mass lesion
  • ECOG performance status 0-3
  • Adequate organ function
  • absolute neutrophil count > 1,500/μL
  • platelet count > 75,000/μL
  • hemoglobin greater than 9 g/dL or 900g/L
  • serum creatinine less than 1.5 times the upper limit of laboratory normal
  • total serum bilirubin less than 1.5 times the upper limit of laboratory normal
  • AST or ALT less than three times the upper limit of laboratory normal

Exclusion Criteria:

  • Prior course of temozolomide
  • Combined glioblastoma
  • Pregnant woman

Sites / Locations

  • Seoul National University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Temozolomide

Arm Description

Temozolomide 200 mg/m2/d in a fasting state for 5 consecutive days

Outcomes

Primary Outcome Measures

Progression free survival (PFS)
PFS will be examined with Kaplan-Meier method.

Secondary Outcome Measures

Objective response rate (ORR)
ORR will be evaluated through the frequency analysis with 95% confidence interval.
Overall survival (OS)
OS will be examined with Kaplan-Meier method.
progression-free survival (PFS)
PFS will be examined with Kaplan-Meier method.
Number of Participants with Adverse Events
Regarding safety endpoints, all adverse events will be individually graded based on the CTCAE version 4.03. The number of participants with adverse events will be summarized using descriptive statistics.

Full Information

First Posted
April 29, 2013
Last Updated
April 22, 2016
Sponsor
Seoul National University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01847235
Brief Title
Temozolomide in Relapsed or Advanced Anaplastic Oligodendroglioma and Oligoastrocytoma: Single-arm, Phase II Trial
Official Title
The Efficacy and Safety of Temozolomide in Patients With Relapsed or Advanced Anaplastic Oligodendroglioma and Oligoastrocytoma: a Multicenter, Single-arm, Phase II Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
May 2013 (undefined)
Primary Completion Date
September 2015 (Actual)
Study Completion Date
March 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine the efficacy and safety of temozolomide in patient with relapsed or advanced anaplastic oligodendroglioma and anaplastic oligoastrocytoma.
Detailed Description
Patient with relapsed or advanced anaplastic oligodendroglioma and anaplastic oligoastrocytoma will be enrolled. Enrolled patients will begin on temozolomide 200 mg/m2/d in a fasting state for 5 consecutive days (1,000 mg/m2 per 28-day cycle). Patients who were previously treated with any chemotherapy initially received temozolomide 150 mg/m2/d for 5 days (750 mg/m2 per cycle).Patients will be receving a total 6 cycles of chemotheray (4weeks/cycle * 6cycles = 24weeks). If the patients shows responses to Temozolomide, treatment can be continued by the investigator's discretion. During the administration of Temozolomide, vital signs, physical examination, ECOG performance status, height, weight, hematology and chemistry test, adverse events and concomitant drugs will be evaluated every four weeks. Brain MRI for tumor assessment will be performed once every 12 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anaplastic Oligodendroglioma, Anaplastic Oligoastrocytoma
Keywords
Temozolomide

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
23 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Temozolomide
Arm Type
Experimental
Arm Description
Temozolomide 200 mg/m2/d in a fasting state for 5 consecutive days
Intervention Type
Drug
Intervention Name(s)
Temozolomide
Other Intervention Name(s)
Temodal
Intervention Description
Temozolomide 200 mg/m2/d in a fasting state for 5 consecutive days (1,000 mg/m2 per 28-day cycle).
Primary Outcome Measure Information:
Title
Progression free survival (PFS)
Description
PFS will be examined with Kaplan-Meier method.
Time Frame
6 month
Secondary Outcome Measure Information:
Title
Objective response rate (ORR)
Description
ORR will be evaluated through the frequency analysis with 95% confidence interval.
Time Frame
1 year
Title
Overall survival (OS)
Description
OS will be examined with Kaplan-Meier method.
Time Frame
1 years
Title
progression-free survival (PFS)
Description
PFS will be examined with Kaplan-Meier method.
Time Frame
1 year
Title
Number of Participants with Adverse Events
Description
Regarding safety endpoints, all adverse events will be individually graded based on the CTCAE version 4.03. The number of participants with adverse events will be summarized using descriptive statistics.
Time Frame
1 years
Other Pre-specified Outcome Measures:
Title
Predictive biomarker study
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven anaplastic oligodendroglioma or oligoastrocytoma Progressed or relapsed after surgery or radiation therapy Female or male aged 20 years or over At least 1 measurable mass lesion ECOG performance status 0-3 Adequate organ function absolute neutrophil count > 1,500/μL platelet count > 75,000/μL hemoglobin greater than 9 g/dL or 900g/L serum creatinine less than 1.5 times the upper limit of laboratory normal total serum bilirubin less than 1.5 times the upper limit of laboratory normal AST or ALT less than three times the upper limit of laboratory normal Exclusion Criteria: Prior course of temozolomide Combined glioblastoma Pregnant woman
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tae Min Kim, MD, PhD
Organizational Affiliation
Seoul National University Hospital, Seoul, South Korea
Official's Role
Study Chair
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
ZIP/Postal Code
110-744
Country
Korea, Republic of

12. IPD Sharing Statement

Citations:
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15758009
Citation
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PubMed Identifier
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Citation
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PubMed Identifier
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Temozolomide in Relapsed or Advanced Anaplastic Oligodendroglioma and Oligoastrocytoma: Single-arm, Phase II Trial

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