Clinical trial · Interventional
Study of Temozolomide to Treat Newly Diagnosed Brain Metastases
A Phase II Study of Temozolomide (TMZ) Following Stereotactic Radiosurgery (SRS) for Patients With Newly Diagnosed Brain Metastases
NCT00717275CI-TRIAL-00008175terminatedPhase 2Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Slow accrual.
Summary
Brief summary (as posted)
The purpose of this study is to determine if administering temozolomide after completion of stereotactic radiosurgery helps control existing brain metastases and prevents the developement of new brain metastases.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Brain Metastases | Brain Neoplasm | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Temozolomide | Drug | Temozolomide | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Temozolomide
- interventionNames
- Drug: Temozolomide
Primary outcomes (1)
- measure
- Number of Participants Who Developed Distant Brain Failure at One Year.
- timeFrame
- 1 Year
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria:
Tumor characteristics adequate for stereotactic radiosurgery:
1. 1-3 newly diagnosed, previously untreated, brain metastases
2. Each tumor measuring a size less than or equal to 3 cm
3. No other contraindications to stereotactic radiosurgery
Systemic parameters adequate for temozolomide following stereotactic radiosurgery:
1. Histological confirmation of systemic malignancy (brain confirmation not required)
2. Male or female 18 years of age or older
3. Negative pregnancy test (if of childbearing potential)
4. Any number of previous recurrences will be allowed
5. Karnofsky Performance Status \> 60
6. Hematocrit \> 30,000
7. White blood cell count \> 1,500
8. Platelet \> 100,000
9. Absolute Neutrophil Count \> 1,000
10. Bilirubin \< 1.5 x upper limits of normal
11. Transaminases (ALT and AST) \< 1.5 x upper limits of normal
12. Creatinine \< 1.5 x upper limits of normal
13. Adequate medical health to participate in this study
14. Adequate documentation of menopause (natural/surgical) or patient commitment to routine use of reliable birth control (barrier/hormonal)
15. Ability to read and understand the informed consent document
16. Ability and willingness to follow all requirements of the study including following all directions, taking medication as prescribed and completing all diaries and forms
17. No other contraindications to temozolomide (severe organ dysfunction, immunosuppression, etc.)
18. Medical stability and/or recovery from effects of stereotactic radiosurgery
Exclusion Criteria:
1. Karnofsky Performance Status \< 60
2. Hematocrit \< 30,000
3. White blood cell count \< 1,500
4. Platelet \< 100,000
5. Absolute Neutrophil Count \< 1,000
6. Bilirubin \>1.5 x upper limits of normal
7. Transaminases (ALT and AST) \> 1.5 x upper limits of normal
8. Creatinine \> 1.5 x upper limits of normal
9. Inability to undergo gadolinium-contrasted MRIs, including severe claustrophobia or insufficient allergy prophylaxis
10. Germ cell, leukemia, and lymphoma histologies will be excluded
11. Prior chemotherapy or radiotherapy for brain metastases (prior resection and steroids are allowed)
12. Contraindications to radiosurgery or temozolomide chemotherapy
13. Uncontrolled systemic malignancy
14. Chemotherapy or other systemic therapy for systemic malignancy within a specified time of temozolomide initiation, depending on half-life of agent:
1. Cytotoxic chemotherapy within the previous 4 weeks
2. Nitrosurea (CCNU, BCNU) within the previous 6 weeks
3. Gliadel or temozolomide within the previous 4 weeks
4. Bevacizumab or other antiangiogenic agent within the previous 4 weeks
5. Other targeted molecular or antibody agent within the previous 4 weeks
6. Hormonal agent within the previous 2 weeksReferences
Publications (0)
Data not yet available
No reference posted for this study.