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Phase 2 N=26 Treatment

Temozolomide and Radiation Therapy in Treating Patients With Brain Metastasis Secondary to Non-Small Cell Lung Cancer

Lung Cancer · Metastatic Cancer

Enrolled (actual)
26
Serious AEs
40.0%
Results posted
Sep 2011
Primary outcome: Primary: Number of Patients With Intracranial Response — 3 participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Temozolomide (Drug); Radiation therapy (Radiation)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Eastern Cooperative Oncology Group
Primary completion
Aug 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Patients With Intracranial Response
3
SECONDARY
1-year Neurologic (Central Nervous System, CNS) Progression Free Rate
90.5
SECONDARY
Time to Non-CNS (Systemic) Progression
3.2
SECONDARY
Overall Survival Time
7

Summary

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs such as temozolomide may make the tumor cells more sensitive to radiation therapy. Combining temozolomide with radiation therapy may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving temozolomide together with whole-brain radiation therapy works in treating patients with brain metastasis secondary to non-small cell lung cancer.

Eligibility Criteria

Inclusion Criteria

  • Histologically confirmed non-small cell lung cancer (NSCLC), including the following histologies:
  • Squamous cell carcinoma
  • Adenocarcinoma
  • Large cell carcinoma
  • Bronchoalveolar carcinoma
  • All variants of NSCLC
  • At least 1 bidimensionally measurable brain metastasis
  • Confirmed by MRI within the past two weeks, and computed tomography (CT) scan is not acceptable
  • Biopsy is not required
  • Not eligible for surgical resection or radiosurgery of brain metastasis
  • Systemic disease not in immediate need of chemotherapy
  • Age>=18 years
  • ECOG Performance status of 0-1
  • More than 12 weeks of life expectancy
  • Adequate hematologic, renal, and liver function as demonstrated by laboratory values performed within two weeks, inclusive, prior to administration of study drug or registration
  • Absolute neutrophil count ≥ 1,500/mm^3
  • Platelet count ≥ 100,000/mm^3
  • Hemoglobin ≥ 10 g/dL
  • Bilirubin ≤ 2 times upper limit of normal (ULN)
  • Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) ≤ 2 times upper limit of normal (5 times ULN if liver metastases are present)
  • Alkaline phosphatase ≤ 2 times ULN (5 times ULN if liver metastases are present)
  • Creatinine ≤ 1.6 mg/dL
  • Fertile patients must use effective contraception
  • Prior biologic therapy allowed
  • More than 4 weeks since prior chemotherapy
  • Prior radiotherapy for local control or palliative therapy for painful bony lesions allowed
  • Prior surgery for brain metastasis allowed
  • At least 4 weeks since prior radiotherapy to ≥ 15% of bone marrow (2 weeks for < 15% of bone marrow) and recovered
  • No prior radiotherapy to ≥ 50% of bone marrow
  • Concurrent radiotherapy to painful bony lesions allowed provided no more than 15% of bone marrow is irradiated

Exclusion Criteria

  • HIV positive
  • AIDS-related illness
  • Poor medical risks due to active nonmalignant systemic disease
  • Frequent vomiting
  • There is medical condition that would interfere with oral medication intake (e.g., partial bowel obstruction)
  • Pregnant or nursing
  • Prior temozolomide
  • Prior radiotherapy to the brain, including stereotactic radiosurgery to a different lesion
  • Concurrent intensity modulated radiotherapy or 3-D cranial radiotherapy
  • Other concurrent investigational agents
  • Other concurrent treatment for brain metastasis
  • Other concurrent chemotherapy during study radiotherapy
  • Concurrent growth factors to induce elevations in blood counts for the purposes of administration of study drug at scheduled dosing interval or to allow treatment with study drug at a higher dose
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00080938). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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