Lung Cancer and Breast Cancer Patients With Brain Metastases Clinical Trial
Official title:
A Phase II, Open-label, Single-arm, Multi-center Pilot Study to Evaluate the Efficacy and Safety of Whole-brain Radiotherapy With Concomitant Temozolomide in Lung Cancer and Breast Cancer Patients With Brain Metastases
Brain metastasis (BM) is among the most feared complications in cancer because even small tumors may cause incapacitating neurologic symptoms. It is observed in more than 50% of patients with lung cancer and 15% to 25% of patients with breast cancer. Temozolomide (TMZ) is an oral alkylating agent that crosses blood-brain barrier (BBB). This pilot study aims to evaluate the efficacy, safety and tolerability of whole-brain radiotherapy (WBRT) plus concomitant TMZ in lung cancer and breast cancer patients with BM.
| Status | Not yet recruiting |
| Enrollment | 24 |
| Est. completion date | May 2016 |
| Est. primary completion date | May 2015 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 20 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - Histologically or cytologically confirmed lung cancer or breast cancer at primary site - Patient with inoperable brain metastases - Female or male, = 20 and < 65 years of age - Karnofsky performance status (KPS) = 70% - Life expectancy = 12 weeks - Adequate organ function - Willing and able to provide a written informed consent Exclusion Criteria: - Female of childbearing potential* who is pregnant/lactating or planning to be pregnant - Male whose partner is planning to be pregnant - Inability to swallow - Meningeal carcinomatosis - History of hypersensitivity to iodinated contrast media, temozolomide or any component of the study drugs - Prior use of temozolomide - Use of systemic chemotherapy within 2 weeks prior to the initiation of study treatment - Prior surgery, chemotherapy or radiotherapy for a brain neoplasm - Current use of valproic acid - Use of any investigational product within 4 weeks prior to the initiation of study treatment - Patient with any condition or disease which is considered not suitable for this study by investigator |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Taiwan | Far Eastern Memorial Hospital | New Taipei City |
| Lead Sponsor | Collaborator |
|---|---|
| Far Eastern Memorial Hospital |
Taiwan,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Safety | Change in lab data Adverse event(s) (AE) Serious adverse event(s) (SAE) |
safety of study treatments will be assessed by physician at each return. The safety for individual subject will be followed till 2 weeks after EOT. | Yes |
| Primary | objective response rate (ORR) | To evaluate the objective response rate (ORR) of WBRT plus concomitant TMZ treatment in lung cancer and breast cancer patients with BM. | assessments will be conducted between 10 to 14 weeks after the end of treatment, all subjects will be followed every 3 months since Month 6 until completion of study (12 months after the last patient is enrolled) or death, whichever comes first. | No |
| Secondary | Progression free survival (PFS) | Progression free survival (PFS), Overall survival (OS), Change from baseline in MMSE scores, Change from baseline in SF-36 | assessments will be conducted between 10 to 14 weeks after the end of treatment, all subjects will be followed every 3 months since Month 6 until completion of study (12 months after the last patient is enrolled) or death, whichever comes first. | No |