Overview

Whole Brain Radiation With or Without Erlotinib for Brain Metastases From Non-Small Cell Lung Cancer

Status:
Terminated
Trial end date:
2018-12-10
Target enrollment:
0
Participant gender:
All
Summary
To determine if erlotinib given orally along with concurrent whole brain irradiation in lung cancer patients with brain metastases improves median overall survival and enhances local control compared to those treated with WBRT alone, without significantly increasing the risk of side effects or lowering quality of life.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Oslo University Hospital
Treatments:
Erlotinib Hydrochloride
Criteria
Inclusion Criteria: Histologically or cytologically confirmed advanced non-small cell lung
cancer (NSCLC) meeting 1 of the following criteria:

- Newly diagnosed multiple brain metastases not suitable for first-line chemotherapy

- Relapsed NSCLC with newly diagnosed multiple brain metastases

- Relapsed NSCLC after second-line or more chemotherapy regimens with newly diagnosed
multiple brain metastases

- Diagnosis of brain metastases confirmed by MRI (or CT if MRI is not
available/possible) within the past 4 weeks

- Symptoms attributable to brain metastases

- Patients who have undergone craniotomy with incomplete resection are eligible

- Clinician's opinion that whole-brain radiotherapy (WBRT) will be beneficial

- ECOG PS 0-2

- Age above 18 years

- Serum bilirubin < 2 times upper limit of normal (ULN)

- AST and ALT < 2 times ULN (< 5 times ULN if liver metastases are present)

- Creatinine < 1.5 times ULN

- Able to take oral medication

- Not pregnant or nursing

- Negative pregnancy test

- Fertile patients must use effective contraception

- No other prior or concurrent malignant disease likely to interfere with study
treatment or comparisons

Exclusion Criteria:

- More than 3 sites (organ systems) of extracranial metastases

- Evidence of solitary brain metastasis on MRI that can be treated with surgical
resection, radiosurgery, or stereotactic radiotherapy

- Evidence of other significant laboratory finding or concurrent uncontrolled medical
illness, that in the opinion of the investigator, would interfere with study treatment
or results comparison or render the patient at high risk for treatment complications