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

University of Oslo (UIO)

Status and phase

Terminated

Phase 2

Conditions

Cancer

Treatments

Radiation: Radiation

Drug: Radiation plus erlotinib

Study type

Interventional

Funder types

Other

Identifiers

NCT01518621

RadEr

Details and patient eligibility

About

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.

Full description

Endpoints

Primary:

• To determine if erlotinib given orally along with concurrent WBRT in lung cancer patients with brain metastases, improves median overall survival compared to those treated with WBRT alone.

Secondary:

To confirm the safety profile of erlotinib along with concurrent WBRT, in the context of treating central nervous system malignancies.
To evaluate if erlotinib along with concurrent WBRT increases local control rate as measured by MRI at 8 weeks, compared to WBRT alone.
To evaluate if erlotinib along with concurrent WBRT increases time to neurologic progression of disease based on neuropsychological assessment at baseline, at 8 and 20 weeks after WBRT.
To evaluate quality of life parameters in patients treated with WBRT alone vs concomitant erlotinib and WBRT
To evaluate if mutation status has impact on the above mentioned parameters Trial design Open multicenter randomized phase II trial. Patients Patients > 18 years with histologically confirmed NSCLC and brain metastases verified on either CT or MRI, not eligible for neurosurgery or stereotactic radiation therapy.

Trial treatment Patients will be randomized 1:1 to either treatment arm A or B.

Arm A: WBRT 3 Gy x10 alone.
Arm B: WBRT 3 Gy x10 and erlotinib given concomitantly, 150 mg p.o. daily from the day before radiation, until the last day of radiation.

Number of patients 150 patients will be included, 75 in each arm

Enrollment

25 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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