Study of Osimertinib + SRS vs Osimertinib Alone for Brain Metastases in EGFR Positive Patients With NSCLC
- Conditions
- Lung Cancer Non-small Cell Stage IVBrain Metastases
- Interventions
- Radiation: Stereotactic radiotherapy
- Registration Number
- NCT03769103
- Lead Sponsor
- British Columbia Cancer Agency
- Brief Summary
This open-label, multicenter, randomized phase II study will evaluate the usage of osimertinib alone for brain metastases compared to SRS and osimertinib in patients with newly diagnosed, treatment naiive EGFR positive lung cancer.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 40
- Able to provide written informed consent by patient or legally acceptable representative
- Meets the criteria in the approved regulatory indication for first line treatment with osimertinib and agree to the restrictions, monitoring, and dose-adjustment criteria stipulated in the associated product label
- Epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 (L858R) substitution mutations (either alone or in combination with other EGFR mutations)
- No prior systemic therapy except neoadjuvant, adjuvant or concurrent chemotherapy given greater than 3 months prior to enrollment on study
- Asymptomatic or minimally symptomatic brain metastases (ie. Headache, nausea, or seizure responsive to dexamethasone/analgesic/antiepileptic on stable doses of medications for a minimum of 3 days)
- Brain metastases must meet the following criteria on a diagnostic MRI: at least one lesion can be classified as measurable disease per RANO-BM, ≤ 10 brain or brainstem metastases, ≤ 30 mm and brainstem metastases must be ≤ 5 mm, metastases > 5 mm from the optic nerve or chiasm
- ECOG performance status 0-2
- Life expectancy > 6 months
- Willing to abstain from sexual activity or willing to use double-barrier method during sexual intercourse
- Previous treatment with osimertinib, or any other EGFR TKI
- Patient with symptomatic brain metastases causing any neurologic deficit (not including headache, nausea, or medically controlled seizure)
- Multiple sclerosis
- Pacemaker or MRI-incompatible metal in the body
- Allergy to gadolinium MRI contrast
- Brain metastasis requiring surgery for decompression
- Leptomeningeal disease
- Previous cranial RT, or surgery for brain metastases
- Uncontrolled systemic lupus erythematosis, scleroderma or other connective tissue disorders considered a contraindication for radiotherapy
- Active cancer from another anatomical site within 5 years (non-melanomatous skin and cervical cancers permitted)
- Any medical or non-medical issue that would render patient unable to reliably complete regular QOL and neurocognitive assessments
- Judgment by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions and requirements
- Treatment with an investigational drug within five half-lives of the compound or 3 months, whichever is greater
- Patients with symptomatic CNS metastases who are neurologically unstable
- Patients currently receiving (or unable to stop use prior to receiving the first dose of study treatment) medications or herbal supplements known to be potent inducers of cytochrome P450 (CYP) 3A4
- Patients taking any drugs that are known to prolong QT interval that can't be withdrawn prior to Osimertinib
- Pregnant or breastfeeding
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description SRS + Osimertinib Stereotactic radiotherapy Stereotactic radiotherapy will be delivered in 1-5 fractions to each brain metastases according to the volume and location of the metastases and clinician discretion. Osimertinib will start 1-7 days post radiotherapy. SRS + Osimertinib Osimertinib Stereotactic radiotherapy will be delivered in 1-5 fractions to each brain metastases according to the volume and location of the metastases and clinician discretion. Osimertinib will start 1-7 days post radiotherapy. Osimertinib alone Osimertinib Osimertinib 80mg PO daily
- Primary Outcome Measures
Name Time Method Intracranial progression free survival 1 year Absence of progressive brain metastases according to the Response Assessment in Neuro-Oncology Brain Metastasis (RANO-BM criteria)
- Secondary Outcome Measures
Name Time Method Exposure to osimertinib 2 years Osimertinib dose (40mg or 80mg) for x number of days (max=730 days)
Intracranial overall response rate 2 years partial or complete response to therapy based on RANO-BM criteria
Time to distant progression 2 years time from randomization to progression of extracranial metastases or development of new sites of disease per RECIST 1.1
Time to whole brain radiotherapy (WBRT) 2 years time from randomization to WBRT
Overall survival 2 years defined as time from randomization to death by any cause
Quality of life 2 years Assessed by European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (QLQ) C30. Subscales for: general presence of symptoms in patients with cancer question 1-28 (1=Not at all; 4=very much); overall health/quality of life question 29-30 (1=very poor; 7=excellent) \& EORTC-QLQ Brain Neoplasm (BN)20: Subscales for presence of symptoms in patients with brain tumours question 31-50 (1=Not at all; 4=very much)
Time to stereotactic radiosurgery (SRS) 2 years time from randomization to SRS (not including initial SRS in the SRS + osimertinib treatment arm)
Rate of radionecrosis 2 years according to institutional standards based on radiologic findings with or without pathologic confirmation and multidisciplinary review when required
Neurocognitive function 2 years Assessed by Montreal Cognitive Assessment. Total score:30. 1=poor function; 30=good function
Trial Locations
- Locations (3)
BC Cancer, Vancouver Centre
🇨🇦Vancouver, British Columbia, Canada
Princess Margaret Hospital
🇨🇦Toronto, Ontario, Canada
Sunnybrook Health Sciences Centre
🇨🇦Toronto, Ontario, Canada