Vemurafenib Plus Cobimetinib After Radiosurgery in Patients With BRAF-mutant Melanoma Brain Metastases

NCT ID: NCT03430947

Last Updated: 2023-09-14

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-07-01
• Study Completion Date: 2023-02-10

Brief Summary

This is a phase II, open label, non-randomised study of vemurafenib and cobimetinib after radiosurgery in adult patients with BRAFV600-mutant melanoma brain metastases. All patients will receive vemurafenib 960 mg twice a day on days 1 - 28 combined with cobimetinib 60 mg once a day on days 1 - 21 of each 28-day treatment cycle until disease progression, drug toxicity or death.

The primary objective of this study is to determine the best overall response rate (BORR) in the brain. The extracranial BORR, intra- and extracranial duration of response, progression-free survival and overall survival, adverse events, quality of life and radiomics features predicting long-term local control of brain metastases and treatment-related toxicity will also be examined.

Conditions

Malignant Melanoma Stage IV; BRAF V600 Mutation; Brain Metastases

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment

all patients will be treated with Vemurafenib + Cobimetinib

Group Type: EXPERIMENTAL

Vemurafenib

Intervention Type: DRUG

Vemurafenib (960 mg twice a day) will be taken on days 1 - 28 of each 28-day treatment cycle.

Cobimetinib

Intervention Type: DRUG

Cobimetinib (60 mg once a day) will be taken on days 1 - 21 of each 28-day treatment cycle.

Interventions

Vemurafenib

Vemurafenib (960 mg twice a day) will be taken on days 1 - 28 of each 28-day treatment cycle.

Intervention Type: DRUG

Cobimetinib

Cobimetinib (60 mg once a day) will be taken on days 1 - 21 of each 28-day treatment cycle.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Signed informed consent
• Female and male patients ≥ 18 years of age
• Histologically confirmed metastatic melanoma (stage IV, per AJCC staging), carrying BRAF V600-mutation
• Performed SRS 14 ±7 days before baseline using a harmonized protocol in patients with at least one measurable intracranial target lesion for which the following criteria are met:

• Previously untreated (Lesions in previously irradiated area should not be selected)
• Largest diameter of ≥ 0.5 but ≤ 4 cm as determined by contrast-enhanced MRI and
• ≤ 10 brain metastases
• ECOG performance status 0 - 2
• Life expectancy ≥ 12 weeks
• Adequate bone marrow function as indicated by the following:

• ANC ≥ 1500/µL,
• Platelets ≥ 100,000/µL and
• Hemoglobin ≥ 9 g/dL
• Adequate renal function, as indicated by creatinine ≤ 1.5 x ULN
• Adequate liver function, as indicated by bilirubin < 1.5 x ULN and AST and ALT < 3 x ULN (documented liver metastases: AST and ALT < 5 x ULN)
• Adequate coagulation within 28 days prior to baseline visit

• Patients without therapeutic anticoagulation: INR or aPTT ≤ 1.5 x ULN
• Patients receiving therapeutic anticoagulation: stable anticoagulation regimen and stable INR
• Able to swallow pills

Exclusion Criteria

• Symptomatic brain metastases requiring immediate local interventions such as neurosurgery or radiosurgery
• Leptomeningeal disease (also synchronous with brain metastases)
• Prior therapy with BRAF or MEK inhibitors within 12 weeks prior to baseline visit (prior therapies for metastatic melanoma including chemo-, cytokine-, immuno-, biological and vaccine-therapy will be al-lowed) A period of at least 6 weeks must be observed between the last dose of ipilimumab and the first administration of the study treatments. Prior treatment with anti-programmed cell death (PD)-1 or anti-PD ligand 1 (PD-L1) is allowed.
• Prior whole brain irradiation (Patients with prior local therapy of brain metas-tases are eligible)
• Patients receiving therapeutic steroids are not stable on corticoster-oids 2 weeks before SRS
• Active and uncontrolled infection
• Known HIV infection or active HBV or HCV infection

• Active HBV infection (chronic and acute), defined as having a posi-tive hepatitis B surface antigen (HBsAg) test at screening (past or resolved HBV infection, defined as negative HBsAg test and a posi-tive total hepatitis B core antibody test at screening, are eligible)
• Active HCV infection, defined as positive HCV antibody test and positive HCV RNA test at screening
• Intracranial radiation therapy within 14 days prior to SRS
• Extracranial radiation therapy within the last 14 days prior to baseline visit
• Treatment with strong CYP3A4/5 inhibitors (e.g. ketoconazole) and inducers (e.g. phenytoin, carbamazepine). (anticonvulsant levetiracetam is allowed; patient should be stable on levetiracetam for 2 weeks)
• Unresolved toxicity of National Cancer Institute Common Terminology Crite-ria for Adverse Events, version 4.0 (NCI v4.0) [NCI, 2009] Grade 2 or higher from previous anti-cancer therapy, except alopecia.
• Conditions that will interfere significantly with the absorption of drugs (e.g. Colitis ulcerosa)
• Inability to undergo MRI secondary to:

• Metal,
• Claustrophobia, or
• Gadolinium contrast allergy
• Previous malignancies active within the last 3 years, with the exception of locally curable cancers that have been treated to complete remis-sion or untreated stage I chronic lymphoid leukemia.
• Unwillingness or inability to comply with study and follow-up procedures
• Known hypersensitivity to any of the excipients of cobimetinib and vemuraf-enib
• The following foods/supplements are prohibited at least 7 days prior to initia-tion of and during study treatment:

• St. John's wort or hyperforin (potent cytochrome P450 CYP3A4 enzyme inducer)
• Grapefruit juice (potent cytochrome P450 CYP3A4 enzyme inhibitor)
• Patient is included in another interventional trial
• Use of any investigational or non-registered product within 4 weeks prior to baseline visit
• Woman of childbearing age with the exception they meet at least one of the following criteria:

• Post-menopausal,
• Sterilization,
• Consistently & correct application of contraceptives (Pearl Index < 1%),
• sexual abstinence, or
• vasectomy of the partner
• Pregnant or lactating women
• History, risk factor or retinal pathology that increases the risk of retinal vein occlusion (RVO) or central serous retinopathy (CSR): evidence of retinal pathology that is considered a risk factor for RVO or CSR, or a history of retinal detachment, central serous chorioretinopathy or reti-nal vein thrombosis. The risk factors for RVO are listed below:

• Uncontrolled glaucoma with intraocular pressures > 21 mm Hg,
• Serum cholesterol ≥ Grade 2 (≥ 7.75 mmol/L),
• Hypertriglyceridemia ≥ Grade 2 (≥ 3.42 mmol/L), Hyperglycemia (fasting) ≥ Grade 2 (≥ 8.9 mmol/L).
• History of clinically significant cardiac dysfunction including:

• Myocardial infarction,
• Severe/unstable angina pectoris,
• Symptomatic congestive heart failure (NYHA stage ≥ 2),
• cerebrovascular accident or transient ischemic attack within the previous 6 months,
• History of congenital long QT syndrome or mean QTcF > 450 msec or uncorrectable electrolyte abnormalities,
• Hypertension > Grade 2 not controlled by medications
• Left ventricular ejection fraction (LVEF) < 50%, or
• Uncontrolled arrhythmias

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Technische Universität Dresden

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Friedegund Meier, MD

Role: PRINCIPAL_INVESTIGATOR

Technische Universität Dresden

Locations

Technische Universität Dresden

Dresden, , Germany

Ruprecht-Karls-University of Heidelberg, Faculty of Medicine

Heidelberg, , Germany

Eberhard Karls University of Tübingen, University Medical Center

Tübingen, , Germany

Countries

Germany

Other Identifiers

2017-000768-13

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

TUD-CoBRIM-67

Identifier Type: -

Identifier Source: org_study_id