NCT02537600已完成2 期
Evaluation of Cobimetinib + Vemurafenib Combination Treatment in Patients With Brain Metastasis BRAFV600 Mutated Cutaneous Melanoma
适应症
干预措施
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 43
- 试验地点
- 17
- 主要终点
- Complete or partial intracranial response rate in cohort A on the evaluation of each patient's best tumor response by the centralized review committee according to modified Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 criteria.
研究概览
简要总结
The purpose of this study is to determine wether cobimetinib + vemurafenib combination treatment is effective in the treatment of BRAFV600-mutated melanoma patients with brain metastasis
详细描述
Patients will be enrolled into 3 cohorts:
- Cohort A : Neurologically asymptomatic patients who have not received prior local treatment ;
- Cohort B. Neurologically asymptomatic patients who have received prior local treatment;
- Cohort C. Neurologically symptomatic patients who have or have not received prior local treatment Every patients will be treated with Vemurafenib 960 mg PO, twice daily from D1 to D28, continuously
Cobimetinib 60 mg PO, once daily, from D1 to D21 - 1 cycle = 28 days
Treatment will be administered until progression (intracranial or extracranial), unacceptable toxicity, withdrawal of consent, death or decision of the treating investigator.
Patients who develop intracranial or extracranial progression and who, in the opinion of the treating investigator, could benefit from continuing treatment may continue treatment with vemurafenib and cobimetinib after approval from the principal investigator.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Men and women ≥ 18 years of age.
- •Histologically confirmed metastatic cutaneous melanoma, mucous melanoma, or melanoma of unknown primary origin (stage IV).
- •Documented BRAFV600 mutation determined in a hospital center specializing in the molecular genetics of cancer that is certified by the French national cancer institute (INCa).
- •Presence of Brain Metastases (BM) for which surgical resection is not a reasonable treatment option but that may be amenable to treatment with targeted therapy, to be decided in the onco-dermatology and/or neuro-oncology multidisciplinary team meeting (MDTM).
- •At least one measurable BM in at least one dimension between 5 and 40 mm on magnetic resonance imaging (MRI) with gadolinium (modified RECIST 1.1).
- •Patients having previously received a maximum of two systemic therapies during the metastatic phase, except BRAF, Map ERK Kinase (MEK) or Extracellular signal Regulated Kinase (ERK) inhibitors or tyrosine kinase pan-inhibitors (TKIs); prior ipilimumab therapy is allowed if patients have documented cerebral progression 12 weeks after the last injection of treatment and if MRI confirms progression at least 4 weeks later. 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.
- •For patients who have received prior whole brain radiotherapy or radiosurgery and/or surgery for BM (cohorts B and C) demonstration of a significant progression of at least one lesion according to RECIST 1.1 criteria, . after at least 4 weeks have elapsed since this treatment has ended, and MRI at inclusion must demonstrate a significant progression of at least one lesion according to RECIST 1.1 criteria.
- •Patients with symptomatic or asymptomatic BM.
- •Eastern Cooperative Oncology Group (ECOG) performance status ≤
- •Patients must have recovered from all the side effects (grade ≤ 1 according to the National Cancer Institute Common Terminology Criteria for Adverse Events, NCI-Common Toxicity Criteria for Adverse Event (CTCAE), version 4.03) of their most recent systemic or local treatment (except alopecia).
- •Signed and dated informed consent before carrying out any procedures that are specific to the trial and are not procedures (examinations) conducted as part of normal patient care.
- •Patients willing and able to comply with scheduled visits, treatment schedule, laboratory testing and other trial procedures.
- •Negative serum pregnancy test within 10 days of the first dose of the study treatment for women of childbearing age. Women of non-childbearing potential may be included if they are surgically sterile or postmenopausal for ≥ 1 year.
- •Fertile men and women must use an effective method of contraception during treatment and for at least 6 months after the last administration of the study treatment. Effective methods of contraception are defined as those that have a low failure rate (i.e. less than 1% per year) when used consistently and correctly, such as injectable implants combined with oral contraception or intra-uterine devices, or as total abstinence in cases where the lifestyle of the patient ensures compliance.
- •Adequate hematologic, renal and hepatic function within 14 days of the administration of treatment:
- •Hematologic Leucocytes > 2.0 x 109/L Neutrophils > 1.0 x 109/L Hemoglobin (transfusion allowed) > 9 g/dL Platelets > 100 x 109/L Liver Total bilirubin < 1.5 x upper limit of normal (ULN) (< 3.0 mg/dL for patients with Gilbert syndrome) Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 3 x ULN (< 5 x ULN if there is liver metastasis) Alkaline phosphatase (ALP) < 3 x ULN (< 5 x ULN if there is liver or bone metastasis) Kidney Creatinine Or creatinine clearance < 1.5 x ULN ≥ 40 mL/min (Cockcroft-Gault formula)
排除标准
- •Uveal melanoma. Patients with mucous melanoma or melanoma of unknown primary origin are eligible if BRAFV600 mutation is confirmed.
- •Symptomatic or diffuse leptomeningeal involvement.
- •Symptoms of uncontrolled intracranial pressure. Increasing corticosteroid dose during the 7 days prior to the first dose of the study treatment is an exclusion criterion. Patients receiving corticosteroids and patients presenting intermittent seizures may be enrolled if the dose of corticosteroids and anti-epileptic treatments has been stable for at least 2 weeks before inclusion.
- •Indication for urgent neurosurgery or radiotherapy.
- •Prior malignancy active within the previous 3 years except for locally curable cancers that have been treated to complete remission or untreated stage I chronic lymphoid leukemia.
- •Known human immunodeficiency virus (HIV) infection.
- •Prior treatment with BRAF, MEK, or ERK inhibitors or pan-TKIs.
- •Concurrent administration of any anticancer therapies other than those administered in this study.
- •Treatment with any cytotoxic and/or investigational drug or targeted therapy within 4 weeks of the first dose of the study treatment, or ipilimumab, anti-PD-1 or anti-PD-L1 immunotherapy within 8 weeks of the study treatment and/or radiation therapy within 2 weeks of the study treatment.
- •Pregnant or breastfeeding women.
- •Refractory nausea and vomiting, intestinal malabsorption, or significant bowel resection that would preclude adequate absorption or cause an inability to swallow tablets.
- •Ulcerative colitis, erosive esophagitis or gastritis, infectious or inflammatory bowel disease, diverticula or other gastrointestinal condition increasing the risk of perforation.
- •Any of the following within the 6 months prior to the first dose of study treatment:
- •myocardial infarction,
- •severe/unstable angina,
- •symptomatic congestive heart failure (New York Heart Association grade ≥2),
- •cerebrovascular accident or transient ischemic attack,
- •pulmonary embolism,
- •grade > 2 hypertension not controlled by medications.
- •History or presence of clinically significant ventricular or atrial arrhythmia ≥ grade 2 (NCI-CTCAE Version 4.03).
- •Corrected QT (cQT) interval ≥ 450 ms and left ventricular ejection fraction (LVEF) below the lower limit of normal (LLN) or < 50% (scintigraphy or ultrasound).
- •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 retinal 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).
- •Serious or uncontrolled medical disorders that, in the opinion of the investigator, may increase the risk associated with study participation or study drug administration, impair the ability of the patient to follow the protocol, or interfere with the interpretation of study results.
- •Patients Under guardianship or curators, maintenance of justice, non-informed about diagnosis, unable to follow study medical requirement for geographical, social or psychic reasons.
- •Patients with abnormal blood electrolyte test (Ca, Mg, K and Na) that could not be corrected.
研究组 & 干预措施
Cobimetinib + Vemurafenib combination
Experimental
Every patients will be treated with :
Vemurafenib 1920 mg / day from day 1 to day 28 continuously Cobimetinib 60 mg / day from day 1 to day 21 One cycle = 28 days Intervention = Cobimetinib + Vemurafenib combination treatment. Only one arm.
干预措施: Cobimetinib + Vemurafenib combination treatment (Drug)
结局指标
主要结局
Complete or partial intracranial response rate in cohort A on the evaluation of each patient's best tumor response by the centralized review committee according to modified Response Evaluation Criteria In Solid Tumors (RECIST) 1.1 criteria.
时间窗: From baseline up to 36 months
次要结局
- Intracranial duration of response (DR) in cohorts A, B and C.(Up to 36 months)
- Overall response rate of cohorts A, B and C(Up to 36 months)
- Complete or partial intracranial response rates in cohorts B and C based on the evaluation of each patient's best tumor response by the centralized review committee according to modified RECIST 1.1 criteria.(Up to 36 months)
- Overall survival in cohorts A, B and C(Up to 36 months)
- Frequency of Adverse events(Up to 36 months)
- Overall duration of response (DR) in cohorts A, B and C.(Up to 36 months)
- Patient free survival in cohorts A, B and C(Up to 36 months)
研究者
研究点 (17)
Loading locations...
相似试验
进行中（未招募）
1 期
Vemurafenib and Cobimetinib combination in BRAF mutated melanoma with brain metastasisPatients with brain metastasis (BM) from BRAFV600-mutated cutaneous melanoma. Patients will be enrolled into three cohorts: A. Neurologically asymptomatic patients who have not received prior local treatment (cohort A)B. Neurologically asymptomatic patients who have received prior local treatment (cohort B)C. Neurologically symptomatic patients who have or have not received prior local treatment (cohort C).MedDRA version: 18.0 Level: LLT Classification code 10027481 Term: Metastatic melanoma System Organ Class: 100000004864EUCTR2014-001671-30-FRCentre Eugène Marquis137
终止
2 期
Phase II Study of Cobimetinib in Combination With Vemurafenib in Active Melanoma Brain MetastasesActive Melanoma Brain MetastasesNCT02230306Melissa Burgess, MD5
已完成
3 期
A Study Comparing Vemurafenib Versus Vemurafenib Plus Cobimetinib in Participants With Metastatic MelanomaMalignant MelanomaNCT01689519Hoffmann-La Roche495
进行中（未招募）
1 期
A phase II trial of vemurafenib plus cobimetinib in patients treated with prior first-line systemic immunotherapy for inoperable locally advanced or metastatic melanomaPatients with advanced melanoma who have received one prior immunotherapy systemic regimen for advanced disease, for whom vemurafenib/cobimetinib treatment has been scheduled by the treating physician.MedDRA version: 21.1Level: LLTClassification code 10053571Term: MelanomaSystem Organ Class: 100000004864EUCTR2017-000504-20-ITFONDAZIONE MELANOMA ONLUS62
招募中
2 期
DETERMINE Trial Treatment Arm 05: Vemurafenib in Combination With Cobimetinib in Adult Patients With BRAF Positive Cancers.Colorectal NeoplasmsGliomaMultiple MyelomaMelanomaNCT05768178Cancer Research UK30