Evaluating the Efficacy and Safety of a Sequencing Schedule of Cobimetinib Plus Vemurafenib Followed by Immunotherapy With an Anti- PD-L1 Antibody in Patients With Unresectable or Metastatic BRAF V600 Mutant Melanoma

NCT ID: NCT02902029

Last Updated: 2025-04-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 186 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-11-30
• Study Completion Date: 2024-03-31

Brief Summary

Most patients with locally advanced or metastatic tumors succumb to their disease. Thus, there is a substantial need for novel therapeutic strategies to improve the outcome for patients with advanced or metastatic melanoma. Targeting the the Ras/Raf signalling pathway by BRAF and MEK inhibition as well as targeting immunologic checkpoint control with an antiPD-L1 antibody have emerged as treatment option.

In this study the best timing for sequential use of both treatment options (BRAF/MEK inhibition and antiPD-L1 antibody) in patients with unresectable or metastatic BRAFV600 mutant melanoma will be assessed.

Detailed Description

At this time there is no experience concerning the sequencing strategy when using the two effective therapeutical approaches as targeting the Ras/Raf signalling pathway by BRAF and MEK inhibition or targeting immunologic checkpoint control with an antiPD-L1 antibody.

This is a prospective, open, multicenter, randomized phase II study in patients with unresectable or metastatic BRAFV600 mutant melanoma. In this study the scheduling of the treatment with a combined BRAF/MEK inhibition and the treatment with an anti-PD-L1 antibody will be assessed.

After a 3 months run-in period with vemurafenib and cobimetinib, all patients who did not show disease progression or treatment interruption for more than 28 days during run-in phase will be randomized in a 1:1 ratio:

• either to proceed vemurafenib and cobimetinib until disease progression and subsequently cross-over to atezolizumab treatment until disease progression (Arm A).
• or to receive the anti-PD-L1 antibody atezolizumab until disease progression and subsequently cross-back to vemurafenib and cobimetinib until disease progression (Arm B). In a translational research program tumor tissue, blood plasma and peripheral blood mononuclear cell will be analyzed to evaluate the biologic effects of treatment sequence on the molecular profile and biomarker expression in tissue and plasma.

Conditions

Malignant Melanoma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm A

After a 3 months run-in period with vemurafenib and cobimetinib [960 mg vemurafenib twice daily (BID), 28/0; 60 mg cobimetinib daily (QD), 21/7], all patients who do not show disease progression or definite treatment interruption (e.g. due to unacceptable toxicity) for more than 28 days will be randomized.

Further treatment with vemurafenib and cobimetinib (960 mg vemurafenib BID, 28/0; 60 mg cobimetinib QD, 21/7).

After progression of disease patients in Arm A will subsequently receive atezolizumab treatment (1200 mg/ q3w).

Group Type: EXPERIMENTAL

Vemurafenib

Intervention Type: DRUG

960 mg vemurafenib BID until progression or unacceptable toxicity develops

Cobimetinib

Intervention Type: DRUG

60 mg cobimetinib QD, 21/7 until progression or unacceptable toxicity develops

Atezolizumab

Intervention Type: DRUG

1200 mg atezolizumab administered intravenously on day 1 of each 21 day-cycle. Will be given until progression or unacceptable toxicity develops

Arm B

After a 3 months run-in period with vemurafenib and cobimetinib (960 mg vemurafenib BID, 28/0; 60 mg cobimetinib QD, 21/7), all patients who do not show disease progression or definite treatment interruption (e.g. due to unacceptable toxicity) for more than 28 days will be randomized.

Further treatment with atezolizumab. Atezolizumab will be administered intravenously at a fixed dose of 1200 mg on day 1 of each 21 day-cycle.

After progression of disease patients in Arm B will cross back to vemurafenib and cobimetinib treatment (960 mg vemurafenib BID, 28/0; 60 mg cobimetinib QD, 21/7).

Group Type: EXPERIMENTAL

Vemurafenib

Intervention Type: DRUG

960 mg vemurafenib BID until progression or unacceptable toxicity develops

Cobimetinib

Intervention Type: DRUG

60 mg cobimetinib QD, 21/7 until progression or unacceptable toxicity develops

Atezolizumab

Intervention Type: DRUG

1200 mg atezolizumab administered intravenously on day 1 of each 21 day-cycle. Will be given until progression or unacceptable toxicity develops

Interventions

Vemurafenib

960 mg vemurafenib BID until progression or unacceptable toxicity develops

Intervention Type: DRUG

Cobimetinib

60 mg cobimetinib QD, 21/7 until progression or unacceptable toxicity develops

Intervention Type: DRUG

Atezolizumab

1200 mg atezolizumab administered intravenously on day 1 of each 21 day-cycle. Will be given until progression or unacceptable toxicity develops

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Be willing and able to provide written informed consent for the trial.
• Male or female patient being ≥18 years of age on day of signing informed consent.
• Histologically confirmed diagnosis of locally advanced, unresectable or metastatic melanoma AJCC (unresectable stage IIIB, IIIC, IVM1a, IVM1b, or IVM1c) without active or untreated brain metastases; all known CNS lesions must have been treated with stereotactic therapy or surgery at least 4 weeks prior to the first dose of trial treatment AND the patient must be without evidence of clinical or radiographic disease progression in the CNS for at least 4 weeks prior to the first dose of trial treatment and any neurologic symptoms must have returned to baseline, the patient must have no evidence of new or enlarging brain metastases, and the patient must not have used steroids for at least 3 weeks prior to trial treatment.
• No previous therapy for the advanced or metastatic stage. Prior adjuvant therapy is permitted (e.g. Interferon, Interleukin-2-therapy, chemo- or radiotherapy). Prior adjuvant therapy has to be terminated (last dose) at least 28 days before enrolment. Patients who are in follow-up period of a clinical trial in adjuvant setting and progressing may be enrolled / randomized.
• Measurable disease, i.e., present with at least one measurable lesion per RECIST, version 1.1, for the definition of a measureable lesion.
• Presence of BRAF mutation (V600) in tumor tissue.
• Performance status of 0 or 1 on the ECOG Performance Scale.
• Adequate organ function.
• Adequate cardiac function.
• Able to take oral medications.
• Female subject of childbearing potential should have a negative pregnancy test within 72 hours prior to receiving the first dose of study medication.
• Female patients of childbearing potential and male patients with partners of childbearing potential must agree to always use a highly effective form of contraception according to CTFG during the course of this study and for at least 6 months after completion of study therapy.

Exclusion Criteria

• Use of any investigational or non-registered product within the 30 days before registration.
• Diagnosis of immunodeficiency or receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to study Day 1.
• Prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-Cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) antibody (including ipilimumab or any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways).
• Prior therapy with a BRAF inhibitor (including but not limited to vemurafenib, dabrafenib, encorafenib and / or MEK inhibitor
• Prior major surgery.
• Known additional malignancy that is progressing or requires active treatment within 5 years prior to the study.
• Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
• History of leptomeningeal metastases.
• History or current evidence of central serous retinopathy (CSR) or retinal vein occlusion (RVO) or predisposing factors to RVO or CSR.
• History of retinal degenerative disease.
• History of allogenic bone marrow transplantation or organ transplantation.
• History of Gilbert's syndrome.
• Impaired cardiovascular function or clinically significant cardiovascular diseases.
• Uncontrolled arterial hypertension despite medical treatment.
• Impairment of gastrointestinal function or gastrointestinal disease.
• Evidence of interstitial lung disease or active, non-infectious pneumonitis.
• Active infection requiring systemic therapy.
• Positive test for Human Immunodeficiency Virus (HIV).
• Positive test for Hepatitis B or Hepatitis C.
• Known hypersensitivity reaction to any of the components of study treatment.
• Medical, psychiatric, cognitive or other conditions, including known alcohol or drug abuse.
• Patients having received a live, attenuated vaccine within 4 weeks prior to the first dose of trial treatment.
• Legal incapacity or limited legal capacity.

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

Sponsors

University Hospital, Essen

OTHER

Sponsor Role: lead

Responsible Party

Prof. Dr. med. Dirk Schadendorf

Prof. Dr. med.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Dirk Schadendorf, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Essen

Locations

Hôpital Ambroise-Paré

Boulogne-Billancourt, , France

Hospital Claude Huriez

Lille, , France

Hôpital de la Timone

Marseille, , France

CHU de Nantes

Nantes, , France

Centre Hospitalier Lyon Sud

Pierre-Bénite, , France

National Centre for Tumour Diseases (NCT)

Heidelberg, Baden-Wurttemberg, Germany

SLK-Kliniken Heilbronn GmbH

Heilbronn, Baden-Wurttemberg, Germany

University Hospital Mannheim, Clinic for Dermatology

Mannheim, Baden-Wurttemberg, Germany

University Hospital Essen, Department of Dermatology, Skin Cancer Center

Essen, North Rhine-Westphalia, Germany

HELIOS Klinikum Erfurt

Erfurt, Thuringia, Germany

Charité-Universitätsmedizin Berlin

Berlin, , Germany

Elbe Kliniken Stade - Buxtehude

Buxtehude, , Germany

Universitätsklinikum Köln

Cologne, , Germany

Universitätsklinik Dresden

Dresden, , Germany

Medizinische Hochschule Hannover

Hanover, , Germany

Universitätsklinikum des Saarlandes

Homburg/Saar, , Germany

Universitäts-Hautklinik Kiel

Kiel, , Germany

Universitätsklinikum Leipzig

Leipzig, , Germany

Gesellschaft für Klinische Forschung Ludwigshafen mbH

Ludwigshafen, , Germany

Universitätsklinikum Schleswig-Holstein

Lübeck, , Germany

Universitätsklinikum Mainz

Mainz, , Germany

Johannes Wesling Klinikum Minden

Minden, , Germany

Klinikum der Universität München

München, , Germany

Universitätsklinikum Tübingen

Tübingen, , Germany

Uniklinikum Würzburg

Würzburg, , Germany

"LAIKO" General Hospital of Athens

Athens, , Greece

Military Medical Academy

Belgrade, , Serbia

Countries

France; Germany; Greece; Serbia

Other Identifiers

ImmunoCobiVem_2015

Identifier Type: -

Identifier Source: org_study_id