ENCOrafenib With Binimetinib in bRAF NSCLC

Non Small Cell Lung Cancer Clinical Trial

— ENCO-BRAF  

Official title:

A Phase II Study of the BRAF Inhibitor Encorafenib in Combination With the MEK Inhibitor Binimetinib in Patients With BRAFV600E-mutant Metastatic Non-small Cell Lung Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04526782
• Other study ID #: IFCT-1904
• Status: Recruiting
• Phase: Phase 2
• Start date: January 19, 2021
• Est. completion date: March 2026

Study information

• Verified date: March 2024
• Source: Intergroupe Francophone de Cancerologie Thoracique
• Contact: Elodie Amour
• Phone: +33156811045
• Email: contact[@]ifct.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A Phase II study of the BRAF inhibitor Encorafenib in combination with the MEK inhibitor Binimetinib in Patients with BRAFV600E-mutant metastatic Non-small Cell Lung Cancer

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 119
• Est. completion date: March 2026
• Est. primary completion date: September 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Subjects must have signed and dated an IRB/IEC approved written informed consent form in accordance with regulatory and institutional guidelines. This must be obtained before the performance of any protocol related procedures that are not part of normal subject care.

Subjects must be willing and able to comply with scheduled visits, treatment schedule, and laboratory testing.

2. Male or female aged at least 18 years old.

3. Histologically confirmed diagnosis of NSCLC that is currently Stage IV (M1a, M1b or M1c AJCC 8th edition).

4. ECOG performance status of 0-1.

5. Able to swallow and retain oral medication.

6. Presence of a BRAFV600E mutation in lung cancer tissue as determined by a local laboratory assay.

7. The Investigator must confirm prior to enrolment that the patient has adequate tumor tissue available to determine BRAFV600E mutation status by central laboratory for confirmation.

Note: Tumor tissue collected after the patient was diagnosed with metastatic disease is preferred.

Tumor tissue sample must not be from locations previously radiated. Tumor sample must be 1 block or 10 to 15 unstained slides of analyzable tissue and one H&E slide.

8. Patients i) (COHORT A) who are either treatment-naïve (e.g., no prior systemic therapy for advanced/metastatic disease), ii) (COHORT B) who are in progression after having received 1) first-line platinum-based chemotherapy OR 2) first-line treatment with an anti-PD-1/L-1 inhibitor given alone or in combination with platinum-based chemotherapy or in combination with immunotherapy (e.g, ipilimumab) with or without platinum-based chemotherapy.

Note: Alternative chemotherapy regimens are acceptable if the patient was platinum intolerant or ineligible.

Patients with early stage disease (e.g., Stages I-III) who have had surgery followed by chemotherapy (e.g., treatment in the adjuvant setting), and present with new lesions or evidence of disease recurrence (e.g., metastatic disease), within 12 months of completing chemotherapy, would be considered as had received a first-line therapy.

Maintenance therapy given after first-line therapy in the metastatic setting will not be considered a separate regimen, provided there was no documentation of disease progression between completion of first-line therapy and the start of maintenance therapy.

9. Presence of measurable disease based on RECIST v1.1.

10. Adequate bone marrow function characterized by the following at screening:

i) ANC = 1.5 × 109/L; ii) Platelets = 100 × 109/L; iii) Hemoglobin = 8.5 g/dL (with or without blood transfusions).

11. Adequate hepatic and renal function characterized by the following at screening:

i) Total bilirubin = 1.5 × ULN and < 2 mg/dL; OR total bilirubin >1.5 × ULN with indirect bilirubin < 1.5 × ULN; ii) ALT and AST = 2.5 × ULN, or = 5 × ULN in presence of liver metastases; iii) Serum creatinine = 1.5 × ULN; or calculated creatinine clearance = 50 mL/min by Cockcroft-Gault formula; or estimated glomerular filtration rate>50 mL/min/1.73m2.

12. Female patients of childbearing potential as described in Appendix 1, must have a negative serum ß HCG test result.

13. Female patients of childbearing potential must agree to use methods of contraception that are highly effective or acceptable, as described in Appendix 1, and to not donate ova from Screening until 30 days after the last dose of study treatment.

14. Male patients must agree to use methods of contraception that are highly effective or acceptable, as described in Appendix 1, and to not donate sperm from Screening until 90 days after the last dose of encorafenib and binimetinib.

15. Patient covered by a national health insurance

Exclusion Criteria:

1. Patients with nonsquamous carcinoma who have documentation of any of the following:

EGFR mutation, ALK fusion oncogene or ROS1 rearrangement.

2. Previous treatment with any other BRAF inhibitor (e.g., dabrafenib, vemurafenib…), or any other MEK inhibitor (e.g., trametinib, cobimetinib…) prior to screening and enrolment.

4. Patients who have received more than 1 prior line of systemic therapy in the advanced/metastatic setting for Cohort B.

Note: Generally, treatments that are separated by an event of progression are considered to represent another line of therapy.

Any therapeutic intervention including systemic therapy, surgery concurrent with or followed by systemic therapy, radiation concurrent with systemic therapy, or stereotactic radiation/radiosurgery, initiated or added to an existing therapy for oligometastatic disease will be considered a new line of therapy.

Palliative radiation to solitary lesions is permitted and will not be considered a new line of therapy.

Surgery/radiosurgery for CNS metastases is permitted and will not be considered a line of therapy as long as the surgery/radiosurgery was not given with systemic therapy (neoadjuvant or adjuvant).

Surgery followed by chemotherapy in the metastatic setting will be considered a line of therapy.

5. Receipt of anticancer therapies or investigational drugs within the following intervals before the first administration of study treatment: i) =14 days for chemotherapy, targeted small molecule therapy, radiation therapy, immunotherapy, or antineoplastic biologic therapy (e.g., erlotinib, crizotinib, bevacizumab etc.).

ii) =14 days or 5 half-lives (minimum of 14 days) for investigational agents or devices. For investigational agents with long half-lives (e.g., > 5 days), enrolment before the fifth half-life requires sponsor approval.

iii) Palliative radiation therapy must be complete 7 days prior to the first dose of study treatment.

6. Patients who have had major surgery (e.g., inpatient procedure with regional or general anesthesia) = 6 weeks prior to start of study treatment.

7. For cohort B : Patient has not recovered to =Grade 1 from toxic effects of prior therapy and/or complications from prior surgical intervention before starting study treatment.

Note: Stable chronic conditions (= Grade 2) that are not expected to resolve (e.g., neuropathy, myalgia, alopecia, and prior therapy-related endocrinopathies) are exceptions.

8. Current use of a prohibited medication (including herbal medications, supplements, or foods), or use of a prohibited medication =1 week prior to the start of study treatment.

9. Impairment of gastrointestinal function or disease which may significantly alter the absorption of oral study treatment (e.g., uncontrolled nausea, vomiting or diarrhea, malabsorption syndrome, small bowel resection).

10. Impaired cardiovascular function or clinically significant cardiovascular diseases, including any of the following: i) History of acute myocardial infarction, acute coronary syndromes (including unstable angina, coronary artery bypass graft, coronary angioplasty or stenting) = 6 months prior to start of study treatment; ii) Congestive heart failure requiring treatment (New York Heart Association Grade =2); iii) LVEF < 50% as determined by MUGA or ECHO; iv) Uncontrolled hypertension defined as persistent systolic blood pressure =150 mmHg or diastolic blood pressure =100 mmHg despite optimal therapy; v) History or presence of clinically significant cardiac arrhythmias (including uncontrolled atrial fibrillation or uncontrolled paroxysmal supraventricular tachycardia); vi) Baseline QTcF interval =480 ms or a history of prolonged QT syndrome. 11. History of thromboembolic or cerebrovascular events =12 weeks prior to the first dose of study treatment. Examples include transient ischemic attacks, cerebrovascular accidents, hemodynamically significant (i.e. massive or sub-massive) deep vein thrombosis or pulmonary emboli. Note: Patients with either deep vein thrombosis or pulmonary emboli that does not result in hemodynamic instability are allowed to enrol as long as they are on a stable dose of anticoagulants for at least 4 weeks. Note: Patients with thromboembolic events related to indwelling catheters or other procedures may be enrolled.

12. History or current evidence of RVO (Retinal Vein Occlusion) or current risk factors for RVO (e.g., uncontrolled glaucoma or ocular hypertension, history of hyper viscosity or hypercoagulability syndromes); history of retinal degenerative disease.

13. Concurrent neuromuscular disorder that is associated with the potential of elevated CK (e.g., inflammatory myopathies, muscular dystrophy, amyotrophic lateral sclerosis, spinal muscular atrophy).

14. Evidence of active, noninfectious pneumonitis, history of interstitial lung disease that required oral or intravenous glucocorticoid steroids for management.

15. Evidence of HBV or HCV infection. Note: Patients with laboratory evidence of cleared HBV or HCV infection may be enrolled. Note: Patients with no prior history of HBV infection who have been vaccinated against HBV and who have a positive antibody against hepatitis B surface antigen as the only evidence of prior exposure may enrol.

16. Patient who aas has a known history of a positive test for HIV or known AIDS.

17. Active infection requiring systemic therapy. 18. Patients with symptomatic brain metastasis, leptomeningeal disease or other active CNS metastases are not eligible.

Note: Patients with previously treated or not treated brain metastases may participate provided they are stable (e.g., without evidence of progression by radiographic imaging for at least 28 days before the first dose of study treatment and neurologic symptoms have returned to baseline) Patients must have no evidence of new or enlarging brain metastases or CNS edema.

Patient must have discontinued use of steroids at least 7 days before the first dose of study treatment.

19. Concurrent or previous other malignancy within 2 years of study entry, except curatively treated basal or squamous cell skin cancer, prostate intraepithelial neoplasm, carcinoma in-situ of the cervix, Bowen's disease and Gleason 6 prostate cancer.

20. Known sensitivity or contraindication to any component of study treatment or their excipients.

21. Pregnancy confirmed by a positive ß-HCG laboratory test result, or breastfeeding (lactating).

22. Other severe, acute or chronic medical or psychiatric condition(s) or laboratory abnormality that may increase the risk associated with study participation or study treatment administration or that may interfere with the interpretation of study results and, in the judgment of the Investigator, would make the patient an inappropriate candidate for the study.

Related Conditions & MeSH terms

• BRAF V600E
• Carcinoma, Non-Small-Cell Lung
• Lung Neoplasms
• Non Small Cell Lung Cancer

Intervention

Drug:
• Encorafenib 75 MG
450 mg (6 × 75 mg capsule) per day
• Binimetinib 15 MG
45 mg (3 × 15 mg tablet) twice daily

Locations

Country	Name	City	State
France	Annemasse - CH	Ambilly
France	Angers - CHU	Angers
France	Hôpital Privé d'Antony	Antony
France	Avignon - Institut Sainte-Catherine	Avignon
France	Bordeaux - Institut Bergonié	Bordeaux
France	Boulogne - Ambroise Paré	Boulogne-Billancourt
France	Brest - CHU	Brest
France	Caen - CHU Côte de Nacre	Caen
France	CH	Colmar
France	Centre Hospitalier Intercommunal de Créteil	Créteil
France	Centre Georges François Leclerc	Dijon
France	CHRU Grenoble	Grenoble
France	La Roche Sur Yon - CH	La Roche Sur Yon
France	CH Le Mans	Le Mans
France	CHRU de Lille	Lille
France	CHU Dupuytren	Limoges
France	Centre Léon Bérard	Lyon
France	AP-HM Hôpital Nord	Marseille
France	Institut Paoli Calmettes	Marseille
France	Montpellier - CHRU	Montpellier
France	Mulhouse - GHRMSA	Mulhouse
France	Nancy - Institut de Cancérologie de Lorraine	Nancy
France	Centre Antoine LACASSAGNE	Nice
France	AP-HP Hôpital Cochin	Paris
France	AP-HP Hôpital Tenon	Paris
France	Hôpital BICHAT	Paris
France	Paris - Institut Curie	Paris
France	Centre Hospitalier Général - Pau	Pau
France	Lyon - URCOT	Pierre-Bénite
France	CHU Rennes - Hôpital Pontchaillou	Rennes
France	CHU Charles Nicolle	Rouen
France	Saint Quentin - CH	Saint Quentin
France	Nouvel Hôpital Civil - Hôpitaux Universitaires de Strasbourg	Strasbourg
France	CHU Toulouse - Pneumologie	Toulouse
France	Tours - CHU	Tours
France	Villefranche-Sur-Saône - Hôpital Nord-Ouest	Villefranche-Sur-Saône
France	Gustave Roussy	Villejuif

Sponsors (1)

Lead Sponsor	Collaborator
Intergroupe Francophone de Cancerologie Thoracique

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective response rate	Objective Response Rate at 6 months using RECIST1.1 criteria	6 months
Secondary	Duration Response Rate	Time from the date of the first documented response (CR or PR) to the earliest date of disease progression (RECIST 1.1), or death due to any cause.	about 12 months
Secondary	Progression-free Survival	Time from enrollment to first observation of progression (RECIST1.1) or date of death (from any cause)	about 24 months
Secondary	Overall Survival	Time from enrollment until death due to any cause	about 24 months
Secondary	Incidence, type and severity of adverse events	Descriptive statistics of safety will be presented using National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE), version 5.0	From time of informed consent through treatment period and up to 30 days post last dose of study treatment (about 24 months)

External Links

•   IFCT website