Ceritinib and Trametinib in Treating Patients with ALK Positive Stage IIIB-IV Non-small Cell Lung Cancer
- Able to swallow and retain orally administered medication and does not have any clinically significant gastrointestinal abnormalities that may alter absorption such as malabsorption syndrome or major resection of the stomach or bowels
- Women of childbearing potential must have a negative serum pregnancy test within 3 days prior to cycle 1 day 1 and agree to use effective contraception, throughout the treatment period, and for 4 months after the last dose of study treatment
- Patients must have histologically or cytological confirmed stage IIIB or IV non-small cell lung cancer
- Documented ALK-rearrangement (or ROS1 rearrangement for phase I only) break-apart fluorescence in situ hybridization (FISH) (in >= 15% or tumor cells), or next generation sequencing assay performed on tumor sample or cell-free DNA in Clinical Laboratory Improvement Amendments (CLIA)-approved laboratory
- Measurable disease defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
- Life expectancy of at least 3 months
- Resolution of all acute toxic effects of prior chemotherapy, immunotherapy, radiotherapy or surgical procedures to =< grade 2 (Common Terminology Criteria for Adverse Events [CTCAE] version [v] 4.03); exception to this criterion: patients with any grade of alopecia are allowed to enter the treatment
- Absolute neutrophil count (ANC) >= 1.5 x 10^ 9/L
- Hemoglobin (Hgb) >= 9 g/dL
- Platelets >= 75 x 10^9/L
- Prothrombin time (PT)/international normalized ratio (INR) and partial thromboplastin time (PTT) =< 1.5 x upper limit of normal (ULN)
- Serum creatinine =< 1.5 mg/dL and /or calculated creatinine clearance (using Cockcroft-Gault formula) >= 30 mL/min
- Albumin >= 2.5 g/dL
- Total bilirubin =< 1.5 x upper limit of normal (ULN), except for patients with Gilbert’s syndrome who may be included if total bilirubin =< 3.0 x ULN or direct bilirubin =< 1.5 x ULN
- Aspartate transaminase (AST) =< 2.5 x ULN; alanine transaminase (ALT) =< 2.5 x ULN, except for patients with liver metastasis, who are only included if AST and ALT < 5 x ULN
- Alkaline phosphatase (ALP) =< 5.0 x ULN
- Fasting plasma glucose =< 175 mg/dL (=< 9.8 mmol/L)
- Serum amylase =< 2 x ULN
- Serum lipase =< ULN in the absence of another known extrapancreatic cause of elevated serum lipase, including recent appendicitis, cholecystis, or severe gastroenteritis
- Patient must have the following laboratory values or have the following laboratory values corrected with supplements to be within normal limits before the first dose of ceritinib + trametinib: * Potassium * Magnesium * Phosphorus * Total calcium (corrected for serum albumin)
- Left ventricular ejection fraction (LVEF) >= lower limit of normal (LLN) by echocardiogram (ECHO) or multigated acquisition scan (MUGA)
- Patient has the ability to understand and provide signed informed consent
- Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests and other study procedure
- PHASE II DOSE EXPANSION COHORTS: * Documented ALK-rearranged stage IIIB or IV NSCLC and: ** Cohort A: No prior ALK inhibitor therapy (prior chemotherapy or immunotherapy is allowed) ** Cohort B: Prior treatment with crizotinib and documented disease progression by RECIST 1.1 criteria ** Cohort C: Prior treatment with 2nd generation ALK inhibitor (ALKi) (e.g. ceritinib, alectinib, loratinib, or brigatinib) and documented disease progression by RECIST 1.1 criteria
- Patients with known hypersensitivity to any of the excipients of ceritinib (microcrystalline cellulose, mannitol, crospovidone, colloidal silicon dioxide and magnesium stearate)
- Patient has history of interstitial lung disease or interstitial pneumonitis, including clinically significant radiation pneumonitis (i.e., affecting activities of daily living or requiring therapeutic intervention)
- Patient who has received thoracic radiotherapy to lung fields =< 4 weeks prior to starting the study treatment or patients who have not recovered from radiotherapyrelated toxicities; for all other anatomic sites (including radiotherapy to thoracic vertebrae and ribs) radiotherapy =< 2 weeks prior to starting the study treatment or has not recovered from radiotherapyrelated toxicities; palliative radiotherapy for bone lesions =< 2 weeks prior to starting study treatment is allowed
- Prior systemic anti-cancer treatment (chemotherapy, immunotherapy, biologic therapy, vaccine therapy, or investigational treatment) within the last 3 weeks, or chemotherapy without delayed toxicity within the last 2 weeks preceding the first dose of the combination; prior systemic treatment in the adjuvant setting is allowed
- Patient has clinically significant, uncontrolled heart disease and/or recent cardiac event (within 6 months), such as: * Unstable angina within 6 months prior to screening; * Myocardial infarction within 6 months prior to screening; * History of documented congestive heart failure (New York Heart Association functional classification III-IV); * Uncontrolled hypertension defined by a systolic blood pressure (SBP) >= 160 mm Hg and/or diastolic blood pressure (DBP) >= 100 mm Hg, with or without antihypertensive medication. * Initiation or adjustment of antihypertensive medication(s) is allowed prior to screening; * Ventricular arrhythmias * Supraventricular and nodal arrhythmias not controlled with medication; * Other cardiac arrhythmia not controlled with medication; * Corrected QT (QTcF) > 470 ms using Fridericia’s correction on the screening electrocardiography (ECG)
- Patient has impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of orally administered medication (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, or malabsorption syndrome)
- Receiving medications that meet one of the following criteria and that cannot be discontinued at least 1 week prior to the start of treatment with ceritinib and for the duration of participation: * Medication with a known risk of prolonging the QT interval or inducing torsades de pointes * Strong inhibitors or strong inducers of CYP3A4/5 * Medications with a low therapeutic index that are primarily metabolized by CYP3A4/5, and/or CYP2C9 * Therapeutic doses of warfarin sodium (Coumadin) or any other coumadin-derived anticoagulant * Anticoagulants not derived from warfarin are allowed (eg, dabigatran, rivaroxaban, apixaban) * Unstable or increasing doses of corticosteroids; If patients are on corticosteroids for endocrine deficiencies or tumor-associated symptoms, dose must have been stabilized (or decreasing) for at least 5 days before first dose of study treatment * Enzyme-inducing anticonvulsive agents * Herbal supplements
- Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive human chorionic gonadotropin (hCG) laboratory test
- Women of childbearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during dosing and for 3 months after the last dose of study treatment; highly effective contraception methods include: * Total abstinence (when this is in line with the preferred and usual lifestyle of the subject); periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception * Female sterilization (have had surgical bilateral oophorectomy with or without hysterectomy) or tubal ligation at least six weeks before taking study treatment; in case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment * Male sterilization (at least 6 months prior to screening) with the appropriate post-vasectomy documentation of the absence of sperm in the ejaculate; for female subjects on the study the vasectomized male partner should be the sole partner for that subject * Combination of any two of the following: ** Use of oral, injected or implanted hormonal methods of contraception or other forms of hormonal contraception that have comparable efficacy (failure rate < 1%), for example hormone vaginal ring or transdermal hormone contraception ** Placement of an intrauterine device (IUD) or intrauterine system (IUS) ** Barrier methods of contraception: condom or occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/vaginal suppository
- In case of use of oral contraception, women should have been stable on the same pill for a minimum of 3 months before taking study treatment
- Women are considered post-menopausal and not of child bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile. (e.g., age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks prior to screening; in the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment is she considered not of child bearing potential
- Sexually active males unless they use a condom during intercourse while taking drug and for 3 months after the last dose of study treatment; male patients for 3 months should not father a child in this period; a condom is required to be used also by vasectomized men in order to prevent delivery of the drug via seminal fluid
- Patient has a history of pancreatitis or history of increased amylase or lipase that was due to pancreatic disease
- Patient has other severe, acute, or chronic medical conditions including uncontrolled diabetes mellitus or psychiatric conditions or laboratory abnormalities that, in the opinion of the investigator, may increase the risk associated with study participation or may interfere with the interpretation of study results
- Patient has had major surgery (e.g., intrathoracic, intraabdominal or intrapelvic) within 4 weeks prior to starting study treatment or has not recovered from side effects of such procedure; video-assisted thoracic surgery (VATS) and mediastinoscopy will not be counted as major surgery and patients can receive study treatment >= 1 week after these procedures
- History of another malignancy; exception: subjects who have been disease-free for 3 years, or subjects with a history of completely resected non-melanoma skin cancer and/or subjects with indolent (early stage breast cancer or prostate cancer) second malignancies are eligible after discussion with the study principal investigator (PI)
- History of retinal vein occlusion (RVO)
- Symptomatic brain metastases or leptomeningeal (LM) disease requiring corticosteroids for symptom management; asymptomatic brain metastases or LM will be allowed on study
- Known human immunodeficiency virus (HIV), hepatitis B Virus (HBV), or hepatitis C Virus (HCV) infection (subjects with laboratory evidence of cleared HBV and HCV infection will be permitted)
I. To determine the safety and tolerability of the combination of ceritinib and trametinib in stage IIIB or IV ALK or ROS-1 rearranged non-small cell lung cancer (NSCLC).
I. To describe any preliminary efficacy of ceritinib in combination with trametinib in patients with stage IIIB or IV ALK-rearranged NSCLC in the first, second, or third line setting.
II. To describe the pharmacokinetics associated with ceritinib when administered combination with study drug trametinib.
I. To identify biomarkers of clinical benefit and mechanisms of resistance (de novo resistance, incomplete response, and acquired resistance) to ceritinib + trametinib combination therapy in ALK + NSCLC.
II. Assess circulating tumor deoxyribonucleic acid (DNA) (ctDNA) for biomarkers of response and/or resistance to ceritinib + trametinib.
OUTLINE: This is a phase I, dose-escalation study followed by a phase II study.
Patients receive ceritinib orally (PO) once daily (QD) and trametinib PO QD on days 1-28. Cycles repeat every 28 days for up to 24 months in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up every 3 months for up 1 year.
Trial Phase Phase I/II
Trial Type Treatment
University of California San Francisco
Collin Michael Blakely
- Primary ID 166512
- Secondary IDs NCI-2017-01318, 16-20614
- Clinicaltrials.gov ID NCT03087448