Anetumab Ravtansine in Treating Patients with Mesothelin Expressing Stage IIIB-IV Lung Cancer That Cannot Be Removed by Surgery
This phase I/II trial studies the side effects and best dose of anetumab ravtansine and to see how well it works in treating patients with mesothelin expressing stage IIIB-IV lung cancer that cannot be removed by surgery. Monoclonal antibodies, such as anetumab ravtansine, may find tumor cells and help kill them.
Inclusion Criteria
- Subjects must have histologically or cytologically confirmed previously treated unresectable mesothelin expressing advanced lung adenocarcinoma (stage IIIB or IV) as confirmed by the Laboratory of Pathology, National Cancer Institute (NCI)
- Subjects must have positive mesothelin expression in the archival tumor tissue, defined as the mesothelin membrane intensity score of 2+ or 3+ (on the 0-3 scale) expressed on the membrane of >= 10% of tumor cells
- Subjects must provide sample of archival tumor tissue (tissue block preferred, at least 5 formalin-fixated, paraffin-embedded [FFPE] slides acceptable) collected any time before the general screening; a fresh biopsy will be collected if archival sample is unavailable or insufficient
- Subjects must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded for non-nodal lesions and short axis for nodal lesions) as >= 20 mm with conventional techniques or as >= 10 mm with spiral computed tomography (CT) scan
- Subjects with resected primary tumors who have documented metastases are eligible
- Subjects should have received at least one prior platinum based chemotherapy and an immune checkpoint targeted agent; subjects with epidermal growth factor receptor (EGFR)-mutated and anaplastic lymphoma kinase (ALK)-translocated non-small cell lung cancer (NSCLC) should have received Food and Drug Administration (FDA)-approved targeted therapies as appropriate
- Eastern Cooperative Oncology Group (ECOG) performance status =< 2
- Hemoglobin >= 9.0 g/dL or >= 5.6 mmol/L
- Absolute neutrophil count (ANC) >= 1,500/mm^3 or >= 1.5 x 10^9/L
- Platelet count >= 100,000/mm^3 or >= 100 x 10^9/L
- Subjects must have adequate kidney function, with serum creatinine < 1.5 x upper limit of normal (ULN) or calculated glomerular filtration rate (GFR) of > 45/mL/min/1.73 m^2
- Total bilirubin =< 1.5 times the upper limit of normal (ULN)
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =< 3.0 times ULN in subjects without liver metastases or =< 5.0 times ULN in subjects with liver metastases
- International normalized ratio (INR) or prothrombin time (PT) =< 1.5 x ULN
- Partial thromboplastin time (PTT) =< 1.5 x ULN
- Subjects must use 2 forms of highly effective contraception concomitantly from the initiation of study therapy until 6 months after the last dose of study therapy; additionally, the use of condoms is required; it should also be noted that, where 2 forms of effective contraception are required, a subject may choose to use a double-barrier method consisting of condom and cervical occlusive cap / diaphragm with spermicide
- Ability of subject to understand and the willingness to sign a written informed consent document
- Subjects must provide a signed informed consent before any screening procedures
Exclusion Criteria
- Subjects who have a previous or concurrent cancer that is distinct in primary site or histology from lung adenocarcinoma, except cervical carcinoma in situ, treated basal cell carcinoma, superficial noninvasive bladder tumors or any previous cancer curatively treated < 2 years before the start of study treatment
- Subjects who have a history or current evidence of bleeding disorder, i.e. any hemorrhage/bleeding event of Common Terminology Criteria for Adverse Events (CTCAE) grade >= 2 within 4 weeks before the start of study treatment
- History of symptomatic metastatic brain or meningeal tumors unless the subject is > 3 months from definitive therapy and has no evidence of tumor growth on an imaging study within 2 weeks prior to study entry; subjects with brain metastases must not be undergoing acute corticosteroid therapy or steroid taper; chronic steroid therapy is acceptable provided that the dose is stable for one month prior to screening
- Subjects who have a history or current evidence of uncontrolled cardiovascular disease including but not limited to the following conditions: * Congestive heart failure of New York Heart Association (NYHA) class III or IV * Unstable angina (symptoms of angina at rest) or new-onset angina within < 3 months before the start of study treatment * Arterial thrombosis, deep vein thrombosis, or pulmonary embolism within < 3 months before the start of study treatment * Myocardial infarction or stroke within < 3 months before the start of study treatment * Pericarditis (any CTCAE grade), pericardial effusion (CTCAE grade >= 2) or pleural effusion (CTCAE grade >= 2) * Cardiac arrhythmia requiring anti-arrhythmic therapy; subjects receiving digoxin, calcium channel blockers except verapamil, or beta-adrenergic blockers except propranolol are eligible at the investigator’s discretion if the dose has been stable for at least 2 weeks before the start of study treatment; subjects with sinus arrhythmia and infrequent premature ventricular contractions are eligible at the investigator’s discretion
- Subjects who have a left ventricular ejection fraction (LVEF) < 50%, as assessed by echocardiogram performed at screening
- Subjects who have a corrected QT (Fridericia's correction formula [QTcF]) interval > 480 milliseconds (ms) (CTCAE grade > 1) determined by the electrocardiogram (ECG) recorder’s algorithm on the screening ECG
- Subjects who have a history or current evidence of uncontrolled hypertension defined as systolic blood pressure > 150 mmHg or diastolic blood pressure > 95 mmHg at screening despite optimal medical management; subjects with a history of mild to moderate hypertension are eligible at the investigator’s discretion if the hypertension is adequately controlled by antihypertensive treatment used at a stable dose for at least 2 weeks before the start of study treatment
- Subjects who have a heart rate >= 100 beats per minute (bpm) or =< 45 bpm determined by the ECG recorder’s algorithm on the screening ECG
- Women who are pregnant or breast-feeding; women of reproductive potential must have a negative serum beta human chorionic gonadotropin (beta-HCG) pregnancy test obtained within 7 days before the start of study treatment
- Subjects who have had a major surgery or significant trauma within 4 weeks before the start of study treatment
- Subjects who have had solid organ or bone marrow transplantation
- Subjects who have a history of hypersensitivity to any of the study drugs or their excipients, or a history of severe hypersensitivity to any other antigen
- Subjects who have a history of human immunodeficiency virus (HIV) infection or subjects who have an active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection requiring treatment due to a theoretical concern that the degree of immune suppression associated with the treatment may result in progression of HIV infection; subjects with chronic HBV or HCV infection are eligible at the investigator’s discretion if the subject is considered non-infectious based on serological markers
- Subjects who have an active clinically serious infection of CTCAE grade >= 2
- Subjects with a non-healing serious wound, ulcer, or bone fracture unrelated to the primary tumor
- Subjects with corneal epitheliopathy or any eye disorder that may predispose the subjects to drug-induced corneal epitheliopathy, or may interfere with diagnosis of treatment-emergent corneal epitheliopathy at the discretion of the investigator in consultation with the ophthalmologist/optometrist; low grades of superficial punctate keratitis, within the range seen in the normal population, should not lead to the exclusion of the patient
- Subjects experiencing unresolved toxicity of previous antitumor therapy which is CTCAE grade > 1 before the start of study treatment, except for alopecia or hemoglobin >= 9.0 g/dL or >= 5.6 mmol/L
- Subjects with any clinical condition that is considered unstable or might jeopardize the safety of the subject and/or influence the subject’s compliance in the study
- Subjects who have received systemic anticancer therapy within 3 weeks before the start of study treatment; mitomycin C or nitrosoureas must be excluded within 6 weeks before the start of study treatment
- Subjects who have received radiotherapy to tumor lesions that would be chosen as target lesions (measurable disease) within 4 weeks before the start of treatment, except if there is objective evidence of progression of the lesion by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 between the prior radiotherapy and the screening CT or magnetic resonance imaging (MRI) scan; palliative radiotherapy to non-target lesions is allowed at the investigator’s discretion
- Use of drugs that inhibit renal tubular secretion (e.g. probenecid and cimetidine) within 2 weeks before the start of study treatment
- Use of strong cytochrome P450 family 3 subfamily A member 4 (3A4) (CYP3A4) inhibitors or strong CYP3A4 inducers within 2 weeks before the start of study treatment
- Subjects who have previously received anetumab ravtansine
- Subjects who are concurrently receiving any other investigational agents
Additional locations may be listed on ClinicalTrials.gov for NCT02839681.
See trial information on ClinicalTrials.gov for a list of participating sites.
PRIMARY OBJECTIVES:
I. To evaluate safety and tolerability of anetumab ravtansine in patients with previously treated unresectable mesothelin expressing advanced lung adenocarcinoma (stage IIIB or IV). (Safety Run-in)
II. To determine the efficacy (objective response rate) of anetumab ravtansine in patients with previously treated, unresectable, advanced (stage IIIB) or metastatic (stage IV) mesothelin expressing lung adenocarcinoma. (Phase II)
SECONDARY OBJECTIVES:
I. To determine the duration of response, progression free survival, overall survival in the study population.
II. To correlate mesothelin expression with clinical activity defined as partial response and complete response.
TERTIARY OBJECTIVES:
I. To determine if treatment with anetumab ravtansine induces a humoral response to mesothelin and to correlate a response (if any) with tumor characteristics.
II. To characterize the molecular changes that occur within the tumors following treatment with anetumab ravtansine.
III. To assess myeloid derived suppressor cells in subjects with lung adenocarcinoma.
OUTLINE: This is a phase I, dose de-escalation study of anetumab ravtansine, followed by a phase II study.
Patients receive anetumab ravtansine intravenously (IV) over 1 hour on day 1. Courses repeat every 3 weeks until disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up at 30 days, every 6 weeks in the first 6 months, every 9 weeks until the end of year 2, and every 12 weeks thereafter.
Trial PhasePhase I/II
Trial Typetreatment
Lead OrganizationNCI - Center for Cancer Research
Principal InvestigatorRaffit Hassan
- Primary ID16-C-0145
- Secondary IDsNCI-2016-01153
- ClinicalTrials.gov IDNCT02839681