BGJ398 in Combination With Imatinib Mesylate in Patients With Untreated Advanced Gastrointestinal Stromal Tumor (GIST)

• Status: Completed
• Trial end date: 2019-03-25
• Target enrollment: 0
• Participant gender: All

Summary

The goal of a phase Ib clinical trial is to find the doses of drugs that are safe. Although BGJ398 has been given to patients safely on its own, it has never been given together with imatinib mesylate. In this study, we will test the safety of taking BGJ398 with imatinib mesylate. The investigators will learn this by closely checking for side effects that the patient may experience. Side effects can be seen in laboratory studies, on physical examination, or by asking the patient.Once a dose has been determined to be safe, a larger Phase II study will be done in patients with advanced GIST who have never received any prior treatments.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Memorial Sloan Kettering Cancer Center
• Collaborators: Dana-Farber Cancer Institute; M.D. Anderson Cancer Center; University of Pittsburgh
• Treatments: Imatinib Mesylate; Infigratinib

Criteria

Inclusion Criteria:

• Patients must have pathologically confirmed GIST.

• In the Phase Ib portion, must have locally advanced or metastatic GIST and have progressed on imatinib.

• In the Phase II portion, patients must be newly diagnosed or imatinib treatment naïve in the advanced/metastatic setting. Prior adjuvant imatinib therapy is allowed as long as disease recurrence was documented ≥90 days after last dose of imatinib and imatinib has not yet been restarted.

• Patients must be at least 18 years of age.

• Disease must be measurable by RECIST 1.1.

• ECOG Performance Status 0 or 1. Adequate renal, hepatic, and hematologic function as the following: Serum Creatinine ≤ 1.5 mg/dL, Total Serum Bilirubin ≤ 1.5 x upper limit of normal (ULN) unless due to Gilbert's Disease, Serum AST (SGOT) and/or ALT (SGPT) ≤ 2.5 x ULN (or ≤ 5.0 x ULN if considered due to tumor), ANC ≥ 1500/mm3, Platelets ≥ 100,000/mm3, and hemoglobin ≥ 10g/dL.

• Patients of childbearing potential must have a negative blood pregnancy test within 14 days of treatment. Patients must agree to use a reliable barrier method of birth control during and for 3 months following the last dose of study drug.

• Patient must have adequate cardiac function (left ventricular ejection fraction (LVEF) ≥50% as determined by a multigated acquisition (MUGA) scan or echocardiogram; and QTc interval ≤480 ms by Fridericia's formula (QTcF).

• Patient must be able to take oral medications.

• Patients must sign an informed consent document.

Exclusion Criteria:

• For phase I, prior intolerance to imatinib at a dose of 400 mg daily.

• For phase II, any receipt of cytotoxic, biologic, or immune therapy aimed to treat GIST except for adjuvant imatinib systemic therapy that concluded at least 90 days prior to registration. For Phase I, patients are eligible regardless of prior therapy.

• Chronic liver disease (e.g., cirrhosis)

• Known positive serology for HIV, active Hepatitis B, and/or active Hepatitis C infection.

• Patients have a history or current evidence of Central Serous Retinopathy (CSR) or retinal vein occlusion (RVO) or major predisposing factors to CSR or RVO (e.g. uncontrolled glaucoma or ocular hypertension) in the opinion of the study ophthalmologist.

• History of retinal degenerative disease

• Active corneal disorder or keratopathy (e.g. corneal abrasion, bullous keratopathy)

• Severe and/or uncontrolled medical disease, including:

• Uncontrolled diabetes mellitus (A1c >8)

• Chronic Kidney Disease Stage III or higher (Creatinine Clearance <60mL/min/m2 by Modified Diet in Renal Disease (MDRD) calculation)

• Active, uncontrolled infection Known active brain metastasis unless they have been treated and shown documented radiographic stability for 28 days.

• Known other active malignancy (other than malignancies which the investigator determines are unlikely to interfere with treatment and safety analysis).

• Patients have clinically significant cardiovascular disease, including any of the following

• Any history of acute coronary syndrome including myocardial infarction, stable or unstable angina, CABG, coronary angioplasty or stenting or known obstructive coronary artery disease.

• Symptomatic chronic heart failure (New York Heart Association Criteria, Class II-IV)

• Evidence of clinically significant cardiac arrhythmias and/or conduction abnormalities < 6 months prior to screening except atrial fibrillation (AF) and paroxysmal supraventricular tachycardia (PSVT)

• Any history of thrombotic cerebrovascular accident or other arterial thrombosis

• Uncontrolled arterial hypertension (systolic blood pressure >155 mmHg or diastolic >95 mmHg) despite appropriate medical therapy.

• History and/or current evidence of uncontrolled endocrine alterations of calcium/phosphate homeostasis, e.g., parathyroid disorders, history of parathyroidectomy, tumor lysis, tumoral calcinosis, etc.

• Impairment of gastrointestinal function or gastrointestinal disease (e.g., uncontrolled ulcerative disease; uncontrolled nausea, vomiting, diarrhea; chronic malabsorption syndrome).

• Patients with major surgery within 3 weeks prior to study entry or who have not recovered from side effects of such procedure.

• Women who are pregnant or lactating.

• Sexually active males, unless they use a condom during intercourse while taking the drug and for 15 days after stopping treatment. They 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.

• Patients with any significant history of non-adherence to medical regimens or with inability to grant reliable informed consent.