Bemcentinib with Chemotherapy in Treating Patients with Metastatic or Recurrent Pancreatic Cancer

Inclusion Criteria

• Ability to understand and the willingness to sign a written informed consent
• Patients must have histologically or cytologically confirmed recurrent or metastatic pancreatic adenocarcinoma
• No prior systemic therapy for metastatic or recurrent disease * Prior adjuvant therapy, if completed more than 6 months prior to date of enrollment, is acceptable * Radiosensitizing chemotherapy, if completed at least 4 weeks from date of enrollment, is acceptable
• Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria
• Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
• Have resolution of toxic effect(s) or intervention complication to grade 1 or less (except alopecia) from any prior chemotherapy, major surgery or radiation therapy of > 30 Gy
• Hemoglobin >= 10 g/dL (within 14 days of date of enrollment)
• Absolute neutrophil count (ANC) >= 1,500/uL (within 14 days of date of enrollment)
• Platelets >= 100,000/uL (within 14 days of date of enrollment)
• Total bilirubin < 1.5 x institutional upper limit of normal (ULN) (within 14 days of date of enrollment)
• Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 2.5 x institutional ULN in patients without known liver metastasis; =< 5 x institutional ULN in patients with known liver metastasis (within 14 days of date of enrollment)
• Serum creatinine =< 1.5 times ULN, and calculated creatinine clearance >= 60 mL/min using the Cockcroft-Gault equation) (within 14 days of date of enrollment)
• International normalized ratio (INR) or prothrombin time (PT) =< 1.5 times the ULN (within 14 days of date of enrollment)
• Albumin >= 3.0 g/dL (within 14 days of date of enrollment)
• Female patients of childbearing potential must have a negative pregnancy test (either urine or serum pregnancy test). If the urine pregnancy test is positive or cannot be confirmed as negative, a serum pregnancy test will be required. A female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria: * Has not undergone a hysterectomy or bilateral oophorectomy; or * Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months)
• Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and for 120 days following completion of therapy. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician, or study team member, immediately

Exclusion Criteria

• Is currently participating and receiving study therapy in a first line setting for metastatic or reccurrent pancreatic adenocarcinoma
• Participated in a study of an investigational agent or used an investigational device within 4 weeks of the first dose of study treatment.
• Patients with known untreated brain metastases. Patients without known brain metastases do not require radiologic imaging prior to enrollment
• Has a known additional malignancy that is progressing or requires active treatment. Note: Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, significant pulmonary disease (shortness of breath at rest or mild exertion), or uncontrolled infection or psychiatric illness/social situations that would limit compliance with study requirements
• History of the following cardiac conditions: * Congestive cardiac failure of > grade II severity according to the New York Heart Association (NYHA) (defined as symptomatic at less than ordinary levels of activity) * Ischemic cardiac event including myocardial infarction within 3 months prior to date of enrollment * Uncontrolled cardiac disease, including unstable angina pectoris, uncontrolled hypertension (i.e. sustained systolic blood pressure [BP] > 160 mmHg or diastolic BP > 90 mmHg), cardiac arrhythmia, or need to change medication due to lack of disease control within 6 weeks prior to date of enrollment * History or presence of sustained bradycardia (=< 55 beats per minute [BPM]), left bundle branch block, cardiac pacemaker or ventricular arrhythmia. Note: Patients with a supraventricular arrhythmia requiring medical treatment, but with a normal ventricular rate are eligible * Known family history or personal history of long corrected QT (QTc) syndrome or previous drug-induced QTc prolongation of at least grade 3 (QTc > 500 ms)
• Abnormal left ventricular ejection fraction (LVEF) on echocardiography (ECHO) or multigated acquisition (MUGA) (less than the lower limit of normal for a patient of that age at the treating institution or < 45%)
• Current treatment with any agent known to cause Torsades de Pointes which cannot be discontinued at least five half-lives or two weeks prior to the first dose of study treatment
• Screening 12-lead electrocardiogram (ECG), in triplicate, with a measurable QTc interval according to Fridericia’s correction > 450 ms
• Known active infection with human immunodeficiency virus (HIV), hepatitis B or C viruses (screening not required, follow institutional practice): * Patients who have a history of hepatitis B infection are eligible provided they are hepatitis B surface antigen negative * Patients who have a history of hepatitis C infection are eligible provided they have no evidence of hepatitis C ribonucleic acid using a quantitative polymerase chain reaction assay at least 6 months after completing treatment for hepatitis C infection
• Active, clinically significant serious infection requiring treatment with antibiotics, anti-virals or anti-fungals
• Treatment with any medication which is predominantly metabolized by CYP3A4 and has a narrow therapeutic index
• Major surgery within 4 weeks prior to date of enrollment; excluding skin biopsies and procedures for insertion of central venous access devices
• Inability to tolerate oral medication
• Existing gastrointestinal disease affecting drug absorption such as celiac disease or Crohn’s disease, or previous bowel resection which is considered to be clinically significant or could interfere with absorption
• Known lactose intolerance
• Is pregnant or breastfeeding
• Any significant medical condition lab abnormality, or psychiatric illness, in the opinion of the investigator, that might interfere with the patient's participation in the study or in the evaluation of the study results
• Unwillingness or inability to comply with study procedures