Metastatic Pancreas Adenocarcinoma Clinical Trial
— FABLOxOfficial title:
An Open Label, Multicenter, Single Arm, Phase 1/2 Trial of Metronomic 5-fluorouracil in Combination With Nab-paclitaxel, Bevacizumab, Leucovorin, and Oxaliplatin in Patients With Metastatic Pancreatic Adenocarcinoma.
| Verified date | October 2019 |
| Source | Celgene |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this study is to learn about the safety and potential benefit of metronomic 5-fluorouracil in combination with nab®1-paclitaxel, bevacizumab, leucovorin, and oxaliplatin in treating patients with metastatic pancreatic adenocarcinoma.
| Status | Completed |
| Enrollment | 12 |
| Est. completion date | October 29, 2018 |
| Est. primary completion date | October 29, 2018 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: A subject will be eligible for inclusion in this study only if all of the following criteria are met: 1. Male or female subject is between 18 and 65 years of age at the time of signing the Informed Consent Form (ICF). 2. Subject has definitive histologically or cytologically confirmed metastatic pancreatic adenocarcinoma. 3. Subject has an Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0-1. 4. Subject has one or more tumors measurable by CT scan (or (MRI), if allergic to CT contrast media) as defined by Response Evaluation Criteria In Solid Tumors (RECIST) 1.1. 5. Subject has the following blood counts / Hemoglobin (Hgb) at screening: - Absolute neutrophil count (ANC) = 1.5 × 10^9/L; - Platelet count = 100,000/mm3 (100 × 10^9/L); - Hgb = LLN or 10 g/dL. 6. Subject has the following blood chemistry levels at screening: - AST (SGOT), ALT (SGPT) = 2.5 x upper limit of normal range (ULN); if hepatic metastases present = 5.0 x ULN - Total bilirubin = 1.5 X ULN - Creatinine clearance = 60 mL/min (by Cockroft-Gault) - Albumin = 3.5 grams/dL7. 7. Females of childbearing potential (FOCBP) [defined as a sexually mature woman who (1) have not undergone hysterectomy (the surgical removal of the uterus) or bilateral oophorectomy (the surgical removal of both ovaries) or (2) have not been naturally postmenopausal for at least 24 consecutive months (ie, has had menses at any time during the preceding 24 consecutive months)] must: - Have a negative pregnancy test (ß-human chorionic gonadotropin [ß -hCG]) as verified by the study doctor within 72 hours prior to starting study therapy - Commit to complete abstinence from heterosexual contact, or agree to use medical doctor-approved contraception throughout the study without interruption; while receiving study medication and for at least 6 months following last dose of study IP. 8. Males must practice complete abstinence or agree to use a condom (even if he has undergone a successful vasectomy) during sexual contact with a pregnant female or a female of childbearing potential while participating in the study, during dose interruptions and for at least 6 months following last dose of study IP. 9. Subject has no clinically significant abnormalities in urinalysis results at baseline. 10. Subject is able to adhere to the study visit schedule and other protocol requirements. 11. Subject understands the nature of the study, and has agreed to participate in the study, and has voluntarily signed the ICF prior to participation in any study-related activities. 12. Subject must consent to provide protocol-mandated tumor and blood samples for molecular analysis. 13. Subject is willing and able to adhere to the study visit schedule and other protocol requirements Exclusion Criteria: A subject will not be eligible for inclusion in this study if any of the following criteria apply: 1. Subject has received previous systemic chemotherapy or investigational therapy (other than that as a radiosensitizer concomitant with radiotherapy) for the treatment of pancreatic adenocarcinoma, including neo-adjuvant or adjuvant therapy. 2. Subject has known brain metastases unless previously treated and controlled for a minimum of 2 weeks prior to enrollment. Subject is not receiving corticosteroids with no evidence of cerebral edema. 3. Pre-existing peripheral neuropathy > Grade 1 4. Subject with unstable stent. 5. History of malignancy in the last 3 years. Subjects with prior history of in situ cancer or basal or squamous cell skin cancer are eligible. Subjects with other malignancies are eligible if they were cured by surgery alone or surgery plus radiotherapy and have been continuously disease-free for at least 3 years. 6. Subject has active, uncontrolled bacterial, viral, or fungal infection(s) requiring systemic therapy , defined as ongoing signs/symptoms related to the infection without improvement despite appropriate antibiotics, antiviral therapy, and/or other treatment. 7. Subject has known historical or active infection with human immunodeficiency virus (HIV), hepatitis B, or hepatitis C or subject receiving immunosuppressive or myelosuppressive medications that would, in the opinion of the Investigator, increase the risk of serious neutropenic complications. 8. Subject has undergone major surgery, other than diagnostic surgery (ie, surgery done to obtain a biopsy for diagnosis without removal of an organ), within 4 weeks prior to Day 1 of treatment in this study or surgical wound has not fully healed. 9. Subject has a history of allergy or hypersensitivity to any of the IP or any of their excipients, or the subject exhibits any of the events outlined in the Contraindications or Special Warnings and Precautions sections for and of the products' Summary of Product Characteristics or Prescribing Information. 10. History of connective tissue disorders (eg, lupus, scleroderma, arteritis nodosa). 11. Subject with a history of interstitial lung disease, history of slowly progressive dyspnea and unproductive cough, sarcoidosis, silicosis, idiopathic pulmonary fibrosis, pulmonary hypersensitivity pneumonitis or multiple allergies that in the opinion of the Investigator may put them at increased risk of interstitial pneumonitis. 12. Subject with high cardiovascular risk, including, but not limited to: - uncontrolled hypertension - unstable angina - diagnosis of ischemic heart disease - heart disease of New York Heart Association functional classification = 3 (see Appendix C) - prior history of hemorrhagic or thrombolytic stroke - prior exposure to anthracycline - history of peripheral artery disease (eg, claudication, Leo Buerger's disease) - any of the following within the prior 6 months - coronary stenting - myocardial infarction - coronary bypass surgery 13. Recent history of clinically significant hemoptysis. 14. Pregnant and nursing (lactating) women. 15. Any significant medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from participating in the study. 16. Subject has any condition including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study. 17. Subject has any condition that confounds the ability to interpret data from the study. |
| Country | Name | City | State |
|---|---|---|---|
| United States | University of Michigan | Ann Arbor | Michigan |
| United States | Tufts - New England Medical Center | Boston | Massachusetts |
| United States | Northwestern University | Chicago | Illinois |
| United States | Karmanos Cancer Center Wayne State University | Detroit | Michigan |
| United States | Cornell University Weill Medical College | New York | New York |
| United States | Virginia Mason Cancer Center | Seattle | Washington |
| United States | Gibbs Cancer Center and Research Institute | Spartanburg | South Carolina |
| Lead Sponsor | Collaborator |
|---|---|
| Celgene |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Dose limiting toxicities (Phase 1) | • Any toxicity starting during the first 28 days of treatment and requiring 14 days or more of treatment interruption • Grade 3 or 4 neutropenia associated with fever > 38.5°C • Grade 3 anemia requiring a transfusion • Any Grade 4 hematological toxicity lasting > 7 days • Grade 4 thrombocytopenia or a Grade 3 or 4 thrombocytopenia associated with clinically significant bleeding • Grade 3 or 4 non-hematological toxicity with the exception of fatigue, due to any of the study drugs and unresponsive to medical treatment within 4 days of onset • Subjects who experience Grade = 3 hyperbilirubinemia as an apparent DLT. If a Phase 1 subject experiences a Grade = 3 hyperbilirubinemia due principally to unconjugated bilirubin, it will not be defined as a DLT. The subject will be removed from the study and the Phase 1 subject will be replaced. • Any non-hematologic toxicity delaying the initiation of cycle 2 by > 21 days • Grade = 2 pneumonitis or interstitial lung disease | Up to Day 1 of Cycle 2 | |
| Primary | 1 year survival rate (Phase II portion) | 1 year survival rate is defined as the time interval between the date of first dose of Investigational Product (IP) and the date of death. | Up to 1 year | |
| Primary | Number of subjects experiencing Adverse Events (AEs) by severity and overall tabulations by cohort and overall including treatment emergent and Serious AEs | An AE is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a subject during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the subject's health, including laboratory test values, regardless of etiology. All AEs will be recorded by the Investigator from the time the subject signs informed consent until 28 days after the last dose of IP as well as those SAEs made known to the Investigator at any time thereafter that are suspected of being related to Investigational Product. | Up to 4 years | |
| Secondary | Summary for the number of subjects experiencing Adverse Events (AEs) by severity and overall in tabulations by cohort and overall including treatment emergent AEs and Serious AEs | An AE is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a subject during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the subject's health, including laboratory test values, regardless of etiology. All AEs will be recorded by the Investigator from the time the subject signs informed consent until 28 days after the last dose of IP as well as those SAEs made known to the Investigator at any time thereafter that are suspected of being related to IP | Up to 4 years | |
| Secondary | Objective Response Rate using Response Evaluation Criteria In Solid Tumours (Recist) v1.1 presented by frequency and percentages | Subjects with confirmed complete or partial response (CR and PR) will be presented by 95% Confidence Intervals (CIs) around the proportion of (CR+PR)/N where N is the total number of subjects who are evaluable for response by RECIST criteria. | Up to 4 years | |
| Secondary | Progression free survival (PFS) | The time interval between the date of first dose of IP until disease progression or death, whichever occurs first. | Up to 4 years | |
| Secondary | Overall Survival (OS) | OS is defined as the time interval between the date of first dose of IP and the date of death. | Up to 4 years | |
| Secondary | Percentage of subjects with symptom improvement | The Pancreatic cancer symptom management using: Functional Assessment Solid Tumors Hepatobiliary Symptom Index-8 (FHSI-8) questionaire will evaluate individual symptom improvement from baseline will be analyzed by different levels of improvement separately, ie, by reduction of score 1, 2, 3, and 4. At any given follow-up time point, the subject is classified having symptom improvement if the subject has reduced symptom severity compared to baseline regardless of subsequent symptom score. | Up to 4 years | |
| Secondary | Percentage of subjects with symptom improvement between subjects who experienced at least partial response and those without partial response | The FHSI-8 assessment will measure the correlation of symptom improvement between those who experienced a Partial Response (PR) to those without a PR. | Up to 4 years | |
| Secondary | Percentage of subjects who experienced symptom improvement by a score of = 2 | The FHSI-8 assessment will measure the correlation of symptom improvement with Eastern Cooperative Oncology Group (ECOG) performance status (PS) over the course of treatment | Up to 4 years |