A Study of Regorafenib in Advanced Pancreatic Cancer Patients

Phase 2CompletedNCT02080260

Wake Forest University Health Sciences20 enrolled

Overview

This study tests regorafenib as a single agent in the treatment of metastatic pancreatic cancer patients who have progressed after prior chemotherapy with gemcitabine. The prognosis for these patients is particularly grim, no other standard treatment options exist, and novel approaches are desperately needed.

This is a single arm, single stage Phase II study designed to evaluate progression free survival (PFS) in patients with metastatic pancreatic cancer who have failed at least one prior line of therapy and treatment with gemcitabine. This study is open at the Levine Cancer Institute (LCI). A total of 32 patients will be enrolled over a two years. Following informed consent and eligibility check, all patients will start oral regorafenib therapy (120 mg daily for 3 weeks on / 1 week off; 28 day cycle) with a built-in dose escalation to 160mg after the first cycle as tolerated, and will continue therapy until progression or patient withdrawal. Patients will undergo radiological staging after the first two cycles of regorafenib therapy. Patients with progressive disease will be removed from the study. Patients who have at least stable disease will continue regorafenib therapy, at the Investigator's discretion, and will be radiologically restaged bimonthly.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Pancreatic Cancer

Interventions

regorafenibDRUG

Single agent drug therapy with regorafenib

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Adenocarcinoma of the exocrine pancreas with metastatic disease. * The site of the primary tumor confirmed to have been within the pancreas. * Progression on at least one prior line of chemotherapy for locally-advanced or metastatic pancreatic cancer. * Progression while on treatment with a gemcitabine regimen for advanced pancreatic cancer, or within 12 months of treatment with gemcitabine as part of adjuvant therapy. * Measurable disease on axial imaging. * Age greater than or equal to 18 years. * Life expectancy of at least 8 weeks. * Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0-2. Enrollment of patients with PS = 2 will be capped at 7 patients. * Subjects must be able to understand and be willing to sign the written informed consent form. * Acute toxic effects except alopecia of any prior treatment must have resolved to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.0 Grade 1 or less. * Adequate bone marrow, renal, and liver function. * Warfarin or heparin will be allowed provided that there is no prior evidence of underlying coagulation abnormality. * Women of childbearing potential must have a negative pregnancy test performed within 7 days prior to the start of study drug. Post-menopausal women (defined as no menses for at least 1 year) and surgically sterilized women are not required to undergo a pregnancy test. * Patients (men and women) of childbearing potential must agree to use adequate contraception * Patient must be able to swallow and retain oral medication. Exclusion Criteria: * Previous assignment to treatment during this study. * Uncontrolled hypertension. * Active clinically significant cardiac disease. * Cerebrovascular arterial event within 6 months. * Evidence or history of bleeding diathesis or coagulopathy. * Any bleeding event greater than or equal to NCI CTCAE Grade 3 within 4 weeks. * New venous thrombotic or embolic events, such as deep vein thrombosis or pulmonary embolism within 3 months. * Previously untreated or concurrent cancer that is distinct in primary site or histology except cervical cancer in-situ, treated basal cell carcinoma, or superficial bladder tumor. Patients surviving a cancer that was curatively treated and without evidence of disease for more than 3 years are allowed. * Patients with pheochromocytoma. * Known history of HIV infection or current chronic or active hepatitis B or C, requiring antiviral medication. * Ongoing infection greater than or equal to Grade 2 NCI-CTCAE v4.0. * Symptomatic metastatic brain or meningeal tumors. * Presence of a non-healing wound, non-healing ulcer, or bone fracture. * Renal failure requiring dialysis. * Dehydration Grade greater than or equal to 1 NCI-CTCAE v4.0. * Patients with seizure disorder requiring medication. * Persistent proteinuria greater than or equal to Grade 3 NCI-CTCAE v4.0. * Symptomatic interstitial lung disease. * Pleural effusion or ascites that cause respiratory compromise. * History of organ allograft except corneal transplant. * Known or suspected allergy or hypersensitivity to the study drugs. * Any severe, uncontrolled malabsorption condition. * Women who are pregnant or breast-feeding. * Substance abuse, medical, psychological or social conditions that may interfere with the subject's participation in the study. * Concurrent anti-cancer therapy other than study treatment (regorafenib). * Prior use of regorafenib. * Concurrent use of another investigational drug or device therapy (i.e., outside of study treatment) during, or within 4 weeks. * Major surgical procedure, open biopsy, or significant traumatic injury within 28 days. * Prior radiation therapy or hepatic arterial therapy is permitted if more than 4 weeks have passed since completion and measurable disease outside of the treated area is present, or if progression since treatment has occurred. * Use of St. John's Wort.

Locations (12)

Levine Cancer Institute-Albemarle

Albemarle, North Carolina, United States

Levine Cancer Institute-South Tryon

Charlotte, North Carolina, United States

Levine Cancer Institute

Charlotte, North Carolina, United States

Outcomes

Primary Outcomes

Number of Patients Progression Free and Surviving at 16 Weeks as a Percent of All Enrolled Subjects

16-week progression free survival was determined for each subject as a binary variable indicating whether or not the subject is alive and progression free at 16 weeks after treatment start, with progression defined radiographically using RECIST v1.1 or clinically based upon investigator assessment.

Time frame: 16 weeks after enrollment

Secondary Outcomes

Progression Free Survival

PFS is defined as duration of time from enrollment to the study to time of progression or death. Disease progression (PD) can be objectively determined as per RECIST v1.1 (Response Evaluation Criteria in Solid Tumors, where PD is defined as a 20% increase in the sum of the longest diseased of target lesions, or a measurable increase in non-target lesion, or the appearance of new lesions) or progression can be subjective as determined by the investigator. Evidence for subjective progressions must be documented in medical records. For surviving subjects who do not have documented PD, PFS will be censored at last radiologic assessment. For subjects who receive subsequent anti-cancer therapy prior to documented PD, PFS will be censored at last radiologic assessment prior to commencement of subsequent therapy. Subjects who experience a PFS event following an interval equal to two or more scheduled CT assessments will be censored at date of last assessment prior to first missed assessment.

Time frame: From date of treatment start to date of progression or death, or censored as described above; assessed for approximately 3 years.

Overall Survival

Overall survival is defined as the duration from enrollment date to the date of death from any cause. Subjects who are alive or lost to follow-up at the time of the analysis will be censored at the last known date they were alive.

Time frame: From date of treatment start to date of death, or censored as described above; assessed for approximately 3 years.

Overall Response

Data from ClinicalTrials.gov

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