Celecoxib, Recombinant Interferon Alfa-2b, and Rintatolimod in Treating Patients With Colorectal Cancer Metastatic to the Liver

• Status: Completed
• Trial end date: 2021-08-29
• Target enrollment: 0
• Participant gender: All

Summary

This early phase IIA trial studies how well celecoxib, recombinant interferon alfa-2b, and rintatolimod work in treating patients with colorectal cancer that as spread to the liver. Celecoxib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Recombinant interferon alfa-2b is a substance that can improve the body's natural response and may interfere with the growth of tumor cells. Rintatolimod may stimulate the immune system. Giving celecoxib, recombinant interferon alfa-2b, and rintatolimod may work better at treating colorectal cancer that has spread to the liver.

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

Details

• Lead Sponsor: Roswell Park Cancer Institute
• Collaborator: National Cancer Institute (NCI)
• Treatments: Benzenesulfonamide; Celecoxib; Interferon alpha-2; Interferon-alpha; Interferons; Poly I-C; poly(I).poly(c12,U)

Criteria

Inclusion Criteria:

• Recurrent and/or metastatic unresectable colorectal cancer with hepatic metastases

• Hepatic metastases present which are amenable to biopsy

• Prior treatment with, contra-indication to or refusal of a fluoropyrimidine, irinotecan, oxaliplatin and an anti-EGFR targeted therapy (if RAS wild-type [wt]) as well as a PD-1 or PD-L1 targeted drug if MSI-H/dMMR

• No chemotherapy, radiotherapy, major surgery, or biologic therapy within 3 weeks of protocol treatment

• An Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2

• Have measurable disease per RECIST 1.1 criteria present

• Ability to swallow and retain oral medication

• Participants of child-bearing potential must agree to use adequate contraceptive methods (e.g., hormonal or barrier method of birth control; abstinence) prior to study entry; should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately

• Platelet >= 75,000/uL

• Hemoglobin >= 9 g/dL

• Hematocrit >= 27%

• Absolute neutrophil count (ANC) >= 1500/uL

• Creatinine < = institutional upper limit of normal (ULN) OR

• Creatinine clearance >= 50 mL/min for patients with creatinine levels greater than ULN

• Total bilirubin =< 1.5 X institutional ULN or for patients with known Gilbert's Syndrome total bilirubin <= 3 x ULN

• Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 2.5 X institutional ULN

• Plasma amylase =< 1.5 X institutional ULN

• Lipase =< 1.5 X institutional ULN

• Participant or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure

Exclusion Criteria:

• Patients currently treated with systemic immunosuppressive agents, including steroids, are ineligible until 3 weeks after removal from immunosuppressive treatment

• Patients with active autoimmune disease, requiring ongoing immunosuppressive therapy or history of transplantation

• Patients who are pregnant or nursing; women of childbearing potential (WOCBP) will have to undergo a urine pregnancy test as part of screening

• Untreated central nervous system (CNS) metastases

• Cardiac risk factors including:

• Patients experiencing cardiac event(s) (acute coronary syndrome, myocardial infarction, or ischemia) within 3 months of signing consent

• Patients with a New York Heart Association classification of III or IV

• History of upper gastrointestinal ulceration, upper gastrointestinal bleeding, or upper gastrointestinal perforation within the past 3 years; patients with ulceration, bleeding or perforation in the lower bowel are not excluded

• Prior allergic reaction or hypersensitivity to celecoxib, or non-steroidal antiinflammatory drugs (NSAIDs) or any study agents which would prevent completion of protocol therapy

• Patients are ineligible if they plan on regular use of NSAIDs at any dose more than 2 times per week (on average) or aspirin at more than 325 mg at least three times per week, on average; low-dose aspirin not exceeding 100 mg/day is permitted; patients who agree to stop regular NSAIDs or higher dose aspirin are eligible and no wash out period is required

• Received an investigational agent within 30 days prior to enrollment

• Unwilling or unable to follow protocol requirements

• Patients with known serious mood disorders

• Any additional condition which in the investigator?s opinion deems the participant an unsuitable candidate to receive the study drugs