This phase IB trial tests the safety and side effects of transarterial chemoembolization (TACE) in combination with axitinib and hydroxychloroquine (HCQ) in treating patients with colorectal cancer that has spread to the liver. TACE is a procedure which delivers chemotherapy to blood vessels surrounding a tumor, simultaneously treating the cancer cells and interrupting blood flow to them. Axitinib is an enzyme inhibitor which may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. HCQ is an immunosuppressive drug that may cause cancer cell death. Giving axitinib and HCQ in combination with TACE may increase the amount of cancer cells killed by TACE.
Additional locations may be listed on ClinicalTrials.gov for NCT04873895.
See trial information on ClinicalTrials.gov for a list of participating sites.
PRIMARY OBJECTIVE:
I. To evaluate the safety of combined TACE + axitinib + HCQ, using a composite threshold of drug discontinuation and Society of Interventional Radiology (SIR) complications class 3-5.
SECONDARY OBJECTIVES:
I. To estimate the objective response rate (ORR) in the liver after TACE + axitinib/HCQ in patients with liver-dominant adenocarcinoma of colon or rectum metastatic to liver.
II. To estimate hepatic progression-free survival after combined TACE + axitinib + HCQ.
III. To estimate overall progression-free survival including extrahepatic sites.
IV. To estimate overall survival following chemoembolization + axitinib + HCQ.
V. To evaluate tolerance and therapeutic intensity of axitinib when combined with TACE.
TERTIARY/EXPLORATORY OBJECTIVES:
I. To examine RAS mutation status as a biomarker for treatment outcome.
II. To examine hypertension as a biomarker for treatment outcome.
III. To measure serum VEGF levels before and after TACE as a biomarker for treatment outcome.
IV. To perform flow cytometry of serial blood samples for immune profiling
OUTLINE:
Patients receive axitinib orally (PO) twice daily (BID) and hydroxychloroquine PO BID in the absence of disease progression or unacceptable toxicity. Patients undergo TACE at weeks 2 and 6. Patients may also undergo TACE at week 12 if needed.
Patients are followed up at week 24 and then every 3 months until progression.
Lead OrganizationUniversity of Pennsylvania/Abramson Cancer Center
Principal InvestigatorMichael C. Soulen