The goal of this clinical trial is to learn if DOC1021 + pIFN will be safe and will lead to tumor responses in patients with refractory melanoma. DOC1021 is a dendritic cell immunotherapy derived from a patient's own blood cells and loaded with antigens from the patient's tumor in the form of tumor lysate and mRNA. The goal is to stimulate a T cell immune response that eliminates tumor cells. The study consists of two components: an initial phase I safety study to confirm safety/tolerability of the treatment regimen, and, subsequently, a single-arm phase II cohort to assess efficacy of the treatment regimen. All participants will: * Undergo a leukapheresis collection (take filgrastim subcutaneously x 5 doses, if clinically necessary, leading up to collection) * Receive two doses of DOC1021 under image guidance 2 weeks apart * Receive subcutaneous pIFN injections weekly for a total of 4 doses in parallel with the DOC1021 injections * Undergo an optional image-guided perinodal DOC1021 booster injection approximately 6 months after the first DOC1021 dose along with additional subcutaneous pIFN injections at time of the booster and the subsequent week for a total of 2 pIFN doses * Visit the clinic regularly to assess quality of life, symptoms, medication use, imaging, bloodwork, and to receive optional treatment with anti-PD1 agents
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
35
Double-loaded dendritic cell vaccine, loaded with tumor lysate and mRNA using proprietary method
Tumor resection or biopsy
pIFN 180 mcg subcutaneously every week for 4 total doses
The University of Alabama at Birmingham
Birmingham, Alabama, United States
RECRUITINGBanner MD Anderson Cancer Center
Gilbert, Arizona, United States
RECRUITINGArizona State University-Honor Health Research Institute
Scottsdale, Arizona, United States
RECRUITINGCity of Hope
Duarte, California, United States
RECRUITINGMassachusetts General Hospital Cancer Institute
Boston, Massachusetts, United States
RECRUITINGAtlantic Health
Morristown, New Jersey, United States
RECRUITINGUniversity of North Carolina
Chapel Hill, North Carolina, United States
RECRUITINGUT Southwestern
Dallas, Texas, United States
RECRUITINGPhase I: To evaluate the number of dose limiting toxicities reported
Time frame: From time of first DOC1021 dose administration to 6 weeks later
Phase II: To evaluate the objective response rate (ORR) as the proportion of patients with a confirmed complete response (CR) or partial response (PR) to treatment, as per RECIST 1.1 criteria
Time frame: 5 years
Overall survival (time in months from the date of study enrollment until death for from any cause)
Time frame: 5 years
Time in months from the first documentation of complete or partial response to disease progression by RECIST 1.1 criteria or death, whichever occurs first.
Duration of Response (DOR)
Time frame: 5 years
Time in months from date of study enrollment to disease progression by RECIST 1.1 criteria or death from any cause
Progression-free survival (PFS)
Time frame: 5 years
The proportion of participants with complete response, partial response, or stable disease out of the total eligible and evaluable participants.
Disease control rate (DCR)
Time frame: 5 years
Number of participants with adverse events as assessed by CTCAE v5.0
Time frame: 3 years
To evaluate the objective response rate (ORR) as the proportion of patients with a confirmed complete response (CR) or partial response (PR) to treatment, as per immune-related response criteria (iRECIST)
Time frame: 5 years
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