Study Name |
|
Modified Immune Cells (Autologous Dendritic Cells) and a Vaccine (Prevnar) After High-Dose External Beam Radiation Therapy in Treating Patients With Unresectable Liver Cancer |
ClinicalTrials.gov Identifier (if applicable) |
|
NCT03942328 |
Clinical Trial Category (check all that apply) |
|
- Radiation Therapy
- Other Novel Therapy
|
Study Center |
Institution Name |
|
Mayo Clinic |
Institution Address |
|
200 First Street SW |
City |
|
Rochester |
State |
|
Minnesota |
Zip Code |
|
55905 |
Country |
|
United States |
Phone |
|
(507) 284-2511 |
Website |
|
https://www.mayoclinic.org |
Study Contacts |
Principal Investigator |
|
Lewis R Roberts, M.B., Ch.B., Ph.D |
P.I. Phone |
|
(507) 266-3239 |
P.I. Email |
|
Roberts.Lewis@mayo.edu |
List additional Principal Investigators (include phone number and email) |
|
Allan B Dietz, Ph.D.
(Dietz.Allan@mayo.edu)
5072664258Christopher Leigh Hallemeier, M.D. (Hallemeier.Christopher@mayo.edu)
5072665232Joleen Marie Hubbard, M.D. (Hubbard.Joleen@mayo.edu)
5072930487
Yi Lin, M.D.
(Lin.Yi@mayo.edu)
5072845096
Sean S Park, M.D.
(Park.Sean@mayo.edu)
5072848227
Thomas D Atwell, M.D.
(Atwell.Thomas@mayo.edu) |
Study Coordinator |
|
Jaclynn Maria Wessling |
Study Coordinator Phone |
|
(507) 538-4545 |
Study Coordinator Email |
|
Wessling.Jaclynn@mayo.edu |
OVERVIEW – in layman’s terms (150 words max) |
|
Early phase 1 study evaluating the safety of autologous dendritic cells (immune cells generated from patients’ own white blood cells, grown in a special lab, and trained to stimulate the immune system against the tumor) and a vaccine (Prevnar) in treating patients with liver cancer that cannot be removed by surgery after undergoing radiotherapy. |
Enrollment |
|
26 |
Study Start Date |
|
05/17/2019 |
Estimated Completion Date |
|
12/31/2026 |
Purpose of the Study – in Layman’s Terms (use the “+” to add more list items) |
|
- Evaluate the safety of autologous dendritic cells and a vaccine (Prevnar) in treating patients with liver cancer that cannot be removed by surgery after undergoing radiotherapy.
- Identify and characterize responses of the immune system in patients with liver cancer treated with radiotherapy followed by autologous dendritic cells and a vaccine (Prevnar).
|
Inclusion Criteria – Patients Must: |
|
- Age ≥18 years
- Histologic confirmation of intrahepatic cholangiocarcinoma
- Unresectable intrahepatic cholangiocarcinoma
- Measurable or evaluable disease
- All lesions should be treatable by radiotherapy while meeting normal tissue constraints.
- Tumor lesions should be accessible using an ultrasound-guided approach for dendritic cell injection into the tumor
- No evidence of tumor outside of the liver (excluding tumor clots) by computed tomography (CT) or magnetic resonance imaging (MRI) scan
- Patients who are not candidates for surgical treatment or for ablation with curative intent Adequate organ functions
- ECOG Performance Status (PS) 0 or 1
|
Exclusion Criteria – Patients Must NOT: |
|
- Co-morbid systemic illnesses or other severe concurrent disease
- Immunocompromised patients and patients known to be HIV positive and currently receiving antiretroviral therapy.
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
- Other active malignancy ≤3years prior to registration. EXCEPTIONS: Non-melanotic skin cancer or carcinoma-in-situ of the cervix.
- Active autoimmune disease such as autoimmune hepatitis, Crohn’s disease, rheumatoid arthritis, Sjögrens’ disease, systemic lupus erythematosus, or similar conditions.
- Child Pugh class B or C cirrhosis of the liver
- Barcelona Clinic Liver Cancer (BCLC) stage D disease
- Previously received immune modulating therapies
- Corticosteroids ≤2 weeks prior to registration, including oral, IV, subcutaneous, or inhaled routes of administration. NOTE: Patients on chronic corticosteroids may enroll if they receive less than 10 mg/day of prednisone (or equivalent)
- Prior liver radiation, including radioembolization
|
REQUIRED TESTS PRIOR TO BEGINNING STUDY TREATMENT – in layman’s terms |
|
- Computed tomography (CT) or magnetic resonance imaging (MRI) scan
- Bloodwork to determine baseline organ functions, tumor markers, and immune cells
- Apheresis (isolation) of immature white blood from a patient’s own blood
|
POTENTIAL SIDE-EFFECTS – in layman’s terms |
|
- Inflammatory symptoms such as fever, chills, nausea, vomiting, diarrhea, rash, can occur
- Pain at injection site
|