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New treatment option for Locally Advanced Intrahepatic Cholangiocarcinoma
Official title Radioembolization With Tremelimumab and Durvalumab for Locally Advanced Unresectable or Oligo-Metastatic Intrahepatic Cholangiocarcinoma
ClinicalTrials.gov ID: NCT06058663
What this study is testing
What is Durvalumab?
Durvalumab is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for locally advanced intrahepatic cholangiocarcinoma.
Also referred to as Imfinzi, Immunoglobulin G1, Anti-(Human Protein B7-H1) (Human Monoclonal MEDI4736 Heavy Chain), Disulfide with Human Monoclonal MEDI4736 Kappa-chain, Dimer.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- This phase I trial tests the safety and side effects of yttrium-90 (Y90) radioembolization combined with immunotherapy drugs tremelimumab and durvalumab in treating patients with intrahepatic cholangiocarcinoma (cancer of the bile ducts in the liver) that has spread to nearby tissue or lymph nodes (locally advanced) and cannot be removed by surgery (unresectable) who are not candidates for curative therapy or that has spread from where it first started (primary side) to multiple other places in the body (oligo-metastatic). Cholangiocarcinoma is a rare but aggressive cancer with limited curative options outside of surgery.
- Phase 1: an early, usually small safety study
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Age \>= 18 years with body weight \> 30 kg
- Histologically or cytologically confirmed, locally advanced intrahepatic cholangiocarcinoma that is not amenable to resection, transplantation, or...
- Measurable disease
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1
- Hemoglobin \>= 9.0 g/dL (=\< 14 days prior to registration)
You likely can't join if
- Concurrent enrollment in another clinical study, unless it is an observational clinical study or during the follow up period of an treatment study
- Surgery =\< 28 days prior to registration
- Chemotherapy =\< 4 weeks prior to registration
- History of \> 1 prior systemic therapy for cholangiocarcinoma not including that in the adjuvant setting. Patients who progressed during or =\< 6...
- Any unresolved toxicity National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) grade \>= 2 from previous anticancer...
- Patients with grade \>= 2 neuropathy will be evaluated on a case-by-case basis after consultation with the study physician
See the full eligibility criteria
Who can join
- Age \>= 18 years with body weight \> 30 kg
- Histologically or cytologically confirmed, locally advanced intrahepatic cholangiocarcinoma that is not amenable to resection, transplantation, or thermal ablation. Oligometastatic intrahepatic cholangiocarcinoma is...
- Measurable disease
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1
- Hemoglobin \>= 9.0 g/dL (=\< 14 days prior to registration)
- Absolute neutrophil count (ANC) \>= 1000/mm\^3 (=\< 14 days prior to registration)
- Platelet count \>= 75,000/mm\^3 (=\< 14 days prior to registration)
- Total bilirubin =\< 1.5 x upper limit of normal (ULN) (patients with known Gilbert disease who have serum bilirubin level 3 x ULN may be enrolled) (=\< 14 days prior to registration)
- Alanine aminotransferase (ALT) and aspartate transaminase (AST) =\< 5 x ULN (=\< 14 days prior to registration)
- Calculated creatinine clearance \>= 40 ml/min using the Cockcroft- Gault formula or measured creatinine clearance \> 40 ml/min (=\< 14 days prior to registration)
- International normalized ratio (INR) =\< 1.6. Note: INR prolongation due
- Anticoagulation (INR \>= 2.0 but =\< 3.0)) for prophylaxis in patients without liver cirrhosis could be exception
- Adequate hepatic function Child Pugh A and albumin-bilirubin (ALBI) 1 or 2
- Patients with concurrent hepatitis B (HBV) or hepatitis C virus (HCV) infection should meet the following criteria:
- Patient with HBV or should be monitored for viral levels during study participation
- Patient with detectable hepatitis B surface antigen (HBsAg) or detectable HBV DNA should have HBV DNA \< 100 IU/ml and should be managed per local guidelines
- Controlled hepatitis B people will be allowed if they have started treatment prior to or by the time point of enrollment into the study and treatment is continued during study participation and for \>= 6 months after...
- Patients positive for HCV antibody are eligible only if polymerase chain reaction is negative for HCV RNA.
- Negative urine pregnancy test done prior =\< 7 days registration, for persons of childbearing potential only
- NOTE: If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
What rules you out
- Concurrent enrollment in another clinical study, unless it is an observational clinical study or during the follow up period of an treatment study
- Surgery =\< 28 days prior to registration
- Chemotherapy =\< 4 weeks prior to registration
- History of \> 1 prior systemic therapy for cholangiocarcinoma not including that in the adjuvant setting. Patients who progressed during or =\< 6 months from completion of adjuvant therapy are excluded
- Any unresolved toxicity National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) grade \>= 2 from previous anticancer therapy with the exception of alopecia, vitiligo, and the laboratory...
- Patients with grade \>= 2 neuropathy will be evaluated on a case-by-case basis after consultation with the study physician
- Patients with irreversible toxicity not reasonably expected to be exacerbated by treatment with durvalumab or tremelimumab may be included only after consultation with the study physician
- History of previous locoregional therapy
- Previous use of therapeutic cancer vaccines
- Unstable liver function and/ or a change in Child Pugh score during screening
- Child Pugh B or greater
- ALBI grade \> 2
- Model for End-Stage Liver Disease (MELD) \> 10
- Patient is unable to undergo mapping angiography or mapping angiography demonstrates tumor blood supply that does not lend itself to transarterial therapy
- A lung shunt fraction greater than 30 Gy within a single session, or cumulative does greater than 50Gy
- Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper...
- Immunocompromised patients and patients known to be human immunodeficiency virus (HIV) positive and currently receiving antiretroviral therapy
- NOTE: Patients known to be HIV positive, but without clinical evidence of an immunocompromised state, are eligible for this trial
- Active or uncontrolled autoimmune or inflammatory disorders (including Inflammatory bowel disease, systemic lupus erythematosus, rheumatoid arthritis, granulomatosis with polyangiitis, sarcoidosis, Grave's disease)
- History of another primary malignancy except for:
- Malignancy treated with curative intent and with no known active disease \>= 5 years prior to registration and of low potential of recurrence
- Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease
- Adequately treated carcinoma in situ without evidence of disease
- Uncontrolled intercurrent illness including, but not limited to:
- Ongoing uncontrolled infections including tuberculosis (clinical evaluation that includes clinical history, physical examination and radiographic findings, and tuberculosis (TB) testing in line with local practice)...
- Serious chronic gastrointestinal condition associated with diarrhea
- Symptomatic congestive heart failure
- Unstable angina pectoris, cardiac arrhythmia and uncontrolled hypertension
- Chronic pulmonary disease including interstitial lung disease requiring oxygen
- Psychiatric illness/social situations limiting compliance that would limit compliance with study requirement, substantially increase risk of incurring adverse events (AEs) or compromise the ability of the patient to...
- Uncontrolled hypertension
- History of leptomeningeal carcinomatosis
- History of allogeneic transplantation
- Current or prior use of immunosuppressive medication \< 14 days before registration. The following are exceptions to this criterion:
- Intranasal, inhaled, topical steroids, or local steroid injections
- Systemic corticosteroids at physiologic doses not to exceed 10mg/day of
- Prednisone or its equivalent
- Known allergy or hypersensitivity to durvalumab and tremelimumab or any of the constituents of the products
- Receiving any other investigational agent which would be considered as a treatment for the primary neoplasm
- Pregnant or lactating female
- Life expectancy \< 3 months
- Intolerance to contrast agents that is refractory to medical management
- Any other condition which the investigator believes would make participation in the study not acceptable
- History of primary immunodeficiency
- Patients who are unable to consent because they do not understand the nature, significance and implications of the clinical trial and therefore cannot form a rational intention in the light of the facts
- Receipt of live attenuated vaccine \< 30 days prior to registration and without need to receive any live attenuated vaccines during study conduct and for up to 30 days after end of durvalumab treatment or 90 days after...
- Prior immunotherapy such as durvalumab or pembrolizumab is allowed as long as patient does not have progressive disease on it
The study team makes the final eligibility decision.
Where it's taking place
- Jacksonville, Florida, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Jacksonville, Florida, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.