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Anti-metabolites

Gemcitabine/Cisplatin/Nab-Paclitaxel and Rilvegostomig for Cholangiocarcinoma (NEOLANGIO Trial)

Phase 2
Waitlist Available
Research Sponsored by University Health Network, Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
1. Patient must be capable of providing written informed consent.
2. Age \>18 years at time of study entry
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 years
Awards & highlights

Summary

Biliary tract cancer is a highly aggressive and heterogeneous group of gastrointestinal cancers that arise from the intra- or extrahepatic bile ducts (CCA), or the gallbladder (GBC)(1-3). While it accounts for only 0.7% of all malignant tumors and 3% of all gastrointestinal malignancies in adults, both incidence and mortality are increasing. Biliary tract cancers usually present at an advanced stage, with only approximately 20% of patients being diagnosed with an early-stage disease (1, 2, 4). There is a high risk of recurrence post curative radical resection, with 60-70% of patients recurring within 5 years, with 5-year survival of around 25% (1, 2, 5). There is evidence for use of adjuvant chemotherapy with fluoropyrimidine- based regimens as per the BILCAP and ASCOT phase III trials \[(5-7).However, despite advances in adjuvant treatment, recurrence rates after resection of BTC remain high even with adjuvant chemotherapy. For example, in the BILCAP study, 5-year RFS was reported as 33.9% (95% CI: 27.6 to 40.2) (1). Therefore, an unmet need exists to optimize peri-operative treatment to reduce recurrence and improve outcomes in patients with resectable BTC.

Who is the study for?
This trial is for patients with a type of bile duct cancer known as iCCA that can be surgically removed. Participants must have not undergone any previous treatments for their condition and should be physically fit enough to handle surgery and chemotherapy.
What is being tested?
The study tests a combination of chemotherapy drugs (Gemcitabine, Cisplatin, Nab-Paclitaxel) with an investigational drug called Rilvegostomig in patients undergoing surgery for iCCA. The goal is to see if this regimen can prevent the cancer from coming back.
What are the potential side effects?
Possible side effects include nausea, vomiting, hair loss, numbness or tingling in hands and feet due to nerve damage (neuropathy), low blood cell counts leading to increased infection risk or bleeding problems, kidney issues, and liver toxicity.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 years for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Major pathological response (MPR), defined as >70% tumor necrosis
Secondary study objectives
Objective response rate (ORR)
Rate of R0
The number of patients who experience a surgical delay and/or drop off due to treatment related adverse events (TRAEs) or progressive disease
+1 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Gemcitabine/Cisplatin/Nab-Paclitaxel and RilvegostomigExperimental Treatment1 Intervention

Find a Location

Who is running the clinical trial?

University Health Network, TorontoLead Sponsor
1,498 Previous Clinical Trials
490,818 Total Patients Enrolled
4 Trials studying Cholangiocarcinoma
98 Patients Enrolled for Cholangiocarcinoma
Sunnybrook Health Sciences CentreOTHER
668 Previous Clinical Trials
1,563,825 Total Patients Enrolled
1 Trials studying Cholangiocarcinoma
8 Patients Enrolled for Cholangiocarcinoma
Hamilton Health Sciences CorporationOTHER
372 Previous Clinical Trials
338,531 Total Patients Enrolled
~27 spots leftby Dec 2027