Gemcitabine/Cisplatin/Nab-Paclitaxel and Rilvegostomig in Resectable iCCA

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Health Network, Toronto

About this trial

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.

Eligibility criteria

Qualifiers

Patient must be capable of providing written informed consent.

Age >18 years at time of study entry

Histologically proven intrahepatic cholangiocarcinoma

Complete surgical resection of the tumor must be achievable*. Resection should include a portal lymphadenectomy as per standard of care.

Disqualifiers

Radiological evidence suggesting inability to resect with curative intent whilst maintaining adequate vascular inflow and outflow

Radiological evidence of direct invasion into adjacent organs.

Radiological evidence of extrahepatic metastatic disease (except regional lymph nodes - stations 9 and 12

Contraindication to any of the study drugs

Trial design

Treatments tested in this trial

  • Gemcitabine/Cisplatin/Nab-Paclitaxel and Rilvegostomig

Treatment groups

40 Participants
are divided into 1 treatment group

Sponsors and collaborators

University Health Network, Toronto

Lead sponsor

Sunnybrook Health Sciences Centre

Collaborator

Hamilton Health Sciences Corporation

Collaborator