Durable Responses in Patients With Advanced Cholangiocarcinoma on Sequential Dual-agent Immunotherapy After Progressing on Single-agent Immunotherapy

Am J Clin Oncol. 2022 Oct 1;45(10):410-414. doi: 10.1097/COC.0000000000000941. Epub 2022 Sep 14.

Abstract

Objectives: Biliary tract tumors have a poor prognosis despite advancements in targeted therapies. More recent studies have started to investigate the use of combination immunotherapy in advanced biliary cancers. However, currently, there are no clinical trials investigating the use of dual-agent immunotherapy with ipilimumab and nivolumab as a sequential treatment after patients have progressed on single-agent immunotherapy. In this case series, we discussed 3 patients with advanced cholangiocarcinoma who have an objective response to dual-agent immunotherapy with ipilimumab and nivolumab after having disease progression on pembrolizumab and multiple other failed lines of treatment.

Materials and methods: A case series, including 3 patients treated at the University of California, Irvine Chao Family Comprehensive Cancer Center, was completed.

Results: Although none of the 3 patients had microsatellite instability or high tumor-mutation burden and were not necessarily predicted to have a response to dual-agent immunotherapy, all 3 patients had an objective radiographic and/or tumor-marker response to a combination of ipilimumab and nivolumab.

Conclusions: This case series serves as proof of the concept that sequential immunotherapy can be beneficial after progression on single-agent immunotherapy for patients with advanced cholangiocarcinoma. This study can also serve as the foundation to build further tests on the true effectiveness and ideal duration of sequential therapy with dual immunotherapy agents.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cholangiocarcinoma* / drug therapy
  • Humans
  • Immunologic Factors
  • Immunotherapy
  • Ipilimumab
  • Microsatellite Instability
  • Nivolumab* / therapeutic use

Substances

  • Immunologic Factors
  • Ipilimumab
  • Nivolumab