# Case Report: Prolonged response to cabozantinib and pembrolizumab in treatment-refractory metastatic pancreatic ductal adenocarcinoma

## TL;DR

A patient with advanced pancreatic cancer responded well to a combination of cabozantinib and pembrolizumab for 25 months.

## Contribution

This case report highlights a durable response to a novel combination therapy in treatment-refractory metastatic pancreatic cancer.

## Key findings

- A patient with metastatic PDAC showed a prolonged response to pembrolizumab and cabozantinib.
- The patient's tumor exhibited immune features that may have enhanced the effectiveness of immunotherapy.
- The case suggests potential for combination immunotherapy in rare PDAC subtypes like UCOGC.

## Abstract

Immunotherapy has yet to demonstrate durable efficacy in pancreatic ductal adenocarcinoma (PDAC) despite the fact that pancreatic cancer cells have higher levels of immune checkpoint expression than other cancer cell types in which immunotherapy efficacy has been well established. We observed effective cytotoxicity with the combination therapy of pembrolizumab (an anti-PD-1 monoclonal antibody, mAb) and cabozantinib (an anti-MET small molecule) in vivo. This served as the basis for an investigator-initiated phase II clinical trial (NCT05052723). The trial was open to patients with treatment-refractory metastatic PDAC with a single-arm treatment protocol of pembrolizumab and cabozantinib. Here, we report the case of a patient with metastatic PDAC who had received two prior lines of systemic therapy and was enrolled in our trial after presenting with pulmonary metastasis. She had a durable response to cabozantinib and pembrolizumab and remained on the trial for 25 months before demonstrating radiographic signs of disease progression. Notably, her initial pathology revealed poorly differentiated adenocarcinoma with features of undifferentiated carcinoma with osteoclast-like giant cells (UCOGC), which is an established rare variant of PDAC. Subsequent biopsies at metastatic sites revealed adenocarcinoma consistent with a pancreatic primary tumor. We hypothesize that the immune features of UCOGC, including increased PD-1 and PD-L1 expression and tumor-infiltrating lymphocytes, may have contributed to the effectiveness of this combination immunotherapy regimen in this patient’s response.