Optimizing Pancreatic Cancer Therapy: The Promise of Immune Stimulatory Oncolytic Viruses

Author:

Thoidingjam Shivani1,Bhatnagar Aseem Rai1ORCID,Sriramulu Sushmitha1,Siddiqui Farzan123,Nyati Shyam124ORCID

Affiliation:

1. Department of Radiation Oncology, Henry Ford Health, Detroit, MI 48202, USA

2. Henry Ford Health + Michigan State University Health Sciences, Detroit, MI 48202, USA

3. Department of Medicine, Michigan State University, East Lansing, MI 48824, USA

4. Department of Radiology, Michigan State University, East Lansing, MI 48824, USA

Abstract

Pancreatic cancer presents formidable challenges due to rapid progression and resistance to conventional treatments. Oncolytic viruses (OVs) selectively infect cancer cells and cause cancer cells to lyse, releasing molecules that can be identified by the host’s immune system. Moreover, OV can carry immune-stimulatory payloads such as interleukin-12, which when delivered locally can enhance immune system-mediated tumor killing. OVs are very well tolerated by cancer patients due to their ability to selectively target tumors without affecting surrounding normal tissues. OVs have recently been combined with other therapies, including chemotherapy and immunotherapy, to improve clinical outcomes. Several OVs including adenovirus, herpes simplex viruses (HSVs), vaccinia virus, parvovirus, reovirus, and measles virus have been evaluated in preclinical and clinical settings for the treatment of pancreatic cancer. We evaluated the safety and tolerability of a replication-competent oncolytic adenoviral vector carrying two suicide genes (thymidine kinase, TK; and cytosine deaminase, CD) and human interleukin-12 (hIL12) in metastatic pancreatic cancer patients in a phase 1 trial. This vector was found to be safe and well-tolerated at the highest doses tested without causing any significant adverse events (SAEs). Moreover, long-term follow-up studies indicated an increase in the overall survival (OS) in subjects receiving the highest dose of the OV. Our encouraging long-term survival data provide hope for patients with advanced pancreatic cancer, a disease that has not seen a meaningful increase in OS in the last five decades. In this review article, we highlight several preclinical and clinical studies and discuss future directions for optimizing OV therapy in pancreatic cancer. We envision OV-based gene therapy to be a game changer in the near future with the advent of newer generation OVs that have higher specificity and selectivity combined with personalized treatment plans developed under AI guidance.

Funder

NCI R21

HFHS Research Administration Start Up

HFHS Proposal Development Award

Game on Cancer Award

HFHS-Radiation Oncology Start Up to Shyam Nyati

Publisher

MDPI AG

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