» Articles » PMID: 36874130

Perioperative Oncolytic Virotherapy to Counteract Surgery-induced Immunosuppression and Improve Outcomes in Pancreatic Ductal Adenocarcinoma

Overview
Journal Front Oncol
Specialty Oncology
Date 2023 Mar 6
PMID 36874130
Authors
Affiliations
Soon will be listed here.
Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a high fatality cancer with one of the worst prognoses in solid tumors. Most patients present with late stage, metastatic disease and are not eligible for potentially curative surgery. Despite complete resection, the majority of surgical patients will recur within the first two years following surgery. Postoperative immunosuppression has been described in different digestive cancers. While the underlying mechanism is not fully understood, there is compelling evidence to link surgery with disease progression and cancer metastasis in the postoperative period. However, the idea of surgery-induced immunosuppression as a facilitator of recurrence and metastatic spread has not been explored in the context of pancreatic cancer. By surveying the existing literature on surgical stress in mostly digestive cancers, we propose a novel practice-changing paradigm: alleviate surgery-induced immunosuppression and improve oncological outcome in PDAC surgical patients by administering oncolytic virotherapy in the perioperative period.

Citing Articles

Defining and Predicting Early Recurrence for Optimal Treatment Strategies for Intraductal Papillary Mucinous Neoplasm-Derived Pancreatic Cancer: An International Multicenter Study.

Habib J, Javed A, Rompen I, Hidalgo Salinas C, Sorrentino A, Campbell B Ann Surg Oncol. 2024; 32(3):1879-1886.

PMID: 39666193 DOI: 10.1245/s10434-024-16649-z.


Gaining insights into virotherapy with canine models.

Leger J, Tai L Mol Ther Oncolytics. 2023; 31:100754.

PMID: 38075242 PMC: 10701345. DOI: 10.1016/j.omto.2023.100754.

References
1.
Ma X, Wang M, Yin T, Zhao Y, Wei X . Myeloid-Derived Suppressor Cells Promote Metastasis in Breast Cancer After the Stress of Operative Removal of the Primary Cancer. Front Oncol. 2019; 9:855. PMC: 6746963. DOI: 10.3389/fonc.2019.00855. View

2.
Bayne L, Beatty G, Jhala N, Clark C, Rhim A, Stanger B . Tumor-derived granulocyte-macrophage colony-stimulating factor regulates myeloid inflammation and T cell immunity in pancreatic cancer. Cancer Cell. 2012; 21(6):822-35. PMC: 3575028. DOI: 10.1016/j.ccr.2012.04.025. View

3.
Beatty G, Eghbali S, Kim R . Deploying Immunotherapy in Pancreatic Cancer: Defining Mechanisms of Response and Resistance. Am Soc Clin Oncol Educ Book. 2017; 37:267-278. DOI: 10.1200/EDBK_175232. View

4.
Harrington K, Freeman D, Kelly B, Harper J, Soria J . Optimizing oncolytic virotherapy in cancer treatment. Nat Rev Drug Discov. 2019; 18(9):689-706. DOI: 10.1038/s41573-019-0029-0. View

5.
Holbrook M, Goad D, Grdzelishvili V . Expanding the Spectrum of Pancreatic Cancers Responsive to Vesicular Stomatitis Virus-Based Oncolytic Virotherapy: Challenges and Solutions. Cancers (Basel). 2021; 13(5). PMC: 7963195. DOI: 10.3390/cancers13051171. View