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Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Optimizing Pancreatic Cancer Therapy: The Promise of Immune Stimulatory Oncolytic Viruses
Shivani Thoidingjam1, Aseem Rai Bhatnagar1, Sushmitha Sriramulu1
1Department of Radiation Oncology, Henry Ford Health, Detroit, MI 48202, 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.
Insights
Oncolytic viruses (OVs) show promise for pancreatic cancer treatment. A novel OV therapy was safe, well-tolerated, and improved overall survival in a phase 1 trial for metastatic pancreatic cancer patients.
Area of Science:
- Oncology
- Virology
- Immunotherapy
Background:
- Pancreatic cancer is aggressive and resistant to current treatments.
- Oncolytic viruses (OVs) selectively destroy cancer cells and stimulate anti-tumor immunity.
- OVs offer a well-tolerated approach with potential for combination therapies.
Purpose of the Study:
- To evaluate the safety and tolerability of a novel oncolytic adenoviral vector in patients with metastatic pancreatic cancer.
- To assess the impact of this OV therapy on overall survival.
Main Methods:
- Phase 1 clinical trial of a replication-competent oncolytic adenoviral vector carrying suicide genes (TK, CD) and human interleukin-12 (hIL12).
- Evaluation of safety, tolerability, and adverse events in metastatic pancreatic cancer patients.
- Long-term follow-up to determine overall survival (OS).
Main Results:
- The oncolytic adenoviral vector was safe and well-tolerated at all tested doses.
- No significant adverse events (SAEs) were observed.
- Long-term follow-up revealed an increase in overall survival (OS) in patients receiving the highest OV dose.
Conclusions:
- This oncolytic virus therapy demonstrates a favorable safety profile and potential to improve survival in advanced pancreatic cancer.
- OV-based gene therapy holds significant promise for future pancreatic cancer treatment strategies.
- Further research and development of next-generation OVs, potentially guided by AI, could revolutionize pancreatic cancer care.
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