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Talimogene Laherparepvec (T-VEC): A Review of the Recent Advances in Cancer Therapy
Tiantian Zhang1, Tony Hong-Ting Jou2, Jerline Hsin3
1Toni Stephenson Lymphoma Center, Department of Hematology and Hematopoietic Stem Cell Transplantation, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Abstract:
The landscape of melanoma treatment has undergone a dramatic revolution in the past decade. The use of oncolytic viruses (OVs) represents a novel therapeutic approach that can selectively infect and lyse tumor cells and induce local and systemic antitumor immune responses. As the first OV approved by the Food and Drug Administration (FDA) for melanoma treatment, talimogene laherparepvec (T-VEC), a genetically modified herpes simplex virus (HSV), has shown promising therapeutic effects in the treatment of advanced melanoma, both as a monotherapy or in combination with other immunotherapies, such as the immune checkpoint inhibitors (ICIs). With proven efficacy, T-VEC has been evaluated against a variety of other cancer types in a clinical trial setting. In this article, we will provide a review on OVs and the application of T-VEC in melanoma monotherapy and combination therapy. In addition, we will review the recent progress of T-VEC application in other cutaneous cancer types. Moreover, we will briefly describe our experience of T-VEC therapy at City of Hope, aiming to provide more insight for expanding its future application.
Insights
Oncolytic viruses (OVs), like talimogene laherparepvec (T-VEC), are revolutionizing melanoma treatment by targeting tumor cells and boosting immune responses. T-VEC shows promise in advanced melanoma and other cancers.
Area of Science:
- Oncology
- Virology
- Immunotherapy
Background:
- Melanoma treatment has advanced significantly with novel therapeutic strategies.
- Oncolytic viruses (OVs) offer a new approach, selectively destroying tumor cells and stimulating antitumor immunity.
- Talimogene laherparepvec (T-VEC), a modified herpes simplex virus (HSV), is the first FDA-approved OV for melanoma.
Purpose of the Study:
- To review the role of OVs and T-VEC in melanoma monotherapy and combination treatments.
- To explore the application of T-VEC in other cutaneous cancers.
- To share clinical experiences with T-VEC therapy to guide future applications.
Main Methods:
- Literature review of oncolytic virus therapy in melanoma.
- Analysis of T-VEC efficacy in monotherapy and combination with immune checkpoint inhibitors (ICIs).
- Review of ongoing clinical trials evaluating T-VEC for various cancers.
Main Results:
- T-VEC demonstrates promising therapeutic effects in advanced melanoma.
- Combination therapy with T-VEC and ICIs shows enhanced antitumor responses.
- T-VEC is being investigated for efficacy across a spectrum of other cancer types.
Conclusions:
- Oncolytic virus therapy, particularly T-VEC, represents a significant advancement in melanoma treatment.
- T-VEC holds potential for treating various cutaneous cancers beyond melanoma.
- Further research and clinical experience are crucial for optimizing T-VEC's therapeutic utility.
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