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Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine
Published on: February 24, 2023
Tumor-Infiltrating Lymphocyte and Other Cell Therapies for Metastatic Melanoma
Christy Los1, Sebastian Klobuch2, John B A G Haanen
1From the Division of Molecular Oncology and Immunology, Oncode Institute, Netherlands Cancer Institute.
Abstract:
Major progress in prolonging survival of patients with advanced melanoma has been made in the past decade because of the development and approval of immune checkpoint inhibitor and targeted therapies. However, for nonresponding or relapsing patients, their prognosis is still dismal. Based on clinical trial data, treatment with adoptive cell therapies holds great promise. In patients with metastatic melanoma progressing on or nonresponsive to single-agent anti-programmed cell death 1, infusion of tumor-infiltrating lymphocytes can produce responses in up to half of patients, with durable complete responses in up to 20%. Genetic modification of peripheral blood T cells with T-cell receptors derived from tumor-specific T cells, or with chimeric antigen receptors, has the potential to further improve treatment outcomes in this refractory population. In this review, we will discuss the historical development, current status, and future perspectives of adoptive T-cell therapies in melanoma.
Insights
Adoptive cell therapies, including tumor-infiltrating lymphocytes, show promise for advanced melanoma patients who do not respond to other treatments. Further advancements in genetically modified T cells may improve outcomes for refractory cases.
Area of Science:
- Oncology
- Immunology
- Cell Therapy
Background:
- Advanced melanoma survival has improved with immune checkpoint inhibitors and targeted therapies.
- Patients with nonresponding or relapsing melanoma still face a poor prognosis.
Approach:
- This review discusses adoptive T-cell therapies for melanoma, including historical development, current status, and future directions.
- Tumor-infiltrating lymphocytes (TILs) can induce responses in up to 50% of patients with metastatic melanoma refractory to anti-programmed cell death 1 therapy.
- Genetically engineered T cells, such as those with chimeric antigen receptors (CARs) or engineered T-cell receptors (TCRs), are being explored.
Key Points:
- Adoptive cell therapy, particularly TILs, offers a promising treatment avenue for advanced melanoma patients unresponsive to standard therapies.
- Durable complete responses are achievable with TIL therapy, reaching up to 20% in refractory populations.
- Genetically modifying T cells represents a next-generation approach to enhance efficacy in difficult-to-treat melanoma.
Conclusions:
- Adoptive T-cell therapies are a significant advancement for advanced melanoma, especially for patients with limited options.
- Further research into genetically modified T-cell therapies holds potential for improved outcomes in refractory melanoma.
- The review highlights the evolving landscape and future potential of cell-based treatments in melanoma management.
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