Tumor infiltrating lymphocyte therapy for ovarian cancer and renal cell carcinoma
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Updated: Apr 5, 2026

Flow Cytometry-Based Isolation and Therapeutic Evaluation of Tumor-Infiltrating Lymphocytes in a Mouse Model of Pancreatic Cancer
Published on: January 17, 2025
Rikke Andersen1,2, Marco Donia1,2, Marie Christine Wulff Westergaard1
1a Center for Cancer Immune Therapy ; Department of Hematology; Herlev Hospital; Copenhagen University ; Copenhagen , Denmark.
Abstract:
Personalized cancer immunotherapy based on infusion of T cells holds the promise to specifically target a patient's individual tumor. Accumulating evidence indicates that the T cells mediating these tumor regressions after cancer immunotherapies may primarily target patient-specific mutations expressed by the patients' tumors and that the presence of these "neo-antigen" specific T-cells may be related to a high number of mutations in the tumor. In melanoma, treatment with autologous tumor-infiltrating lymphocytes (TILs) can mediate durable complete responses. Previous trials investigating TIL therapy in solid tumors other than melanoma have shown limited success, however none of these early trials used current preparative chemotherapy regimens, and the methods for in vitro lymphocyte expansion have changed considerably. New advances and understandings in T cell based immunotherapies have stimulated the interest in developing this approach for other indications. Here, we summarize the early clinical data in the field of adoptive cell transfer therapy (ACT) using tumor-infiltrating lymphocytes for patients with renal cell carcinoma (RCC) and ovarian cancer (OC). In addition we describe the major advances in the characterization and application of TIL therapy for patients with RCC and OC.
Insights
Personalized cancer immunotherapy using tumor-infiltrating lymphocytes (TILs) shows promise for treating renal cell carcinoma (RCC) and ovarian cancer (OC). Advances in T cell therapies are improving patient outcomes by targeting unique tumor mutations.
Area of Science:
- Oncology
- Immunology
- Cancer Therapy
Background:
- Adoptive cell transfer (ACT) therapy, particularly with tumor-infiltrating lymphocytes (TILs), is a promising personalized cancer immunotherapy.
- TILs may target patient-specific mutations (neoantigens) driving tumor regression, with higher mutation burdens correlating with T-cell presence.
- While effective in melanoma, TIL therapy has shown limited success in other solid tumors historically.
Purpose of the Study:
- To summarize early clinical data on TIL-based ACT for renal cell carcinoma (RCC) and ovarian cancer (OC).
- To describe recent advances in the characterization and application of TIL therapy for these specific cancer types.
Main Methods:
- Review of early clinical trial data for adoptive cell transfer therapy using tumor-infiltrating lymphocytes.
- Summary of advancements in the characterization and application of TIL therapy.
Main Results:
- TIL therapy has demonstrated potential in treating solid tumors beyond melanoma.
- Early data suggests efficacy in renal cell carcinoma and ovarian cancer, warranting further investigation.
- Improved methodologies in T cell expansion and preparative chemotherapy regimens enhance treatment potential.
Conclusions:
- Adoptive cell transfer therapy with tumor-infiltrating lymphocytes represents a significant advancement in personalized cancer immunotherapy.
- Further research and clinical trials are essential to optimize TIL therapy for renal cell carcinoma and ovarian cancer patients.
- The targeting of neoantigens by TILs offers a rational basis for expanding this approach to new indications.
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