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[Adoptive immunotherapy with interleukin 2 in oncology]
M Favrot1, E Bouffet, S Négrier
1Unité fonctionnele de greffes de moelle, Centre anticancéreux Léon-Bérard, Lyon, France.
Bulletin Du Cancer
|January 1, 1990
Summary
Interleukin-2 (IL2) immunotherapy showed a 26% response rate in renal carcinoma patients and varied outcomes in neuroblastoma, with toxicity depending on prior treatments and patient status.
Area of Science:
- Oncology
- Immunotherapy
- Biomedical Research
Background:
- Immunotherapy utilizing Interleukin-2 (IL2) is being explored for various cancers.
- The efficacy and toxicity of IL2, alone or in combination with other agents, require further investigation, particularly in different patient populations and treatment contexts.
Purpose of the Study:
- To evaluate the efficacy and toxicity of Interleukin-2 (IL2) based immunotherapy in patients with renal carcinoma and neuroblastoma.
- To assess the influence of combination therapies and prior treatments on IL2's immunomodulatory effects and clinical outcomes.
Main Methods:
- Retrospective analysis of 47 renal carcinoma patients receiving IL2 with or without LAK cells, INF alpha, or TNF.
- Analysis of 19 neuroblastoma patients treated with IL2 alone or with LAK cells, considering prior high-dose chemotherapy and autologous bone marrow transplantation (ABMT).
Main Results:
- Renal carcinoma patients showed a 26% response rate with mild toxicity and 2% mortality.
- Neuroblastoma patients with end-stage disease experienced higher morbidity/mortality, while those treated post-ABMT had mild, transient toxicity.
- One complete response in a neuroblastoma patient treated with IL2 post-ABMT.
Conclusions:
- IL2 immunotherapy demonstrates a moderate response rate in renal carcinoma with acceptable toxicity.
- The immunomodulatory effects and clinical outcomes of IL2 are significantly influenced by combination therapies, patient's immunological status, and prior treatment history, especially in neuroblastoma.
- IL2 can be beneficial in specific contexts, such as post-ABMT, but careful patient selection and treatment sequencing are crucial.