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'You give me fever!': are health services ready for immune cell engager therapy in advanced solid malignancies?
Claire Pettinger1,2, Claire Livings1,2, Rafael Grochot1,2
1Drug Development Unit, Royal Marsden NHS Foundation Trust, London, UK.
Abstract:
Immune cell engager therapeutic strategies using bioengineered molecules to redirect immune cells into tumor are starting to demonstrate promising clinical activity in multiple early phase trials across numerous targets and a range of solid tumor types. These therapies, however, carry the risk of exaggerated cytokine-mediated on-target off-tumor adverse events that require highly specialized inpatient facilities. We report here the Royal Marsden experience of treating patients with advanced solid tumors on early phase immune engager clinical trials in a dedicated inpatient facility, focusing specifically on patterns of cytokine-mediated toxicity seen and proposing a risk-mitigation algorithm for the safe, feasible and scalable delivery of these therapies.
Insights
Immune cell engagers show promise for solid tumors but risk severe side effects. This study details managing these toxicities in a specialized inpatient setting to ensure safe treatment delivery.
Area of Science:
- Oncology
- Immunotherapy
- Biotechnology
Background:
- Immune cell engagers are emerging as a promising therapeutic strategy for various solid tumors.
- These therapies redirect immune cells to target cancer cells, showing early clinical activity.
- However, they pose risks of severe cytokine-mediated adverse events, necessitating specialized care.
Purpose of the Study:
- To report the experience of treating advanced solid tumors with early-phase immune engager clinical trials.
- To analyze patterns of cytokine-mediated toxicity observed in patients treated in a dedicated inpatient facility.
- To propose a risk-mitigation algorithm for the safe and scalable administration of these novel therapies.
Main Methods:
- Retrospective analysis of patients with advanced solid tumors treated on early-phase immune engager trials.
- Focus on treatment in a dedicated inpatient facility equipped for managing complex toxicities.
- Detailed review of cytokine-mediated adverse events and their management.
Main Results:
- Immune engager therapies demonstrated clinical activity in advanced solid tumors.
- Specific patterns of cytokine-mediated toxicities were identified.
- The dedicated inpatient facility facilitated the management of these adverse events.
Conclusions:
- Early-phase immune engager trials require specialized inpatient facilities due to potential toxicities.
- Effective management strategies and risk mitigation are crucial for the safe delivery of these therapies.
- The proposed algorithm aims to enhance the feasibility and scalability of immune engager treatments.
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