OnCo
ideasIdea

Select patients for cell therapy by whether their tumour holds reactive T cells

Growing a patient's own tumour-fighting cells only works if those cells are there to start with. A test for them would spare futile treatment.

Tumour-infiltrating lymphocyte therapy is approved in melanoma but works in a minority, and manufacturing takes weeks and costs a great deal. Markers of genuinely tumour-reactive T cells, notably CD39 and CD69 co-expression and CXCL13 expression, distinguish reactive from bystander cells in human tumours. A pre-manufacture biopsy assay could predict product potency and patient benefit.

Hypothesis
A pre-manufacture reactivity assay predicts objective response to tumour-infiltrating lymphocyte therapy, allowing at least a third of patients unlikely to benefit to avoid a costly and toxic procedure.
Rationale
Bystander T cells dominate many tumours, so total lymphocyte density is a poor proxy for reactivity. Product potency assays are standard in cell therapy manufacture in other diseases, and the markers here are well characterised in human tissue.
What would test it
Retrospective analysis of banked pre-manufacture biopsies from treated patients for association with response; if positive, use the assay prospectively as an eligibility criterion in one arm of a trial.
Maturity
preclinical evidence
Who has to act
industry
Cost to try
Medium ($1M to $50M)
Years to first evidence
5
Bottlenecks it attacks

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