OnCo
ideasIdea

Grow each trial patient's tumour as organoids to decide which platform arm opens next

While patients are treated in a platform trial, their tumour cells grow in a dish and are tested against dozens of drug pairs. The pairs that win in the dish become the next arms.

Co-clinical organoid programmes (for example in pancreatic and colorectal cancer) have tested whether dish responses predict patient responses. The proposal inverts the use: a platform trial's organoid bank becomes a combination discovery engine, testing hundreds of pairs on the same tumours that are being treated, so the next arm is chosen from data on the trial population itself rather than on generic cell lines.

Hypothesis
Arms nominated by co-clinical organoid screening achieve a higher objective response rate than arms nominated by investigator choice in the same platform, with the difference visible after two rounds of arm selection.
Rationale
Organoid sensitivity correlates with patient response for cytotoxics and some targeted agents. Pairs tested on the actual trial population avoid the mismatch between cell-line panels and the patients enrolled.
What would test it
Add a co-clinical organoid screen to an existing pancreatic or colorectal platform; nominate two arms by organoid data and two by steering committee; compare response rates after 40 patients per arm.
Maturity
preclinical evidence
Who has to act
research
Cost to try
Medium ($1M to $50M)
Years to first evidence
4
Bottlenecks it attacks

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