3513 Background: In unresectable mCRC, meta-analysis of RCTs suggests triplet therapy consisting of fluorouracil, oxaliplatin, and irinotecan (FOLFOXIRI) + bevacizumab (bev) may improve survival outcomes over doublet regimens of fluorouracil with irinotecan (FOLFIRI) or oxaliplatin (FOLFOX) + bev, at the expense of increased toxicity. Adoption of triplet therapy remains low. A histology-based biomarker to predict outcomes in mCRC treated with triplet vs doublet regimens could optimize treatment selection. We aimed to use the previously described CHAI platform to develop and validate a histology-based predictive biomarker for doublet vs triplet therapy in mCRC with participant-level data from 3 RCTs. Methods: Development used diagnostic H NCT00719797 (TRIBE); NCT02339116 (TRIBE2).
Ciracì et al. (Wed,) studied this question.