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Abstract
Pancreatic ductal adenocarcinoma (PDAC) ranks as the 5th leading cause of cancer death in Western countries. Recent therapeutic advances have yielded limited success, necessitating more personalized treatment protocols based on tumour molecular and functional characteristics. Our recent work allowed us to establish an original model of pancreatic patient-derived tumor organoids (PDTO) treated with the FOLFIRINOX regimen, revealing critical time points in the acquisition of chemoresistance to this combination of drugs and potentially new opportunities for targeted therapies such as PARP inhibitors. The use of PDTO models in general could lead to new treatment strategies for a significant proportion of patients, offering potential alternative sequences through guided second-line treatment decisions.
Source : Open Agenda
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