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Revisiting the ALA/N (a-Lipoic Acid/Low-Dose Naltrexone) protocol for people with metastatic and nonmetastatic pancreatic cancer: A report of 3 new cases

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In parallel, DTP cells exploit compensatory signaling circuits, including pathways such as AURKB, JNK, PI3K, and FAK-YAP, which remain active when major oncogenic drivers such as EGFR, BRAF, or MEK are inhibited ( DTP states can arise under different therapeutic exposure paradigms, including acute high-dose treatment and chronic, continuous drug exposure

37 Overall, the traditional limitation of all these observational clinical studies is that, by design, they can only show association, not causation