Search for Mutations Connected With Non-Response to Anti-EGFR Therapy in mCRC in the Morphologically Defined Regions of Primary Tumours
| Autoři | |
|---|---|
| Rok publikování | 2025 |
| Druh | Článek v odborném periodiku |
| Časopis / Zdroj | Cancer Medicine |
| Fakulta / Pracoviště MU | |
| Citace | |
| www | https://onlinelibrary.wiley.com/doi/10.1002/cam4.70910 |
| Doi | http://dx.doi.org/10.1002/cam4.70910 |
| Klíčová slova | anti-EGFR therapy; <italic>BRAF</italic>; invasion front; <italic>KRAS</italic>; metastatic cancer; morphological sampling; <italic>NRAS</italic>; <italic>PIK3CA</italic>; PTEN; tumour heterogeneity |
| Přiložené soubory | |
| Popis | BackgroundEmerging evidence suggests that tumour morphological heterogeneity may influence mutational profiles relevant to therapy response. In this pilot study, we aimed to assess whether mutations identified within specific morphological patterns or at the invasion front correlate with shorter time to progression after anti-EGFR therapy, as compared to whole-tissue analysis.MethodsWe investigated genetic mutations in 142 samples from primary tumours of 39 KRAS wild-type metastatic colorectal cancer (CRC) patients receiving anti-EGFR therapy. Deep next-generation sequencing was performed on whole-tumour sections and six morphology-defined tumour regions.ResultsMutations in genes linked to anti-EGFR therapy response (KRAS, BRAF, NRAS, PTEN and PI3KCA) were found uniquely in the non-responder group, with substantial variability across morphological sub-regions. BRAF mutations were aligned with serrated and mucinous morphologies, while KRAS mutations (p.Lys147Glu and p.Ala146Thr) were associated with mucinous and desmoplastic morphologies. In all cases, the cumulative mutational profile from sub-regions provided more details than that of the whole-tumour profile.ConclusionOur findings highlight that comprehensive analysis, considering morphological heterogeneity, is crucial for personalised CRC treatment strategies. |
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