The development of MRTX1133, zoldonrasib, zoldonrasib (RMC-9805), VS-7375, RMC-5127, and daraxonrasib (RMC-6236) demonstrates that direct targeting of previously undruggable KRAS alleles is becoming clinically feasible, and anti-EGFR combination strategies particularly important in CRC.
T. Sagawa, Masahiro Hirakawa, H. Nagashima et al.· Journal of Gastrointestinal...· 1 citation
Treatment selection in the post- BREAKWATER era should integrate molecular context, patient fitness, and remaining evidence gaps, as well as the management of frail or oxaliplatin-ineligible patients, maintenance therapy, local treatment integration, and sequencing after frontline encorafenib exposure.
T. Sagawa, H. Nagashima, K. Fujikawa· Journal of Gastrointestinal...· 0 citations
This review discusses recent advances in EGFR-targeted therapies within the molecular landscape of classical and uncommon EGFR mutations, focusing on frontline intensification strategies in metastatic disease—specifically TKI combinations with chemotherapy or bispecific antibodies or bispecific antibodies—and emerging...
L. Lucente, Lucrezia Barcellini, Beatrice Ramella Pollone et al.· Expert Opinion on Pharmacoth...· 0 citations
This structured narrative review separately examines mismatch repair-deficient/microsatellite instability-high (dMMR/MSI-H) and microsatellite-stable/mismatch repair-proficient (MSS/pMMR) disease and distinguish established treatments from investigational strategies and identify the remaining evidence gaps.
Alireza Tojjari, Shamim Pourbahrighesmat, Shahd Alkhazna et al.· Critical reviews in oncology...· 0 citations
This narrative review focuses on the practical integration of HER2 testing and HER2-directed treatment into mCRC care and proposes a clinician-oriented framework for early patient identification, treatment sequencing, and resistance assessment.
T. Sagawa, H. Nagashima, K. Fujikawa· Journal of Gastrointestinal...· 0 citations
The rapid evolution of KRAS-targeted therapeutic agents represents a shift from allele-specific inhibition towards a strategy that is mutation/context-dependent, thereby creating further clinical translation opportunities and increased patient benefit.
Srijita Chatterjee, S. Arya, Nidhi Sharma et al.· Medical Oncology· 0 citations
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