Expanding the Reach of Precision Oncology by Drugging All KRAS Mutants
Boehringer Ingelheim (Austria) · Memorial Sloan Kettering Cancer Center
Abstract
KRAS is the most frequently mutated oncogene, harboring mutations in approximately one in seven cancers. Allele-specific KRASG12C inhibitors are currently changing the treatment paradigm for patients with KRASG12C-mutated non-small cell lung cancer and colorectal cancer. The success of addressing a previously elusive KRAS allele has fueled drug discovery efforts for all KRAS mutants. Pan-KRAS drugs have the potential to address broad patient populations, including KRASG12D-, KRASG12V-, KRASG13D-, KRASG12R-, and KRASG12A-mutant or KRAS wild-type-amplified cancers, as well as cancers with acquired resistance to KRASG12C inhibitors. Here, we review actively pursued allele-specific and pan-KRAS inhibition…
Citation impact
- FWCI
- 23.73
- Percentile
- 100%
- References
- 94
Authors
5- MHMarco H. HofmannCorresponding
Boehringer Ingelheim (Austria)
- DGDaniel Gerlach
Boehringer Ingelheim (Austria)
- SMSandra Misale
Memorial Sloan Kettering Cancer Center
- MPMark Petronczki
Boehringer Ingelheim (Austria)
- NKNorbert Kraut
Boehringer Ingelheim (Austria)
Topics & keywords
- KRAS
- Precision oncology
- Precision medicine
- Mutant
- Mutation
- Cancer