BRAF-directed therapy outperforms EGFR inhibition in metastatic BRAF-mutant CRC Skip to content The CRC Digest ◆ TRIAL DATA BRAF-directed therapy outperforms EGFR inhibition in metastatic BRAF-mutant CRC Meta-analysis of 18 randomized trials (11,931 participants) found pooled median overall survival of 22.3 months for BRAF-directed regimens versus 10.1 months for EGFR-directed therapy in first-line treatment. (Journal of Gastrointestinal
Molecular profiling study identifies clinicopathological factors linked to dMMR/MSI-H status Skip to content The CRC Digest Molecular profiling study identifies clinicopathological factors linked to dMMR/MSI-H status In 272 resected colorectal cancers, dMMR/MSI-H was present in 9.6% of tumors and independently associated with younger age, proximal tumor location, and poor differentiation. (Clinical Therapeutics) This content is informational only
KRAS, NRAS, and BRAF mutation frequencies reported in Iranian metastatic CRC cohort Skip to content The CRC Digest KRAS, NRAS, and BRAF mutation frequencies reported in Iranian metastatic CRC cohort Among 83 patients with metastatic colorectal cancer, mutation frequencies were 47% for KRAS, 14.5% for NRAS, and 6% for BRAF; BRAF mutations were significantly more frequent in patients under 50 years
Phase II trial tests anti-EGFR rechallenge in ctDNA-selected metastatic CRC Skip to content The CRC Digest ▸ TREATMENT Phase II trial tests anti-EGFR rechallenge in ctDNA-selected metastatic CRC The ROMANCE trial is randomizing 150 patients with circulating tumor DNA-negative hyperselected metastatic colorectal cancer to irinotecan plus cetuximab rechallenge versus trifluridine/tipiracil plus bevacizumab as third-line therapy, aiming to improve objective response
PIK3CA and BRAF mutations linked to worse outcomes in RAS wild-type mCRC on anti-EGFR therapy Skip to content The CRC Digest PIK3CA and BRAF mutations linked to worse outcomes in RAS wild-type mCRC on anti-EGFR therapy A meta-analysis of 1,478 RAS wild-type mCRC patients found PIK3CA mutations were associated with significantly worse PFS (HR 1.38) and OS (HR 1.58), while BRAF mutations