Clinical features associated with NeoRAS wild-type metastatic colorectal cancer A SCRUM-Japan GOZILA substudy.
Hiroki OsumiEiji ShinozakiYoshiaki NakamuraTaito EsakiHisateru YasuiHiroya TaniguchiHironaga SatakeYu SunakawaYoshito KomatsuYoshinori KagawaTadamichi DendaManabu ShiozawaTaroh SatohTomohiro NishinaMasahiro GotoNaoki TakahashiTakeshi KatoHideaki BandoKensei YamaguchiTakayuki YoshinoPublished in: Nature communications (2024)
"NeoRAS WT" refers to the loss of RAS mutations (MTs) following first-line treatment in metastatic colorectal cancer (mCRC). We evaluate the incidence and clinicopathological characteristics of NeoRAS WT mCRC using next-generation sequencing of plasma circulating tumor DNA. Patients with mCRC enrolled in the GOZILA study initially diagnosed with tissue RAS MT mCRC and received subsequent systemic therapy are eligible. NeoRAS WT is defined as the absence of detectable RAS MT in plasma and assessed in all eligible patients (Group A) and in a subgroup with at least one somatic alteration detected in plasma (Group B). Overall, 478 patients are included. NeoRAS WT prevalence is 19.0% (91/478) in Group A and 9.8% (42/429) in Group B. Absence of liver or lymph node metastasis and tissue RAS MTs other than KRAS exon 2 MTs are significantly associated with NeoRAS WT emergence. Overall, 1/6 and 2/6 patients with NeoRAS WT treated with anti-EGFR monoclonal antibodies (mAbs) show partial response and stable disease for ≥6 months, respectively. NeoRAS WT mCRC is observed at a meaningful prevalence, and anti-EGFR mAb-based therapy may be effective.
Keyphrases
- wild type
- circulating tumor
- metastatic colorectal cancer
- end stage renal disease
- lymph node metastasis
- newly diagnosed
- ejection fraction
- chronic kidney disease
- small cell lung cancer
- risk factors
- peritoneal dialysis
- squamous cell carcinoma
- epidermal growth factor receptor
- gene expression
- stem cells
- tyrosine kinase
- circulating tumor cells
- dna methylation
- open label
- mesenchymal stem cells
- papillary thyroid
- patient reported outcomes
- placebo controlled