Clinical features associated with NeoRAS wild-type metastatic colorectal cancer A SCRUM-Japan GOZILA substudy

Author:

Osumi HirokiORCID,Shinozaki EijiORCID,Nakamura YoshiakiORCID,Esaki Taito,Yasui HisateruORCID,Taniguchi Hiroya,Satake HironagaORCID,Sunakawa YuORCID,Komatsu YoshitoORCID,Kagawa Yoshinori,Denda Tadamichi,Shiozawa Manabu,Satoh Taroh,Nishina Tomohiro,Goto Masahiro,Takahashi Naoki,Kato Takeshi,Bando HideakiORCID,Yamaguchi Kensei,Yoshino TakayukiORCID

Abstract

Abstract“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.

Publisher

Springer Science and Business Media LLC

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