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

Author

Listed:
  • Hiroki Osumi

    (Cancer Institute Hospital of Japanese Foundation for Cancer Research)

  • Eiji Shinozaki

    (Cancer Institute Hospital of Japanese Foundation for Cancer Research)

  • Yoshiaki Nakamura

    (National Cancer Center Hospital East)

  • Taito Esaki

    (National Hospital Organization Kyushu Cancer Center)

  • Hisateru Yasui

    (Kobe City Medical Center General Hospital)

  • Hiroya Taniguchi

    (Aichi Cancer Center Hospital)

  • Hironaga Satake

    (Kochi Medical School)

  • Yu Sunakawa

    (St. Marianna University School of Medicine)

  • Yoshito Komatsu

    (Hokkaido University Hospital)

  • Yoshinori Kagawa

    (Osaka General Medical Center)

  • Tadamichi Denda

    (Chiba Cancer Center)

  • Manabu Shiozawa

    (Kanagawa Cancer Center)

  • Taroh Satoh

    (Osaka University Hospital)

  • Tomohiro Nishina

    (National Hospital Organization Shikoku Cancer Center)

  • Masahiro Goto

    (Osaka Medical and Pharmaceutical University Hospital)

  • Naoki Takahashi

    (Saitama Cancer Center)

  • Takeshi Kato

    (National Hospital Organization Osaka National Hospital)

  • Hideaki Bando

    (National Cancer Center Hospital East)

  • Kensei Yamaguchi

    (Cancer Institute Hospital of Japanese Foundation for Cancer Research)

  • Takayuki Yoshino

    (National Cancer Center Hospital East)

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.

Suggested Citation

  • Hiroki Osumi & Eiji Shinozaki & Yoshiaki Nakamura & Taito Esaki & Hisateru Yasui & Hiroya Taniguchi & Hironaga Satake & Yu Sunakawa & Yoshito Komatsu & Yoshinori Kagawa & Tadamichi Denda & Manabu Shio, 2024. "Clinical features associated with NeoRAS wild-type metastatic colorectal cancer A SCRUM-Japan GOZILA substudy," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-50026-4
    DOI: 10.1038/s41467-024-50026-4
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