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Metastatic colorectal cancer with RAS wild-type status: KRAS exon 2 (codons 12, 13), exon...

Детермінований перегляд YAML-сутності з джерельної бази. Клінічний авторитет лишається за вказаними source ID та статусом клінічного sign-off.

IDRF-CRC-RAS-WT
ТипТривожна ознака
Статуспереглянуто 2026-04-27 | очікує клінічного підпису
ХворобиDIS-CRC
ДжерелаSRC-ESMO-COLON-2024 SRC-NCCN-COLON-2025

Походження тривожної ознаки

ВизначенняMetastatic colorectal cancer with RAS wild-type status: KRAS exon 2 (codons 12, 13), exon 3 (codons 59, 61), exon 4 (codons 117, 146) AND NRAS exon 2/3/4 ALL wild-type by NGS or extended-RAS PCR. Defines the ~50% of mCRC eligible for anti-EGFR monoclonal antibody therapy (cetuximab, panitumumab) when combined with chemotherapy backbone. Left-sided RAS-WT mCRC particularly benefits from 1L anti-EGFR + FOLFOX/ FOLFIRI (CALGB/SWOG-80405, FIRE-3, PRIME, CRYSTAL — survival benefit driven by left-sided primaries; right-sided RAS-WT does NOT benefit and routes to bevacizumab + chemo).
Клінічний напрямintensify
Категоріяhigh-risk-biology

Логіка спрацьовування

{
  "all_of": [
    {
      "any_of": [
        {
          "finding": "kras_status",
          "value": "wild_type"
        },
        {
          "finding": "kras_mutation",
          "value": false
        },
        {
          "finding": "kras_extended_status",
          "value": "wild_type"
        }
      ]
    },
    {
      "any_of": [
        {
          "finding": "nras_status",
          "value": "wild_type"
        },
        {
          "finding": "nras_mutation",
          "value": false
        }
      ]
    },
    {
      "any_of": [
        {
          "finding": "ras_status",
          "value": "wild_type"
        },
        {
          "finding": "extended_ras_status",
          "value": "wild_type"
        }
      ]
    }
  ],
  "type": "biomarker"
}

Нотатки

Sidedness modifier: left-sided primary (splenic flexure to rectum) + RAS-WT — anti-EGFR + chemo strongly preferred (mOS ~38 mo with cetux+ FOLFOX vs ~33 mo with bev+FOLFOX, FIRE-3 left-sided). Right-sided primary (cecum to transverse) + RAS-WT — bev + chemo preferred (anti- EGFR no benefit or harm in right-sided despite RAS-WT). MSI-H still takes priority (RF-CRC-MSI-H-ACTIONABILITY) — pembrolizumab 1L regardless of RAS status. BRAF V600E mutation (RF-CRC-BRAF-V600E) is a DIFFERENT axis — even RAS-WT BRAF-V600E does NOT respond to anti-EGFR alone; routes to encorafenib + cetuximab (BEACON-CRC). HER2 amplification (~3% RAS-WT) — trastuzumab + tucatinib or T-DXd second-line option (MOUNTAINEER, DESTINY-CRC01). Left-sided + RAS-WT + BRAF-WT + HER2-WT + MSS = canonical anti-EGFR target population (~30% of mCRC). Resistance evolution: ctDNA monitoring at progression for emerging RAS or EGFR-ECD (S492R) mutations — anti-EGFR rechallenge after a TKI-free interval (CHRONOS, Sartore-Bianchi 2022) is feasible if ctDNA shows RAS-WT clonal reset.

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Algorithms