OpenOnco
UA EN

Onco Wiki / Red flag

MCL with acquired BTK C481S (rarely C481R/F/Y) mutation after progression on covalent BTK...

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDRF-MCL-POST-BTKI-C481-ACTIONABLE
TypeRed flag
Statusreviewed 2026-04-30 | pending_clinical_signoff
DiseasesDIS-MCL
SourcesSRC-ESMO-MCL-2024 SRC-NCCN-BCELL-2025

Red Flag Origin

DefinitionMCL with acquired BTK C481S (rarely C481R/F/Y) mutation after progression on covalent BTK inhibitor (ibrutinib, acalabrutinib, zanubrutinib). C481S abolishes covalent binding of cBTKi to BTK; non-covalent BTKi pirtobrutinib retains activity (BRUIN MCL-321, Wang Lancet Oncol 2024; pirtobrutinib in cBTKi-pretreated MCL ORR 51%, mPFS 7.4 mo). Routes 3L+ post-cBTKi MCL with confirmed C481-axis resistance to pirtobrutinib over chemoimmunotherapy or alternative cBTKi (which would not regain activity given the on-target resistance mechanism).
Clinical directionintensify
Categoryprior-therapy-class
Shifts algorithmALGO-MCL-2L

Trigger Logic

{
  "all_of": [
    {
      "any_of": [
        {
          "finding": "prior_btki_received",
          "value": true
        },
        {
          "finding": "prior_cbtki_received",
          "value": true
        }
      ]
    },
    {
      "any_of": [
        {
          "finding": "btk_c481s_mutation",
          "value": true
        },
        {
          "finding": "btk_c481_mutation",
          "value": "positive"
        },
        {
          "finding": "btk_resistance_mutation",
          "value": "C481S"
        },
        {
          "finding": "plcg2_mutation",
          "value": true
        }
      ]
    }
  ],
  "type": "biomarker"
}

Notes

Distinguish from RF-PRIOR-BTKI-PROGRESSION (universal, broad) — that flag fires on any cBTKi PD; this flag is mutation-confirmed C481S resistance, the canonical mechanism of acquired cBTKi resistance in MCL (similar prevalence to CLL ~80% on cBTKi PD). PLCG2 mutations (R665W, S707F/Y, L845F) are an alternative resistance mechanism (~15%) — also responds to pirtobrutinib. Test at PD by ddPCR or NGS on peripheral-blood mononuclear cells. Brexucabtagene autoleucel (CAR-T, ZUMA-2) is the alternative for CAR-T-eligible post-cBTKi MCL; pirtobrutinib preferred for CAR-T-ineligible (age, comorbidity, organ dysfunction). Access UA: pirtobrutinib not yet NSZU-listed; international early-access pathways.

Used By

Algorithms

Indications