Progressão do IMT em crizotinib de primeira linha (mutação de resistência ao domínio da quinase ALK adquirida...
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| ID | RF-IMT-TRANSFORMATION-PROGRESSION |
|---|---|
| Tipo | Sinal de alerta |
| Estado | reviewed 2026-04-27 | pending_clinical_signoff |
| Doenças | DIS-IMT |
| Fontes | SRC-NCCN-SARCOMA |
Origem da bandeira vermelha
| Definição | IMT progression on first-line crizotinib (acquired ALK kinase-domain resistance mutation L1196M / G1202R / I1171N), dedifferentiation into high-grade sarcoma (epithelioid inflammatory myofibroblastic sarcoma variant), new metastatic disease, or rapid local progression — triggers switch to lorlatinib / alectinib (next-gen ALK), repotrectinib (ROS1), or salvage cytotoxic chemotherapy. |
|---|---|
| Direcção clínica | aguentar |
| Categoria | transformação-progressão |
Lógica de Desencadeamento
{
"any_of": [
{
"finding": "BIO-ALK-G1202R",
"value": "positive"
},
{
"finding": "BIO-ALK-L1196M",
"value": "positive"
},
{
"finding": "alk_resistance_mutation",
"value": true
},
{
"finding": "epithelioid_inflammatory_sarcoma_dedifferentiation",
"value": true
},
{
"finding": "new_metastatic_disease",
"value": true
},
{
"finding": "rapid_progression_on_tki",
"value": true
}
],
"type": "composite_clinical"
}
Notas
Most IMT is intermediate-behavior; epithelioid inflammatory myofibroblastic sarcoma (EIMS) is an aggressive variant with exclusively ALK-fusion (typically RANBP2-ALK) that behaves like high-grade sarcoma — distinct prognosis, often metastatic at diagnosis, requires aggressive systemic therapy + surgery. Acquired ALK resistance mutations (L1196M gatekeeper, G1202R solvent-front, I1171N) drive crizotinib failure within 12-18 mo — switch to lorlatinib (covers most resistance variants) or alectinib (covers L1196M, less G1202R). ROS1+ progression: repotrectinib (TRIDENT-1). Re-biopsy at progression strongly recommended for resistance genotyping.
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