Paciente con diinmunes o inflamatorias preexistentes activas o incompletamente controladas.
Vista determinista de la entidad fuente YAML. La autoridad clínica sigue con los ID de fuente citados y estado de firma del revisor.
| ID | RF-ACTIVE-AUTOIMMUNE-DISEASE-ICI-RISK |
|---|---|
| Tipo | Señal de alerta |
| Situación | reviewed 2026-05-04 | pending_clinical_signoff |
| Enfermedades | DIS-BREAST DIS-CERVICAL DIS-CHL DIS-CRC DIS-ENDOMETRIAL DIS-ESOPHAGEAL DIS-GASTRIC DIS-HCC DIS-HNSCC DIS-MELANOMA DIS-MESOTHELIOMA DIS-NSCLC DIS-PMBCL DIS-RCC DIS-UROTHELIAL |
| Fuentes | SRC-ESMO-ICI-TOXICITY-2022 SRC-SITC-ICI-IRAEMANAGEMENT-2021 |
Origen de la bandera roja
| Definición | Se considera que el paciente con enfermedad autoinmune o inflamatoria preexistente activa o incompletamente controlada (sarcoidosis, artritis reumatoide, EII, hepatitis autoinmunitaria, miopatía inflamatoria, miastenia grave o similar) se trata de un tratamiento con inhibidores de puntos de control inmunitarios (ICI) que presenta un riesgo elevado de reacciones adversas relacionadas con la inmunización (IRAE) o de un aumento de la IRA de grado de novo 3-4. Requiere revisión previa al tratamiento por especialistas (reeumatología / pneumología / gastroenterología); prefiera la columna vertebral de carga inferior de irAE cuando existan opciones (pembrolizumab mono > ipilimumab+nivolumab). |
|---|---|
| Dirección clínica | decreciente |
| Categoría | idoneidad para la aptitud |
Lógica de activación
{
"any_of": [
{
"finding": "active_autoimmune_disease",
"value": true
},
{
"finding": "autoimmune_disease_active",
"value": true
},
{
"finding": "active_sarcoidosis",
"value": true
},
{
"finding": "pulmonary_sarcoidosis_active",
"value": true
},
{
"finding": "active_rheumatoid_arthritis",
"value": true
},
{
"finding": "active_inflammatory_bowel_disease",
"value": true
},
{
"finding": "active_crohn_disease",
"value": true
},
{
"finding": "active_ulcerative_colitis",
"value": true
},
{
"finding": "active_autoimmune_hepatitis",
"value": true
},
{
"finding": "active_lupus",
"value": true
},
{
"finding": "active_sle",
"value": true
},
{
"finding": "active_inflammatory_myopathy",
"value": true
},
{
"finding": "active_myasthenia_gravis",
"value": true
},
{
"finding": "active_multiple_sclerosis",
"value": true
},
{
"finding": "active_psoriasis_systemic",
"value": true
}
],
"type": "composite_clinical"
}
Notas
Pre-existing autoimmune disease is present in ~10-15% of patients eligible for ICI therapy; historically excluded from pivotal trials. Real-world data (Abdel-Wahab 2018, 3557 pts) shows 55% experienced irAE flare and ~29% required systemic immunosuppression beyond steroids. Risk stratification by SITC 2021: - **Low risk** (generally safe to proceed with monitoring): thyroiditis, vitiligo, stable psoriasis, type 1 diabetes — irAE flare mild, manageable. - **Moderate risk** (proceed with specialist input): RA, IBD (Crohn/UC), sarcoidosis, sicca syndrome, psoriatic arthritis — flare rate ~50%; baseline DMARDs often OK to continue (methotrexate, HCQ but NOT high-dose steroids or anti-TNF at start). - **High risk** (strongest caution; consider alternative if available): active autoimmune hepatitis, myasthenia gravis, inflammatory myopathy, neuromyelitis optica — flare can be life-threatening; benefit-risk discussion mandatory. Pulmonary sarcoidosis specifically: ICI-induced sarcoid-like reactions are well-documented (5-7% of patients on ICI), often mimicking disease progression on imaging. Active pulmonary sarcoidosis + ICI raises risk of severe pulmonary irAE (gr 3 pneumonitis). Pre-I...
Utilizado por
Algoritmos
ALGO-MELANOMA-METASTATIC-2L- ALGO-MELANOMA-METASTATIC-2L
Indicación
IND-CERVICAL-2L-TISOTUMAB-VEDOTIN- IND-CERVICAL-2L-TISOTUMAB-VEDOTINAIND-CERVICAL-METASTATIC-1L-PEMBRO-CHEMO-BEV- IND-CERVICAL-METASTATIC-1L-PEMBRO-CHEMO-BEVIND-CHL-1L-N-AVD- IND-CHL-1L-N-AVDIND-CHL-2L-BRENTUXIMAB-MAINTENANCE- IND-CHL-2L-BRENTUXIMAB-MAINTENANCEIND-CHL-2L-PEMBROLIZUMAB- IND-CHL-2L-PEMBROLIZUMABIND-CRC-METASTATIC-1L-MSI-H-PEMBRO- IND-CRC-METASTATIC-1L-MSI-H-PEMBROIND-CRC-METASTATIC-2L-MSI-H-PEMBRO- IND-CRC-METASTATIC-2L-MSI-H-PEMBROIND-ENDOMETRIAL-2L-DOSTARLIMAB-DMMR- IND-ENDOMETRIAL-2L-DOSTARLIMAB-DMMRIND-ENDOMETRIAL-2L-PEMBRO-LENVA-PMMR- IND-ENDOMETRIAL-2L-PEMBRO-LENVA-PMMRIND-ENDOMETRIAL-ADVANCED-1L-DOSTARLIMAB-CHEMO- IND-ENDOMETRIAL-ADVANCED-1L-DOSTARLIMAB-CHEMOIND-ENDOMETRIAL-ADVANCED-1L-PEMBRO-CHEMO- IND-ENDOMETRIAL-ADVANCED-1L-PEMBRO-CHEMOIND-ESOPH-ADJUVANT-NIVOLUMAB-POST-CROSS- IND-ESOPH-ADJUVANT-NIVOLUMAB-POST-CROSSIND-ESOPH-METASTATIC-2L-NIVO-SQUAMOUS- IND-ESOPH-METASTATIC-2L-NIVO-SQUAMOUSIND-ESOPH-METASTATIC-2L-PEMBRO-CPS10- IND-ESOPH-METASTATIC-2L-PEMBRO-CPS10IND-HCC-SYSTEMIC-1L-ATEZO-BEV- IND-HCC-SYSTEMIC-1L-ATEZO-BEVIND-HCC-SYSTEMIC-1L-DURVA-TREME- IND-HCC-SYSTEMIC-1L-DURVA-TREMEIND-NK-T-NASAL-2L-AVELUMAB- IND-NK-T-NASAL-2L-AVELUMABIND-PENILE-SCC-METASTATIC-1L-MSI-H-PEMBRO- IND-PENILE-SCC-METASTATIC-1L-MSI-H-PEMBROIND-SCLC-EXTENSIVE-1L- IND-SCLC-EXTENSIVE-1LIND-VULVAR-VAGINAL-SCC-METASTATIC-1L-PEMBRO- IND-VULVAR-VAGINAL-SCC-METASTATIC-1L-PEMBRO
Fuentes
SRC-ESMO-ICI-TOXICITY-2022- Gestión de toxicidades de la inmunoterapia: Guía de Práctica Clínica ESMO para diagnósticos...