Patient mit aktiven oder unvollständig kontrollierten vorbestehenden Autoimmun- oder Entzündungs- störungen.
Deterministische Ansicht der Quelle YAML Entität. Klinische Autorität bleibt mit den zitierten Quell-IDs und Rezensenten Sign-off Zustand.
| ID | RF-ACTIVE-AUTOIMMUNE-DISEASE-ICI-RISK |
|---|---|
| Art | Warnhinweis |
| Status | reviewed 2026-05-04 | pending_clinical_signoff |
| Erkrankungen | 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 |
| Quellen | SRC-ESMO-ICI-TOXICITY-2022 SRC-SITC-ICI-IRAEMANAGEMENT-2021 |
Ursprung der Roten Flagge
| Begriffsbestimmung | Patienten mit aktiver oder unvollständig kontrollierter vorbestehender Autoimmunerkrankung oder entzündlicher Erkrankung (Sarkoidose, rheumatoide Arthritis, IBD, SLE, Autoimmunhepatitis, entzündliche Myopathie, Myasthenia gravis oder ähnliches) werden für die Immunkontrollpunkt-Hemmer-Therapie (ICI) in Betracht gezogen – ein erhöhtes Risiko für immunbedingte unerwünschte Ereignisse (irAE) mit einer Flare oder einem de-novo Grad 3-4 irAE. Benötigt eine Fachprüfung vor der Behandlung (Rheumatologie / Pulmonologie / Gastroenterologie); bevorzugt das untere irAE-Bürden-Rückgrat, wenn Optionen vorhanden sind (Pembrolizumab mono > Ipilimumab+nivolumab). |
|---|---|
| Klinische Richtung | Eskalation |
| Kategorie | Eignungsvoraussetzungen |
Logik auslösen
{
"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"
}
Anmerkungen
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...
Verwendet von
Algorithmen
ALGO-MELANOMA-METASTATIC-2L- ALGO-MELANOMA-METASTATIC-2L
Anwendungsgebiet
IND-CERVICAL-2L-TISOTUMAB-VEDOTIN- IND-CERVICAL-2L-TISOTUMAB-VEDOTININD-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
Quellen
SRC-ESMO-ICI-TOXICITY-2022- Management von Toxizitäten aus der Immuntherapie: ESMO-Leitfaden für klinische Praxis...