Sociedad Americana de Hirudoterapia

Burden of illness of non-hematopoietic stem cell transplant-related hepatic sinusoidal obstruction syndrome: A systematic review

Fan L, Stewart F, Ruiz K, Devani D, Fusco N, Gill M, Amber V, Su W, Gangi A, Hanvesakul R (2024) · Heliyon · n=0

Detalle de evidencia de RCTReferencia del ensayo

Perfil del estudio

Diseño
systematic review of 92 studies (2002-2023) on non-HCT SOS/VOD burden of illness and management
Tamaño de la muestra (n)
Intervención
Defibrotide and other treatments for non-HCT-related sinusoidal obstruction syndrome/veno-occlusive disease
Comparador
Standard of care or natural history
Punto final primario
Incidence, diagnosis, management, clinical and economic burden of non-HCT SOS/VOD
Resultado primario
Non-HCT SOS/VOD occurs in ~35% of oxaliplatin-treated colorectal liver metastases (CRLM) patients and ~5% of acute leukemia patients; defibrotide most frequently reported treatment; significant unmet need for diagnostic and treatment guidelines
Duración del seguimiento
Variable across included studies (2002-2023 window)

Hallazgos clave

  • 35% non-HCT SOS/VOD incidence in oxaliplatin-treated CRLM patients
  • 5% incidence in acute lymphoblastic and acute myeloid leukemia
  • Defibrotide most frequently reported treatment
  • Wide diagnostic criteria variability across disease settings
  • Identifies unmet need for guidelines

Limitaciones

  • 57% retrospective cohort studies (low evidence quality)
  • Industry-affiliated authorship (Jazz Pharmaceuticals)
  • Excluded pulmonary VOD and pyrrolizidine alkaloid cases
  • Methodological quality varied across included studies
  • Not applicable to whole-leech hirudotherapy

Implicaciones clínicas

Fan 2024 quantifies the substantial off-label use of defibrotide for non-HSCT VOD, particularly in oncology populations. For ASH, this systematic review illustrates how the pharmaceutical pathway expands beyond approved indications through clinical adoption rather than regulatory action - a phenomenon also visible in the K040187 device-leech US clinical practice but with different scale and economic implications.

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