Clínicos > Estudos Clínicos do HCC > SARAH >
Diagrama CONSORT


Os 8 pacientes retiraram o consentimento após serem randomizados (SIRT n = 2, sorafenibe n = 6). Segundo a lei francesa, os dados desses pacientes não podem ser usados na análise.

† Desvio pulmonar (n = 14), agravamento da doença (n = 4), shunt arterio-portal (n = 2), doença extra-hepática (n = 1), captação extra-hepática de MAA (n = 1), não captação do tumor no MAA (n = 1), razões técnicas (n = 3: ausência de cateterização seletiva n = 2, pseudo-aneurisma ilíaco n = 1).

‡ Embolia pulmonar (n = 1), agravamento da doença (n = 8), morte precoce (n = 2), motivos técnicos (n = 5: shunt arterio-portal n = 1, trombose arterial hepática n = 1, extra-hepática captação de MAA n = 1, ausência de captação tumoral em MAA n = 1 e shunt de pulmão n = 1).

§ Pacientes adicionais também não atenderam aos critérios de inclusão (n = 2) e receberam sorafenibe em vez de SIRT (n = 1).

Vilgrain V et al.  Lancet Oncol 2017; 18: 1624–36.




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