2019
DOI: 10.1016/j.clinthera.2019.04.036
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Apatinib Combined With Transarterial Chemoembolization in Patients With Hepatocellular Carcinoma and Portal Vein Tumor Thrombus: A Multicenter Retrospective Study

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Cited by 38 publications
(36 citation statements)
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“…The patients who were included in this study were ( 1 ) patients who were diagnosed with HCC according to a pathologic examination or noninvasive criteria in accordance with the American Association for the study of Liver Disease guidelines ( 17 )/European Association for the Study of Liver, ( 2 ) patients with HCC in BCLC stage C, ( 3 ) patients with liver function graded at Child–Pugh A or B, ( 4 ) patients with Eastern Cooperative Oncology Group (ECOG) score of ≤2 points ( 18 ), ( 5 ) patients with platelet count ≥60 × 10 9 platelets per liter, neutrophil count >1.5 × 10 9 cells per liter, and hemoglobin >9 g/dl ( 19 ), and ( 6 ) patients with aspartate aminotransferase and alanine aminotransferase <200 U/L and total bilirubin ≤50 umol/l ( 19 ).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The patients who were included in this study were ( 1 ) patients who were diagnosed with HCC according to a pathologic examination or noninvasive criteria in accordance with the American Association for the study of Liver Disease guidelines ( 17 )/European Association for the Study of Liver, ( 2 ) patients with HCC in BCLC stage C, ( 3 ) patients with liver function graded at Child–Pugh A or B, ( 4 ) patients with Eastern Cooperative Oncology Group (ECOG) score of ≤2 points ( 18 ), ( 5 ) patients with platelet count ≥60 × 10 9 platelets per liter, neutrophil count >1.5 × 10 9 cells per liter, and hemoglobin >9 g/dl ( 19 ), and ( 6 ) patients with aspartate aminotransferase and alanine aminotransferase <200 U/L and total bilirubin ≤50 umol/l ( 19 ).…”
Section: Methodsmentioning
confidence: 99%
“…The patients who were excluded from the study were ( 1 ) patients with complete occlusion of the main portal vein ( 18 ), ( 2 ) patients with moderate or severe ascites, ( 3 ) patients who had previously undergone a treatment of oral sorafenib, liver resection, systemic chemotherapy, transarterial chemoinfusion, or TACE, ( 4 ) patients with serious comorbidities, such as severe dysfunction of the kidney, lung, or heart, and ( 5 ) patients who received other therapies during this study, such as iodine 125 seed implantation, radiofrequency ablation, external beam radiotherapy, or percutaneous ethanol injection.…”
Section: Methodsmentioning
confidence: 99%
“…Sample size of the study is calculated using log-rank test. The estimated OS is 11 months for the study arm and 7 months for the control arm (8,(19)(20)(21). The estimated study duration will be 3.5 years, including 2 years of recruitment, and 1.5 years of follow-up.…”
Section: Sample Sizementioning
confidence: 99%
“…After inclusion, 11 patients received 1 TACE session, 10 received 2 sessions, and 30 received 3 or more sessions. The median number of TACE treatments per patient was 3.6 ± 2.8 (range, [1][2][3][4][5][6][7][8][9][10][11][12][13][14].…”
Section: Treatment Processmentioning
confidence: 99%