A clinical study on transcatheter arterial chemoembolization plus portal vein chemoembolization after partial hepatectomy for patients with hepatocellular carcinoma with portal vein tumor thrombosis
Shujuan Su, Hong Li, Shiteng Zhang
Abstract
Shujuan Su, Hong Li, Shiteng Zhang
Abstract
Objective To study the short and long term outcomes in patients after partial hepatectomy carried out for primary hepatocellular carcinoma (PHC) with portal vein tumor thrombosis (PVTT) who were treated with transcatheter arterial chemoembolization (TACE) plus portal vein chemoembolization (PVCE). Methods 57 patients who underwent partial hepatectomy for PHC with PVTT were treated with TACE+ PVCE. These patients formed the study group. Another 55 such patients who received TACE only were matched by age and gender to form the control group. Blood samples before and after treatment for these 2 groups were collected to study the serum tumor markers. Any chemotherapy-related toxicity and complications were recorded. The hepatocellular carcinoma recurrence rate and recurrence time were recorded on follow up. Survival analysis was conducted. Results There was no significant difference between the two groups in TACE treatment times (P>0.05). In the study group, the levels of AFP, IGF-Ⅱ, and IGFBP-2 were significantly lower than those in the control group at 1 month after chemotherapy [respectively, (4.3±0.5) μg/L vs. (4.8±0.6) μg/L, (3.3±0.4) μg/L vs. (4.0±0.5) μg/L, (5.3±0.6) μg/L vs. (5.8±0.6) μg/L; all P 0.05). In the study group, 2 patients (3.5%) developed bleeding from esophageal and gastric fundus vein rupture, while there were no such cases in the control group. Conclusion Compared with TACE alone, the combination of PVCE and TACE after partial hepatectomy for patients with PHC with PVTT effectively reduced tumor burden, prevented liver recurrence and improved long-term survival rates, with no significant increase in toxicity and complication rates. Key words: Hepatocellular carcinoma; Portal vein tumor thrombus; Portal vein chemoembolization; Transcatheter arterial chemoembolization; Survival rate
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Objective To study the short and long term outcomes in patients after partial hepatectomy carried out for primary hepatocellular carcinoma (PHC) with portal vein tumor thrombosis (PVTT) who were treated with transcatheter arterial chemoembolization (TACE) plus portal vein chemoembolization (PVCE). Methods 57 patients who underwent partial hepatectomy for PHC with PVTT were treated with TACE+ PVCE. These patients formed the study group. Another 55 such patients who received TACE only were matched by age and gender to form the control group. Blood samples before and after treatment for these 2 groups were collected to study the serum tumor markers. Any chemotherapy-related toxicity and complications were recorded. The hepatocellular carcinoma recurrence rate and recurrence time were recorded on follow up. Survival analysis was conducted. Results There was no significant difference between the two groups in TACE treatment times (P>0.05). In the study group, the levels of AFP, IGF-Ⅱ, and IGFBP-2 were significantly lower than those in the control group at 1 month after chemotherapy [respectively, (4.3±0.5) μg/L vs. (4.8±0.6) μg/L, (3.3±0.4) μg/L vs. (4.0±0.5) μg/L, (5.3±0.6) μg/L vs. (5.8±0.6) μg/L; all P 0.05). In the study group, 2 patients (3.5%) developed bleeding from esophageal and gastric fundus vein rupture, while there were no such cases in the control group. Conclusion Compared with TACE alone, the combination of PVCE and TACE after partial hepatectomy for patients with PHC with PVTT effectively reduced tumor burden, prevented liver recurrence and improved long-term survival rates, with no significant increase in toxicity and complication rates. Key words: Hepatocellular carcinoma; Portal vein tumor thrombus; Portal vein chemoembolization; Transcatheter arterial chemoembolization; Survival rate
Key concepts: Medicine, Hepatocellular carcinoma, Transcatheter arterial chemoembolization, Portal vein thrombosis, Hepatectomy, Gastroenterology, Thrombosis, Carcinoma