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Abstract The aim of this work was to evaluate the effectiveness and safety of trans-arterial chemoembolization with and without gel foam for the management of HCC. This study was conducted on 40 cirrhotic patients with primary HCC . All patients had HCV infection. The patients were classified into 2 groups; Group I, ٢٠ patients treated with transcatheter arterial chemoembolization (TACE) by lipidol and adriamycin. Group II, 20 patients were treated with TACE by lipidol and adriamycin followed by gel foam. The patients of each group were classified according to Child-Pough classification to Child A, B & C. All patients included in the study were subjected to pre treatment evaluation in the form of detailed clinical history, thorough clinical assessment, complete blood pictre, liver profile, AFP, kidney function tests, upper endoscopy, colonoscopy, chest X-ray, abdominal ultrasonography and doppler study of the portal vein, abdominal triphasic spiral CT, bone scan, selective hepatic angiography, celiac arteriography and digital subtraction angiography. After proper assessment of the two groups, all patients underwent 1-3 sessions of TACE, 1-2 months apart & evaluated after sessions by CT after 2 weeks to determine the response to treatment. TACE was then repeated according to the response. This program of follow up continued for six months after TACE intervention to evaluate the effect of TACE on liver functions and alfafetoprotein as well as, the response rate of tumor necrosis, size and newly formed tumors and evaluate the survival rate between the studied groups . Results of the current study showed that, the post-embolization syndrome (fever, vomiting and/or right hypochondrial pain) was experiences in 40% of patients in group I and in 65% of patients in group II (P<0.001) following chemoembolization for 3-5 days. However, no major life-threatening treatment related complications were encountered in any of the patients. Regarding liver function tests, there was initial worsening in both groups 2 weeks after treatment as there was significant elevation of AST and ALT in both groups plus significant elevation of bilirubin in group II only. No significant change was noted regarding albumin and prothrombin concentration. Analysis of AFP values before and after treatment in the studied groups showed that, there was a highly significant reduction of its levels during the follow up period being maximal at the end of 6 months. Mean ultrasonographic measurement of the longest diameter of the focal lesions was 5.25 ± 1.06 cm in group I and 5.40 ± 1.0 in group II (P>0.05) before TACE treatment. Six months after treatment, there was a highly significant reduction in tumor size in both groups, where mean longest diameter was 2.20 ± 1.16 cm in group I (percent reduction = 58.1%) and 1.89 ± 0.93 cm in group II (percent reduction = 63.2%) (P<0.001) with no significant difference when comparing between group I and group II. Regarding CT scan, the mean baseline longest diameter of the focal lesion in group I was 5.43±1.06 cm and in group II was 5.50±0.85cm. Six months after treatment, there was a highly significant reduction in tumor size where the mean longest diameter was2.00±1.20 in group I (percent reduction = 65%) and1.50±0.85 cm in group II (percent reduction = 72.7%) (P<0.001). There was no significant difference between both groups. Results showed that, 45.5% of lesions in group I showed complete response to treatment, 37.5% showed partial response and 17% showed stationary response. In group II, 56.5% of lesions showed complete response, 30.5% showed partial response and 13% showed stationary response with no significant difference between the two studied groups. Regarding overall survival, out of the studied 40 patients, 9 died during the 6 months course of follow up with a survival rate of 77.5%. In group 1, the 6-months survival rate was 75%, while, in group 2 it was 80% with no significant difference between both studied groups (P>0.05). In conclusion, we found a trend toward greater survival when gelfoam was used as the embolic agent for TACE for HCC although not reaching significant level when compared with lipiodol. |