Single dose dexamethasone prophylaxis of postembolisation syndrome after chemoembolisation in hepatocellular carcinoma patient: A randomised, double-blind, placebo-controlled study

被引:10
作者
Sainamthip, Panot [1 ]
Kongphanich, Chutcharn [2 ]
Prasongsook, Naiyarat [3 ]
Chirapongsathorn, Sakkarin [4 ]
机构
[1] Chulalongkorn Univ, Dept Pharmacol, Bangkok 10330, Thailand
[2] Phramongkutklao Coll Med, Dept Radiol, Bangkok 10400, Thailand
[3] Phramongkutklao Coll Med, Div Med Oncol, Dept Med, Bangkok 10400, Thailand
[4] Phramongkutklao Coll Med, Div Gastroenterol & Hepatol, Dept Med, 315 Rajvithee, Jatujak 10900, Thailand
关键词
Hepatocellular carcinoma; Chemoembolization; Dexamethasone; Double blind method; Prevention; Postembolization syndrome; HEPATIC TRANSARTERIAL CHEMOEMBOLIZATION; POSTEMBOLIZATION SYNDROME; SURVIVAL;
D O I
10.12998/wjcc.v9.i30.9059
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Even in the immuno-oncology era, transca theter arterial chemoembolisation (TACE) is the most effective way to treat intermediate stage hepatocellular carcinoma (HCC). Postembolisation syndrome (PES) is the most common side effect from TACE and there is still no standard prevention guideline. AIM To evaluate the efficacy of single dose intravenous dexamethasone regimen to prevent PES after TACE among patients with HCC. METHODS This study enrolled patients with HCC who had eligible indication for TACE without macrovascular invasion/extrahepatic metastasis. Patients were randomly assigned to either an intravenous single dose of dexamethasone 8 mg or placebo one hour before TACE. The primary outcome was a negative result of PES at 48 h after TACE, which was defined as score < 2 of Southwest Oncology Group toxicity coding criteria using fever, nausea, vomiting and pain to calculated. And the secondary end point was duration of admission between two groups. RESULTS One hundred patients were randomly assigned 1:1. Under intention-to-treat analysis, 49 patients were randomly assigned to the dexamethasone and 51 to the placebo groups. Both groups were similar for baseline characteristics. The negative PES rate was significantly higher in the dexamethasone group than in the placebo group (63.3% vs 29.4%; P = 0.005). Mean Southwest Oncology Group toxicity coding PES was 2.14 (95%CI: 1.41-2.8) vs 3.71 (95%CI: 2.97-4.45) between the dexamethasone and placebo groups, respectively. Cumulative incidence of fever was significantly lower in dexamethasone group with P < 0.001, pain, nausea and vomiting were also lower in the dexamethasone group compared with the placebo group (P = 0.16, P = 0.11, and P = 0.49). The dexamethasone regimen was generally well tolerated by patients with HCC patients including those with hepatitis B virus infection and well-controlled diabetes mellitus. CONCLUSION Single dose dexamethasone was effective at preventing PES among patients with HCC treated with TACE. The study showed no adverse events of special interest related to dexamethasone.
引用
收藏
页码:9059 / 9069
页数:11
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