载药微球经导管动脉化疗栓塞术联合肠系膜上动脉灌注化疗治疗肝细胞癌合并门静脉癌栓的效果分析
DOI: 10.12449/JCH241216
Efficacy of drug-eluting beads-transarterial chemoembolization combined with infusion chemotherapy via superior mesenteric artery in treatment of hepatocellular carcinoma complicated by portal vein tumor thrombus
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摘要:
目的 对比分析载药微球经导管动脉化疗栓塞术(D-TACE)联合肠系膜上动脉灌注化疗与单纯D-TACE治疗肝细胞癌合并门静脉癌栓(PVTT)的效果。 方法 回顾性分析徐州医科大学附属医院2022年1月—2023年12月行介入治疗的肝细胞癌合并PVTT的患者资料,其中采用D-TACE联合肠系膜上动脉灌注化疗的患者15例(观察组)。按1∶1进行倾向性匹配后入选单纯D-TACE治疗的患者15例(对照组)。术后1、2、3个月及以后每3个月行上腹部增强MRI评估肝脏肿瘤及PVTT情况。对比分析两组患者客观缓解率(ORR)、疾病控制率(DCR)。计量资料两组间比较采用成组t检验或Mann-Whitney U检验,术前、术后资料比较采用配对t检验或Wilcoxon检验。计数资料两组间比较采用χ2检验。采用Kaplan-Meier曲线计算累积生存率,并使用Log-rank检验比较两组差异。 结果 两组患者治疗技术成功率100%,术后均无严重并发症。全部患者随访3~26个月,平均(10.5±6.7)个月。术后3个月,观察组和对照组肝脏肿瘤的ORR(73.3% vs 53.3%)和DCR(93.3% vs 80.0%)差异均无统计学意义(P值均>0.05);观察组PVTT的ORR(46.7% vs 13.3%)和DCR(100% vs 73.3%)均显著高于对照组(χ2值分别为3.968、4.615,P值分别为0.046、0.032)。观察组和对照组患者累积3、6、12个月无进展生存率分别为93.3%、86.2%、68.9%和80.0%、62.2%、24.9%(P=0.028);累积3、6、12个月总生存率分别为100%、88.9%、88.9%和93.3%、85.6%、70.0%(P=0.340)。 结论 与单纯D-TACE相比,D-TACE联合肠系膜上动脉灌注化疗在治疗肝细胞癌合并PVTT方面显示了更好的近期疗效。 Abstract:Objective To investigate the efficacy of drug-eluting beads-transarterial chemoembolization (D-TACE) combined with infusion chemotherapy via superior mesenteric artery versus D-TACE alone in the treatment of hepatocellular carcinoma (HCC) complicated by portal vein tumor thrombus (PVTT). Methods A retrospective analysis was performed for the data of patients with HCC and PVTT who underwent interventional treatment in The Affiliated Hospital of Xuzhou Medical University from January 2022 to December 2023, among whom 15 patients received D-TACE combined with infusion chemotherapy via superior mesenteric artery and were enrolled as observation group, and after propensity score matching at a ratio of 1∶1, 15 patients who received D-TACE alone were enrolled as control group. Contrast-enhanced MRI of the upper abdomen was performed at 1, 2, and 3 months after surgery and every 3 months thereafter to evaluate the conditions of liver tumor and PVTT. Objective response rate (ORR) and disease control rate (DCR) were compared between the two groups. The independent-samples t test or the Mann-Whitney U test was used for comparison of continuous data between two groups, and the paired t-test or the Wilcoxon test was used for comparison of preoperative and postoperative data; the chi-square test was used for comparison of categorical data between two groups. The Kaplan-Meier curve was used to calculate the cumulative survival rate, and the Log-rank test was used for comparison between two groups. Results Both groups had a technical success rate of 100%, with no serious complications after surgery. The patients were followed up for 3-26 months (mean 10.5±6.7 months). At 3 months after surgery, there were no significant differences between the observation group and the control group in ORR (73.3% vs 53.3%, χ2=1.292, P=0.256) and DCR (93.3% vs 80.0%, χ2=1.154, P=0.283) for liver tumors, and compared with the control group, the observation group had significantly higher ORR and DCR for PVTT (ORR: 46.7% vs 13.3%, χ2=3.968, P=0.046; DCR: 100% vs 73.3%, χ2=4.615, P=0.032). The 3-, 6-, and 12-month cumulative progression-free survival rates were 93.3%, 86.2%, and 68.9%, respectively, for the observation group and were 80.0%, 62.2%, and 24.9%, respectively, for the control group (P=0.028), and the 3-, 6-, and 12-month cumulative overall survival rates were 100%, 88.9%, and 88.9%, respectively, for the observation group and were 93.3%, 85.6%, and 70.0%, respectively, for the control group (P=0.340). Conclusion Compared with D-TACE alone, D-TACE combined with infusion chemotherapy via the superior mesenteric artery shows better short-term efficacy in the treatment of HCC complicated by PVTT. -
表 1 两组患者基线资料情况比较
Table 1. Comparison of baseline characteristics between the two groups of patients
指标 观察组(n=15) 对照组(n=15) 统计值 P值 年龄(岁) 58.5±10.7 57.7±8.9 t=0.315 0.755 性别[例(%)] χ2=0.370 0.543 男 14(93.3) 13(86.7) 女 1(6.7) 2(13.3) Child-Pugh评分(分) 6.3±0.9 6.1±1.1 t=0.374 0.711 Child-Pugh分级[例(%)] χ2=0.144 0.705 A 9(60.0) 10(66.7) B 6(40.0) 5(33.3) 肿瘤最大径(mm) 101.5±44.9 95.8±35.6 t=0.323 0.750 肿瘤数量[例(%)] χ2=0.536 0.464 单个 7(46.7) 9(60.0) 多个 8(53.3) 6(40.0) PVTT分型[(%)] χ2=0.311 0.958 Ⅰ型 2(13.3) 3(20.0) Ⅱ型 7(46.7) 7(46.7) Ⅲ型 5(33.3) 4(26.7) Ⅳ型 1(6.7) 1(6.7) AFP[例(%)] χ2=1.222 0.269 <400 ng/mL 7(46.7) 10(66.7) ≥400 ng/mL 8(53.3) 5(33.3) 表 2 两组患者术后1个月肝功能指标变化情况
Table 2. Changes in liver function indicators one month after treatment in the two groups of patients
指标 观察组(n=15) 对照组(n=15) 统计值 P值 AST(U/L) 术前 66.5(45.8~202.8) 61.0(33.0~117.0) Z=-0.952 0.341 术后1个月 86.0(34.0~119.0) 54.0(33.8~89.0) Z=-0.986 0.324 ALT(U/L) 术前 44.5(35.0~73.8) 42.0(22.5~80.0) Z=-0.762 0.446 术后1个月 43.5(23.3~60.3) 28.5(15.8~53.8) Z=-1.059 0.290 白蛋白(g/L) 术前 35.4±3.4 37.6±4.1 t=1.462 0.157 术后1个月 35.1±5.5 36.2±7.1 t=0.388 0.702 总胆红素(μmol/L) 术前 17.6(12.7~25.2) 14.5(11.6~23.0) Z=-0.653 0.514 术后1个月 22.5(9.9~26.7) 24.9(14.9~54.5) Z=-1.021 0.307 表 3 两组患者术后3个月疗效评价
Table 3. Assessment of efficacy at three months postoperatively in the two groups of patients
组别 例数 肝脏肿瘤[例(%)] PVTT[例(%)] 观察组 15 CR 1(6.7) 0(0.0) PR 10(66.7) 7(46.7) SD 3(20.0) 8(53.3) PD 1(6.7) 0(0.0) 对照组 15 CR 1(6.7) 0(0.0) PR 7(46.7) 2(13.3) SD 4(26.7) 9(60.0) PD 3(20.0) 4(26.7) -
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