背景
本研究旨在探讨阿帕替尼联合经动脉化疗栓塞(TACE)和射频消融(RFA)治疗肝细胞癌(HCC)患者的疗效和安全性。
方法
从 2015 年 12 月到 2018 年 6 月,我们的研究纳入了 175 名符合条件的参与者。24 例接受阿帕替尼联合 TACE 和 RFA 的患者被分类为 TACE + RFA-A 组,82 名接受阿帕替尼联合 TACE 的患者被分类为 TACE-A 组,69 名单独接受 TACE 的患者被分类为 TACE团体。记录治疗并发症、治疗反应、总生存期(OS)和进展时间(TTP)。比较了生存分析。进行单变量和多变量 Cox 分析以研究 OS 和 TTP 的预测因素。进行了亚组分析。
结果
TACE + RFA-A 组的中位 TTP 为 8.0 个月(95% CI 6.7-9.3),比 TACE-A 组(6.0 个月,95% CI 4.8-7.2)和 TACE 组(3.0 个月,95 % CI 2.3–3.7);差异有统计学意义(P < 0.001)。TACE + RFA-A 组的中位 OS 为 23.0 个月(95% CI 12.6-33.4),TACE-A 组为 18.0 个月(95% CI 16.2-19.8)和 8.0 个月(95% CI 5.3-10.7) ) 在 TACE 组中;差异有统计学意义(P < 0.001)。TACE + RFA-A t 组的客观缓解率 (ORR) 更高(M1,70.8% vs 65.9% vs. 46.4%,P = 0.023;M3,58.3% vs. 53.7% vs. 26.1%,P = 0.001)。多变量 Cox 分析表明,治疗策略和肿瘤大小是 OS 和 TTP 的独立预后因素,而 Child-Pugh 分期是 OS 的预测因素。没有观察到与治疗相关的死亡。两组之间的毒性相当。
结论
TACE联合RFA加阿帕替尼是治疗中晚期HCC的安全三联疗法,其疗效优于TACE联合阿帕替尼或单独TACE。
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Comparison of the Efficacy Among Transcatheter Arterial Chemoembolization (TACE)–Radiofrequency Ablation Plus Apatinib, TACE Plus Apatinib, and TACE Alone for Hepatocellular Carcinoma: A Retrospective Study
Background
This study aimed to investigate the efficacy and safety of apatinib plus transarterial chemoembolization (TACE) and radiofrequency ablation (RFA) in the therapy of hepatocellular carcinoma (HCC) patients.
Methods
From December 2015 to June 2018, 175 eligible participants were included in our research. Twenty-four patients who received apatinib plus TACE and RFA were categorized as the TACE + RFA-A group, 82 patients who received apatinib plus TACE were categorized as the TACE-A group, and 69 patients who received TACE alone were categorized as the TACE group. Treatment complications, treatment response, overall survival (OS), and time to progression (TTP) were recorded. Survival analyses were compared. Univariate and multivariate Cox analyses were conducted to investigate the predictive factors for OS and TTP. A subgroup analysis was carried out.
Results
The median TTP was 8.0 months (95% CI 6.7–9.3) in the TACE + RFA-A, which was longer than the TACE-A group (6.0 months, 95% CI 4.8–7.2) and TACE group (3.0 months, 95% CI 2.3–3.7); the difference was statistically significant (P < 0.001). The median OS was 23.0 months (95% CI 12.6–33.4) in the TACE + RFA-A group, 18.0 months (95% CI 16.2–19.8) in the TACE-A group, and 8.0 months (95% CI 5.3–10.7) in the TACE group; the difference was statistically significant (P < 0.001). The objective response rate (ORR) was higher in TACE + RFA-A t group (M1, 70.8% vs 65.9% vs. 46.4%, P = 0.023; M3, 58.3% vs. 53.7% vs. 26.1%, P = 0.001). Multivariate Cox analysis demonstrated that treatment strategy and tumor size were independent prognostic factors for the OS and TTP, whereas the Child–Pugh stage was predictive factor of OS. No treatment-related death was observed. The toxicity was comparable between the two groups.
Conclusion
TACE combined with RFA plus apatinib is a safe three-modality treatment for the intermediate or advanced HCC, and it demonstrated better efficacy than TACE plus apatinib or TACE alone.