不同治疗模式对肝细胞癌合并门静脉癌栓患者预后及安全性影响的多中心研究

Effect of different treatment modalities on prognosis and safety in hepatocellular carcinoma patients with portal vein tumor thrombus: a multicenter study

  • 摘要:
    目的 探讨不同治疗模式对肝细胞癌合并门静脉癌栓(PVTT)患者预后及安全性的影响。
    方法 采用回顾性队列研究方法。收集2021年9月至2023年12月海军军医大学第三附属医院等全国19家医学中心收治的269例肝细胞癌合并PVTT患者的临床病理资料;男237例,女32例;年龄为(53±11)岁。269例患者中,75例行单纯系统治疗设为系统治疗组,155例行系统联合介入治疗设为联合治疗组,39例行放疗联合系统及介入治疗设为放疗+联合治疗组。观察指标:(1)倾向评分匹配及匹配后患者临床病理特征比较。(2)患者预后情况。(3)患者预后的影响因素分析。(4)治疗安全性分析。正态分布的计量资料组间比较采用单因素方差分析。偏态分布的计量资料组间比较采用 Kruskal‑Wallis H检验。计数资料组间比较采用χ2检验或Fisher确切概率法。采用Kaplan‑Meier法计算生存率并绘制生存曲线,Log‑rank检验进行生存分析。两两比较采用Bonferroni法校正。单因素及多因素分析采用Cox比例风险回归模型。倾向评分匹配按1∶2∶3最优完全匹配法进行匹配,卡钳值为0.30。
    结果 (1)倾向评分匹配及匹配后患者临床病理特征比较:269例患者中,216例匹配成功,系统治疗组72例,联合治疗组108例,放疗+联合治疗组36例。倾向评分匹配后,消除体质量指数、血小板、疾病进展混杂因素的影响,具有可比性。(2)患者预后情况:倾向评分匹配后患者随访时间为20.1(0.6~43.2)个月。放疗+联合治疗组1、2、3年总生存率和无进展生存率分别为97.0%、61.5%、43.9%和57.6%、31.5%、25.2%,联合治疗组分别为 80.7%、64.4%、61.9%和50.1%、29.2%、22.4%,系统治疗组分别为66.8%、47.4%、34.6%和43.3%、35.3%、19.6%,3组总生存率比较,差异有统计学意义(χ²=11.10,P<0.05);无进展生存率比较,差异无统计学意义(χ²=3.32,P>0.05)。进一步两两比较结果显示:放疗+联合治疗组与联合治疗组总生存率比较,差异无统计学意义(χ²=0.04,P>0.05);放疗+联合治疗组、联合治疗组分别与系统治疗组总生存率比较,差异均有统计学意义(χ²=5.75、8.52,P<0.05)。(3)患者预后的影响因素分析:倾向评分匹配后,多因素分析结果示中性粒细胞与淋巴细胞比值≥2.5、肿瘤数目≥3个、疾病进展均为影响肝细胞癌合并PVTT患者总生存率的独立危险因素(风险比=1.81,1.82,4.66,95%可信区间为1.09~3.01,1.05~3.15,2.74~7.92,P<0.05),联合治疗相对系统治疗是影响肝细胞癌合并PVTT患者总生存率的保护因素(风险比=0.58,95%可信区间为0.34~0.99,P<0.05)。甲胎蛋白≥400 μg/L和疾病进展均是影响肝细胞癌合并PVTT患者无进展生存率的独立危险因素(风险比=1.52,7.39,95%可信区间为1.06~2.18,4.70~11.60,P<0.05)。(4)治疗安全性分析:269例患者中,251例出现不良反应,其中96例出现3~4级不良反应。系统治疗组、联合治疗组、放疗+联合治疗组分别有70、145、36例出现不良反应,3组比较,差异无统计学意义(χ²=0.08,P>0.05)。3组患者疲劳、放射性皮炎、中性粒细胞减少、血小板降低、蛋白尿比较,差异均有统计学意义(P<0.05)。系统治疗组、联合治疗组及放疗+联合治疗组分别有22、51、23例出现3~4级不良反应,3组比较,差异有统计学意义(χ²=11.04,P<0.05)。
    结论 与单纯系统治疗比较,系统联合介入治疗、放疗联合系统及介入治疗可改善肝细胞癌合并PVTT患者预后,但在系统联合介入治疗基础上叠加放疗并未带来额外生存获益,还增加部分不良反应的发生和严重程度。

     

    Abstract:
    Objective To investigate the effects of different treatment modalities on prognosis and safety in hepatocellular carcinoma(HCC) patients with portal vein tumor thrombus(PVTT).
    Methods The retrospective cohort study was conducted. The clinicopathological data of 269 HCC patients with PVTT who were admitted to 19 medical centers in China, including Third Affiliated Hospital of Naval Medical University et al, from September 2021 to December 2023 were collected. There were 237 males and 32 females, aged (53±11) years. Among the 269 patients, 75 cases undergoing systemic therapy alone were assigned to the systemic therapy group, 155 cases undergoing systemic therapy combined with interventional therapy were assigned to the combined therapy group, and 39 cases undergoing radiotherapy combined with systemic therapy and interventional therapy were assigned to the radiotherapy plus combined therapy group. Observation indicators: (1) propensity score matching (PSM) and comparison of clinicopathological characteristics after matching; (2) patient prognosis; (3) prognostic factors analysis of patients; (4) treatment safety analysis. Comparison of measurement data with normal distribution among groups was conducted using the ANOVA. Comparison of measurement data with skewed distribution among groups was conducted using the Kruskal‑Wallis H test. Comparison of count data among groups was conducted using the chi‑square test or Fisher exact probability. The Kaplan-Meier method was used to calculate survival rates and plot survival curves, and survival analysis was performed using the Log‑rank test. Pairwise comparison was adjusted using the Bonferroni method. Univariate and multivariate analyses were performed using the Cox proportional hazards regression model. PSM was performed using a 1:2:3 optimal full matching method with a caliper of 0.30.
    Results (1) PSM and comparison of clinicopathological characteristics after matching: among the 269 patients, 216 cases were successfully matched, with 72 cases in the systemic therapy group, 108 cases in the combined therapy group, and 36 cases in the radiotherapy plus combined therapy group. After PSM, the elimination of body mass index, platelet and disease progression confounding bias ensured comparability. (2) Patient prognosis: the follow‑up time of patients after PSM was 20.1(range, 0.6-43.2) months. The 1‑, 2‑, and 3‑year overall survival and progression‑free survival rates were 97.0%, 61.5%, 43.9% and 57.6%, 31.5%, 25.2% for the radiotherapy plus combined therapy group, 80.7%, 64.4%, 61.9% and 50.1%, 29.2%, 22.4% for the combined therapy group, 66.8%, 47.4%, 34.6% and 43.3%, 35.3%, 19.6% for the systemic therapy group, respectively. Significant difference was observed in overall survival rate among the 3 groups (χ²=11.10, P<0.05), whereas no significant difference was found in progression‑free survival rate (χ²=3.32, P>0.05). Further pairwise comparisons showed no significant difference in overall survival rate between the radiotherapy plus combined therapy group and combined therapy group (χ²=0.04, P>0.05). There was a significant difference in overall survival rate between the radiotherapy plus combined therapy group and systemic therapy group, between the combined therapy group and systemic therapy group (χ²=5.75, 8.52, P<0.05). (3) Prognostic factors analysis of patients: after PSM, multivariate analysis showed that the neutrophil-to-lymphocyte ratio ≥2.5, the number of tumors ≥3, and disease progression were independent risk factors for overall survival rate in HCC patients with PVTT (hazard ratio=1.81, 1.82, 4.66, 95% confidence interval as 1.09-3.01, 1.05-3.15, 2.74-7.92, P<0.05). Combined therapy was identified as a protective factor for overall survival rate compared with systemic therapy alone (hazard ratio=0.58, 95% confidence interval as 0.34-0.99, P<0.05). Alpha‑fetoprotein ≥400 μg/L and disease progression were risk factors for progression‑free survival rate in HCC patients with PVTT (hazard ratio=1.52, 7.39, 95% confidence interval as 1.06-2.18, 4.70-11.6, P<0.05). (4) Treatment safety analysis: among the 269 patients, 251 cases had adverse reactions, of which 96 cases were classified as grade 3-4. There were 70, 145, and 36 patients with adverse reactions in the systemic therapy group, combined therapy group, and radiotherapy plus combined therapy group, respectively, showing no significant difference among the 3 groups (χ²=0.08, P>0.05). There were significant differences in the fatigue, radiation dermatitis, neutropenia, thrombocytopernia, proteinuria among the 3 groups (P<0.05). There were 22, 51, and 23 patients with grade 3-4 adverse reactions in the systemic therapy group, combined therapy group, and radiotherapy plus combined therapy group, respectively, showing a significant difference among the 3 groups (χ²=11.04, P<0.05).
    Conclusions Compared with systemic therapy, systemic therapy combined with interventional, radiotherapy plus both systemic therapy and interventional can improve prognosis of HCC patients with PVTT. However, the addition of radiotherapy to the systemic combined with interventional therapy does not further improve patient prognosis, and increases the incidence and severity of certain adverse reactions.

     

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