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经载多柔比星微球的肝动脉化疗栓塞术疗效评估:5 年移植队列中的肿瘤生物学与肝细胞癌复发。

Assessment of Response to Transcatheter Arterial Chemoembolization with Doxorubicin-eluting Microspheres: Tumor Biology and Hepatocellular Carcinoma Recurrence in a 5-year Transplant Cohort.

机构信息

From the Departments of Radiology (T.A.S., S.E.A., A.A.A., D.A.D., D.S.K., J.M.G., P.J.G., D.K., P.M.G.), Transplant Surgery (H.E.B., A.J.C.), and Pathology (G.A.G.), and the Institute of Translational Research (P.T.T., K.G.N.), Ochsner Health System, 1514 Jefferson Hwy, New Orleans, LA 70121; and The University of Queensland School of Medicine, Ochsner Clinical School, New Orleans, La (D.A.D., D.S.K., J.M.G., H.E.B., P.J.G., G.A.G., A.J.C., D.K., P.M.G.).

出版信息

Radiology. 2018 Mar;286(3):1072-1083. doi: 10.1148/radiol.2017170731. Epub 2017 Dec 4.

Abstract

Purpose To assess response to transcatheter arterial chemoembolization (TACE) based on immune markers and tumor biology in patients with hepatocellular carcinoma (HCC) who were bridged to liver transplantation, and to produce an optimized pretransplantation model for posttransplantation recurrence risk. Materials and Methods In this institutional review board-approved HIPAA-compliant retrospective analysis, 93 consecutive patients (73 male, 20 female; mean age, 59.6 years; age range, 23-72 years) underwent TACE with doxorubicin-eluting microspheres (DEB) (hereafter, DEB-TACE) and subsequently underwent transplantation over a 5-year period from July 7, 2011, to May 16, 2016. DEB-TACE response was based on modified Response Evaluation Criteria in Solid Tumors. Imaging responses and posttransplantation recurrence were compared with demographics, liver function, basic immune markers, treatment dose, and tumor morphology. Treatment response and recurrence were analyzed with uni- and multivariate statistics, as well as internal validation and propensity score matching of factors known to affect recurrence to assess independent effects of DEB-TACE response on recurrence. Results Low-grade tumors (grade 0, 1, or 2) demonstrated a favorable long-term treatment response in 87% of patients (complete response, 49%; partial response, 38%; stable disease [SD] or local disease progression [DP], 13%) versus 33% of high-grade tumors (grade 3 or 4) (complete response, 0%; partial response, 33%; SD or DP, 67%) (P < .001). Of the 93 patients who underwent treatment, 82 were followed-up after transplantation (mean duration, 757 days). Recurrence occurred in seven (9%) patients (mean time after transplantation, 635 days). Poor response to DEB-TACE (SD or DP) was present in 86% of cases and accounted for 35% of all patients with SD or DP (P < .001). By using only variables routinely available prior to liver transplantation, a validated model of posttransplantation recurrence risk was produced with a concordance statistic of 0.83. The validated model shows sensitivity of 83.6%, specificity of 82.6%, and negative predictive value of 98.4%, which are pessimistic estimates. Conclusion Response to DEB-TACE is correlated with tumor biology and patients at risk for posttransplantation recurrence, and it may be associated with HCC recurrence after liver transplantation. RSNA, 2017 Online supplemental material is available for this article.

摘要

目的 在经导管肝动脉化疗栓塞术(TACE)基础上评估免疫标志物和肿瘤生物学在接受肝移植桥接治疗的肝细胞癌(HCC)患者中的反应,并为移植后复发风险制定优化的移植前模型。

材料与方法 本研究为机构审查委员会批准的符合 HIPAA 规定的回顾性研究,共纳入 93 例连续患者(73 例男性,20 例女性;平均年龄 59.6 岁;年龄范围 23-72 岁),于 2011 年 7 月 7 日至 2016 年 5 月 16 日接受多柔比星洗脱微球(DEB)的 TACE(简称 DEB-TACE)治疗,随后接受移植。DEB-TACE 反应基于实体瘤反应评估标准修订版。比较影像学反应和移植后复发与患者人口统计学、肝功能、基本免疫标志物、治疗剂量和肿瘤形态。采用单变量和多变量统计分析以及内部验证和倾向评分匹配已知影响复发的因素,以评估 DEB-TACE 反应对复发的独立影响。

结果 低级别肿瘤(0 级、1 级或 2 级)患者的长期治疗反应良好,在 87%的患者(完全缓解 49%;部分缓解 38%;稳定疾病[SD]或局部疾病进展[DP] 13%)中优于高级别肿瘤(3 级或 4 级)患者(完全缓解 0%;部分缓解 33%;SD 或 DP 67%)(P<0.001)。在 93 例接受治疗的患者中,82 例在移植后进行了随访(平均随访时间 757 天)。7 例(9%)患者发生复发(平均移植后时间 635 天)。DEB-TACE 反应不良(SD 或 DP)的比例为 86%,占所有 SD 或 DP 患者的 35%(P<0.001)。仅使用移植前常规可用的变量,即可建立移植后复发风险的验证模型,其一致性统计量为 0.83。验证模型的灵敏度为 83.6%,特异性为 82.6%,阴性预测值为 98.4%,这些都是悲观的估计值。

结论 DEB-TACE 的反应与肿瘤生物学和移植后复发风险相关,可能与肝移植后 HCC 复发相关。RSNA,2017 年。本文提供在线补充材料。

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