Friedrich Stefanie, Busch Felix, Jonczyk Martin, Wieners Gero, Böning Georg, Lüdemann Willie Magnus, Meddeb Aymen, Collettini Federico, Gebauer Bernhard
Department of Radiology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt Universität zu Berlin, Campus Virchow-Klinikum, Berlin, Germany.
Department of Anesthesiology, Division of Operative Intensive Care Medicine, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt Universität zu Berlin, Campus Virchow-Klinikum, Berlin, Germany.
J Contemp Brachytherapy. 2023 Feb;15(1):15-26. doi: 10.5114/jcb.2023.125480. Epub 2023 Feb 28.
To compare the effectivity and toxicity of monotherapy with computed tomography-guided high-dose-rate brachytherapy (CT-HDRBT) vs. combination therapy of transarterial chemoembolization with irinotecan (irinotecan-TACE) and CT-HDRBT in patients with large unresectable colorectal liver metastases (CRLM) with a diameter of > 3 cm.
Forty-four retrospectively matched patients with unresectable CRLM were treated either with mono-CT-HDRBT or with a combination of irinotecan-TACE and CT-HDRBT ( = 22 in each group). Matching parameters included treatment, disease, and baseline characteristics. National Cancer Institute Common Terminology Criteria for Adverse Events (version 5.0) were used to evaluate treatment toxicity and the Society of Interventional Radiology classification was applied to analyze catheter-related adverse events. Statistical analysis involved Cox regression, Kaplan-Meier estimator, log-rank test, receiver operating characteristic curve analysis, Shapiro-Wilk test, Wilcoxon test, paired sample -test, and McNemar test. -values < 0.05 were deemed significant.
Combination therapy ensued longer median progression-free survival (PFS: 5/2 months, = 0.002) and significantly lower local (23%/68%, < 0.001) and intrahepatic (50%/95%, < 0.001) progress rates compared with mono-CT-HDRBT after a median follow-up time of 10 months. Additionally, tendencies for longer local tumor control (LTC: 17/9 months, = 0.052) were found in patients undergoing both interventions. After combination therapy, aspartate and alanine aminotransferase toxicity levels increased significantly, while total bilirubin toxicity levels showed significantly higher increases after monotherapy. No catheter-associated major or minor complications were identified in each cohort.
Combining irinotecan-TACE with CT-HDRBT can improve LTC rates and PFS compared with mono-CT-HDRBT in patients with unresectable CRLM. The combination of irinotecan-TACE and CT-HDRBT shows satisfying safety profiles.
比较计算机断层扫描引导下高剂量率近距离放射治疗(CT-HDRBT)单药治疗与伊立替康经动脉化疗栓塞术(伊立替康-TACE)联合CT-HDRBT治疗直径>3 cm的不可切除大肠肝转移瘤(CRLM)患者的有效性和毒性。
44例回顾性匹配的不可切除CRLM患者接受了CT-HDRBT单药治疗或伊立替康-TACE联合CT-HDRBT治疗(每组22例)。匹配参数包括治疗、疾病和基线特征。采用美国国立癌症研究所不良事件通用术语标准(第5.0版)评估治疗毒性,并应用介入放射学会分类法分析导管相关不良事件。统计分析包括Cox回归、Kaplan-Meier估计、对数秩检验、受试者工作特征曲线分析、Shapiro-Wilk检验、Wilcoxon检验、配对样本t检验和McNemar检验。P值<0.05被认为具有统计学意义。
中位随访时间为10个月后,与CT-HDRBT单药治疗相比,联合治疗的中位无进展生存期更长(PFS:5/2个月,P=0.002),局部(23%/68%,P<0.001)和肝内(50%/95%,P<0.001)进展率显著更低。此外,接受两种干预措施的患者出现局部肿瘤控制时间更长的趋势(LTC:17/9个月,P=0.052)。联合治疗后,天冬氨酸和丙氨酸转氨酶毒性水平显著升高,而单药治疗后总胆红素毒性水平升高更为显著。每个队列中均未发现与导管相关的严重或轻微并发症。
与CT-HDRBT单药治疗相比,伊立替康-TACE联合CT-HDRBT可提高不可切除CRLM患者的LTC率和PFS。伊立替康-TACE与CT-HDRBT联合显示出令人满意的安全性。