经动脉化疗栓塞联合靶向治疗结直肠癌术后复发伴肝转移的临床观察。

IF 1.7 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Jian-Yu Liu, Zhi-Hui Liang, Jing-Lei Liu, Liang Li, Bao Cui, Tie-Gang Li
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引用次数: 0

摘要

背景:结直肠癌(CRC)伴肝转移仍然是一个重大的治疗挑战,特别是在术后复发的情况下。虽然经动脉化疗栓塞(TACE)和靶向治疗单独显示出希望,但联合治疗术后复发性结直肠癌伴肝转移的疗效有待进一步研究。目的:评价TACE联合靶向治疗结直肠癌术后复发伴肝转移的疗效和安全性。方法:本观察性研究纳入了2020年1月至2023年12月期间75例伴有肝转移的术后复发结直肠癌患者。所有患者均接受TACE联合靶向治疗:贝伐单抗(40例,53.3%)、西妥昔单抗(25例,33.3%)或帕尼单抗(10例,13.3%)。使用实体瘤反应评价标准1.1标准评估治疗反应,以总生存期(OS)和无进展生存期作为主要终点。在基线和治疗六个月后,使用欧洲癌症研究和治疗组织的生活质量问卷对生活质量进行评估。结果:中位OS为28个月(95%置信区间:24-32个月),中位无进展生存期为12个月(95%置信区间:10-14个月)。贝伐单抗治疗患者的生存结果明显优于西妥昔单抗/帕尼单抗治疗患者(中位生存期,30个月vs 24个月,P = 0.015)。总有效率为58.7%,疾病控制率为86.7%。生活质量评分在所有领域均有显著改善,贝伐单抗组的改善更大。治疗相关不良事件可控,13.3%的患者发生3-4级不良事件,无治疗相关死亡。结论:TACE联合靶向治疗,特别是贝伐单抗治疗术后复发性结直肠癌合并肝转移的疗效和安全性良好。这种多模式方法不仅改善了生存结果,而且提高了患者的生活质量,这表明它有潜力成为这种具有挑战性的疾病的有价值的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical observation of combined transarterial chemoembolization and targeted therapy in postoperative recurrent colorectal cancer with liver metastasis.

Background: Colorectal cancer (CRC) with liver metastasis remains a significant therapeutic challenge, particularly in cases of postoperative recurrence. While transarterial chemoembolization (TACE) and targeted therapies have shown promise individually, the efficacy combining these for treating postoperative recurrent CRC with liver metastasis requires further investigation.

Aim: To evaluate the efficacy and safety of TACE combined with targeted therapies for postoperative recurrent CRC with liver metastasis.

Methods: This observational study enrolled 75 patients with postoperative recurrent CRC accompanied by liver metastasis between January 2020 and December 2023. All patients received combined treatment with TACE and targeted therapy: Bevacizumab (40 patients, 53.3%), cetuximab (25 patients, 33.3%), or panitumumab (10 patients, 13.3%). Treatment response was evaluated using the Response Evaluation Criteria in Solid Tumors 1.1 criteria, with overall survival (OS) and progression-free survival as the primary endpoints. Quality of life was assessed using the European Organization for Research and Treatment of Cancer quality of life questionnaire at baseline and after six months of treatment.

Results: The median OS was 28 months (95% confidence interval: 24-32 months), and the median progression-free survival was 12 months (95% confidence interval: 10-14 months). Patients treated with bevacizumab showed significantly better survival outcomes than those treated with cetuximab/panitumumab (median OS, 30 vs 24 months, P = 0.015). The overall response rate was 58.7%, with a disease control rate of 86.7%. Quality of life scores improved significantly across all domains, with greater improvements observed in the bevacizumab group. Treatment-related adverse events were manageable, with grade 3-4 events occurring in 13.3% of the patients and no treatment-related mortality.

Conclusion: The combination of TACE with targeted therapy, particularly bevacizumab, has demonstrated promising efficacy and acceptable safety for the treatment of postoperative recurrent CRC with liver metastasis. This multimodal approach not only improved survival outcomes but also enhanced the patients' quality of life, suggesting its potential as a valuable treatment strategy for this challenging condition.

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