The Impact of Radiation Dose and Tumour Burden on Outcomes in Hepatocellular Carcinoma: 11-Year Experience in a 413-Patient Cohort Treated with Yttrium-90 Resin Microsphere Radioembolisation.

IF 11.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Liver Cancer Pub Date : 2024-09-19 eCollection Date: 2025-04-01 DOI:10.1159/000541539
Kaina Chen, Aaron K T Tong, Fiona N N Moe, David C E Ng, Richard H G Lo, Apoorva Gogna, Sean X Yan, Sue Ping Thang, Kelvin S H Loke, Nanda Karaddi Venkatanarasimha, Hian Liang Huang, Chow Wei Too, Timothy S K Ong, Eng Xuan Yeo, Daniel Yang Yao Peh, Ashley W Y Ng, Lu Yang, Wan Ying Chan, Jason P E Chang, Brian K P Goh, Han Chong Toh, Pierce K H Chow
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引用次数: 0

Abstract

Introduction: Transarterial radioembolisation (RE) using yttrium-90 (Y-90) microspheres is a widely used locoregional therapy for a broad spectrum of hepatocellular carcinoma (HCC) given its favourable safety profile. We evaluated the real-world outcomes of unresectable HCC treated with resin Y-90 RE and the relationship between tumour absorbed dose and subsequent curative therapy with survival.

Methods: Included were consecutive patients treated with Y-90 resin microspheres RE for unresectable HCC between January 2008 and May 2019 at the National Cancer Centre Singapore/Singapore General Hospital. The outcomes were stratified by tumour burden, distribution, presence of portal vein invasion (PVI) and liver function to improve prognostication.

Results: The median overall survival (OS) evaluated on 413 included patients was 20.9 months (95% CI: 18.2-24.0). More than half of the patients (214/413, 51.8%) had HCC beyond up-to-seven criteria, and 37.3% had portal vein invasion (154/413, 37.3%). Majority (71.7%) had dosimetry calculated based on the partition model. Patients who received ≥150 Gy to tumour had significantly better outcomes (OS 32.2 months, 95% CI: 18.3-46.4) than those who did not (OS 17.5 months, 95% CI: 13.7-22.7, p < 0.001). Seventy patients (17%) received curative therapies after tumour was downstaged by Y-90 RE and had better OS of 79.7 months (95% CI: 40.4 - NE) compared to those who did not receive curative therapies (OS 17.1 months; 95% CI: 13.5-20.4, p < 0.001). RE-induced liver injury was observed in 5.08% of the patients while 3.2% of the patients had possible radiation pneumonitis but none developed Grade 3-4 toxicity. For HCC without PVI, OS differed significantly with performance status, albumin-bilirubin grade, tumour distribution, and radiation dose; for HCC with PVI, Child-Pugh class and AFP were significant predictors of survival.

Conclusions: Treatment outcomes for unresectable HCC using Y-90 RE were favourable. Incorporating tumour burden and distribution improved prognostication. Patients who received tumour absorbed dose above 150 Gy had better OS. Patients who subsequently received curative therapies after being downstaged by Y-90 RE had remarkable clinical outcomes.

放射剂量和肿瘤负荷对肝细胞癌预后的影响:413例接受钇-90树脂微球放射栓塞治疗的患者11年的经验
导论:使用钇-90 (Y-90)微球经动脉放射栓塞(RE)是广泛应用于广泛范围的肝细胞癌(HCC)的局部治疗方法,因为它具有良好的安全性。我们评估了树脂Y-90 RE治疗不可切除HCC的实际结果,以及肿瘤吸收剂量和随后的治愈治疗与生存的关系。方法:纳入2008年1月至2019年5月在新加坡国家癌症中心/新加坡总医院连续接受Y-90树脂微球RE治疗不可切除HCC的患者。根据肿瘤负荷、分布、门静脉侵犯(PVI)的存在和肝功能对结果进行分层,以改善预后。结果:纳入的413例患者的中位总生存期(OS)为20.9个月(95% CI: 18.2-24.0)。超过一半的患者(214/413,51.8%)HCC≥7级,37.3%的患者有门静脉侵犯(154/413,37.3%)。大多数(71.7%)采用分区模型计算剂量。接受≥150gy肿瘤治疗的患者的预后(生存期32.2个月,95% CI: 18.3-46.4)明显优于未接受治疗的患者(生存期17.5个月,95% CI: 13.7-22.7, p < 0.001)。70例患者(17%)在接受Y-90放射治疗后接受了根治性治疗,与未接受根治性治疗的患者(OS 17.1个月;95% CI: 13.5-20.4, p < 0.001)。5.08%的患者出现re性肝损伤,3.2%的患者可能出现放射性肺炎,但没有发生3-4级毒性。对于无PVI的HCC, OS与运动状态、白蛋白胆红素分级、肿瘤分布和辐射剂量有显著差异;对于合并PVI的HCC, Child-Pugh分级和AFP是生存率的重要预测指标。结论:使用Y-90 RE治疗不可切除的HCC效果良好。结合肿瘤负荷和分布可改善预后。肿瘤吸收剂量大于150gy的患者OS较好。经Y-90 RE降阶后接受根治性治疗的患者临床效果显著。
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来源期刊
Liver Cancer
Liver Cancer Medicine-Oncology
CiteScore
20.80
自引率
7.20%
发文量
53
审稿时长
16 weeks
期刊介绍: Liver Cancer is a journal that serves the international community of researchers and clinicians by providing a platform for research results related to the causes, mechanisms, and therapy of liver cancer. It focuses on molecular carcinogenesis, prevention, surveillance, diagnosis, and treatment, including molecular targeted therapy. The journal publishes clinical and translational research in the field of liver cancer in both humans and experimental models. It publishes original and review articles and has an Impact Factor of 13.8. The journal is indexed and abstracted in various platforms including PubMed, PubMed Central, Web of Science, Science Citation Index, Science Citation Index Expanded, Google Scholar, DOAJ, Chemical Abstracts Service, Scopus, Embase, Pathway Studio, and WorldCat.
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