Chin Re-I, Bommireddy Anirudh, Fraum Tyler J, Ludwig Daniel R, Huang Yi, Zoberi Jacqueline E, Garcia-Ramirez Jose L, Maughan Nichole M, Chapman William, Korenblat Kevin, Henke Lauren E, Kim Hyun, Badiyan Shahed N
Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
St. Louis University School of Medicine, St. Louis, Missouri.
Adv Radiat Oncol. 2022 Mar 21;7(4):100948. doi: 10.1016/j.adro.2022.100948. eCollection 2022 Jul-Aug.
Yttrium-90 (90Y) radioembolization with an escalated dose has been shown to improve clinical outcomes compared with standard dose radioembolization, but there are few data on the local control of primary liver tumors. We reported the clinical outcomes of patients with unresectable primary liver tumors treated with 90Y radioembolization with an escalated dose.
Clinical data of patients with unresectable hepatocellular carcinoma (HCC), cholangiocarcinoma (CC), and biphenotypic tumors (cHCC-CC) treated with radioembolization with an escalated dose (≥150 Gy) between 2013 and 2020 with >3 months follow-up were retrospectively reviewed. The primary endpoint was freedom from local progression. Clinical response was defined by Modified Response Evaluation Criteria in Solid Tumours and toxic effects were assessed using Common Terminology Criteria for Adverse Events version 5.0.
Fifty-three patients with HCC and 15 patients with CC/cHCC-CC were analyzed. The median dose delivered was 205 Gy (interquartile range, 183-253 Gy) and 198 Gy (interquartile range, 154-234 Gy) for patients with HCC and CC/cHCC-CC, respectively. The 1-year freedom from local progression rate was 54% (95% confidence interval [CI], 38%-78%) for patients with HCC and 66% (95% CI, 42%-100%) for patients with CC/cHCC-CC. For patients with HCC, United Network for Organ Sharing nodal stage 1 ( = .01), nonsolitary tumors ( = .02), pretreatment α-fetoprotein of >7.7 ng/mL ( = .006), and ≤268 Gy dose delivered ( = .003) were predictors for local progression on multivariate Cox analysis. No patients with HCC who received a dose >268 Gy had a local tumor progression. The 1-year overall survival for patients with HCC was 74% (95% CI, 61%-89%). After radioembolization, 5 (7%) patients had grade 3 ascites, and 4 (6%) patients had grade 3/4 hyperbilirubinemia.
Treatment of unresectable primary liver tumors with 90Y radioembolization with an escalated dose was safe and well tolerated. Delivery of >268 Gy may improve local tumor control of HCC. Determination of the maximum tolerated dose needs to be performed in the context of future prospective dose-escalation trials to further evaluate the safety and efficacy of such an approach.
与标准剂量放射性栓塞相比,高剂量钇-90(90Y)放射性栓塞已显示可改善临床结果,但关于原发性肝肿瘤局部控制的数据较少。我们报告了接受高剂量90Y放射性栓塞治疗的不可切除原发性肝肿瘤患者的临床结果。
回顾性分析了2013年至2020年间接受高剂量(≥150 Gy)放射性栓塞治疗且随访超过3个月的不可切除肝细胞癌(HCC)、胆管癌(CC)和双表型肿瘤(cHCC-CC)患者的临床资料。主要终点是无局部进展。临床反应根据实体瘤改良反应评估标准定义,毒性作用使用不良事件通用术语标准5.0版进行评估。
分析了53例HCC患者和15例CC/cHCC-CC患者。HCC和CC/cHCC-CC患者的中位给药剂量分别为205 Gy(四分位间距,183 - 253 Gy)和198 Gy(四分位间距,154 - 234 Gy)。HCC患者的1年无局部进展率为54%(95%置信区间[CI],38% - 78%),CC/cHCC-CC患者为66%(95%CI,42% - 100%)。对于HCC患者,多因素Cox分析显示,器官共享联合网络淋巴结分期1期(P = .01)、非孤立肿瘤(P = .02)、治疗前甲胎蛋白>7.7 ng/mL(P = .006)以及给药剂量≤268 Gy(P = .003)是局部进展的预测因素。接受剂量>268 Gy的HCC患者均无局部肿瘤进展。HCC患者的1年总生存率为74%(95%CI,61% - 89%)。放射性栓塞后,5例(7%)患者出现3级腹水,4例(6%)患者出现3/4级高胆红素血症。
高剂量90Y放射性栓塞治疗不可切除原发性肝肿瘤安全且耐受性良好。给药剂量>268 Gy可能改善HCC的局部肿瘤控制。需要在未来的前瞻性剂量递增试验中确定最大耐受剂量,以进一步评估这种方法的安全性和有效性。