From the Division of Interventional Radiology, Department of Radiology (A.S., M.S.M., N.H.V., M.M.T., J.L.W., M.A.); Department of Radiology (L.L.T.); Division of Hepatology and Gastroenterology, Department of Internal Medicine (M.P.C., A.M.C.); Division of Hematology and Medical Oncology (A.J.B.); Division of Nuclear Medicine, Department of Radiology (J.A.P.); Division of Transplantation, Department of Surgery (D.E.E.); and Department of Pathology (I.A.N.), Beth Israel Deaconess Medical Center, Harvard Medical School, 1 Deaconess Rd, Boston, MA 02215.
Radiology. 2024 May;311(2):e231386. doi: 10.1148/radiol.231386.
Background Limited data are available on radiation segmentectomy (RS) for treatment of hepatocellular carcinoma (HCC) using yttrium 90 (Y) resin microsphere doses determined by using a single-compartment medical internal radiation dosimetry (MIRD) model. Purpose To evaluate the efficacy and safety of RS treatment of HCC with Y resin microspheres using a single-compartment MIRD model and correlate posttreatment dose with outcomes. Materials and Methods This retrospective single-center study included adult patients with HCC who underwent RS with Y resin microspheres between July 2014 and December 2022. Posttreatment PET/CT and dosimetry were performed. Adverse events were assessed using the Common Terminology Criteria for Adverse Events, version 5.0. Per-lesion and overall response rates (ie, complete response [CR], objective response, disease control, and duration of response) were assessed at imaging using the Modified Response Evaluation Criteria in Solid Tumors, and overall survival (OS) was assessed using Kaplan-Meier analysis. Results Among 67 patients (median age, 69 years [IQR, 63-78 years]; 54 male patients) with HCC, median tumor absorbed dose was 232 Gy (IQR, 163-405 Gy). At 3 months, per-lesion and overall (per-patient) CR was achieved in 47 (70%) and 41 (61%) of 67 patients, respectively. At 6 months ( = 46), per-lesion rates of objective response and disease control were both 94%, and per-patient rates were both 78%. A total of 88% (95% CI: 79 99) and 72% (95% CI: 58, 90) of patients had a per-lesion and overall duration of response of 1 year or greater. At 1 month, a grade 3 clinical adverse event (abdominal pain) occurred in one of 67 (1.5%) patients. Median posttreatment OS was 26 months (95% CI: 20, not reached). Disease progression at 2 years was lower in the group that received 300 Gy or more than in the group that received less than 300 Gy (17% vs 61%; = .047), with no local progression in the former group through the end of follow-up. Conclusion Among patients with HCC who underwent RS with Y resin microspheres, 88% and 72% achieved a per-lesion and overall duration of response of 1 year or greater, respectively, with one grade 3 adverse event. In patients whose tumors received 300 Gy or more according to posttreatment dosimetry, a disease progression benefit was noted. © RSNA, 2024
背景 利用单室医学内部辐射剂量学(MIRD)模型确定钇 90(Y)树脂微球剂量的放射性肝段切除术(RS)治疗肝细胞癌(HCC)的相关数据有限。目的 评估使用单室 MIRD 模型治疗 HCC 的 RS 疗效和安全性,并将治疗后剂量与结局相关联。材料与方法 本回顾性单中心研究纳入了 2014 年 7 月至 2022 年 12 月期间接受 Y 树脂微球 RS 治疗的 HCC 成年患者。术后进行 PET/CT 和剂量测定。采用通用不良事件术语标准 5.0 评估不良事件。使用实体瘤改良反应评估标准,在影像学上评估每个病灶和总体的反应率(即完全缓解[CR]、客观缓解、疾病控制和缓解持续时间),采用 Kaplan-Meier 分析评估总生存期(OS)。结果 在 67 例 HCC 患者(中位年龄,69 岁[IQR,63-78 岁];54 例男性)中,中位肿瘤吸收剂量为 232 Gy(IQR,163-405 Gy)。术后 3 个月,67 例患者中 47 例(70%)和 41 例(61%)达到了每个病灶的 CR。术后 6 个月(=46),每个病灶的客观缓解率和疾病控制率均为 94%,每个患者的缓解率均为 78%。88%(95%CI:79 99)和 72%(95%CI:58,90)的患者的每个病灶和总体缓解持续时间为 1 年或更长。术后 1 个月,67 例患者中有 1 例(1.5%)发生 3 级临床不良事件(腹痛)。中位随访期 OS 为 26 个月(95%CI:20,未达到)。在接受 300 Gy 或更高剂量治疗的患者中,2 年时疾病进展率低于接受 300 Gy 以下剂量治疗的患者(17%比 61%; =.047),前者在整个随访期内无局部进展。结论 在接受 Y 树脂微球 RS 治疗的 HCC 患者中,88%和 72%的患者分别实现了 1 年或更长的每个病灶和总体缓解持续时间,只有 1 例 3 级不良事件。在根据术后剂量测定结果接受 300 Gy 或更高剂量治疗的患者中,观察到疾病进展获益。 ©RSNA,2024