Interventional Radiology, Memorial Sloan-Kettering Cancer Center, New York, NY.
Interventional Radiology, Memorial Sloan-Kettering Cancer Center, New York, NY.
Clin Colorectal Cancer. 2014 Mar;13(1):27-36. doi: 10.1016/j.clcc.2013.11.010. Epub 2013 Nov 13.
This prospective study assessed the safety and outcomes of selective internal radiation therapy (SIRT) using yttrium-90 ((90)Y) resin microspheres as a salvage therapy for liver-predominant metastases of colorectal cancer in patients with documented progression after hepatic arterial chemotherapy (HAC) and systemic chemotherapy.
We recruited 19 patients who had received a mean of 2.9 prior lines of chemotherapy and ≥ 1 line of HAC. Dose-limiting toxicities (grade 3 or higher) were catalogued using Common Terminology Criteria for Adverse Events version 3.0. At 4 to 8 weeks and 3 to 4 months post SIRT, responses were assessed by carcinoembryonic antigen (CEA), and quantitative imaging using Response Evaluation Criteria in Solid Tumors (RECIST) and PET Response Criteria in Solid Tumors (PERCIST). Liver progression-free survival (LPFS), progression-free survival (PFS), and overall survival (OS) were calculated using Kaplan-Meier methodology.
Median follow-up was 31.2 months after SIRT. Within 6 weeks of SIRT, 3 patients (15.8%) experienced grade 3 toxicity. There was no incidence of radiation-induced liver disease. Responses by RECIST, PERCIST, and CEA were, respectively, 0%, 20%, and 32% at 4 to 8 weeks and 5%, 33%, and 21% at 3 to 4 months post SIRT; 53% of patients had stable disease (by RECIST) at 3 to 4 months. Of 19 patients, 4 (21.1%) had liver ablation, 9 (47%) received additional HAC, and 17 (89%) received systemic chemotherapy after SIRT. Median LPFS, PFS, and OS after SIRT were 5.2 months, 2.0 months, and 14.9 months, respectively.
SIRT was well tolerated and did not prohibit subsequent treatment, resulting in a median OS of 14.9 months in this heavily pretreated population.
本前瞻性研究评估了钇-90((90)Y)树脂微球选择性内放射治疗(SIRT)作为结直肠癌肝转移患者肝动脉化疗(HAC)和系统化疗后记录疾病进展的挽救性治疗的安全性和结果。
我们招募了 19 名患者,这些患者平均接受了 2.9 线化疗和≥1 线 HAC。使用不良事件通用术语标准 3.0 版(CTCAE)对剂量限制毒性(3 级或更高)进行分类。在 SIRT 后 4 至 8 周和 3 至 4 个月,通过癌胚抗原(CEA)和实体瘤反应评估标准(RECIST)和实体瘤 PERCIST 标准评估反应。采用 Kaplan-Meier 方法计算肝无进展生存期(LPFS)、无进展生存期(PFS)和总生存期(OS)。
SIRT 后中位随访时间为 31.2 个月。SIRT 后 6 周内,3 名患者(15.8%)出现 3 级毒性。无放射性肝损伤发生。4 至 8 周时,根据 RECIST、PERCIST 和 CEA 评估的反应率分别为 0%、20%和 32%,3 至 4 个月时分别为 5%、33%和 21%;3 至 4 个月时,根据 RECIST,53%的患者疾病稳定。19 名患者中,4 名(21.1%)行肝消融术,9 名(47%)接受额外的 HAC,17 名(89%)在 SIRT 后接受全身化疗。SIRT 后 LPFS、PFS 和 OS 的中位数分别为 5.2 个月、2.0 个月和 14.9 个月。
SIRT 耐受性良好,不影响后续治疗,在这一预处理广泛的人群中,中位 OS 为 14.9 个月。