Department of Interventional Radiology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.
Diagn Interv Radiol. 2021 Jan;27(1):50-58. doi: 10.5152/dir.2020.19371.
We aimed to explore the feasibility and clinical effectiveness of percutaneous CT-guided iodine-125 (¹²⁵I) brachytherapy combined with chemotherapy for the treatment of patients with unresectable or locally advanced pancreatic carcinoma (PC).
We retrospectively reviewed 66 patients with Stage III and IV PC who had received chemotherapy. A total of 35 (53%) patients receiving 125I brachytherapy and chemotherapy (gemcitabine + cisplatin, GP) were classified as Group A, and 31 (47%) patients who received GP chemotherapy alone were categorized as Group B. The evaluated indications were local control rate (LCR), local progression-free survival (LPFS), overall survival (OS), treatment-related complications, and the degree of symptom relief. Kaplan-Meier curves, log-rank test and Cox regression models were generated and used for further analysis to identify predictors of outcomes.
The median follow-up time was 6.00±0.84 months. The 1-, 3-, 6-, 12- and 18-month LCRs for Group A were 100% (35/35), 89.3% (25/28), 71.4% (15/21), 37.5% (3/8) and 33.3% (1/3), respectively; and those for Group B were 87.1% (27/31), 69.6% (16/23), 41.2% (7/17), 14.3% (1/7) and 0% (0/3), respectively. The LCR differed at 1-, 3- and 6-months (P = 0.032; P = 0.009; P = 0.030; respectively). The median LPFS was 7.00±0.30 months and 5.00±0.75 months for Groups A and B (P = 0.023), respectively; however, the median OS of the groups were not significantly different (8.00±0.77 months vs. 6.00±1.04 months. P = 0.917). No life-threatening complications occurred during or after the procedures. Patients in Group A experienced better pain control and relief of abdominal distension than those in Group B.
CT-guided 125I brachytherapy is a feasible, safe, and valuable treatment for patients with unresectable PC.
本研究旨在探讨经皮 CT 引导下碘 125(¹²⁵I)近距离放疗联合化疗治疗不可切除或局部进展期胰腺癌(PC)的可行性和临床疗效。
回顾性分析了 66 例接受化疗的 III 期和 IV 期 PC 患者的资料。35 例(53%)接受 ¹²⁵I 近距离放疗联合化疗(吉西他滨+顺铂,GP)的患者被归入 A 组,31 例(47%)仅接受 GP 化疗的患者归入 B 组。评估的指标包括局部控制率(LCR)、局部无进展生存期(LPFS)、总生存期(OS)、治疗相关并发症以及症状缓解程度。采用 Kaplan-Meier 曲线、Log-rank 检验和 Cox 回归模型进行进一步分析,以确定预后的预测因素。
中位随访时间为 6.00±0.84 个月。A 组患者的 1、3、6、12 和 18 个月 LCR 分别为 100%(35/35)、89.3%(25/28)、71.4%(15/21)、37.5%(3/8)和 33.3%(1/3);B 组患者的 1、3、6、12 和 18 个月 LCR 分别为 87.1%(27/31)、69.6%(16/23)、41.2%(7/17)、14.3%(1/7)和 0%(0/3)。1、3 和 6 个月时的 LCR 存在差异(P = 0.032;P = 0.009;P = 0.030;分别)。A、B 两组的中位 LPFS 分别为 7.00±0.30 个月和 5.00±0.75 个月(P = 0.023),但两组的中位 OS 无显著差异(8.00±0.77 个月 vs. 6.00±1.04 个月,P = 0.917)。治疗过程中和治疗后均未发生危及生命的并发症。A 组患者的疼痛控制和腹胀缓解情况明显优于 B 组。
CT 引导下 ¹²⁵I 近距离放疗是一种可行、安全且有价值的治疗不可切除 PC 的方法。