Department of Radiation Oncology, Stanford Cancer Institute, Stanford, California.
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Pract Radiat Oncol. 2020 Jul-Aug;10(4):274-281. doi: 10.1016/j.prro.2020.02.010. Epub 2020 Feb 29.
Our purpose was to report the outcome of stereotactic ablative radiation therapy (SABR) to the primary tumor for patients with metastatic pancreatic cancer.
We examined the records of patients with metastatic pancreatic cancer treated with SABR to the primary tumor between 2002 and 2018. Toxicities were graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.03. Pain intensity pre- and post-SABR was scored according to the Stanford Pain Scale as reported by the patient. Time-to-events were calculated from the date of end of SABR delivery.
In total, 27 patients were identified that met the inclusion criteria. Seventeen (63%) patients received single fraction SABR with a median dose of 25 Gy (range, 12.5-25), and 10 (37%) patients were treated in 5 fractions with a median dose of 33 Gy (range, 25-40). Before the start of SABR, 17 (63%) patients reported having abdominal pain, with a median intensity of 5 in the 0 to 10 pain scale (range, 1-9), 11 (41%) of them needing continuous opioid use. The median follow-up was 6 months (range, 0-18). Median overall survival was 7 months (95% confidence interval, 3-10), with a cumulative incidence of local failures at 1 year of 25% (95% confidence interval, 10-44). After SABR, there was a significant reduction in the mean intensity of pain (P = .01), and a 46% relative reduction in continuous opioid use. Only 2 patients (7%) presented a grade 3 toxicity that could be attributed to treatment.
In this small series, SABR was a safe and effective option for the local palliation of metastatic pancreatic cancer, with measurable improvements in abdominal pain and the need for opioids.
本研究旨在报告立体定向消融放疗(SABR)治疗转移性胰腺癌患者原发肿瘤的结果。
我们对 2002 年至 2018 年间接受 SABR 治疗的转移性胰腺癌患者的病历进行了检查。毒性反应根据国家癌症研究所不良事件通用术语标准第 4.03 版进行分级。根据患者报告的斯坦福疼痛量表,在 SABR 前后对疼痛强度进行评分。从 SABR 结束日期开始计算时间事件。
共确定了 27 名符合纳入标准的患者。17 名(63%)患者接受单次 SABR 治疗,中位剂量为 25 Gy(范围,12.5-25),10 名(37%)患者接受 5 次分割治疗,中位剂量为 33 Gy(范围,25-40)。在开始 SABR 之前,17 名(63%)患者报告有腹痛,疼痛程度中位数为 0 至 10 疼痛量表中的 5(范围,1-9),其中 11 名(41%)需要持续使用阿片类药物。中位随访时间为 6 个月(范围,0-18)。中位总生存期为 7 个月(95%置信区间,3-10),1 年时局部失败的累积发生率为 25%(95%置信区间,10-44)。SABR 后,疼痛强度的平均水平显著降低(P =.01),连续使用阿片类药物的相对减少了 46%。只有 2 名患者(7%)出现了可归因于治疗的 3 级毒性。
在这项小系列研究中,SABR 是治疗转移性胰腺癌的一种安全有效的局部姑息治疗方法,可显著改善腹痛和阿片类药物的需求。