Department of Radiation Oncology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands; Department of Radiation Oncology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands; Cancer Center Amsterdam, Treatment and Quality of Life, Amsterdam, The Netherlands.
Department of Radiation Oncology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands; Department of Radiation Oncology, Instituut Verbeeten, The Netherlands.
Int J Radiat Oncol Biol Phys. 2024 Feb 1;118(2):352-361. doi: 10.1016/j.ijrobp.2023.08.055. Epub 2023 Aug 28.
Clinical evidence is limited regarding palliative radiation therapy for relieving pancreatic cancer-related pain. We prospectively investigated pain response after short-course palliative radiation therapy in patients with moderate-to-severe pancreatic cancer-related pain.
In this prospective phase 2 single center nonrandomized trial, 30 patients with moderate-to-severe pain (5-10, on a 0-10 scale) of pancreatic cancer refractory to pain medication, were treated with a short-course palliative radiation therapy; 24 Gy in 3 weekly fractions (2015-2018). Primary endpoint was defined as a clinically relevant average decrease of ≥2 points in pain severity, compared with baseline, within 7 weeks after the start of treatment. Secondary endpoint was global quality of life (QoL), with a clinically relevant increase of 5 to 10 points (0-100 scale). Pain severity reduction and QoL were assessed 9 times using the Brief Pain Inventory and European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-C15-PAL, respectively. Both outcomes were analyzed using joint modeling. In addition, acute toxicity based on clinician reporting and overall survival (OS) were assessed.
Overall, 29 of 30 patients (96.7%) received palliative radiation therapy. At baseline, the median oral morphine equivalent daily dose was 129.5 mg (range, 20.0-540.0 mg), which decreased to 75.0 mg (range, 15.0-360.0 mg) after radiation (P = .021). Pain decreased on average 3.15 points from baseline to 7 weeks (one-sided P = .045). Patients reported a clinically relevant mean pain severity reduction from 5.9 to 3.8 points (P = .011) during the first 3 weeks, which further decreased to 3.2 until week 11, ending at 3.4 (P = .006) in week 21 after the first radiation therapy fraction. Global QoL significantly improved from 50.5 to 60.8 during the follow-up period (P = .001). Grade 3 acute toxicity occurred in 3 patients and no grade 4 to 5 toxicity was observed. Median OS was 11.8 weeks, with a 13.3% 1-year actuarial OS rate.
Short-course palliative radiation therapy for pancreatic cancer-related pain was associated with rapid, clinically relevant reduction in pain severity, and clinically relevant improvement in global QoL, with mostly mild toxicity.
关于缓解胰腺癌相关疼痛的姑息性放疗的临床证据有限。我们前瞻性地研究了中重度胰腺癌相关疼痛患者接受短程姑息性放疗后的疼痛反应。
在这项前瞻性的 2 期单中心非随机试验中,30 名中重度疼痛(5-10 分,0-10 分制)且对疼痛药物治疗有抗药性的胰腺癌患者接受了短程姑息性放疗;24 Gy 分 3 周给予(2015-2018 年)。主要终点定义为治疗开始后 7 周内疼痛严重程度相对于基线平均下降≥2 分,具有临床相关性。次要终点为全球生活质量(QoL),有临床意义的增加 5-10 分(0-100 分制)。使用简短疼痛量表和欧洲癌症研究与治疗组织生活质量问卷-C15-PAL 分别在 9 次评估疼痛严重程度减轻和 QoL。使用联合建模分析这两个结果。此外,还评估了基于临床医生报告的急性毒性和总生存期(OS)。
总体而言,30 名患者中有 29 名(96.7%)接受了姑息性放疗。基线时,口服吗啡等效日剂量中位数为 129.5 mg(范围 20.0-540.0 mg),放疗后降至 75.0 mg(范围 15.0-360.0 mg)(P=.021)。疼痛平均从基线下降 3.15 分至 7 周(单侧 P=.045)。患者报告在最初 3 周内疼痛严重程度从 5.9 分平均降低至 3.8 分(P=.011),随后在第 11 周进一步降低至 3.2 分,在接受第一次放疗后第 21 周结束时降至 3.4 分(P=.006)。在随访期间,全球 QoL 显著从 50.5 分提高至 60.8 分(P=.001)。3 名患者出现 3 级急性毒性,未观察到 4-5 级毒性。中位 OS 为 11.8 周,1 年累计生存率为 13.3%。
胰腺癌相关疼痛的短程姑息性放疗与疼痛严重程度的快速、具有临床相关性降低以及全球 QoL 的具有临床相关性改善相关,且毒性主要为轻度。