Department of Radiation Sciences/Oncology, Umeå University, Umeå, Sweden; Department of Neurobiology, Caring Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Regional Cancer Centre Stockholm Gotland, Stockholm, Sweden; Center for Complementary Medicine, Department of Medicine II, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany; Institute for Applied Epistemology and Medical Methodology at Witten/Herdecke University (IFAEMM), Freiburg, Germany; Department of Nursing, Umeå University, Umeå, Sweden; Department of Biomedical and Clinical Sciences, Linköping University, Sweden; Department of Oncology, Västmanlands Hospital, Västerås, Schweden; Department of Oncology, Ryhov County Hospital, Jönköping, Schweden; Palliative Care Unit Västerås, Schweden.
Dtsch Arztebl Int. 2024 May 31;121(11):347-354. doi: 10.3238/arztebl.m2024.0080.
Patients with advanced pancreatic cancer have limited survival and few treatment options. We studied whether mistletoe extract (ME), in addition to comprehensive oncological treatment and palliative care, prolongs overall survival (OS) and improves health-related quality of life (HRQoL).
The double-blind, placebo-controlled MISTRAL trial was conducted in Swedish oncology centers. The main inclusion criteria were advanced exocrine pancreatic cancer and Eastern Cooperative Oncology Group (ECOG) performance status 0-2. The subjects were randomly assigned to ME (n=143) or placebo (n=147) and were stratified by study site and by eligibility (yes/no) for palliative chemotherapy (June 2016-December 2021). ME or placebo was injected subcutaneously three times a week for nine months. The primary endpoint was overall survival (OS); one of the secondary endpoints was the HRQoL dimension global health/QoL (EORTC-QLQ-C30), as assessed at seven time points over nine months. Trial registration: EudraCT 2014-004552-64, NCT02948309.
No statistically significant benefit of adding ME to standard treatment was seen with respect to either OS or global health/ QoL. The adjusted hazard ratio for OS was 1.13 [0.89; 1.44], with a median survival time of 7.8 and 8.3 months for ME and placebo, respectively. The figures for the HRQoL dimension "global health/QoL" were similar in the two groups (p=0.86). The number, severity, and outcome of the reported adverse events were similar as well, except for more common local skin reactions at ME injection sites (66% vs. 1%).
ME is unlikely to have a clinically significant effect on OS or the HRQoL dimension global health/QoL when administered in patients with advanced pancreatic cancer in addition to comprehensive cancer care.
晚期胰腺癌患者的生存时间有限,治疗选择有限。我们研究了在综合肿瘤治疗和姑息治疗的基础上,槲寄生提取物(ME)是否能延长总生存期(OS)并改善健康相关生活质量(HRQoL)。
这项双盲、安慰剂对照的 MISTRAL 试验在瑞典肿瘤中心进行。主要纳入标准为晚期外分泌胰腺癌和东部合作肿瘤组(ECOG)体能状态 0-2。受试者被随机分配到 ME(n=143)或安慰剂(n=147)组,并按研究地点和姑息化疗资格(是/否)进行分层(2016 年 6 月至 2021 年 12 月)。ME 或安慰剂每周皮下注射 3 次,持续 9 个月。主要终点是总生存期(OS);次要终点之一是健康相关生活质量(HRQoL)维度总体健康/生活质量(EORTC-QLQ-C30),在 9 个月内的 7 个时间点进行评估。试验注册:EudraCT 2014-004552-64,NCT02948309。
在标准治疗基础上添加 ME 治疗,在 OS 或总体健康/生活质量方面均未显示出统计学上的获益。OS 的调整危险比为 1.13[0.89;1.44],ME 和安慰剂的中位生存时间分别为 7.8 和 8.3 个月。两组的 HRQoL 维度“总体健康/生活质量”结果相似(p=0.86)。报告的不良反应的数量、严重程度和结局也相似,除了 ME 注射部位更常见的局部皮肤反应(66%比 1%)。
在晚期胰腺癌患者中,在综合癌症治疗的基础上添加 ME 治疗,不太可能对 OS 或 HRQoL 维度的总体健康/生活质量产生临床显著影响。