Rhee John Y, Mastrangelo Carissa, Miller Paul J, Youssef Gilbert, Tentor Zachary, Rothfeld-Wehrwein Zachary R, Dhongade Vrushali A, Nakhate Vihang, Batchelor Tracy, Dhand Amar
Department of Neurology, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Department of Neurology, Harvard Medical School, Boston, Massachusetts, USA.
Neurooncol Pract. 2025 Jan 8;12(3):426-436. doi: 10.1093/nop/npaf002. eCollection 2025 Jun.
Patients with glioblastoma experience high physical and psychosocial symptom burden. Poor social relationships have been shown to increase the risk of neurologic illnesses and decline, and conversely, strong personal social networks (PSN) have been shown to reduce the risk of mortality and improve quality of life. The aim of this pilot study is to determine the feasibility of measuring PSN in glioblastoma patients.
We recruited 25 adult glioblastoma patients between the initial diagnosis and the first cycle of adjuvant chemotherapy from March to September 2023 in the outpatient neuro-oncology clinic and adapted PERSNET, a quantitative PSN assessment tool, to this population. We collected demographics, tumor measures, treatment courses, and the European Organization for Research and Treatment of Cancer QOL for Patients with Brain Tumors (EORTC QLQ-BN20) and conducted qualitative interviews.
The average age was 64.5 years old, 56% were female, and 84% had a Karnofsky Performance Status of 70 or higher. Patients had large network sizes (total size of patient's PSN; mean = 8.8). Participants stressed the importance of social support and how different people filled different roles in their oncology care. Behavioral and/or cognitive changes resulted in delayed presentation, and children, especially daughters, were important in advocating for presentation to the hospital.
This is the first proof-of-concept study showing that PSN can be measured in patients with glioblastoma. Qualitative data showed that patients felt social support was very important, and different people in their networks addressed different domains of care: physical, emotional, and logistical.
胶质母细胞瘤患者承受着较高的身体和心理社会症状负担。研究表明,不良的社会关系会增加患神经疾病和病情恶化的风险,相反,强大的个人社会网络(PSN)则可降低死亡风险并改善生活质量。这项试点研究的目的是确定在胶质母细胞瘤患者中测量PSN的可行性。
我们于2023年3月至9月在门诊神经肿瘤诊所招募了25名成年胶质母细胞瘤患者,这些患者处于初始诊断和辅助化疗的第一个周期之间,并将定量PSN评估工具PERSNET应用于该人群。我们收集了人口统计学信息、肿瘤指标、治疗过程,以及欧洲癌症研究与治疗组织脑肿瘤患者生活质量量表(EORTC QLQ - BN20),并进行了定性访谈。
平均年龄为64.5岁,56%为女性,84%的卡氏评分在70分及以上。患者的社交网络规模较大(患者PSN的总规模;平均值 = 8.8)。参与者强调了社会支持的重要性,以及不同的人在他们的肿瘤护理中如何扮演不同的角色。行为和/或认知变化导致就诊延迟,而子女,尤其是女儿,在促使患者前往医院就诊方面发挥了重要作用。
这是第一项概念验证研究,表明可以在胶质母细胞瘤患者中测量PSN。定性数据显示,患者认为社会支持非常重要,其社交网络中的不同人在不同的护理领域发挥作用:身体、情感和后勤方面。