Department of Nursing, Umeå University, Umeå, 901 87, Sweden.
Department of Oncology, Sundsvall County Hospital, Sundsvall, Sweden.
BMC Palliat Care. 2024 Mar 27;23(1):80. doi: 10.1186/s12904-024-01410-w.
Men with metastatic castration-resistant prostate cancer (mCRPC) have an incurable disease. Along with prolonging life, symptom management is one of the main goals with treatment. This is also important from a palliative care perspective where the life prolonging outcomes should be balanced with quality of life (QoL) in this late phase. It is also essential in symptom management to view different dimensions of symptoms, for example how severe or distressing symptoms are, to support best QoL. Therefore, more knowledge is needed about the symptom experience when these treatments are initiated and thus the aim of this study was to describe different dimensions of symptoms in men with mCRPC starting their first-line of life-prolonging treatment, and to describe the association between symptom burden and QoL.
Baseline data from a prospective longitudinal study of 143 men with mCRPC starting their first-line life-prolonging treatment were used. Symptoms were measured using the Memorial Symptom Assessment Scale (MSAS) and global QoL was measured by the EORTC QLQ C-30. Data was analyzed using descriptive- and multivariable linear regression analyses.
On average, the men had more than 10 symptoms (range 0-31 of 33). 50% or more reported sweats, lack of energy, pain, problems with sexual activity and sexual desire. The symptoms they reported as most severe, or most distressing were not always the ones that were reported as most frequent. There was an association between QoL and physical symptoms, and also between QoL, and analgesic use and prostate-specific antigen (PSA) values.
Even if some men with mCRPC report many symptoms, the dimensions of severity and distress levels vary, and the most frequent symptoms was not always the most burdensome or distressing. There was an association between high physical symptom burden and QoL, suggesting that it is not the number of symptoms that affects QoL but rather the subjective perceived impact of the physical symptoms experienced. The knowledge of how men with mCRPC experience and perceive their symptoms may help health care professionals in symptom management aiming to improve QoL, which is a cornerstone in integrating early palliative care.
患有转移性去势抵抗性前列腺癌(mCRPC)的男性患有无法治愈的疾病。除了延长生命外,症状管理是治疗的主要目标之一。从姑息治疗的角度来看,这也很重要,因为在晚期,延长生命的结果应该与生活质量(QoL)平衡。在症状管理中,还必须从不同维度来看待症状,例如症状的严重程度或困扰程度,以支持最佳的 QoL。因此,需要更多关于开始一线延长生命治疗时这些治疗的症状体验的知识,因此本研究的目的是描述开始一线延长生命治疗的 mCRPC 男性的不同症状维度,并描述症状负担与 QoL 之间的关系。
使用前瞻性纵向研究的基线数据,该研究纳入了 143 名开始一线延长生命治疗的 mCRPC 男性。使用 Memorial Symptom Assessment Scale(MSAS)测量症状,使用 EORTC QLQ C-30 测量总体 QoL。使用描述性和多变量线性回归分析对数据进行分析。
平均而言,男性报告的症状超过 10 种(33 种症状中 0-31 种)。超过 50%的男性报告有出汗、缺乏能量、疼痛、性功能障碍和性欲下降。他们报告的最严重或最困扰的症状并不总是报告频率最高的症状。QoL 与身体症状之间存在关联,与镇痛药物使用和前列腺特异性抗原(PSA)值之间也存在关联。
即使一些 mCRPC 男性报告有许多症状,但其严重程度和困扰程度的维度也各不相同,而且最常见的症状并不总是最负担重或最困扰的症状。身体症状负担较重与 QoL 之间存在关联,这表明影响 QoL 的不是症状的数量,而是身体症状的主观感知影响。了解 mCRPC 男性的症状体验和感知可能有助于医疗保健专业人员进行症状管理,旨在改善 QoL,这是整合早期姑息治疗的基石。