帕金森病对癌症幸存者生存的影响:日本的一项回顾性多中心队列研究

IF 4.5 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2025-09-13 eCollection Date: 2025-01-01 DOI:10.1093/braincomms/fcaf347
Kanako Asai, Yasufumi Gon, Yasuyoshi Kimura, Toshitaka Morishima, Hideki Mochizuki, Isao Miyashiro
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引用次数: 0

摘要

人口老龄化和医疗保健的进步促进了帕金森病患者和癌症幸存者人数的增加。然而,帕金森病对癌症患者生存的影响尚不清楚。我们旨在探讨帕金森病对癌症患者预后的影响。这项回顾性多中心队列研究使用了大阪癌症登记处的数据,该数据与日本2010年至2015年期间获得的行政数据有关。癌症患者确诊后随访5年,根据是否存在帕金森病合并症分为帕金森病组和非帕金森病组。我们使用Kaplan-Meier分析比较两组患者的生存率。采用Cox比例风险模型评估帕金森病全因死亡率的风险比和95%置信区间。倾向评分匹配用于验证分析和处理组间临床特征的差异。该队列包括118999例癌症患者和1049例(0.9%)合并帕金森病患者。帕金森氏病组的患者比非帕金森氏病组的患者年龄更大,活动能力更低。Kaplan-Meier分析显示,帕金森病组癌症诊断后的5年生存率明显低于非帕金森病组(54%比70%,P < 0.001)。共病帕金森病与5年死亡率独立相关[粗风险比(95%可信区间),1.72 (1.56 ~ 1.88),P < 0.001]。在校正潜在混杂因素后,这种关联仍然显著[校正风险比(95%置信区间),1.37 (1.25-1.51),P < 0.001]。当生存分析按活动能力分层时,活动能力受损患者的预后未见组间差异。然而,在具有独立活动能力的患者中,帕金森病组患者的预后差于非帕金森病组[粗风险比(95%可信区间)为1.74 (1.42-2.13),P < 0.001]。倾向-得分匹配后观察到类似的结果。癌症合并合并帕金森病患者的预后比没有合并帕金森病患者的预后差。效果因移动性而异。这些发现强调了仔细管理帕金森病症状和维持帕金森病癌症患者活动能力的重要性,因为这可能会改善他们的预后和生存结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Parkinson's disease on survival in cancer survivors: a retrospective, multicentre cohort study in Japan.

Aging populations and advances in medical care have contributed to an increase in the number of patients with Parkinson's disease and cancer survivors. However, the effects of Parkinson's disease on the survival of patients with cancer remain unclear. We aimed to investigate the effect of Parkinson's disease on the prognosis of patients with cancer. This retrospective multicentre cohort study used data from the Osaka Cancer Registry, which was linked to administrative data obtained between 2010 and 2015 in Japan. Patients with cancer who were followed up for 5 years after cancer diagnosis were categorized into Parkinson's disease and non- Parkinson's disease groups according to the presence of comorbid Parkinson's disease. We compared survival between the two groups using Kaplan-Meier analyses. Cox proportional-hazard models were used to assess the hazard ratio and 95% confidence interval of Parkinson's disease for all-cause mortality. Propensity-score matching was used to validate the analysis and address differences in clinical characteristics between the groups. The cohort included 118 999 patients with cancer and 1049 patients (0.9%) with comorbid Parkinson's disease. The patients in the Parkinson's disease group were older and had lower mobility than those in the non- Parkinson's disease group. Kaplan-Meier analysis revealed that the 5-year survival rate after cancer diagnosis was significantly worse in the Parkinson's disease group than in the non- Parkinson's disease group (54% versus 70%, P < 0.001). Comorbid Parkinson's disease was independently associated with 5-year mortality [crude hazard ratio (95% confidence interval), 1.72 (1.56-1.88), P < 0.001]. This association remained significant after adjusting for potential confounders [adjusted hazard ratio (95% confidence interval), 1.37 (1.25-1.51), P < 0.001]. When the survival analysis was stratified by mobility, no intergroup difference in prognosis was observed among patients with impaired mobility. However, among patients with independent mobility, patients in the Parkinson's disease group had a worse prognosis than those in the non- Parkinson's disease group [crude hazard ratio (95% confidence interval), 1.74 (1.42-2.13), P < 0.001]. Similar results were observed after propensity-score matching. Patients with cancer and comorbid Parkinson's disease had a worse prognosis than those without comorbid Parkinson's disease. The effect varied depending on mobility. These findings highlight the importance of carefully managing Parkinson's disease symptoms and maintaining mobility in cancer patients with Parkinson's disease, as this could potentially improve their prognosis and survival outcomes.

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