Pôle pharmacie, CHU Grenoble Alpes, Grenoble, France.
Université Grenoble Alpes, Grenoble, France.
BMC Cancer. 2023 Jun 23;23(1):585. doi: 10.1186/s12885-023-10939-7.
BACKGROUND: Although polypharmacy has been described among cancer patients, very few studies have focused on those with lung cancer. We aimed to assess whether polypharmacy and comorbidity have an impact on systemic parenteral treatment administration and survival among lung-cancer patients. METHODS: In this retrospective monocenter cohort study, we included patients hospitalized in thoracic oncology for the first time between 2011 and 2015. The Elixhauser score was used to assess comorbidity and polypharmacy was estimated with a threshold of at least five prescribed medications. The Fine and Gray competitive risk model was used to estimate the impact of polypharmacy and comorbidity on systemic parenteral treatment administration within the first two months of hospitalization. The effect of comorbidity and polypharmacy on overall survival was evaluated by Cox proportional hazards analysis. RESULTS: In total, 633 patients were included (71% men), with a median age of 66 years. The median Elixhauser score was 6 and median overall survival was four months. Among the patients, 24.3% were considered to be receiving polypharmacy, with a median number of medications of 3, and 49.9% received systemic parenteral treatment within two months after hospitalization. Severe comorbidity (Elixhauser score > 11), but not polypharmacy, was independently associated with a lower rate of systemic parenteral treatment prescription (SdHR = 0.4 [0.3;0.6], p < 0.01) and polypharmacy, but not a high comorbidity score, was independently associated with poorer four-month survival (HR = 1.4 [1.1;1.9], p < 0.01) CONCLUSIONS: This first study to evaluate the consequences of comorbidity and polypharmacy on the care of lung-cancer patients shows that a high comorbidity burden can delay systemic parenteral treatment administration, whereas polypharmacy has a negative impact on four-month survival.
背景:尽管已有研究描述了癌症患者的多重用药情况,但针对肺癌患者的研究却很少。我们旨在评估肺癌患者的多重用药和合并症是否会影响全身静脉治疗的实施和生存。
方法:本回顾性单中心队列研究纳入了 2011 年至 2015 年期间首次因胸部肿瘤住院的患者。采用 Elixhauser 评分评估合并症,将至少开具 5 种处方药物定义为多重用药。采用 Fine 和 Gray 竞争风险模型评估住院前两个月内全身静脉治疗实施的多重用药和合并症的影响。采用 Cox 比例风险分析评估合并症和多重用药对总生存的影响。
结果:共纳入 633 例患者(71%为男性),中位年龄为 66 岁。中位 Elixhauser 评分 6 分,中位总生存时间为 4 个月。24.3%的患者被认为是多重用药,中位数用药数为 3 种,49.9%的患者在住院后 2 个月内接受全身静脉治疗。严重合并症(Elixhauser 评分>11 分)而非多重用药与全身静脉治疗处方率较低独立相关(SdHR=0.4 [0.3;0.6],p<0.01),而多重用药而非高合并症评分与 4 个月生存较差独立相关(HR=1.4 [1.1;1.9],p<0.01)。
结论:这是第一项评估合并症和多重用药对肺癌患者治疗影响的研究,结果表明高合并症负担会延迟全身静脉治疗的实施,而多重用药会对 4 个月生存产生负面影响。
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