Suppr超能文献

老年癌症患者(70 岁以上)的药物风险及其与治疗相关毒性的关系。

Medication risks in older patients (70 +) with cancer and their association with therapy-related toxicity.

机构信息

Institute of Pharmacy, Department of Clinical Pharmacy, University of Bonn, An der Immenburg 4, 53121, Bonn, Germany.

Department of Geriatrics and Neurology, Johanniter Hospital Bonn, Johanniterstr. 1-3, 53113, Bonn, Germany.

出版信息

BMC Geriatr. 2022 Aug 30;22(1):716. doi: 10.1186/s12877-022-03390-z.

Abstract

BACKGROUND

To evaluate medication-related risks in older patients with cancer and their association with severe toxicity during antineoplastic therapy.

METHODS

This is a secondary analysis of two prospective, single-center observational studies which included patients ≥ 70 years with cancer. The patients' medication lists were investigated regarding possible risks: polymedication (defined as the use of ≥ 5 drugs), potentially inappropriate medication (PIM), and relevant potential drug-drug interactions (rPDDI). The risks were analyzed before and after start of cancer therapy. Severe toxicity during antineoplastic therapy was captured from medical records according to the Common Terminology Criteria for Adverse Events (CTCAE). The association between grade ≥ 3 toxicity and medication risks was evaluated by univariate as well as multivariate regression adjusted by ECOG and age.

RESULTS

The study cohort comprised 136 patients (50% female, mean age 77 years, 42% hematological malignancies). Before the start of cancer therapy, patients took on average 5 drugs as long-term medication and 52% of patients were exposed to polymedication. More than half of patients used at least one PIM. Approximately one third of patients exhibited rPDDI. The prevalence of medication risks increased after start of cancer therapy. rPDDI were significantly associated with severe overall toxicity (OR, 5.07; p = 0.036; 95% Confidence Interval (CI) 1.11-23.14; toxicity in patients with rPDDI 94.1% (32/34) vs 75.9% (60/79) in patients without rPDDI) and hematological toxicity (OR, 3.95; p = 0.010; 95% CI 1.38-11.29; hematological toxicity in patients with rPDDI 85.3% (29/34) vs 59.5% (47/79) in patients without rPDDI). In the multivariate analysis adjusted by ECOG and age, only the association for rPDDI with hematological toxicity remained statistically significant (OR, 4.51; p = 0.007; 95% CI 1.52-13.38). These findings should be further investigated in larger studies.

CONCLUSION

Medication risks are common in older patients with cancer and might be associated with toxicity. This raises the need for tailored interventions to ensure medication safety in this patient cohort.

摘要

背景

评估老年癌症患者的药物相关风险及其与抗肿瘤治疗期间严重毒性的关系。

方法

这是两项前瞻性、单中心观察性研究的二次分析,纳入了≥70 岁的癌症患者。调查了患者的用药清单,以评估潜在风险:多药治疗(使用≥5 种药物)、潜在不适当药物(PIM)和相关潜在药物-药物相互作用(rPDDI)。在开始癌症治疗前后分析了这些风险。根据常见不良事件术语标准(CTCAE)从病历中捕捉抗肿瘤治疗期间的严重毒性。通过单变量和多变量回归分析,在调整 ECOG 和年龄后,评估了≥3 级毒性与药物风险之间的关系。

结果

研究队列包括 136 名患者(50%为女性,平均年龄 77 岁,42%为血液恶性肿瘤)。在开始癌症治疗之前,患者平均服用 5 种长期药物,52%的患者接受了多药治疗。超过一半的患者使用至少一种 PIM。约三分之一的患者存在 rPDDI。开始癌症治疗后,药物风险的发生率增加。rPDDI 与严重总体毒性(OR,5.07;p=0.036;95%置信区间(CI)1.11-23.14;rPDDI 患者的毒性为 94.1%(32/34)vs 无 rPDDI 患者的 75.9%(60/79))和血液学毒性(OR,3.95;p=0.010;95%CI 1.38-11.29;rPDDI 患者的血液学毒性为 85.3%(29/34)vs 无 rPDDI 患者的 59.5%(47/79))显著相关。在调整 ECOG 和年龄的多变量分析中,只有 rPDDI 与血液学毒性的关联具有统计学意义(OR,4.51;p=0.007;95%CI 1.52-13.38)。这些发现需要在更大的研究中进一步探讨。

结论

老年癌症患者的药物风险很常见,可能与毒性有关。这就需要针对这一患者群体进行有针对性的干预措施,以确保药物安全。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0b3/9429305/378b1c0b605b/12877_2022_3390_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验