Popa Mihaela A, Wallace Kristie J, Brunello Antonella, Extermann Martine, Balducci Lodovico
Biovest International, Inc., Tampa, FL, United States.
Edward White Hospital, St. Petersburg, FL, United States.
J Geriatr Oncol. 2014 Jul;5(3):307-14. doi: 10.1016/j.jgo.2014.04.002. Epub 2014 May 10.
Increased risk of drug interactions due to polypharmacy and aging-related changes in physiology among older patients with cancer is further augmented during chemotherapy. No previous studies examined potential drug interactions (PDIs) from polypharmacy and their association with chemotherapy tolerance in older patients with cancer.
This study is a retrospective medical chart review of 244 patients aged 70+ years who received chemotherapy for solid or hematological malignancies. PDI among all drugs, supplements, and herbals taken with the first chemotherapy cycle were screened for using the Drug Interaction Facts software, which classifies PDIs into five levels of clinical significance with level 1 being the highest. Descriptive and correlative statistics were used to describe rates of PDI. The association between PDI and severe chemotoxicity was tested with logistic regressions adjusted for baseline covariates.
A total of 769 PDIs were identified in 75.4% patients. Of the 82 level 1 PDIs identified among these, 32 PDIs involved chemotherapeutics. A large proportion of the identified PDIs were of minor clinical significance. The risk of severe non-hematological toxicity almost doubled with each level 1 PDI (OR=1.94, 95% CI: 1.22-3.09), and tripled with each level 1 PDI involving chemotherapeutics (OR=3.08, 95% CI: 1.33-7.12). No association between PDI and hematological toxicity was found.
In this convenience sample of older patients with cancer receiving chemotherapy we found notable rates of PDI and a substantial adjusted impact of PDI on risk of non-hematological toxicity. These findings warrant further research to optimize chemotherapy outcomes.
老年癌症患者因多种药物联合使用及与衰老相关的生理变化导致药物相互作用风险增加,在化疗期间这种风险进一步加剧。此前尚无研究探讨老年癌症患者多种药物联合使用引起的潜在药物相互作用(PDIs)及其与化疗耐受性的关系。
本研究是一项回顾性病历审查,研究对象为244名年龄在70岁及以上、因实体瘤或血液系统恶性肿瘤接受化疗的患者。使用《药物相互作用事实》软件筛查首个化疗周期所服用的所有药物、补充剂和草药之间的PDIs,该软件将PDIs分为五个临床意义级别,1级为最高级别。采用描述性和相关性统计来描述PDIs的发生率。通过对基线协变量进行调整的逻辑回归分析,检验PDIs与严重化学毒性之间的关联。
共在75.4%的患者中识别出769例PDIs。在这些识别出的PDIs中,82例为1级,其中32例涉及化疗药物。识别出的PDIs中很大一部分临床意义较小。每出现一例1级PDI,严重非血液学毒性的风险几乎增加一倍(比值比[OR]=1.94,95%置信区间[CI]:1.22 - 3.09),每出现一例涉及化疗药物的1级PDI,严重非血液学毒性的风险增加两倍(OR=3.08,95% CI:1.33 - 7.12)。未发现PDIs与血液学毒性之间存在关联。
在这个接受化疗的老年癌症患者便利样本中,我们发现PDIs的发生率较高,且PDIs对非血液学毒性风险有显著的调整影响。这些发现值得进一步研究以优化化疗结果。