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P-520: Association of polypharmacy and potential inappropriate medication with toxicity to anti-neoplastic treatment

机译:P-520:多酚和潜在的不恰当药物与抗肿瘤治疗的潜在不恰当的药物协会

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Background: The prevalence of potential inappropriate medications (PIM) in the geriatric cancer population is 24-54%. The effect of PIMs on outcome in cancer patients is not well studied. We hypothesized that older cancer patients exposed to polypharmacy (PP) and/or PIMs will experience more toxicity and reduced adhesion to cancer treatment. Further CARG (predictive model for chemotherapy toxicity in C 65 years) was assessed. Method: The study was undertaken at the Department of Oncology, Odense University Hospital, Denmark 2017-2018. Prospective observational cohort study including (1) patients with cancer, (2) aged ≥ 70 years, (3) starting taxane-based chemotherapy. Patients were included consecutively during a 12 months period. Baseline PP, PIMs (EU(7)PIM list), potential drug-drug interactions, Charlson comorbidity score (CCIS), ECOG performance status (PS) and CARG score, planned dose and number of treatments and toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) was noted. Primary endpoint was treatment adherence in relation to the above points. Results: 96 patients, median age 75, 62% male were included. PS was 0-1 in 73.7% indicating good functional status, risk of grade C 3 toxicity according to the CARG score was intermediate (6-9) in 62.5%, and, median CCIS 1 (IQR 0-2). Most patients were exposed to major PP at baseline. Only 21% of patients completed treatment as planned. 62% of patients had CTCAE grade 3-4 toxicity. PIM exposure was low and exposure was associated with interrupted or reduced chemotherapy (OR 3.2 (1.12-8.90) (unadjusted). Conclusion: PIMs had a negative influence on the treatment adherence. Many patients had severe toxicity.
机译:背景:老年癌症群体中潜在不恰当药物(PIM)的患病率为24-54%。 PIMS对癌症患者的结果的影响并未得到很好的研究。我们假设暴露于多酚(PP)和/或PIMS的较老的癌症患者将经历更多的毒性和降低对癌症治疗的粘附性。评估进一步的CARG(C 65岁的化疗毒性的预测模型)进行了评估。方法:该研究在丹麦2017-2018丹麦肿瘤学院肿瘤学院进行。预期观察队列研究包括(1)癌症患者,(2)≥70岁,(3)开始紫杉烷基化疗。在12个月期间,患者连续纳入。基线PP,PIMS(欧盟(7)PIM列表),潜在的药物 - 药物相互作用,Charlson合并率评分(CCIS),ECOG性能状态(PS)和Carg评分,计划剂量和治疗次数和毒性,根据常见的术语标准注意事实(CTCAE)被注意到。主要终点是与上述要点相关的治疗依从性。结果:96例患者,中位数75岁,包括62%的男性。 PS为0-1,表1中表明良好的功能状态,根据CC1分数的C 3毒性级毒性的风险是62.5%,中位CCIS 1(IQR 0-2)中中间体(6-9)。大多数患者在基线暴露于主要PP。只有21%的患者按计划完成治疗。 62%的患者具有CTCAE级3-4毒性。 PIM暴露较低,暴露与中断或减少化疗(或3.2(1.12-8.90)(未经调整的)相关联。结论:PIM对治疗依从性产生负面影响。许多患者毒性严重。

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