Pajiep Marie, Conte Cécile, Huguet Françoise, Gauthier Martin, Despas Fabien, Lapeyre-Mestre Maryse
Service de Pharmacologie Médicale et Clinique, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
Equipe PEPSS (Pharmacologie en Population, cohorteS, biobanqueS), Centre d'Investigation Clinique 1436, INSERM, Université de Toulouse 3, Toulouse, France.
Front Oncol. 2021 Sep 30;11:675609. doi: 10.3389/fonc.2021.675609. eCollection 2021.
We analyzed demographic characteristics, comorbidities and patterns of treatment with tyrosine kinase inhibitors (TKIs) in a cohort of 3,633 incident cases of chronic myeloid leukemia (CML) identified across France from 1 January 2011 to 31 December 2014. Patients were identified through a specific algorithm in the French Healthcare Data System and were followed up 12 months after inclusion in the cohort. The estimated incidence rate of CML for this period in France was 1.37 per 100,000 person-years (95% Confidence Interval 1.36-1.38) and was higher in men, with a peak at age 75-79 years. At baseline, the median age of the cohort was 60 years (Inter Quartile Range 47-71), the Male/Female ratio was 1.2, and 25% presented with another comorbidity. Imatinib was the first-line TKI for 77.6% of the patients, followed by nilotinib (18.3%) and dasatinib (4.1%). Twelve months after initiation, 86% of the patients remained on the same TKI, 13% switched to another TKI and 1% received subsequently three different TKIs. During the follow-up, 23% discontinued and 52% suspended the TKI. Patients received a mean of 16.7 (Standard Deviation (SD) 9.6) medications over the first year of follow-up, and a mean of 2.7 (SD 2.3) concomitant medications on the day of first TKI prescription: 24.4% of the patients received allopurinol, 6.4% proton pump inhibitors (PPI) and 6.5% antihypertensive agents. When treatment with TKI was initiated, incident CML patients presented with comorbidities and polypharmacy, which merits attention because of the persistent use of these concomitant drugs and the potential increased risk of drug-drug interactions.
我们分析了2011年1月1日至2014年12月31日期间在法国确定的3633例慢性髓性白血病(CML)新发病例队列中的人口统计学特征、合并症以及酪氨酸激酶抑制剂(TKIs)的治疗模式。患者通过法国医疗数据系统中的特定算法识别,并在纳入队列后随访12个月。在此期间法国CML的估计发病率为每10万人年1.37例(95%置信区间1.36 - 1.38),男性发病率更高,在75 - 79岁达到峰值。基线时,队列的中位年龄为60岁(四分位间距47 - 71),男/女比例为1.2,25%的患者伴有其他合并症。伊马替尼是77.6%患者的一线TKI,其次是尼洛替尼(18.3%)和达沙替尼(4.1%)。开始治疗12个月后,86%的患者仍使用同一种TKI,13%换用了另一种TKI,1%随后接受了三种不同的TKI。随访期间,23%的患者停用了TKI,52%的患者暂停使用。在随访的第一年,患者平均接受了16.7种(标准差(SD)9.6)药物治疗,在首次开具TKI处方当天平均接受了2.7种(SD 2.3)伴随药物治疗:24.4%的患者接受了别嘌醇,6.4%接受了质子泵抑制剂(PPI),6.5%接受了抗高血压药物。当开始使用TKI治疗时,CML新发病例存在合并症和多种药物联用情况,鉴于这些伴随药物的持续使用以及药物相互作用风险可能增加,这值得关注。