Department of Cancer Pharmacology & Pharmacogenomics, Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
Department of Pharmacy, Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
Am J Health Syst Pharm. 2023 Sep 22;80(19):1342-1349. doi: 10.1093/ajhp/zxad117.
To describe the implementation of an in-house genotyping program to detect genetic variants linked to impaired dihydropyrimidine dehydrogenase (DPD) metabolism at a large multisite cancer center, including barriers to implementation and mechanisms to overcome barriers to facilitate test adoption.
Fluoropyrimidines, including fluorouracil and capecitabine, are commonly used chemotherapy agents in the treatment of solid tumors, such as gastrointestinal cancers. DPD is encoded by the DPYD gene, and individuals classified as DPYD intermediate and poor metabolizers due to certain genetic variations in DPYD can experience reduced fluoropyrimidine clearance and an increased risk of fluoropyrimidine-related adverse events. Although pharmacogenomic guidelines provide evidence-based recommendations for DPYD genotype-guided dosing, testing has not been widely adopted in the United States for numerous reasons, including limited education/awareness of clinical utility, lack of testing recommendations by oncology professional organizations, testing cost, lack of accessibility to a comprehensive in-house test and service, and prolonged test turnaround time. Based on stakeholder feedback regarding barriers to testing, we developed an in-house DPYD test and workflow to facilitate testing in multiple clinic locations at Levine Cancer Institute. Across 2 gastrointestinal oncology clinics from March 2020 through June 2022, 137 patients were genotyped, and 13 (9.5%) of those patients were heterozygous for a variant and identified as DPYD intermediate metabolizers.
Implementation of DPYD genotyping at a multisite cancer center was feasible due to operationalization of workflows to overcome traditional barriers to testing and engagement from all stakeholders, including physicians, pharmacists, nurses, and laboratory personnel. Future directions to scale and sustain testing in all patients receiving a fluoropyrimidine across all Levine Cancer Institute locations include electronic medical record integration (eg, interruptive alerts), establishment of a billing infrastructure, and further refinement of workflows to improve the rate of pretreatment testing.
描述在大型多站点癌症中心实施内部基因分型程序以检测与二氢嘧啶脱氢酶(DPD)代谢受损相关的遗传变异的情况,包括实施过程中的障碍以及克服障碍以促进测试采用的机制。
氟嘧啶类药物,包括氟尿嘧啶和卡培他滨,是胃肠道等实体瘤治疗中常用的化疗药物。DPD 由 DPYD 基因编码,由于 DPYD 中的某些遗传变异,某些个体被归类为 DPYD 中间代谢型和弱代谢型,可能会导致氟嘧啶清除率降低,氟嘧啶相关不良反应风险增加。尽管药物基因组学指南为 DPYD 基因型指导剂量提供了循证建议,但由于多种原因,美国尚未广泛采用测试,包括对临床应用的认识/意识有限、肿瘤专业组织缺乏测试建议、测试成本、无法获得全面的内部测试和服务,以及测试周转时间延长。根据利益相关者对测试障碍的反馈,我们开发了一种内部 DPYD 测试和工作流程,以促进在莱文癌症研究所的多个诊所进行测试。在 2020 年 3 月至 2022 年 6 月期间的 2 个胃肠肿瘤学诊所中,对 137 名患者进行了基因分型,其中 13 名(9.5%)患者为杂合变体,被鉴定为 DPYD 中间代谢型。
由于克服了传统测试障碍的工作流程的运作以及包括医生、药剂师、护士和实验室人员在内的所有利益相关者的参与,在多站点癌症中心实施 DPYD 基因分型是可行的。在莱文癌症研究所的所有地点扩大和维持所有接受氟嘧啶治疗的患者的测试,包括电子病历整合(例如,中断警报)、建立计费基础设施以及进一步改进工作流程以提高治疗前测试的比例,是未来的方向。