Furney Terra, Horowitz Amy, Malamakal John, Frei Christopher R
South Texas Veterans Health Care System, San Antonio.
College of Pharmacy, University of Texas at Austin, San Antonio.
Fed Pract. 2023 May;40(Suppl 1):S54-S59. doi: 10.12788/fp.0327. Epub 2022 Nov 17.
Granulocyte colony-stimulating factor prophylaxis has been shown to reduce the risk and duration of chemotherapy-induced neutropenia and febrile neutropenia and is recommended for at-risk patients receiving chemotherapy. Within the South Texas Veterans Health Care System, daily filgrastim injections remain the preferred formulation of granulocyte colony-stimulating factor for primary prophylaxis of febrile neutropenia.
This retrospective, single-center cohort study included 59 patients who received daily filgrastim as primary prophylaxis with a curative cancer diagnosis and a chemotherapy regimen at the South Texas Veterans Health Care System from September 1, 2015 to September 24, 2020. Patients had either a high risk for febrile neutropenia or a chemotherapy regimen with an intermediate risk for febrile neutropenia and additional risk factors. The primary outcome was the incidence of neutropenia/febrile neutropenia leading to treatment delays. Secondary outcomes included chemotherapy dose decreases or discontinuations, hospitalizations, days of hospitalization, infections, extended duration of filgrastim, and transitions to pegfilgrastim due to neutropenia/febrile neutropenia.
Patients received a median (IQR) of 7 (5-10) doses of filgrastim for primary prophylaxis. Overall, 10 patients (17%) experienced treatment delays due to neutropenia/febrile neutropenia. Fifteen patients (25%) were hospitalized with a median (IQR) length of stay of 5 (4-7) days, 9 patients (15%) had documented infections, and 2 patients (3%) required a chemotherapy dose reduction. Additionally, 9 patients (15%) required an additional median (IQR) of 2 (2-5) doses of filgrastim, and 9 (15%) patients were transitioned to pegfilgrastim.
These results suggest that additional measures such as tracking postnadir absolute neutrophil counts should be performed to ensure patients receive an appropriate number of filgrastim doses to prevent complications associated with neutropenia/febrile neutropenia.
粒细胞集落刺激因子预防已被证明可降低化疗引起的中性粒细胞减少症和发热性中性粒细胞减少症的风险及持续时间,推荐用于接受化疗的高危患者。在南德克萨斯退伍军人医疗保健系统中,每日注射非格司亭仍是预防发热性中性粒细胞减少症的首选粒细胞集落刺激因子制剂。
这项回顾性单中心队列研究纳入了2015年9月1日至2020年9月24日期间在南德克萨斯退伍军人医疗保健系统接受每日非格司亭作为原发性预防且患有治愈性癌症诊断并接受化疗方案的59例患者。患者要么有发热性中性粒细胞减少症的高风险,要么有发热性中性粒细胞减少症的中度风险且有其他风险因素的化疗方案。主要结局是导致治疗延迟的中性粒细胞减少症/发热性中性粒细胞减少症的发生率。次要结局包括化疗剂量减少或停药、住院、住院天数、感染、非格司亭使用时间延长以及因中性粒细胞减少症/发热性中性粒细胞减少症转为使用培非格司亭。
患者接受非格司亭进行原发性预防的中位(四分位间距)剂量为7(5 - 10)剂。总体而言,10例患者(17%)因中性粒细胞减少症/发热性中性粒细胞减少症出现治疗延迟。15例患者(25%)住院,中位(四分位间距)住院时间为5(4 - 7)天,9例患者(15%)有记录的感染,2例患者(3%)需要降低化疗剂量。此外,9例患者(15%)需要额外中位(四分位间距)2(2 - 5)剂非格司亭,9例(15%)患者转为使用培非格司亭。
这些结果表明,应采取额外措施,如跟踪最低点后绝对中性粒细胞计数,以确保患者接受适当数量的非格司亭剂量,预防与中性粒细胞减少症/发热性中性粒细胞减少症相关的并发症。