OptumInsight, Eden Prairie, MN, USA.
J Med Econ. 2013;16(1):160-8. doi: 10.3111/13696998.2012.734885. Epub 2012 Oct 11.
Few studies have compared the effectiveness of filgrastim (FIL), pegfilgrastim (PEG), and sargramostim (SAR) to reduce the risk of febrile neutropenia (FN) associated with myelosuppressive chemotherapy (M-CT). Two large commercial database analyses were separately conducted to examine the incidence of neutropenia-related and all-cause hospitalizations associated with FIL, PEG, and SAR prophylaxis for patients receiving M-CT for non-Hodgkin lymphoma (NHL), Hodgkin lymphoma, or solid tumors.
Separate retrospective US claims database analyses utilized patient data from January 1, 2004 to April 30, 2010 using the HealthCore Integrated Research Database (HIRD(SM)) and January 1, 2001 to August 31, 2009 using OptumInsight's (formerly Ingenix) database. Patients were ≥18 years old and treated with M-CT for NHL, Hodgkin lymphoma, and solid tumors. All identified M-CT cycles with prophylactic (first 5 days of cycle) FIL, PEG, or SAR were included in the analysis. Patterns of administration and incidence rates of all-cause and neutropenia-related hospitalization were examined on a per-cycle basis.
In total, 9330 and 8762 patients with cancer, representing 30,264 and 24,215 chemotherapy cycles (28,189 and 22,649 (PEG), 1669 and 1351 (FIL), 406 and 215 (SAR)) from the HIRD(SM) and OptumInsight databases, respectively, were included in the separate database analyses. Both the HIRD(SM) and OptumInsight analysis showed that SAR and FIL prophylaxis had a higher risk of neutropenia-related hospitalization (SAR: OR = 3.48 [95%CI = 2.11, 5.74] and 2.81 [1.62, 4.87]; FIL: 1.78 [1.28, 2.48] and 2.36 [1.82, 3.06], respectively) and all-cause hospitalization (SAR: 2.18 [1.41, 3.36] and 2.41 [1.58, 3.68]; FIL:1.57 [1.25, 1.97] and 1.95 [1.60, 2.38], respectively) vs PEG.
Medical claims do not contain information about chemotherapy dose, and hospitalizations were not validated against the patient's chart.
In this comparative effectiveness study, use of PEG was associated with a lower risk of neutropenia-related and all-cause hospitalizations compared to use of FIL or SAR prophylaxis.
仅有少数研究比较了非格司亭(FIL)、聚乙二醇化非格司亭(PEG)和沙格司亭(SAR)在降低骨髓抑制化疗(M-CT)相关发热性中性粒细胞减少(FN)风险方面的有效性。分别进行了两项大型商业数据库分析,以检查在接受 M-CT 治疗非霍奇金淋巴瘤(NHL)、霍奇金淋巴瘤或实体瘤的患者中,FIL、PEG 和 SAR 预防用药与中性粒细胞减少相关和全因住院的发生率。
使用健康核心综合研究数据库(HIRD(SM))进行了两项独立的美国回顾性索赔数据库分析,使用的患者数据时间为 2004 年 1 月 1 日至 2010 年 4 月 30 日;使用 OptumInsight 的(前身为 Ingenix)数据库进行了另一项分析,使用的患者数据时间为 2001 年 1 月 1 日至 2009 年 8 月 31 日。患者年龄均≥18 岁,接受 NHL、霍奇金淋巴瘤和实体瘤的 M-CT 治疗。所有确定的预防性(周期前 5 天)FIL、PEG 或 SAR 的 M-CT 周期均包含在分析中。按周期分析全因和中性粒细胞减少相关住院的管理模式和发生率。
分别来自 HIRD(SM)和 OptumInsight 数据库的 9330 名和 8762 名癌症患者,代表 30264 个和 24215 个化疗周期(28189 个和 22649 个(PEG)、1669 个和 1351 个(FIL)、406 个和 215 个(SAR)),纳入了这两项独立的数据库分析。这两项分析均显示,SAR 和 FIL 预防用药与中性粒细胞减少相关住院的风险更高(SAR:比值比 [OR] = 3.48 [95%置信区间 [CI] 2.11-5.74] 和 2.81 [1.62-4.87];FIL:1.78 [1.28-2.48] 和 2.36 [1.82-3.06])和全因住院(SAR:2.18 [1.41-3.36] 和 2.41 [1.58-3.68];FIL:1.57 [1.25-1.97] 和 1.95 [1.60-2.38])高于 PEG。
医疗索赔中不包含化疗剂量信息,且住院情况未经患者病历验证。
在这项比较有效性研究中,与使用 FIL 或 SAR 预防用药相比,PEG 与中性粒细胞减少相关和全因住院的风险较低相关。