Sevinç Alper, Özkan Metin, Özet Ahmet, Dane Faysal, Öksüzoğlu Berna, Işıkdoğan Abdurrahman, Özdemir Feyyaz, Uncu Doğan, Gümüş Mahmut, Evrensel Türkkan, Yaren Arzu, Kara Oğuz, Tekin Salim Başol
Department of Medical Oncology, Medical Park Gaziantep Hospital, Gaziantep.
Department of Medical Oncology, Erciyes University Faculty of Medicine, Kayseri.
Onco Targets Ther. 2018 Jan 18;11:419-426. doi: 10.2147/OTT.S106342. eCollection 2018.
We studied the comparative effectiveness of biosimilar filgrastim vs original filgrastim in patients with chemotherapy-induced neutropenia.
This multicenter, observational study was conducted at 14 centers. The study included 337 patients experiencing neutropenia under chemotherapy. Patients were given either filgrastim 30 MIU or 48 MIU (Neupogen) or biosimilar filgrastim 30 MIU (Leucostim). Data regarding age, chemotherapeutic agents used, number of chemotherapy courses, previous diagnosis of neutropenia, neutrophil count of patients after treatment, medications used for the treatment of neutropenia, and duration of neutropenia were collected. Time to absolute neutrophil count (ANC) recovery was the primary efficacy measure.
Ambulatory and hospitalized patients comprised 11.3% and 45.1% of the enrolled patients, respectively, and a previous diagnosis of neutropenia was reported in 49.3% of the patients, as well. Neutropenia occurred in 13.7% (n=41), 45.5% (n=136), 27.4% (n=82), 11.4% (n=34), and 2.0% (n=6) of the patients during the first, second, third, fourth, and fifth cycles of chemotherapy, respectively. While the mean neutrophil count was 0.53±0.48 before treatment, a significant increase to 2.44±0.66 was observed after treatment (=0.0001). While 90.3% of patients had a neutrophil count <1.49 before treatment, all patients had a neutrophil count ≥1.50 after treatment. Neutropenia resolved within ≤4 days of filgrastim therapy in 60.1%, 56.7%, and 52.6% of the patients receiving biosimilar filgrastim 30 MIU, original filgrastim 30 MIU, and original filgrastim 48 MIU, respectively. However, there was no significant difference between the three arms (=0.468). Similarly, time to ANC recovery was comparable between the treatment arms (=0.332).
The results indicate that original filgrastim and biosimilar filgrastim have comparable efficacy in treating neutropenia. Biosimilar filgrastim provides a valuable alternative; however, there is need for further studies comparing the two products in different patient subpopulations.
我们研究了生物类似药非格司亭与原研非格司亭在化疗所致中性粒细胞减少症患者中的相对疗效。
这项多中心观察性研究在14个中心开展。研究纳入了337例在化疗期间出现中性粒细胞减少症的患者。患者被给予非格司亭30 MIU或48 MIU(优保津)或生物类似药非格司亭30 MIU(乐保津)。收集了有关年龄、使用的化疗药物、化疗疗程数、既往中性粒细胞减少症诊断情况、治疗后患者的中性粒细胞计数、用于治疗中性粒细胞减少症的药物以及中性粒细胞减少症持续时间的数据。绝对中性粒细胞计数(ANC)恢复时间是主要疗效指标。
门诊患者和住院患者分别占入组患者的11.3%和45.1%,49.3%的患者也报告有既往中性粒细胞减少症诊断。在化疗的第一、第二、第三、第四和第五周期中,分别有13.7%(n = 41)、45.5%(n = 136)、27.4%(n = 82)、11.4%(n = 34)和2.0%(n = 6)的患者出现中性粒细胞减少症。治疗前平均中性粒细胞计数为0.53±0.48,治疗后显著升高至2.44±0.66(P = 0.0001)。治疗前90.3%的患者中性粒细胞计数<1.49,治疗后所有患者中性粒细胞计数≥1.50。接受生物类似药非格司亭30 MIU、原研非格司亭30 MIU和原研非格司亭48 MIU治疗的患者中,分别有60.1%、56.7%和52.6%的患者在非格司亭治疗后≤4天中性粒细胞减少症得到缓解。然而,三组之间无显著差异(P = 0.468)。同样,各治疗组之间ANC恢复时间相当(P = 0.332)。
结果表明,原研非格司亭和生物类似药非格司亭在治疗中性粒细胞减少症方面疗效相当。生物类似药非格司亭提供了一种有价值的替代选择;然而,需要进一步研究在不同患者亚组中比较这两种产品。