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生物类似物重组人粒细胞集落刺激因子用于自体干细胞移植后的外周血干细胞动员与植入

Peripheral blood stem cell mobilization and engraftment after autologous stem cell transplantation with biosimilar rhG-CSF.

作者信息

Reményi Péter, Gopcsa László, Marton Imelda, Réti Marienn, Mikala Gábor, Pető Mónika, Barta Anikó, Bátai Arpád, Farkas Zita, Borbényi Zita, Csukly Zoltán, Bodó Imre, Fábián János, Király Agnes, Lengyel Lilla, Piukovics Klára, Torbágyi Eva, Masszi Tamás

机构信息

Department of Hematology and Stem Cell Transplantation, St. Istvan and St. Laszlo Hospital of Budapest, Budapest, Hungary,

出版信息

Adv Ther. 2014 Apr;31(4):451-60. doi: 10.1007/s12325-014-0114-z. Epub 2014 Apr 1.

Abstract

INTRODUCTION

Biosimilar versions of filgrastim [recombinant human granulocyte colony-stimulating factor (rhG-CSF)] are now widely available. To date, biosimilar rhG-CSF has demonstrated a comparable quality, safety and efficacy profile to the originator product (filgrastim [Neupogen(®)], Amgen Inc., CA, USA) in the prevention and management of neutropenia. Biosimilar rhG-CSFs have also been used to induce peripheral blood stem cell (PBSC) mobilization in patients undergoing autologous stem cell transplantation (AHSCT). The authors have examined the effectiveness of a biosimilar rhG-CSF (Zarzio(®), Sandoz Biopharmaceuticals, Holzkirchen, Germany) in two retrospective studies across two medical centers in Hungary.

METHODS

In Study 1, 70 patients with hematological malignancies scheduled to undergo AHSCT received chemotherapy followed by biosimilar rhG-CSF (2 × 5 μg) for facilitating neutrophil, leukocyte, and platelet engraftment. In study 2, 40 additional patients with lymphoid malignancies and planned AHSCT received chemotherapy followed by biosimilar rhG-CSF for PBSC mobilization. The effectiveness of treatment was assessed by the average yield of cluster of differentiation (CD) 34+ cells and the number of leukaphereses required.

RESULTS

In Study 1 (patients undergoing AHSCT), the median age was 56 years and most patients were male (60%). The conditioning regimens were mainly high-dose melphalan (n = 41) and carmustine (BiCNU(®), Bristol-Myers Squibb, NJ, USA), etoposide, cytarabine and melphalan BEAM (n = 21). Median times to absolute neutrophil and leukocyte engraftment were 9 (range 8-11 days) and 10 (8-12) days, respectively. Median time to platelet engraftment was 10.5 days (7-19 days). In Study 2, the patients' median age was 54 years and the majority (57.5%) were female. The median time interval between day 1 of mobilizing chemotherapy and first leukapheresis was 12 (9-27) days. In the autologous PBSC grafts, the median number of CD34+ cells harvested was 5.2 × 10(6)/kg (2.22-57.07 × 10(6)/kg). The median yield of CD34+ cells per leukapheresis product was 2.47 × 10(6)/kg. In total, 58 leukaphereses were performed in 40 successfully harvested patients.

CONCLUSIONS

In line with previous studies with originator rhG-CSF, the findings of this study indicate that biosimilar rhG-CSF following AHSCT is effective and generally well tolerated in the engraftment setting. In addition, biosimilar rhG-CSF is comparable to the originator rhG-CSF in terms of kinetics of PBSC mobilization and yield of CD34+ cells. In conclusion, the authors have demonstrated that the use of biosimilar rhG-CSF is effective and safe in autologous PBSC mobilization and engraftment after AHSCT.

摘要

引言

非格司亭的生物类似药[重组人粒细胞集落刺激因子(rhG-CSF)]现已广泛可得。迄今为止,在预防和管理中性粒细胞减少症方面,生物类似药rhG-CSF已证明其质量、安全性和疗效与原研产品(非格司亭[优保津(Neupogen®)],美国加利福尼亚州安进公司)相当。生物类似药rhG-CSF也已用于诱导接受自体干细胞移植(AHSCT)患者的外周血干细胞(PBSC)动员。作者在匈牙利两个医疗中心开展的两项回顾性研究中检验了一种生物类似药rhG-CSF(沙格司亭(Zarzio®),德国霍尔茨基兴山德士生物制药公司)的有效性。

方法

在研究1中,70例计划接受AHSCT的血液系统恶性肿瘤患者接受化疗,随后使用生物类似药rhG-CSF(2×5μg)以促进中性粒细胞、白细胞和血小板植入。在研究2中,另外40例患有淋巴系统恶性肿瘤且计划进行AHSCT的患者接受化疗,随后使用生物类似药rhG-CSF进行PBSC动员。通过分化簇(CD)34+细胞的平均产量和所需白细胞单采术的次数评估治疗效果。

结果

在研究1(接受AHSCT的患者)中,中位年龄为56岁,大多数患者为男性(60%)。预处理方案主要为大剂量美法仑(n = 41)和卡莫司汀(卡氮芥(BiCNU®),美国新泽西州百时美施贵宝公司)、依托泊苷、阿糖胞苷和美法仑BEAM方案(n = 21)。达到绝对中性粒细胞和白细胞植入的中位时间分别为9天(范围8 - 11天)和10天(8 - 12天)。血小板植入的中位时间为10.5天(7 - 19天)。在研究2中,患者的中位年龄为54岁,大多数(57.5%)为女性。动员化疗第1天至首次白细胞单采术的中位时间间隔为12天(9 - 27天)。在自体PBSC移植物中,收获的CD34+细胞的中位数为5.2×10⁶/kg(2.22 - 57.07×10⁶/kg)。每次白细胞单采术产品中CD34+细胞的中位产量为2.47×10⁶/kg。在40例成功采集的患者中总共进行了58次白细胞单采术。

结论

与先前使用原研rhG-CSF的研究一致,本研究结果表明,AHSCT后使用生物类似药rhG-CSF在植入方面是有效的,且一般耐受性良好。此外,在PBSC动员动力学和CD34+细胞产量方面,生物类似药rhG-CSF与原研rhG-CSF相当。总之,作者已证明在AHSCT后的自体PBSC动员和植入中,使用生物类似药rhG-CSF是有效且安全的。

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