Shen Wen-yi, Li Jian-yong, Hong Ming, Zhang Run, Lu Hua, Liu Peng, Qian Si-xuan, Xu Wei, Qiu Hong-xia, Wu Han-xin
Department of Hematology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Zhonghua Xue Ye Xue Za Zhi. 2012 Aug;33(8):628-31.
To explore the effectivity and safety of single high-dose (HD) etoposide (Vp16) with granulocyte colony-stimulating factor (G-CSF) for mobilization of autologous peripheral blood stem cells (PBSC) in patients with hematologic malignancies.
80 patients of hematologic malignancies including 20 patients with acute leukemia (AL), 23 with multiple myeloma (MM), 35 with non-Hodgkin's lymphoma (NHL) and 2 with Hodgkin's lymphoma (HL) received Vp16 (1.6 g/m(2)) continuous intravenous infusion for 10 hrs on day 1. G-CSF at 10 µg/kg once daily subcutaneous injection began to use on day of ANC lower than 1×10(9)/L and continued until PBSC collection was completed. Autologous PBSC (APBSC) was collected on day of WBC greater than 5×10(9)/L and continuing until the collection goal was met (target value: MNC ≥ 6.0×10(8)/kg and CD34(+) ≥ 2.0×10(6)/kg). The patients received APBSC after conditioning regimen. The number of the cells collection, time of hematopoietic reconstruction, adverse effect and so on were observed during the course of stem cell mobilization and collection.
PBSC was collected on day 11 (range: 7 - 25 days) of after Vp16 administration with a median collection time of 2 (range 1 - 5). 3/80 patients with AML got stem cell mobilization failure. 5 of 6 patients who failed to mobilize before got successful stem cell mobilization, 1/6 patient with AML-M(5) got a second failure after the mobilization of VP16 whose first time's mobilization using Ara-C did not succeed. The median number of CD34(+) cells collected in 77 patients who got successful mobilization was 4×10(6)/kg [range (1.59 - 24.68)×10(6)/kg]. The collection of 20 patients with AL and 23 with MM were got detection for minimal residual disease, no pollution of tumor cells were happened. All patients could tolerate the whole course of stem cell mobilization. 29/80 (36.25%) patients got a 4 grade leucopenia, 19/80 (23.75%) patients got infection.
Single high-dose etoposide with G-CSF for mobilization of APBSC has a higher achievement ratio, a controllable adverse effect, a promising hematopoiesis recovery, which is an effective and safe mobilizing regimen for patients with hematologic malignancies.
探讨单次大剂量(HD)依托泊苷(Vp16)联合粒细胞集落刺激因子(G-CSF)动员血液系统恶性肿瘤患者自体外周血干细胞(PBSC)的有效性及安全性。
80例血液系统恶性肿瘤患者,其中急性白血病(AL)20例、多发性骨髓瘤(MM)23例、非霍奇金淋巴瘤(NHL)35例、霍奇金淋巴瘤(HL)2例,于第1天接受Vp16(1.6 g/m²)持续静脉输注10小时。当中性粒细胞绝对值(ANC)低于1×10⁹/L时开始每日1次皮下注射10 μg/kg的G-CSF,并持续至PBSC采集完成。当白细胞计数大于5×10⁹/L时开始采集自体外周血干细胞(APBSC),并持续至采集目标达成(目标值:单个核细胞(MNC)≥6.0×10⁸/kg且CD34⁺≥2.0×10⁶/kg)。患者在预处理方案后接受APBSC。在干细胞动员和采集过程中观察细胞采集数量、造血重建时间、不良反应等。
Vp16给药后第11天(范围:7 - 25天)采集PBSC,中位采集时间为2天(范围1 - 5天)。80例患者中有3例急性髓系白血病(AML)患者干细胞动员失败。6例之前动员失败的患者中有5例成功动员出干细胞,1例AML-M(5)患者在Vp16动员后再次失败,其首次使用阿糖胞苷动员未成功。77例动员成功的患者采集的CD34⁺细胞中位数为4×10⁶/kg [范围(1.59 - 24.68)×10⁶/kg]。对20例AL患者和23例MM患者的采集物进行微小残留病检测,未发生肿瘤细胞污染。所有患者均可耐受整个干细胞动员过程。80例患者中有29例(36.25%)发生4级白细胞减少,19例(23.75%)发生感染。
单次大剂量依托泊苷联合G-CSF动员APBSC成功率较高,不良反应可控,造血恢复良好,是血液系统恶性肿瘤患者一种有效且安全的动员方案。