Huan S D, Hester J, Spitzer G, Yau J C, Dunphy F R, Wallerstein R O, Dicke K, Spencer V, LeMaistre C F, Andersson B S
Division of Oncology, St Louis University Medical Center, MO 63110.
Blood. 1992 Jun 15;79(12):3388-93.
Peripheral blood cells (PBC) can hasten hematopoietic recovery after high-dose chemotherapy. To determine if PBC apheresed after mobilization further enhance hematopoietic recovery over that achieved with autologous bone marrow (ABM) and recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF), 14 patients with metastatic solid tumors were supported by ABM and rhGM-CSF during the first course of high doses of cyclophosphamide, etoposide, and cisplatin (CVP) and 11 of these 14 patients by mobilized PBC with ABM and rhGM-CSF during the second CVP. Each patient served as his or her own control. Identical doses of CVP were administered in both courses: cyclophosphamide 5.25 g/m2, etoposide 1,200 mg/m2, and cisplatin 165 to 180 mg/m2. PBC were collected on day 10 after mobilization with cyclophosphamide (3 g/m2) intravenously (IV) on day 1, doxorubicin (50 mg/m2) as a continuous IV infusion over 48 hours starting day 2, and rhGM-CSF as a daily 4-hour IV infusion starting day 4 at 0.6 mg/m2 for 14 days. Comparing recovery in the 11 patients to receive two cycles of therapy, the median days to an absolute neutrophil count of 0.1 x 10(9)/L and 0.5 x 10(9)/L were not statistically significant between the two courses; neither was there a difference in the incidence of fever and bacteremia. The median number of days to platelet count of 0.02 x 10(12)/L unmaintained by platelet transfusion was 20 from marrow infusion for course 1 and 16 for course 2 (P = .059). The median number of days to a platelet count of 0.05 x 10(12)/L was significantly shortened: 24 and 19 days for courses 1 and 2, respectively (P = .045). Patients who received PBC required fewer number of platelet transfusions. Extramedullary toxicities were not different between the groups. Our finding of enhanced early recovery of platelets and reduced platelet transfusion requirement is in concordance with other studies.
外周血细胞(PBC)可加速大剂量化疗后的造血恢复。为了确定动员后采集的PBC是否比自体骨髓(ABM)和重组人粒细胞巨噬细胞集落刺激因子(rhGM-CSF)更能增强造血恢复,14例转移性实体瘤患者在第一个大剂量环磷酰胺、依托泊苷和顺铂(CVP)疗程中接受ABM和rhGM-CSF支持,这14例患者中的11例在第二个CVP疗程中接受动员后的PBC联合ABM和rhGM-CSF支持。每位患者均以自身作为对照。两个疗程均给予相同剂量的CVP:环磷酰胺5.25 g/m²、依托泊苷1200 mg/m²、顺铂165至180 mg/m²。在第1天静脉注射环磷酰胺(3 g/m²)动员后第10天采集PBC,从第2天开始以48小时持续静脉输注多柔比星(50 mg/m²),从第4天开始每天4小时静脉输注rhGM-CSF,剂量为0.6 mg/m²,共14天。比较接受两个周期治疗的11例患者的恢复情况,两个疗程之间达到绝对中性粒细胞计数0.1×10⁹/L和0.5×10⁹/L的中位天数无统计学差异;发热和菌血症的发生率也无差异。未进行血小板输注维持时,达到血小板计数0.02×10¹²/L的中位天数,第1疗程从骨髓输注开始为20天,第2疗程为16天(P = 0.059)。达到血小板计数0.05×10¹²/L的中位天数显著缩短:第1疗程和第2疗程分别为24天和19天(P = 0.045)。接受PBC的患者所需血小板输注次数较少。两组间的髓外毒性无差异。我们关于血小板早期恢复增强和血小板输注需求减少的发现与其他研究一致。