Zinzani P L, Pavone E, Storti S, Moretti L, Fattori P P, Guardigni L, Falini B, Gobbi M, Gentilini P, Lauta V M, Bendandi M, Gherlinzoni F, Magagnoli M, Venturi S, Aitini E, Tabanelli M, Leone G, Liso V, Tura S
Institute of Hematology Seragnoli, University of Bologna, Italy.
Blood. 1997 Jun 1;89(11):3974-9.
Age is an important prognostic parameter, especially in patients with advanced high-grade non-Hodgkin's lymphoma (HG-NHL) who require more intensive and extensive therapy for any possible chance of cure. We investigated the potential of granulocyte colony-stimulating factor (G-CSF) for reducing myelotoxicity, which is the most important dose-limiting factor for chemotherapy. Between March 1993 and June 1995, 158 previously untreated patients 60 years and older with HG-NHL were included in a cooperative randomized comparative trial and treated with a combination therapy including VNCOP-B (cyclophosphamide, mitoxantrone, vincristine, etoposide, bleomycin, and prednisone) with or without G-CSF. G-CSF was administered at 5 microg/kg/d throughout the treatment starting on day 3 of every week for 5 consecutive days. Of the 158 patients registered for the trial, 149 patients were evaluable: 77 received VNCOP-B plus G-CSF and 72 received VNCOP-B alone. The overall response rate was 81.5%, with complete response in 59%: 60% in the VNCOP-B plus G-CSF group, and 58% in the VNCOP-B group. At 30 months (median 24 months), 68% of all complete responders were alive without disease in the G-CSF group and 65% in the control group. Neutropenia occurred in 18 out of 77 (23%) of the G-CSF treated patients and in 40 out of 72 (55.5%) of the controls (P = .00005). Clinically relevant infections occurred in 4 out of 77 (5%) of the G-CSF group and in 15 out of 72 (21%) of the controls (P = .004). The delivered dose intensity was higher in patients receiving G-CSF (95% v 85%), but the difference was not statistically significant. Our data show that VNCOP-B is a feasible and effective regimen in elderly HG-NHL patients, and that the use of G-CSF reduces infection and neutropenia rates without producing any significant modifications to the dose intensity, CR rate, and relapse-free survival curve.
年龄是一个重要的预后参数,尤其对于晚期高级别非霍奇金淋巴瘤(HG-NHL)患者而言,他们为了获得任何治愈的可能机会都需要更强化和广泛的治疗。我们研究了粒细胞集落刺激因子(G-CSF)降低骨髓毒性的潜力,骨髓毒性是化疗最重要的剂量限制因素。在1993年3月至1995年6月期间,158名60岁及以上未经治疗的HG-NHL患者被纳入一项合作随机对照试验,并接受包括VNCOP-B(环磷酰胺、米托蒽醌、长春新碱、依托泊苷、博来霉素和泼尼松)联合或不联合G-CSF的联合治疗。从每周第3天开始,在整个治疗过程中,G-CSF以5微克/千克/天的剂量连续5天给药。在登记参加该试验的158名患者中,149名患者可进行评估:77名接受VNCOP-B加G-CSF治疗,72名仅接受VNCOP-B治疗。总体缓解率为81.5%,完全缓解率为59%:VNCOP-B加G-CSF组为60%,VNCOP-B组为58%。在30个月时(中位时间为24个月),G-CSF组所有完全缓解者中有68%无病存活,对照组为65%。77名接受G-CSF治疗的患者中有18名(23%)发生中性粒细胞减少,72名对照组患者中有40名(55.5%)发生中性粒细胞减少(P = .00005)。G-CSF组77名患者中有4名(5%)发生临床相关感染,对照组72名患者中有15名(21%)发生临床相关感染(P = .004)。接受G-CSF治疗的患者的给药剂量强度更高(95%对85%),但差异无统计学意义。我们的数据表明,VNCOP-B方案对于老年HG-NHL患者是可行且有效的,并且使用G-CSF可降低感染率和中性粒细胞减少率,而不会对剂量强度、完全缓解率和无复发生存曲线产生任何显著改变。