Hagenbeek Anton, Eghbali Houchingue, Monfardini Silvio, Vitolo Umberto, Hoskin Peter J, de Wolf-Peeters Christiane, MacLennan Ken, Staab-Renner Elvira, Kalmus Joachim, Schott Astrid, Teodorovic Ivana, Negrouk Anastassia, van Glabbeke Martine, Marcus Robert
European Organisation for Research and Treatment of Cancer (EORTC) Lymphoma Group, Amsterdam, The Netherlands.
J Clin Oncol. 2006 Apr 1;24(10):1590-6. doi: 10.1200/JCO.2005.03.7952.
To compare the efficacy and safety of fludarabine phosphate with cyclophosphamide, vincristine, and prednisone (CVP) in 381 previously untreated, advanced-stage, low-grade (lg) non-Hodgkin's lymphoma (NHL) patients in a phase III, multicenter study.
Between 1993 and 1997, patients were randomly assigned to treatment with either fludarabine (25 mg/m2 intravenously [IV] daily for 5 days every 4 weeks) or CVP (cyclophosphamide 750 mg/m2 IV on day 1; vincristine, 1.4 mg/m2 IV on day 1; and prednisone, 40 mg/m2 orally on days 1 through 5 every 4 weeks). Results Overall response (OR) rates were significantly improved in the fludarabine arm versus the CVP arm, both for the intent-to-treat (ITT) population and assessable patients (P < .001). Complete response (CR) rates in the ITT population were also higher after fludarabine treatment. The CR rate was 38.6% for fludarabine compared with 15.0% for CVP. There were no statistically significant differences in time to progression (TTP), time to treatment failure (TTF), and overall survival (OS) between treatment groups. WHO grades 3 and 4 hematologic adverse events were more common in the fludarabine arm. However, concerning the higher incidence of granulocytopenia, this did not translate to more infections in fludarabine-treated patients.
Newly diagnosed lgNHL patients who received fludarabine achieved higher OR and CR rates compared with CVP-treated patients. No differences in TTP, TTF, and OS were noted. Fludarabine is a highly active single agent in lgNHL. Combination therapies incorporating fludarabine are now being further evaluated as first-line therapy in follicular NHL.
在一项III期多中心研究中,比较381例先前未经治疗的晚期低度(lg)非霍奇金淋巴瘤(NHL)患者使用氟达拉滨磷酸盐与环磷酰胺、长春新碱和泼尼松(CVP)的疗效和安全性。
1993年至1997年期间,患者被随机分配接受氟达拉滨(每4周静脉注射[IV]25mg/m²,每日1次,共5天)或CVP(环磷酰胺750mg/m²,第1天静脉注射;长春新碱,第1天静脉注射1.4mg/m²;泼尼松,每4周第1天至第5天口服40mg/m²)治疗。结果在意向性治疗(ITT)人群和可评估患者中,氟达拉滨组的总体缓解(OR)率均显著高于CVP组(P<.001)。氟达拉滨治疗后ITT人群的完全缓解(CR)率也更高。氟达拉滨的CR率为38.6%,而CVP为15.0%。治疗组之间的疾病进展时间(TTP)、治疗失败时间(TTF)和总生存期(OS)无统计学显著差异。WHO 3级和4级血液学不良事件在氟达拉滨组更常见。然而,关于粒细胞减少症的发生率较高,这并未导致氟达拉滨治疗患者发生更多感染。
与接受CVP治疗的患者相比,接受氟达拉滨治疗的新诊断lgNHL患者的OR和CR率更高。TTP、TTF和OS无差异。氟达拉滨在lgNHL中是一种高活性单药。目前正在进一步评估含氟达拉滨的联合疗法作为滤泡性NHL的一线治疗。