Eichhorst Barbara F, Busch Raymonde, Hopfinger Georg, Pasold Rita, Hensel Manfred, Steinbrecher Cordelia, Siehl Siegfried, Jäger Ulrich, Bergmann Manuela, Stilgenbauer Stephan, Schweighofer Carmen, Wendtner Clemens M, Döhner Hartmut, Brittinger Günter, Emmerich Bertold, Hallek Michael
Department of Internal Medicine I, University of Cologne, Kerpener Str 62, D-50924 Köln, Germany.
Blood. 2006 Feb 1;107(3):885-91. doi: 10.1182/blood-2005-06-2395. Epub 2005 Oct 11.
Combination chemotherapy with fludarabine plus cyclophosphamide (FC) was compared with the standard regimen of fludarabine monotherapy in first-line treatment of younger patients with chronic lymphocytic leukemia (CLL). Between 1999 and 2003, a total of 375 patients younger than 66 years who predominantly had advanced CLL were randomly assigned to receive either fludarabine (25 mg/m(2) for 5 days intravenously, repeated every 28 days) or FC combination therapy (fludarabine 30 mg/m(2) plus cyclophosphamide 250 mg/m(2) for 3 days intravenously, repeated every 28 days). Both regimens were administered to a maximum of 6 courses. FC combination chemotherapy resulted in significantly higher complete remission rate (24%) and overall response rate (94%) compared with fludarabine alone (7% and 83%; P < .001 and P = .001). FC treatment also resulted in longer median progression-free survival (48 vs 20 months; P = .001) and longer treatment-free survival (37 vs 25 months; P < .001). Thus far, no difference in median overall survival has been observed. FC caused significantly more thrombocytopenia and leukocytopenia but did not increase the number of severe infections. In summary, first-line treatment with FC increases the response rates and the treatment-free interval in younger patients with advanced CLL.
在年轻慢性淋巴细胞白血病(CLL)患者的一线治疗中,将氟达拉滨联合环磷酰胺(FC)的联合化疗与氟达拉滨单药标准方案进行了比较。1999年至2003年期间,共有375名年龄小于66岁、主要为晚期CLL的患者被随机分配接受氟达拉滨(25mg/m²静脉注射5天,每28天重复一次)或FC联合治疗(氟达拉滨30mg/m²加环磷酰胺250mg/m²静脉注射3天,每28天重复一次)。两种方案均最多给予6个疗程。与单独使用氟达拉滨相比,FC联合化疗导致显著更高的完全缓解率(24%)和总缓解率(94%)(分别为7%和83%;P<0.001和P=0.001)。FC治疗还导致更长的中位无进展生存期(48个月对20个月;P=0.001)和更长的无治疗生存期(37个月对25个月;P<0.001)。迄今为止,未观察到中位总生存期的差异。FC导致的血小板减少症和白细胞减少症明显更多,但未增加严重感染的数量。总之,FC一线治疗可提高晚期CLL年轻患者的缓解率和无治疗间隔时间。