Robak T, Bloński J Z, Kasznicki M, Blasińska-Morawiec M, Krykowski E, Dmoszyńska A, Mrugala-Spiewak H, Skotnicki A B, Nowak W, Konopka L, Ceglarek B, Maj S, Dwilewicz-Trojaczek J, Hellmann A, Urasiński I, Zdziarska B, Kotlarek-Haus S, Potoczek S, Grieb P
Department of Hematology, Medical University of Lodz, Poland.
Blood. 2000 Oct 15;96(8):2723-9.
The efficacy and toxicity of cladribine (2-CdA) + prednisone (P) versus chlorambucil (Chl) + P were compared in previously untreated patients with progressive or symptomatic chronic lymphocytic leukemia (CLL) in a randomized, multicenter prospective trial. Eligible patients were assigned to either 2-CdA 0.12 mg/kg per day in 2-hour infusions and P 30 mg/m(2) per day for 5 consecutive days or Chl 12 mg/m(2) per day and P 30 mg/m(2) per day for 7 consecutive days. Three courses were administered at 28-day intervals or longer if myelosuppression developed. The therapy was finished if complete response (CR) was achieved. Of 229 available patients 126 received 2-CdA+P and 103 received Chl+P as a first-line treatment. CR and overall response rates were significantly higher in the patients treated with 2-CdA+P (47% and 87%, respectively) than in the patients treated with Chl+P (12% and 57%, respectively) (P = .001). Progression-free survival was significantly longer in the 2-CdA-treated group (P = .01), but event-free survival was not statistically different. Thirteen percent of patients were refractory to 2-CdA+P and 43% to Chl+P (P = .001). Drug-induced neutropenia was more frequently observed during 2-CdA+P (23%) than Chl+P therapy (11%) (P = .02), but thrombocytopenia occurred with similar frequency in both groups (36% and 27%, respectively). Infections were seen more frequently in the 2-CdA+P-treated group (56%) than in the Chl+P-treated group (40%; P = .02). Death rates have so far been similar in patients treated with 2-CdA (20%) and with Chl (17%). The probability of overall survival calculated from Kaplan-Meier curves at 24 months was also similar for both groups (78% and 82%, respectively). (Blood. 2000;96:2723-2729)
在一项随机、多中心前瞻性试验中,对未接受过治疗的进展性或有症状的慢性淋巴细胞白血病(CLL)患者,比较了克拉屈滨(2-CdA)+泼尼松(P)与苯丁酸氮芥(Chl)+P的疗效和毒性。符合条件的患者被分配接受以下两种治疗方案之一:一是2-CdA每日0.12mg/kg,静脉输注2小时,P每日30mg/m²,连续5天;二是Chl每日12mg/m²,P每日30mg/m²,连续7天。若出现骨髓抑制,则每28天或更长时间给予3个疗程的治疗。若达到完全缓解(CR),则结束治疗。在229例可评估患者中,126例接受2-CdA+P作为一线治疗,103例接受Chl+P作为一线治疗。接受2-CdA+P治疗的患者CR率和总缓解率显著高于接受Chl+P治疗的患者(分别为47%和87%,以及12%和57%)(P = 0.001)。2-CdA治疗组的无进展生存期显著更长(P = 0.01),但无事件生存期无统计学差异。13%的患者对2-CdA+P耐药,43%的患者对Chl+P耐药(P = 0.001)。2-CdA+P治疗期间比Chl+P治疗更频繁地观察到药物性中性粒细胞减少(分别为23%和11%)(P = 0.02),但两组血小板减少的发生率相似(分别为36%和27%)。2-CdA+P治疗组的感染发生率高于Chl+P治疗组(分别为56%和40%;P = 0.02)。迄今为止,接受2-CdA治疗的患者死亡率(20%)与接受Chl治疗的患者(17%)相似。根据Kaplan-Meier曲线计算的两组24个月总生存率概率也相似(分别为78%和82%)。(《血液》。2000年;96:2723 - 2729)