Robak T, Bloński J Z, Kasznicki M, Konopka L, Ceglarek B, Dmoszyńska A, Soroka-Wojtaszko M, Skotnicki A B, Nowak W, Dwilewicz-Trojaczek J, Tomaszewska A, Hellmann A, Lewandowski K, Kuliczkowski K, Potoczek S, Zdziarska B, Hansz J, Kroll R, Komarnicki M, Holowiecki J, Grieb P
Department of Haematology, Medical University of Lódz, Institute of Haematology and Blood Transfusion, Warsaw, Poland.
Br J Haematol. 2000 Feb;108(2):357-68. doi: 10.1046/j.1365-2141.2000.01850.x.
Between January 1992 and January 1999, we treated 378 B-chronic lymphocytic leukaemia (CLL) patients with cladribine (2-CdA), and 255 of the patients were also treated with prednisone. A total of 194 patients were previously untreated, and 184 had relapsed or refractory disease after previous other therapy. Complete response (CR) was obtained in 111 (29.4%) and partial response (PR) in 138 (36.5%) patients, giving an overall response (OR) rate of 65.9%. CR and OR were achieved more frequently in patients in whom 2-CdA was a first-line treatment (45.4% and 82.5% respectively) than in the pretreated group (12.5% and 48.4% respectively) (P < 0.0001). The median duration of OR for previously untreated patients was 14.7 months and for pretreated patients 13.5 months (P = 0.09). The median survival evaluated from the beginning of 2-CdA treatment was shorter in the pretreated group (16.3 months) than in the untreated group (19.4 months) (P < 0.0001). A total of 117 (63.9%) patients died in the pretreated group and 63 (32.6%) in the untreated group. In pretreated patients, 2-CdA + prednisone (P) and 2-CdA alone resulted in similar OR (51.0% and 45.0% respectively; P = 0.4). In contrast, in untreated patients, 2-CdA + P produced a higher OR (85.4%) than 2-CdA alone (72.1%) (P = 0.04). Infections and fever of unknown origin, observed in 91 (49.4%) pretreated and 74 (38.1%) untreated patients (P = 0.03), were the most frequent toxic effects. Our results indicate that 2-CdA is an effective, relatively well-tolerated drug, especially in previously untreated CLL.
1992年1月至1999年1月期间,我们用克拉屈滨(2-氯脱氧腺苷)治疗了378例B细胞慢性淋巴细胞白血病(CLL)患者,其中255例患者还接受了泼尼松治疗。共有194例患者既往未接受过治疗,184例患者在先前接受其他治疗后出现复发或难治性疾病。111例(29.4%)患者获得完全缓解(CR),138例(36.5%)患者获得部分缓解(PR),总缓解率(OR)为65.9%。与预处理组(分别为12.5%和48.4%)相比,2-氯脱氧腺苷作为一线治疗的患者更频繁地实现CR和OR(分别为45.4%和82.5%)(P<0.0001)。既往未接受治疗的患者OR的中位持续时间为14.7个月,预处理患者为13.5个月(P = 0.09)。从2-氯脱氧腺苷治疗开始评估的中位生存期,预处理组(16.3个月)短于未治疗组(19.4个月)(P<0.0001)。预处理组共有117例(63.9%)患者死亡,未治疗组有63例(32.6%)患者死亡。在预处理患者中,2-氯脱氧腺苷+泼尼松(P)和单用2-氯脱氧腺苷导致相似的OR(分别为51.0%和45.0%;P = 0.4)。相比之下,在未治疗的患者中,2-氯脱氧腺苷+P产生的OR(85.4%)高于单用2-氯脱氧腺苷(72.1%)(P = 0.04)。91例(49.4%)预处理患者和74例(38.1%)未治疗患者出现感染和不明原因发热(P = 0.03),这是最常见的毒性作用。我们的结果表明,2-氯脱氧腺苷是一种有效的、耐受性相对良好的药物,尤其是在既往未治疗的CLL患者中。