Saven A, Burian C, Koziol J A, Piro L D
Division of Hematology/Oncology, Ida M. and Cecil H. Green Cancer Center, Scripps Clinic, La Jolla, CA; The Scripps Research Institute, La Jolla, CA, USA.
Blood. 1998 Sep 15;92(6):1918-26.
Hairy cell leukemia is a chronic B-cell disorder that follows an indolent, but progressive course. Cladribine (2-chlorodeoxyadenosine) induces complete remissions in the majority of patients after a single course. We report the long-term outcomes, including response rates and their duration; time-to-treatment failure (TTF) rates; retreatment results; toxicities; and survival rates of patients treated at Scripps Clinic (La Jolla, CA). A total of 358 patients with hairy cell leukemia were treated with cladribine at 0.087 or 0.1 mg/kg body weight per day by continuous intravenous infusion for 7 days. The expected number of second neoplasms was based on the National Cancer Institute's Surveillance Epidemiology and End Results data. Of 349 evaluable patients, 319 (91%) achieved an initial complete response and 22 (7%) a partial response with an overall median duration of response follow-up of 52 months. Ninety patients (26%) had relapsed at a median of 29 months. The TTF rate for all 341 responders was 19% at 48 months, 16% for complete responders, and 54% for partial responders. Of 53 evaluable patients treated with second courses of cladribine at first relapse, 33 (62%) achieved complete responses and 14 (26%) partial responses. Twenty-seven patients (8%) developed second neoplasms (only 1 hematopoietic) with an observed-to-expected ratio of 1.88 (95% confidence interval, 1.24 to 2.74). The overall survival rate was 96% at 48 months. Single courses of cladribine induced long-lasting complete responses in the vast majority of patients. Relapse rates for complete responders were low. Patients who relapse can be successfully retreated with cladribine. Cladribine has high efficacy and a favorable acute and long-term toxicity profile when administered to patients with hairy cell leukemia.
毛细胞白血病是一种慢性B细胞疾病,病程进展缓慢但呈进行性发展。克拉屈滨(2-氯脱氧腺苷)单次疗程后可使大多数患者获得完全缓解。我们报告了在斯克里普斯诊所(加利福尼亚州拉霍亚)接受治疗的患者的长期预后,包括缓解率及其持续时间、治疗失败时间(TTF)率、再次治疗结果、毒性和生存率。共有358例毛细胞白血病患者接受了克拉屈滨治疗,每天按0.087或0.1mg/kg体重连续静脉输注7天。第二肿瘤的预期数量基于美国国立癌症研究所的监测、流行病学和最终结果数据。在349例可评估患者中,319例(91%)获得初始完全缓解,22例(7%)获得部分缓解,总体缓解期随访的中位持续时间为52个月。90例患者(26%)在中位时间29个月时复发。所有341例缓解者在48个月时的TTF率为19%,完全缓解者为16%,部分缓解者为54%。在53例首次复发时接受克拉屈滨第二疗程治疗的可评估患者中,33例(62%)获得完全缓解,14例(26%)获得部分缓解。27例患者(8%)发生第二肿瘤(仅1例为造血系统肿瘤),观察到的与预期的比例为1.88(95%置信区间,1.24至2.74)。48个月时的总生存率为96%。单次疗程的克拉屈滨可使绝大多数患者获得持久的完全缓解。完全缓解者的复发率较低。复发患者可用克拉屈滨成功再次治疗。克拉屈滨用于毛细胞白血病患者时具有高效以及良好的急性和长期毒性特征。