Rafel M, Cervantes F, Beltrán J M, Zuazu F, Hernández Nieto L, Rayón C, García Talavera J, Montserrat E
Department of Hematology, Hospital Clínic, IDIBAPS, University of Barcelona, Spain.
Cancer. 2000 Jan 15;88(2):352-7. doi: 10.1002/(sici)1097-0142(20000115)88:2<352::aid-cncr15>3.0.co;2-8.
Deoxycoformycin (DCF) has been reported to produce high response rates in patients with hairy cell leukemia (HCL), but to the authors' knowledge data regarding experience with such therapy in a large HCL series are scarce.
Between 1988-1997, DCF (4 mg/m(2)/day, every 2 weeks) was administered to 80 HCL patients in 32 Spanish institutions. In 35 of 78 evaluable patients DCF was the first-line therapy; the remaining 43 patients had received other therapies. Pretreatment variables influencing the achievement of complete remission (CR) and event free survival were identified by multivariate analyses.
The median number of cycles administered was 7 (range, 1-22 cycles). A CR was obtained in 56 patients (72%) and a partial remission was obtained in 13 patients, for an overall response rate of 88%. In the multivariate analysis previous splenectomy and an Eastern Cooperative Oncology Group (ECOG) performance status > or = 2 were the parameters adversely influencing CR achievement. With a median follow-up of 31.2 months (range, 0.4-126.5 months), disease recurrence was observed in 11 of the CR patients, 5 of whom showed a further response to DCF. An ECOG performance status > or = 2 was the only pretreatment variable associated with a shorter event free survival. Seven patients died, four during the treatment period. The actuarial median event free survival was 46 months (95% confidence interval, 22.5-69.5 months), and 48.7% of the 56 patients who achieved a CR were expected to be alive and disease free at 5 years. Hematologic toxicity (marked neutropenia [22 cases], anemia [6 cases], and thrombocytopenia [1 case]) was the main side effect, followed by nausea and emesis (5 cases); 14 patients required hospitalization.
The results of the current study confirm the effectiveness and acceptable toxicity of DCF in the treatment of patients with HCL.
据报道,脱氧助间型霉素(DCF)治疗毛细胞白血病(HCL)患者时缓解率较高,但据作者所知,关于在大量HCL病例中使用该疗法的经验数据较少。
1988年至1997年间,西班牙32家机构的80例HCL患者接受了DCF治疗(4mg/m²/天,每2周一次)。78例可评估患者中,35例将DCF作为一线治疗;其余43例患者曾接受过其他治疗。通过多因素分析确定影响完全缓解(CR)和无事件生存的预处理变量。
给药周期中位数为7个(范围1 - 22个周期)。56例患者(72%)获得CR,13例患者获得部分缓解,总缓解率为88%。多因素分析中,既往脾切除术和东部肿瘤协作组(ECOG)体能状态≥2是影响CR获得的不利因素。中位随访31.2个月(范围0.4 - 126.5个月),11例CR患者出现疾病复发,其中5例对DCF再次产生反应。ECOG体能状态≥2是与无事件生存时间较短相关的唯一预处理变量。7例患者死亡,4例死于治疗期间。精算无事件生存中位数为46个月(95%置信区间,22.5 - 69.5个月),56例获得CR的患者中,48.7%预计在5年时仍存活且无疾病。血液学毒性(明显中性粒细胞减少[22例]、贫血[6例]和血小板减少[1例])是主要副作用,其次是恶心和呕吐(5例);14例患者需要住院治疗。
本研究结果证实DCF治疗HCL患者有效且毒性可接受。