Jehn U, Bartl R, Dietzfelbinger H, Haferlach T, Heinemann V
Klinikum Grosshadern, Ludwig-Maximilians University, Munich, Germany.
Leukemia. 2004 Sep;18(9):1476-81. doi: 10.1038/sj.leu.2403418.
Long-term results of both pretreated and previously untreated patients (pts) with hairy cell leukemia (HCL) using uniformly a single 7-day course of 2-chlorodeoxyadenosine (2-CdA) by continuous infusion are reported. In addition, the probability of obtaining another response with this drug in pts who relapsed after 2-CdA treatment will be addressed. A total of 44 consecutive pts (34 males, 10 females) with a median age of 57 years (range 33-77) at the time of initiation of 2-CdA treatment were analyzed. In all, 11 pts were pretreated with either splenectomy (n=6), interferon alpha (n=9) or deoxycoformycin (dCF) (n=3) or all procedures in sequence. Two pts treated with dCF did not respond to dCF, but only 2-CdA. The median time to the start of 2-CdA treatment of the 11 pretreated pts was 47 months (mo) (10-160). Out of 44, 43 (98%) achieved complete response (CR) (13 pts with residual disease-RD), one pt reached a good partial response with a single cycle of 2-CdA. Out of 44 pts, 13 had no nonhematologic toxicities at all. Toxicities (WHO grade I-IV) were mainly of grade I and II, in one pt grade IV infectious complication. Bone marrow biopsies were performed at the time of recovery of hematopoiesis, thereafter at 2-3 mo intervals, thereafter at 6 mo, and finally annually in 35 pts. The median follow-up is 8.5 years (0.1-12.2). Disease-free survival from the start of 2-CdA treatment is 36% at 12 years (median 8.4 years), 17/44 pts relapsed. Nine of these pts were treated with 2-CdA again, eight achieved a second CR (median 2.5 yrs), one pt did not respond. Eight of our cohort had a second malignancy before receiving 2-CdA. Six pts died in CR due to the second malignancy. The overall survival at 12 years after the start of 2-CdA treatment is 79%. 2-CdA is a safe and effective treatment of HCL inducing complete remissions in the majority of pts with only a single cycle of 2-CdA, and a paucity of toxicities. Responses are durable and long-lasting. Pts who relapsed following treatment with 2-CdA responded to subsequent retreatment with 2-CdA.
报告了采用单一疗程连续输注2-氯脱氧腺苷(2-CdA)7天的方案,对毛细胞白血病(HCL)患者(pts)进行治疗的长期结果,这些患者包括先前接受过治疗的和未经治疗的。此外,还将探讨2-CdA治疗后复发的患者再次使用该药物获得缓解的可能性。共分析了44例连续的患者(34例男性,10例女性),开始2-CdA治疗时的中位年龄为57岁(范围33-77岁)。其中,11例患者曾接受过脾切除术(n = 6)、α干扰素(n = 9)或脱氧助间型霉素(dCF)(n = 3)治疗,或依次接受了所有这些治疗。2例接受dCF治疗的患者对dCF无反应,但对2-CdA有反应。11例接受过治疗的患者开始2-CdA治疗的中位时间为47个月(10-160)。44例患者中,43例(98%)达到完全缓解(CR)(13例有残留疾病-RD),1例患者接受单周期2-CdA治疗后达到良好的部分缓解。44例患者中,13例完全没有非血液学毒性。毒性(世界卫生组织I-IV级)主要为I级和II级,1例患者出现IV级感染并发症。在造血恢复时进行骨髓活检,此后每2-3个月进行一次,然后每6个月进行一次,最后35例患者每年进行一次。中位随访时间为8.5年(0.1-12.2)。从开始2-CdA治疗起,12年时无病生存率为36%(中位8.4年),44例患者中有17例复发。其中9例患者再次接受2-CdA治疗,8例获得第二次CR(中位2.5年),1例无反应。我们队列中的8例患者在接受2-CdA治疗前患有第二种恶性肿瘤。6例患者因第二种恶性肿瘤在CR状态下死亡。2-CdA治疗开始后12年的总生存率为79%。2-CdA是一种安全有效的HCL治疗方法,大多数患者仅需单周期2-CdA即可诱导完全缓解,且毒性较小。缓解持久且长期。2-CdA治疗后复发的患者对随后的2-CdA再治疗有反应。