Gillis S, Amir G, Bennett M, Polliack A
Department of Hematology, Hadassah University Hospital, Ein Kerem, Jerusalem, Israel.
Eur J Haematol. 2001 Jan;66(1):7-10. doi: 10.1034/j.1600-0609.2001.00308.x.
Treatment with the purine analog 2-chlorodeoxyadenosine (2-CDA) achieves a complete response in close to 90% of patients with hairy cell leukemia, with approximately 75% remaining in prolonged remission. Recently, we unexpectedly noted foci of hypoplasia and aplasia in routine follow-up bone marrow biopsies of several hairy cell leukemia patients in remission with normal blood counts. Because of this finding we examined all available biopsies to assess the incidence of this phenomenon. A total of 94 biopsies in 31 patients were reviewed. Of these, 23 were prior to 2-CDA therapy and 71 (in 30 patients) were obtained 2-76 (mean 22) months following one or more courses of treatment. Nine patients had also received prior interferon and 7 (of whom 3 had also received interferon) had undergone splenectomy. Hypocellular foci were found in only 3 (13%) of the pre-therapy biopsies. Forty-seven of the 71 post-therapy biopsies (in 23 patients) (66%) had a total of 176 hypocellular foci. Of these 47 biopsies, 39 were without evidence of disease. A simultaneous complete blood count was normal in 34 of the 47 hypoplastic biopsies (72%). This suggests that these hypoplastic areas may not be representative of the entire bone marrow and that normal hematopoiesis may take place at other sites. However, since the longest follow-up is less than 7 yr, the potential long-term significance of these findings, such as progressive bone marrow aplasia or dysplasia, may still be unrecognised.
嘌呤类似物2-氯脱氧腺苷(2-CDA)治疗可使近90%的毛细胞白血病患者获得完全缓解,约75%的患者可长期缓解。最近,我们意外地在几名血液计数正常且处于缓解期的毛细胞白血病患者的常规随访骨髓活检中发现了发育不全和再生障碍灶。基于这一发现,我们检查了所有可用的活检样本,以评估这种现象的发生率。共对31例患者的94份活检样本进行了回顾。其中,23份是在2-CDA治疗前取得的,71份(来自30例患者)是在一个或多个疗程治疗后的2至76个月(平均22个月)取得的。9例患者还曾接受过干扰素治疗,7例(其中3例也接受过干扰素治疗)接受过脾切除术。在治疗前的活检样本中,仅3份(13%)发现了细胞减少灶。71份治疗后的活检样本中有47份(来自23例患者)(66%)共有176个细胞减少灶。在这47份活检样本中,39份没有疾病证据。47份发育不全的活检样本中有34份(72%)同时全血细胞计数正常。这表明这些发育不全区域可能不代表整个骨髓,正常造血可能在其他部位发生。然而,由于最长随访时间不足7年这些发现的潜在长期意义,如进行性骨髓再生障碍或发育异常,可能仍未被认识到。