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2-氯脱氧腺苷治疗后复发的毛细胞白血病患者对α干扰素的反应

Response to interferon-alpha in patients with hairy cell leukemia relapsing after treatment with 2-chlorodeoxyadenosine.

作者信息

Seymour J F, Estey E H, Keating M J, Kurzrock R

机构信息

Department of Clinical Haematology and Medical Oncology, Royal Melbourne Hospital, Australia.

出版信息

Leukemia. 1995 May;9(5):929-32.

PMID:7769859
Abstract

2-Chlorodeoxyadenosine (2-CdA) has recently established itself as an extremely effective therapy for patients with hairy cell leukemia. To date, the issue of how to treat patients relapsing after 2-CdA has not been adequately addressed. In our initial study, 41 of 46 patients achieved an objective response (complete or partial remission). The only persistent toxicity associated with this agent appears to be significant suppression of CD4+ lymphocyte counts, albeit without evidence of clinical sequelae at a median follow-up of 30 months (range, 7-43). Eight patients have developed recurrent disease 3-23 months (median, 16 months) after 2-CdA. Because of progressive cytopenias, three of these patients were treated with interferon-alpha (IFN-alpha) (3 x 10(6) units subcutaneously three times per week), commencing 2, 9 and 16 months after the documentation of relapse. All three patients have shown an objective response with reduction of marrow hairy cells and amelioration of neutropenia and thrombocytopenia (two patients, complete remission; one patient, partial remission). Responses were maintained while on IFN-alpha, but two patients relapsed shortly (3 and 4 months, respectively) after discontinuation of IFN. There was no significant toxicity. Prior to commencing IFN-alpha, 22-36 months after 2-CdA, these patients' absolute CD4+ counts were suppressed (mean 211/microliters, s.d. +/- 85/microliters), but have not significantly changed after 10, 11 and 18 months of IFN-alpha therapy (mean 225/microliters, s.d. +/- 93/microliters). These results suggest that in hairy cell leukemia patients relapsing after 2-CdA, IFN-alpha may be a reasonable therapeutic option, especially if persistent CD4+ lymphocytopenia is present.

摘要

2-氯脱氧腺苷(2-CdA)最近已成为毛细胞白血病患者极为有效的治疗方法。迄今为止,2-CdA治疗后复发患者的治疗问题尚未得到充分解决。在我们的初步研究中,46例患者中有41例获得了客观缓解(完全或部分缓解)。与该药物相关的唯一持续性毒性似乎是CD4 +淋巴细胞计数的显著抑制,尽管在中位随访30个月(范围7 - 43个月)时没有临床后遗症的证据。8例患者在2-CdA治疗后3 - 23个月(中位时间16个月)出现疾病复发。由于血细胞减少进展,其中3例患者在复发记录后2、9和16个月开始接受α-干扰素(IFN-α)治疗(3×10⁶单位皮下注射,每周3次)。所有3例患者均表现出客观缓解,骨髓毛细胞减少,中性粒细胞减少和血小板减少得到改善(2例患者完全缓解;1例患者部分缓解)。在接受IFN-α治疗期间缓解得以维持,但2例患者在停用IFN后不久(分别为3个月和4个月)复发。没有明显的毒性。在开始IFN-α治疗前,即2-CdA治疗后22 - 36个月,这些患者的绝对CD4 +计数受到抑制(平均211/微升,标准差±85/微升),但在IFN-α治疗10、11和18个月后没有显著变化(平均225/微升,标准差±93/微升)。这些结果表明,对于2-CdA治疗后复发的毛细胞白血病患者,IFN-α可能是一种合理的治疗选择,特别是在存在持续性CD4 +淋巴细胞减少的情况下。

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