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2-氯脱氧腺苷治疗后慢性期费城染色体阳性慢性髓性白血病的完全血液学缓解

Complete hematologic remissions in chronic-phase, Philadelphia-chromosome-positive, chronic myelogenous leukemia after 2-chlorodeoxyadenosine.

作者信息

Saven A, Piro L D, Lemon R H, Figueroa M L, Kosty M, Ellison D J, Beutler E

机构信息

Division of Hematology/Oncology, Cecil H. and Ida M. Green Cancer Center, Scripps Clinic and Research Foundation, La Jolla, CA 92037.

出版信息

Cancer. 1994 Jun 15;73(12):2953-63. doi: 10.1002/1097-0142(19940615)73:12<2953::aid-cncr2820731212>3.0.co;2-v.

Abstract

BACKGROUND

2-Chlorodeoxyadenosine (Cladribine, Leustatin, Ortho Biotech, Raritan, NJ) (2-CdA) is a purine analog with activity in the treatment of lymphoid neoplasms. Interferon induces cytogenetic remissions in chronic myeloid leukemia (CML) and partial remissions in hairy cell leukemia, a disorder in which single courses of 2-CdA induce complete remissions. In vitro clonal growth of immature myeloid progenitors from normal marrow is markedly inhibited by 2-CdA.

METHODS

2-CdA was administered to 12 patients with Philadelphia-chromosome-positive CML, 11 chronic phase, and 1 accelerated phase, at 0.1 mg/kg/day by continuous intravenous infusion for 7 days every 28-35 days, until maximum peripheral hematologic response.

RESULTS

Of 12 patients, 10 (83%) achieved complete hematologic responses and 2 (17%) partial hematologic responses after a median of two courses of 2-CdA. The median first hematologic response duration was 3 months. Of the seven patients who relapsed and were retreated with a median of two further courses of 2-CdA, five obtained responses (four complete and one partial) and two did not respond. The median second hematologic response duration was 4 months. No patient had significant Philadelphia-chromosome suppression. Reversible myelosuppression and severe cumulative T-cell immunosuppression associated with opportunistic infections in four patients were the principal toxicities.

CONCLUSIONS

2-CdA is active in CML, inducing complete hematologic responses, but the absence of cytogenetic responses and severe immunosuppression may limit its clinical use.

摘要

背景

2-氯脱氧腺苷(克拉屈滨,Leustatin,Ortho Biotech公司,新泽西州拉里坦)(2-CdA)是一种嘌呤类似物,对治疗淋巴系统肿瘤具有活性。干扰素可诱导慢性髓性白血病(CML)患者出现细胞遗传学缓解,并可诱导毛细胞白血病患者出现部分缓解,而单疗程的2-CdA可使毛细胞白血病患者获得完全缓解。正常骨髓中未成熟髓系祖细胞的体外克隆生长受到2-CdA的显著抑制。

方法

对12例费城染色体阳性的CML患者(11例慢性期和1例加速期),每28 - 35天连续静脉输注2-CdA,剂量为0.1 mg/kg/天,共7天,直至达到最大外周血液学反应。

结果

12例患者中,中位接受两个疗程的2-CdA治疗后,10例(83%)获得完全血液学缓解,2例(17%)获得部分血液学缓解。首次血液学缓解的中位持续时间为3个月。7例复发患者再次接受中位两个疗程的2-CdA治疗,其中5例获得反应(4例完全缓解和1例部分缓解),2例无反应。第二次血液学缓解的中位持续时间为4个月。无患者出现明显的费城染色体抑制。主要毒性为可逆性骨髓抑制和4例患者出现的与机会性感染相关的严重累积性T细胞免疫抑制。

结论

2-CdA对CML有活性,可诱导完全血液学缓解,但缺乏细胞遗传学反应和严重免疫抑制可能限制其临床应用。

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