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2-氯-2'-脱氧腺苷联合环磷酰胺治疗晚期淋巴增殖性恶性肿瘤患者后并发症的高发生率。

High incidence of complications after 2-chloro-2'-deoxyadenosine combined with cyclophosphamide in patients with advanced lymphoproliferative malignancies.

作者信息

Van Den Neste E, Michaux L, Layios N, Costantini S, Francart J, Lambert C, Sonet A, André M, Robert A, Ferrant A

机构信息

Department of Hematology, Cliniques universitaires Saint-Luc, Université catholique de Louvain, 1200 Brussels, Belgium.

出版信息

Ann Hematol. 2004 Jun;83(6):356-63. doi: 10.1007/s00277-004-0858-7. Epub 2004 Mar 16.

Abstract

The combination of purine analogs with alkylating agents is able to produce a synergistic antitumoral effect. However, the addition of immunosuppressive and DNA-targeting agents might increase purine analog-related complications. The risk for serious complications was evaluated in 38 patients treated with 2-chloro-2'-deoxyadenosine (CDA) and cyclophosphamide (CP). The diagnoses were chronic lymphocytic leukemia (CLL) in 15, Waldenström's macroglobulinemia in 4, mantle cell lymphoma in 6, follicular non-Hodgkin's lymphoma (NHL) in 10, and other low-grade NHL in 3 patients. All patients were pretreated (median: 2 lines, range: 1-5) and 23 (61%) were refractory. The patients received a median of two courses (range: 1-5) of 5.6 mg/m(2) CDA, followed by a median of 200 mg/m(2) CP, for 3 days. The response rate was 51% [complete remission (CR): 14%, partial remission (PR): 38%]. Grade 3/4 infections occurred in 16 (42%) patients. Dose-limiting cytopenias were seen in 22 (58%) patients. In 12 (32%) patients, autoimmune manifestations developed requiring treatment in most of them. Second cancers arose in five (13%) patients (myelodysplastic syndrome/acute myelocytic leukemia in three, lung cancer in two). Multivariate analysis showed that cytopenias, gender (F), prior radiotherapy, and age (>65 years) predicted for the complications seen after CDA-CP. To conclude, because of the high incidence of complications, caution is warranted in selecting patients with advanced lymphoid malignancies for the CDA-CP protocol.

摘要

嘌呤类似物与烷化剂联合使用能够产生协同抗肿瘤作用。然而,添加免疫抑制剂和DNA靶向药物可能会增加嘌呤类似物相关的并发症。对38例接受2-氯-2'-脱氧腺苷(CDA)和环磷酰胺(CP)治疗的患者的严重并发症风险进行了评估。诊断结果为15例慢性淋巴细胞白血病(CLL)、4例瓦尔登斯特伦巨球蛋白血症、6例套细胞淋巴瘤、10例滤泡性非霍奇金淋巴瘤(NHL)以及3例其他低级别NHL。所有患者均接受过预处理(中位值:2线,范围:1 - 5线),23例(61%)为难治性患者。患者接受了中位值为两个疗程(范围:1 - 5个疗程)的5.6 mg/m² CDA治疗,随后中位值为200 mg/m² CP,持续3天。缓解率为51%[完全缓解(CR):14%,部分缓解(PR):38%]。16例(42%)患者发生3/4级感染。22例(58%)患者出现剂量限制性血细胞减少。12例(32%)患者出现自身免疫表现,其中大多数需要治疗。5例(13%)患者发生了第二肿瘤(3例为骨髓增生异常综合征/急性髓细胞白血病,2例为肺癌)。多因素分析表明,血细胞减少、性别(女性)、既往放疗以及年龄(>65岁)可预测CDA - CP治疗后出现的并发症。总之,由于并发症发生率高,在为晚期淋巴系统恶性肿瘤患者选择CDA - CP方案时应谨慎。

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