Van Den Neste E, Michaux L, Layios N, Costantini S, Francart J, Lambert C, Sonet A, André M, Robert A, Ferrant A
Department of Hematology, Cliniques universitaires Saint-Luc, Université catholique de Louvain, 1200 Brussels, Belgium.
Ann Hematol. 2004 Jun;83(6):356-63. doi: 10.1007/s00277-004-0858-7. Epub 2004 Mar 16.
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.
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。