Robak T, Blonski J Z, Gora-Tybor J, Kasznicki M, Konopka L, Ceglarek B, Komarnicki M, Lewandowski K, Hellmann A, Lewandowski K, Moskwa A, Dmoszyńska A, Sokołowska B, Dwilewicz-Trojaczek A, Tomaszewska A, Sułek K, Całbecka M
Department of Haematology, Medical University of Łódź and Copernicus Memorial Hospital, Pabianicka 62, 93-513, ul. Pabianicka 62, Łódź, Poland.
Eur J Cancer. 2004 Feb;40(3):383-9. doi: 10.1016/j.ejca.2003.09.031.
The increased frequency of second malignancies in chronic lymphocytic leukaemia (CLL) is well known. Moreover, antineoplastic therapy additionally increases the risk of secondary cancers. In this study, we analysed whether treatment with cladribine (2-chlorodeoxyadenosine, 2-CdA) during the course of CLL had an impact on the subsequent occurrence of either secondary solid tumours or Richter's syndrome. There were 1487 eligible patients, 251 treated with 2-CdA alone, 913 treated with alkylating agents (AA)-based regimens alone and 323 treated with both 2-CdA and AA. Median time from the start of CLL treatment to the diagnosis of secondary malignancy was 1.9 years (0.5-5.1 years) for the 2-CdA group, 1.8 years (0.3-7.9 years) for the AA group and 3.9 years (0.3-8.4 years) for the 2-CdA+AA group. A total of 68 malignancies were reported in 65 patients. Ten events were non-melanotic skin cancers and were excluded from the analysis, leaving 58 events in 58 patients. In the group of patients treated with 2-CdA alone, there were 15 (6.0%) cases, in the group of patients treated with AA alone there were 26 (2.8%) cases, and in the group treated with 2-CdA+AA there were 17 (5.3%) cases of secondary malignancies. The differences between the frequency of secondary malignancies in the 2-CdA and 2-CdA+AA versus AA alone groups were not significant (P=0.05 and P=0.06, respectively). Only lung cancers occurred significantly more frequently in the 2-CdA (2.8%) and 2-CdA+AA (2.2%) treated groups compared with the AA patients (0.3%) (P<0.001 and P<0.01, respectively). In conclusion, 2-CdA in CLL patients does not seem to increase the risk of secondary malignancies except for lung cancers. However, further studies are necessary to establish the real risk of lung cancer in CLL patients treated with 2-CdA.
慢性淋巴细胞白血病(CLL)患者中第二原发恶性肿瘤的发生率增加是众所周知的。此外,抗肿瘤治疗还会进一步增加患继发性癌症的风险。在本研究中,我们分析了CLL病程中使用克拉屈滨(2-氯脱氧腺苷,2-CdA)治疗是否会对随后继发性实体瘤或 Richter 综合征的发生产生影响。共有1487例符合条件的患者,其中251例仅接受2-CdA治疗,913例仅接受基于烷化剂(AA)的方案治疗,323例同时接受2-CdA和AA治疗。2-CdA组从CLL治疗开始至继发性恶性肿瘤诊断的中位时间为1.9年(0.5 - 5.1年),AA组为1.8年(0.3 - 7.9年),2-CdA + AA组为3.9年(0.3 - 8.4年)。65例患者共报告了68例恶性肿瘤。10例为非黑素瘤皮肤癌,被排除在分析之外,58例患者中有58例事件。仅接受2-CdA治疗的患者组中有15例(6.0%),仅接受AA治疗的患者组中有26例(2.8%),接受2-CdA + AA治疗的患者组中有17例(5.3%)发生继发性恶性肿瘤。2-CdA组和2-CdA + AA组与仅接受AA治疗组的继发性恶性肿瘤发生率差异无统计学意义(P分别为0.05和0.06)。与接受AA治疗的患者(0.3%)相比,接受2-CdA治疗组(2.8%)和2-CdA + AA治疗组(2.2%)的肺癌发生率显著更高(P分别<0.001和<0.01)。总之,CLL患者使用2-CdA似乎不会增加继发性恶性肿瘤的风险,但肺癌除外。然而,需要进一步研究以确定接受2-CdA治疗的CLL患者患肺癌的实际风险。