University of Texas School of Public Health, Houston, TX, USA.
Cancer. 2010 Nov 15;116(22):5279-89. doi: 10.1002/cncr.25525.
The current study was conducted to evaluate the association between colony-stimulating factor (CSF) use and the risk of developing therapy-related myelodysplastic syndromes or acute myeloid leukemia (t-MDS/AML) among a large cohort of elderly patients with non-Hodgkin lymphoma (NHL) who were treated with chemotherapy.
A total of 13,203 NHL patients were identified from the Surveillance, Epidemiology, and End Results-Medicare database who were diagnosed from 1992 through 2002. Patients were followed from their initial chemotherapy date until the date they were diagnosed with t-MDS/AML, death, or last follow-up (October 31, 2006), whichever occurred first.
Overall, 40% (n = 5266) of patients received CSF. During the follow-up period (median follow-up, 2.9 years [range, 1-14.7 years]), 272 (5.2%) patients who were treated with CSF developed t-MDS/AML, compared with 230 (2.9%) patients who did not (P < .0001, log-rank test). The 5-year incidence of t-MDS/AML for patients receiving CSF was 14.1 per 1000 person-years compared with 8.3 per 1000 person-years for patients not receiving CSF. In a multivariable Cox regression analysis adjusted for gender, histology, stage, comorbidities, radiotherapy, and chemotherapy agent, CSF use was found to be independently associated with a 53% increased risk of t-MDS/AML (hazard ratio [HR], 1.53; 95% confidence interval [95% CI], 1.26-1.84). The observed association between CSF use and t-MDS/AML persisted across histologic subgroups (ie, diffuse large B-cell lymphoma, follicular lymphoma, and others). Patients who received both CSF and antimetabolite chemotherapy were found to have a 2.5-fold increased risk of t-MDS/AML (HR, 2.49; 95% CI, 1.91-3.26) compared with patients who received neither agent.
The current study, which to our knowledge is the first large population-based study published to date, demonstrated that the administration of CSF among elderly NHL patients receiving chemotherapy was associated with an increased risk of t-MDS/AML, although the absolute risk was low.
本研究旨在评估在接受化疗的老年非霍奇金淋巴瘤(NHL)患者中,集落刺激因子(CSF)的使用与治疗相关的骨髓增生异常综合征或急性髓系白血病(t-MDS/AML)发生风险之间的关系。
从 1992 年至 2002 年,我们从监测、流行病学和最终结果-医疗保险数据库中确定了 13203 名 NHL 患者。从患者首次接受化疗的日期开始,对其进行随访,直到患者被诊断为 t-MDS/AML、死亡或末次随访(2006 年 10 月 31 日),以先发生者为准。
总体而言,40%(n=5266)的患者接受了 CSF。在随访期间(中位随访时间为 2.9 年[范围为 1-14.7 年]),接受 CSF 治疗的 272 名(5.2%)患者发生 t-MDS/AML,而未接受 CSF 治疗的 230 名(2.9%)患者中仅发生了 230 例(P<0.0001,对数秩检验)。接受 CSF 治疗的患者 5 年 t-MDS/AML 的发生率为每 1000 人年 14.1 例,而未接受 CSF 治疗的患者为每 1000 人年 8.3 例。多变量 Cox 回归分析调整性别、组织学、分期、合并症、放疗和化疗药物后,发现 CSF 的使用与 t-MDS/AML 风险增加 53%相关(风险比[HR],1.53;95%置信区间[95%CI],1.26-1.84)。在观察到的 CSF 与 t-MDS/AML 之间的关联中,观察到的 CSF 与 t-MDS/AML 之间的关联在不同的组织学亚组中仍然存在(即弥漫性大 B 细胞淋巴瘤、滤泡性淋巴瘤和其他)。与未接受两种药物治疗的患者相比,同时接受 CSF 和抗代谢化疗药物治疗的患者发生 t-MDS/AML 的风险增加了 2.5 倍(HR,2.49;95%CI,1.91-3.26)。
本研究是迄今为止发表的第一项大型基于人群的研究,表明在接受化疗的老年 NHL 患者中使用 CSF 与 t-MDS/AML 风险增加相关,尽管绝对风险较低。