Use of White Blood Cell Growth Factors and Risk of Acute Myeloid Leukemia or Myelodysplastic Syndrome Among Elderly Patients With Non-Hodgkin Lymphoma

被引:13
作者
Gruschkus, Stephen K. [1 ]
Lairson, David [2 ,3 ]
Dunn, J. Kay [4 ]
Risser, Jan [1 ,2 ]
Du, Xianglin L. [1 ,2 ,3 ]
机构
[1] Univ Texas Houston, Sch Publ Hlth, Div Epidemiol & Dis Control, Houston, TX 77030 USA
[2] Univ Texas Houston, Sch Publ Hlth, Div Management Policy & Community Hlth, Houston, TX 77030 USA
[3] Univ Texas Houston, Sch Publ Hlth, Ctr Hlth Serv Res, Houston, TX 77030 USA
[4] Univ Texas Houston, Sch Publ Hlth, Div Biostat, Houston, TX 77030 USA
基金
美国医疗保健研究与质量局;
关键词
non-Hodgkin lymphoma; colony-stimulating factor; chemotherapy; myelodysplastic syndromes; acute myeloid leukemia; COLONY-STIMULATING FACTOR; EARLY BREAST-CANCER; 2ND MALIGNANCIES; ADJUVANT CHEMOTHERAPY; DOSE-DENSE; THERAPY; EPIRUBICIN; CYCLOPHOSPHAMIDE; TRIALS;
D O I
10.1002/cncr.25525
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUND. 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. METHODS. 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. RESULTS. 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. CONCLUSIONS. 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. Cancer 2010;116:5279-89. (c) 2010 American Cancer Society.
引用
收藏
页码:5279 / 5289
页数:11
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