Mądry Krzysztof, Lis Karol, Biecek Przemysław, Młynarczyk Magda, Rytel Jagoda, Górka Michał, Kacprzyk Piotr, Dutka Magdalena, Rodzaj Marek, Bołkun Łukasz, Krochmalczyk Dorota, Łątka Ewa, Drozd-Sokołowska Joanna, Waszczuk-Gajda Anna, Knopińska-Posłuszny Wanda, Kopińska Anna, Subocz Edyta, Masternak Anna, Guzicka-Kazimierczak Renata, Gil Lidia, Machowicz Rafał, Biliński Jarosław, Giebel Sebastian, Czerw Tomasz, Dwilewicz-Trojaczek Jadwiga
Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.
Department of Hematology, Oncology and Internal Diseases, Medical University, Warsaw, Poland.
Clin Lymphoma Myeloma Leuk. 2019 May;19(5):264-274.e4. doi: 10.1016/j.clml.2019.01.002. Epub 2019 Jan 23.
Myelodysplastic syndromes (MDS), chronic myelomonocytic leukemia (CMML), and acute myeloid leukemia (AML) patients, including those treated with azacitidine, are at increased risk for serious infections. The aim of our study was to identify patients with higher infectious risk at the beginning of azacitidine treatment.
We performed a retrospective evaluation of 298 MDS/CMML/AML patients and included in the analysis 232 patients who completed the first 3 cycles of azacitidine therapy or developed Grade III/IV infection before completing the third cycle.
Overall, 143 patients (62%) experienced serious infection, and in 94 patients (41%) infection occurred within the first 3 cycles. The following variables were found to have the most significant effect on the infectious risk in multivariate analysis: red blood cell transfusion dependency (odds ratio [OR], 2.38; 97.5% confidence interval [CI], 1.21-4.79), neutropenia <0.8 × 10/L (OR, 3.03; 97.5% CI, 1.66-5.55), platelet count <50 × 10/L (OR, 2.63; 97.5% CI, 1.42-4.76), albumin level <35 g/dL (OR, 2.04; 97.5% CI, 1.01-4.16), and Eastern Cooperative Oncology Group performance status ≥2 (OR, 2.19; 97.5% CI, 1.40-3.54). Each of these variables is assigned 1 point, and the combined score represents the proposed Azacitidine Infection Risk Model. The infection rate in the first 3 cycles of therapy in lower-risk (0-2 score) and higher-risk (3-5 score) patients was 25% and 73%, respectively. The overall survival was significantly reduced in higher-risk patients compared with the lower-risk cohort (8 vs. 29 months).
We selected a subset with high early risk for serious infection and worse clinical outcome among patients treated with azacitidine.
骨髓增生异常综合征(MDS)、慢性粒单核细胞白血病(CMML)和急性髓系白血病(AML)患者,包括接受阿扎胞苷治疗的患者,发生严重感染的风险增加。我们研究的目的是在阿扎胞苷治疗开始时识别出感染风险较高的患者。
我们对298例MDS/CMML/AML患者进行了回顾性评估,分析纳入了232例完成阿扎胞苷治疗前3个周期或在完成第3个周期前发生Ⅲ/Ⅳ级感染的患者。
总体而言,143例患者(62%)发生了严重感染,94例患者(41%)在第1个3周期内发生感染。多因素分析发现以下变量对感染风险影响最为显著:红细胞输注依赖(比值比[OR],2.38;97.5%置信区间[CI],1.21 - 4.79)、中性粒细胞减少<0.8×10⁹/L(OR,3.03;97.5%CI,1.66 - 5.55)、血小板计数<50×10⁹/L(OR,2.63;97.5%CI,1.42 - 4.76)、白蛋白水平<35 g/dL(OR,2.04;97.5%CI,1.01 - 4.16)以及东部肿瘤协作组体能状态≥2(OR,2.19;97.5%CI,1.40 - 3.54)。这些变量每个赋值1分,综合评分代表所提出的阿扎胞苷感染风险模型。低风险(0 - 2分)和高风险(3 - 5分)患者在治疗第1个3周期的感染率分别为25%和73%。与低风险队列相比,高风险患者的总生存期显著缩短(8个月对29个月)。
我们在接受阿扎胞苷治疗的患者中选出了一组早期发生严重感染风险高且临床结局较差的患者亚组。