Schernberg Antoine, Nivet Alexandre, Dhermain Frédéric, Ammari Samy, Escande Alexandre, Pallud Johan, Louvel Guillaume, Deutsch Eric
Radiation Oncology Department, Gustave Roussy Cancer Campus, Villejuif, France.
INSERM1030, Gustave Roussy Cancer Campus, Villejuif, France.
Clin Transl Radiat Oncol. 2018 Apr 13;10:47-52. doi: 10.1016/j.ctro.2018.04.002. eCollection 2018 Mar.
To study the prognostic value of neutrophil disorders in a retrospective cohort of high-grade glioma patients receiving definitive concurrent temozolomide and radiation.
Clinical records of consecutive patients treated in our Institution between January 2005 and December 2010 with concurrent temozolomide (75 mg/m daily) and radiation were collected. The prognostic value of pretreatment neutrophilia on survival, defined as a neutrophil count exceeding 7 G/L, was examined.
We identified 164 patients, all treated with concurrent temozolomide-based chemoradiotherapy. Initial surgery was achieved in most (75%), with resection > 90% in 55 patients (34%). Total 151 patients (92%) had glioblastoma, and 13 patients (8%) had WHO grade III glioma. Eighty-two patients (50%) displayed pretreatment neutrophilia. Neutrophilia was not associated with concurrent or adjuvant temodal discontinuation (p > 0.3). The 2-year actuarial overall survival was 45%. Steroid consumption, i.e. 60 mg or more of daily prednisolone, increased pretreatment neutrophil count (p = 0.005). In univariate analysis, neutrophilia was associated with worse overall survival (p = 0.019), as well as age ≥ 65 years (p = 0.009), surgical resection < 90% (p = 0.003) and prednisolone consumption ≥ 60 mg/day (p = 0.016). In multivariate analysis, neutrophilia (p = 0.013), age ≥ 65 (p = 0.001), and surgical tumor resection < 90% (p = 0.010) independently decreased overall survival, while, steroid consumption was not (p = 0.088).
In high-grade gliomas treated with concurrent temozolomide and radiation, pretreatment neutrophilia may be a significant prognosis factor for overall survival. In addition with previously available markers, this independent cost-effective biomarker could help identifying patients with worsened prognosis.
在接受替莫唑胺同步放化疗的高级别胶质瘤患者回顾性队列研究中,探讨中性粒细胞紊乱的预后价值。
收集2005年1月至2010年12月在本机构接受替莫唑胺(每日75mg/m²)同步放疗的连续患者的临床记录。研究了预处理中性粒细胞增多症(定义为中性粒细胞计数超过7×10⁹/L)对生存的预后价值。
我们确定了164例患者,均接受了基于替莫唑胺的同步放化疗。大多数患者(75%)进行了初始手术,55例患者(34%)切除率>90%。总共151例患者(92%)患有胶质母细胞瘤,13例患者(8%)患有世界卫生组织III级胶质瘤。82例患者(50%)出现预处理中性粒细胞增多症。中性粒细胞增多症与同步或辅助替莫唑胺停药无关(p>0.3)。2年精算总生存率为45%。类固醇使用,即每日泼尼松龙60mg或更多,会增加预处理中性粒细胞计数(p=0.005)。在单因素分析中,中性粒细胞增多症与较差的总生存率相关(p=0.019),以及年龄≥65岁(p=0.009)、手术切除率<90%(p=0.003)和泼尼松龙使用量≥60mg/天(p=0.016)。在多因素分析中,中性粒细胞增多症(p=0.013)、年龄≥65岁(p=0.001)和手术肿瘤切除率<90%(p=0.010)独立降低总生存率,而类固醇使用量则不然(p=0.088)。
在接受替莫唑胺同步放疗的高级别胶质瘤中,预处理中性粒细胞增多症可能是总生存的一个重要预后因素。除了先前可用的标志物外,这种独立的成本效益高的生物标志物有助于识别预后较差的患者。