Radiation oncology department, Gustave Roussy Cancer Campus, Villejuif, France.
INSERM 1030, Gustave Roussy Cancer Campus, Villejuif, France.
PLoS One. 2018 Oct 10;13(10):e0204490. doi: 10.1371/journal.pone.0204490. eCollection 2018.
To study the prognostic value of baseline leukocytosis or neutrophiliain two retrospective cohorts of stage III Non-Small Cell Lung Cancer (NSCLC) patients.
Clinical records of consecutive previously untreated NSCLC patients in our Institution between June 2001 and September 2016 for stage III NSCLC were collected. The prognostic value of pretreatment leucocyte disorders was examined, with focus on patterns of relapse and survival. Leukocytosis and neutrophilia were defined as a leukocyte count or a neutrophil count exceeding 10 and 7 G/L, respectively.
We identified 238 patients, displaying baseline leukocytosis or neutrophilia in 39% and 40% respectively. Most were diagnosed with adenocarcinoma (48%), and stage IIIB NSCLC (58%). 3-year actuarial overall survival (OS) and progression-free survival (PFS) were 35% and 27% respectively. Local relapses were reported in 100 patients (42%), and distant metastases in 132 patients (55%). In multivariate analysis, leukocytosis, neutrophilia, and induction chemotherapy regimen based on carboplatin/paclitaxel were associated with worse OS and PFS (p<0.05). Neutrophilia independently decreased Locoregional Control (LRC) (HR = 2.5, p<0.001) and Distant Metastasis Control (DMC) (HR = 2.1, p<0.001). Neutrophilia was significantly associated with worse brain metastasis control (p = 0.004), mostly in adenocarcinoma patients (p<0.001).
In stage III NSCLC patients, treated with concurrent cisplatin-based chemoradiation, baseline leukocytosis and neutrophilia were associated with worse OS, PFS, LRC, and DMC. In addition with previously available markers, this independent cost-effective biomarker could help to stratify stage III NSCLC population with more accuracy.
研究基线白细胞增多或中性粒细胞增多在两个回顾性 III 期非小细胞肺癌(NSCLC)患者队列中的预后价值。
收集了我院 2001 年 6 月至 2016 年 9 月期间连续未经治疗的 III 期 NSCLC 患者的临床记录。检查了预处理白细胞紊乱的预后价值,重点关注复发和生存模式。白细胞增多和中性粒细胞增多分别定义为白细胞计数或中性粒细胞计数超过 10 和 7 G/L。
我们确定了 238 例患者,分别有 39%和 40%存在基线白细胞增多或中性粒细胞增多。大多数患者被诊断为腺癌(48%)和 IIIB 期 NSCLC(58%)。3 年总生存率(OS)和无进展生存率(PFS)分别为 35%和 27%。100 例患者(42%)出现局部复发,132 例患者(55%)出现远处转移。多变量分析显示,白细胞增多、中性粒细胞增多和基于卡铂/紫杉醇的诱导化疗方案与较差的 OS 和 PFS 相关(p<0.05)。中性粒细胞独立降低局部区域控制(LRC)(HR = 2.5,p<0.001)和远处转移控制(DMC)(HR = 2.1,p<0.001)。中性粒细胞与脑转移控制不良显著相关(p = 0.004),主要见于腺癌患者(p<0.001)。
在接受顺铂为基础的放化疗的 III 期 NSCLC 患者中,基线白细胞增多和中性粒细胞增多与较差的 OS、PFS、LRC 和 DMC 相关。除了以前可用的标志物外,这种独立的具有成本效益的生物标志物可以帮助更准确地分层 III 期 NSCLC 人群。