Schernberg Antoine, Escande Alexandre, Rivin Del Campo Eleonor, Ducreux Michel, Nguyen France, Goere Diane, Chargari Cyrus, Deutsch Eric
Radiotherapy Department, Gustave Roussy Cancer Campus, Villejuif, France.
Université Paris Sud, Université Paris Saclay, Faculté de médecine du Kremlin-Bicetre, Le Kremlin-Bicetre, France; Department of Medical Oncology, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Radiother Oncol. 2017 Jan;122(1):137-145. doi: 10.1016/j.radonc.2016.12.009. Epub 2016 Dec 24.
Leukocytosis and neutrophilia could be the tip of the iceberg in the inflammatory tumor microenvironment. We aimed to validate their prognostic significance in a cohort of patients treated with definitive chemoradiation for anal squamous cell carcinoma (SCC).
MATERIALS & METHODS: Clinical records from all consecutive patients treated in a single institution between 2006 and 2016 with curative-intent radiotherapy were retrospectively analyzed. Leukocytosis and neutrophilia, defined as leukocyte or neutrophil count over 10,000 and 7500/mm, respectively, were studied in terms of overall survival (OS), progression (PFS), locoregional (LFS) and distant (DFS)-free survival.
We identified 103 non-metastatic HIV-negative patients, with concurrent chemotherapy use in 78%. Twelve and 8% displayed baseline leukocytosis and neutrophilia, respectively. Estimated 3-year OS and PFS were 88% and 67%, respectively. In univariate analysis, both leukocytosis and neutrophilia were strongly associated with inferior OS, PFS, LFS and DFS (p<0.01). In multivariate analysis, leukocytosis and neutrophilia remained strongly associated with patient outcome (p<0.01), independently from tumor T and N-stage. Anemia was an independent predictor of worse OS and PFS, while chemoradiation overall treatment time below 50days improved PFS.
Leukocytosis and neutrophilia are strong prognostic factors for OS, PFS, LFS and DFS in anal cancer treated with chemoradiation. These biomarkers could help identify patients with higher risk of tumor relapse that require treatment intensification.
白细胞增多和中性粒细胞增多可能是炎症性肿瘤微环境的冰山一角。我们旨在验证它们在一组接受肛管鳞状细胞癌(SCC)根治性放化疗患者中的预后意义。
回顾性分析了2006年至2016年在单一机构接受根治性放疗的所有连续患者的临床记录。分别将白细胞计数超过10,000/mm³和中性粒细胞计数超过7500/mm³定义为白细胞增多和中性粒细胞增多,并就总生存期(OS)、无进展生存期(PFS)、局部区域无复发生存期(LFS)和远处无复发生存期(DFS)进行研究。
我们纳入了103例非转移性HIV阴性患者,其中78%同时接受了化疗。分别有12%和8%的患者出现基线白细胞增多和中性粒细胞增多。估计3年总生存期和无进展生存期分别为88%和67%。在单因素分析中,白细胞增多和中性粒细胞增多均与较差的总生存期、无进展生存期、局部区域无复发生存期和远处无复发生存期密切相关(p<0.01)。在多因素分析中,白细胞增多和中性粒细胞增多仍然与患者预后密切相关(p<0.01),独立于肿瘤T和N分期。贫血是总生存期和无进展生存期较差的独立预测因素,而放化疗总治疗时间低于50天可改善无进展生存期。
白细胞增多和中性粒细胞增多是接受放化疗的肛管癌患者总生存期、无进展生存期、局部区域无复发生存期和远处无复发生存期的强有力预后因素。这些生物标志物有助于识别肿瘤复发风险较高、需要强化治疗的患者。