| Literature DB >> 30868576 |
Markus Diefenhardt1,2, Ralf-Dieter Hofheinz3, Daniel Martin1,2, Tim Beißbarth4, Dirk Arnold5, Arndt Hartmann6, Jens von der Grün1, Robert Grützmann7, Torsten Liersch8, Philipp Ströbel9, Gerhard G Grabenbauer10, Michael Rieger11,12, Rainer Fietkau13, Ullrich Graeven14, Jürgen Weitz12,15, Gunar Folprecht12,16, Michael Ghadimi8, Franz Rödel1,2,12, Claus Rödel1,2,12, Emmanouil Fokas1,2,12.
Abstract
Peripheral blood leukocytosis and neutrophilia reflect cancer inflammation and have been proposed as prognostic immunological biomarkers in various malignancies. However, previous studies were limited by their retrospective nature and small patient numbers. Baseline peripheral blood leukocytes, neutrophils, hemoglobin, platelets, lactate dehydrogenase and carcinoembryonic antigen (CEA) were correlated with clinicopathologic characteristics, and clinical outcome in 1236 patients with rectal cancer treated with 5-FU-based preoperative chemoradiotherapy (CRT) alone or with oxaliplatin followed by surgery and adjuvant chemotherapy within the CAO/ARO/AIO-04 randomized phase 3 trial. Multivariable analyses were performed using Cox regression models. After a median follow-up of 50 months, baseline leukocytosis remained an independent adverse prognostic factor for disease-free survival (DFS; HR 1.457; 95% CI 1.163-1.825; p = 0.001), distant metastasis (HR 1.696; 95% CI 1.266-2.273; p < 0.001) and overall survival (OS; HR 1.716; 95% CI 1.264-2.329; p = 0.001) in multivariable analysis. Similar significant findings were observed for neutrophilia and high CEA levels. Conversely, treatment-induced leukopenia correlated with favorable DFS (p = 0.037), distant metastasis (p = 0.028) and OS (p = 0.012). Intriguingly, addition of oxaliplatin to 5-FU CRT resulted in a significant DFS improvement only in patients with neutrophilia and leukocytosis (p = 0.028 and p = 0.002). Our findings have important clinical implications and provide high-level evidence on the adverse prognostic role of leukocytes and neutrophils, and the impact of chemotherapy in the context of these biomarkers. These data could help guide patient stratification and should be further validated within prospective studies.Entities:
Keywords: clinical radiotherapeutic studies; clinical trials; colorectal cancer; molecular markers of metastasis and progression; radiochemotherapy
Year: 2019 PMID: 30868576 DOI: 10.1002/ijc.32274
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396