Neutrophil-to-Lymphocyte Ratio in Rectal CancerNovel Biomarker of Tumor Immunogenicity During Radiotherapy or Confounding Variable?

被引:42
作者
Braun, Lore Helene [1 ,2 ]
Baumann, David [1 ,2 ]
Zwirner, Kerstin [1 ,2 ]
Eipper, Ewald [3 ]
Hauth, Franziska [1 ,2 ]
Peter, Andreas [3 ]
Zips, Daniel [1 ,2 ,4 ,5 ,6 ]
Gani, Cihan [1 ,2 ,4 ,5 ,6 ]
机构
[1] Eberhard Karls Univ Tubingen, Univ Hosp, Dept Radiat Oncol, D-72076 Tubingen, Germany
[2] Eberhard Karls Univ Tubingen, Med Fac Tubingen, D-72076 Tubingen, Germany
[3] Univ Hosp Tubingen, Inst Clin Chem & Pathobiochem, D-72076 Tubingen, Germany
[4] German Canc Res Ctr, Heidelberg, Germany
[5] German Canc Consortium DKTK, D-69120 Heidelberg, Germany
[6] Comprehens Canc Ctr Tubingen Stuttgart, Gastrointestinal Canc Ctr, D-72076 Tubingen, Germany
关键词
rectal cancer; inflammation; leukocytosis; neutrophil-to-lymphocyte ratio; pathologic response; neoadjuvant radiotherapy; tumor volume; SUPPRESSOR-CELLS; NEOADJUVANT CHEMORADIOTHERAPY; INFLAMMATION; RELEVANCE; CORRELATE; HALLMARKS; SURVIVAL;
D O I
10.3390/ijms20102448
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to investigate the predictive value of blood-derived makers of local and systemic inflammatory responses on early and long-term oncological outcomes. A retrospective analysis of patients with locally advanced rectal cancer treated with preoperative long-course 5-fluorouracil-based radiochemotherapy was performed. Differential blood counts before neoadjuvant treatment were extracted from the patients' electronic charts. Optimal cut-off values for neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and lymphocyte-to-monocyte ratio (LMR) were determined. Potential clinical and hematological prognostic factors for disease-free survival (DFS) were studied using uni- and multivariate analysis. A total of 220 patients were included in the analysis. Median follow-up was 67 months. Five-year DFS and overall survival (OS) were 70% and 85%, respectively. NLR with a cut-off value of 4.06 was identified as optimal to predict DFS events. In multivariate analysis, only tumor volume (HR 0.33, 95% CI (0.14-0.83), p = 0.017) and NLR (HR 0.3, 95% CI (0.11-0.81), p = 0.017) remained significant predictors of DFS. Patients with a good histological response (Dworak 3 and 4) to radiotherapy also had a lower NLR than patients with less pronounced tumor regression (3.0 vs. 4.2, p = 0.015). A strong correlation between primary tumor volume and NLR was seen (Pearson's r = 0.64, p < 0.001). Moreover, patients with T4 tumors had a significantly higher NLR than patients with T1-T3 tumors (6.6 vs. 3.3, p < 0.001). An elevated pretherapeutic NLR was associated with higher T stage, inferior DFS, and poor pathological response to neoadjuvant radiochemotherapy. A strong correlation between NLR and primary tumor volume was seen. This association is important for the interpretation of study results and for the design of translational studies which are warranted.
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页数:9
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共 36 条
[1]   Cancer-related inflammation: Common themes and therapeutic opportunities [J].
Balkwill, Frances R. ;
Mantovani, Alberto .
SEMINARS IN CANCER BIOLOGY, 2012, 22 (01) :33-40
[2]   Polymorphonuclear Neutrophils and Cancer. Intense and Sustained Neutrophilia as a Treatment Against Solid Tumors [J].
Carlos Souto, Juan ;
Vila, Luis ;
Bru, Antonio .
MEDICINAL RESEARCH REVIEWS, 2011, 31 (03) :311-363
[3]   Systemic inflammatory response is a predictor of outcome in patients undergoing preoperative chemoradiation for locally advanced rectal cancer [J].
Carruthers, R. ;
Tho, L. M. ;
Brown, J. ;
Kakumanu, S. ;
McCartney, E. ;
McDonald, A. C. .
COLORECTAL DISEASE, 2012, 14 (10) :E701-E707
[4]   Cancer-related inflammation and treatment effectiveness [J].
Diakos, Connie I. ;
Charles, Kellie A. ;
McMillan, Donald C. ;
Clarke, Stephen J. .
LANCET ONCOLOGY, 2014, 15 (11) :E493-E503
[5]   Increased circulating myeloid-derived suppressor cells correlate with clinical cancer stage, metastatic tumor burden, and doxorubicin-cyclophosphamide chemotherapy [J].
Diaz-Montero, C. Marcela ;
Salem, Mohamed Labib ;
Nishimura, Michael I. ;
Garrett-Mayer, Elizabeth ;
Cole, David J. ;
Montero, Alberto J. .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2009, 58 (01) :49-59
[6]   Leukocytosis and neutrophilia as independent prognostic immunological biomarkers for clinical outcome in the CAO/ARO/AIO-04 randomized phase 3 rectal cancer trial [J].
Diefenhardt, Markus ;
Hofheinz, Ralf-Dieter ;
Martin, Daniel ;
Beissbarth, Tim ;
Arnold, Dirk ;
Hartmann, Arndt ;
von Der Gauein, Jens ;
Gruetzmann, Robert ;
Liersch, Torsten ;
Stroebel, Philipp ;
Grabenbauer, Gerhard G. ;
Rieger, Michael ;
Fietkau, Rainer ;
Graeven, Ullrich ;
Weitz, Juergen ;
Folprecht, Gunar ;
Ghadimi, Michael ;
Roedel, Franz ;
Roedel, Claus ;
Fokas, Emmanouil .
INTERNATIONAL JOURNAL OF CANCER, 2019, 145 (08) :2282-2291
[7]   Immunomonitoring and prognostic relevance of neutrophils in clinical trials [J].
Donskov, Frede .
SEMINARS IN CANCER BIOLOGY, 2013, 23 (03) :200-207
[8]   Neutrophils and granulocytic myeloid-derived suppressor cells: immunophenotyping, cell biology and clinical relevance in human oncology [J].
Dumitru, Claudia A. ;
Moses, Katrin ;
Trellakis, Sokratis ;
Lang, Stephan ;
Brandau, Sven .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2012, 61 (08) :1155-1167
[9]   Pathological features of rectal cancer after preoperative radiochemotherapy [J].
Dworak, O ;
Keilholz, L ;
Hoffmann, A .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 1997, 12 (01) :19-23
[10]   Polarization of Tumor-Associated Neutrophil Phenotype by TGF-β: "N1" versus "N2" TAN [J].
Fridlender, Zvi G. ;
Sun, Jing ;
Kim, Samuel ;
Kapoor, Veena ;
Cheng, Guanjun ;
Ling, Leona ;
Worthen, G. Scott ;
Albelda, Steven M. .
CANCER CELL, 2009, 16 (03) :183-194