Peripheral Neutrophil to Lymphocyte Ratio Improves Prognostication in Colon Cancer.
Peripheral Neutrophil to Lymphocyte Ratio Improves Prognostication in Colon Cancer.
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DOI:
10.1016/j.clcc.2017.01.008
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发表时间:
2017-06
影响因子:
3.4
通讯作者:
Boardman LA
中科院分区:
文献类型:
--
作者:
Rashtak S;Ruan X;Druliner BR;Liu H;Therneau T;Mouchli M;Boardman LA
We studied the role of peripheral Neutrophil to Lymphocyte Ratio (NLR) on survival outcomes in colon and rectal cancer to determine if its inclusion improved prognostication within existing staging systems. Disease free and overall survival (DFS and OS) Hazard Ratios (HR) of pretreatment NLR were calculated for 2536 stage I-III colon or rectal cancer patients and adjusted for age, positive/total number of nodes, T stage, and grade. The association of NLR with clinicopathologic features and survival was evaluated and compared to American Joint Committee on cancer (AJCC) TNM staging and Memorial Sloan Kettering Cancer Center (MSKCC) models. High NLR was significantly associated with worse DFS (HR: 1.36 [95% CI 1.08–1.70] p: 0.009) and OS (HR: 1.65 [95%CI 1.29–2.10] p<0.0005) in all stages for colon, but not rectal cancer patients. High NLR was significantly associated with site-specific worse prognosis which was stronger in the left vs right colon; an inverse relationship with grade was found. The impact of high NLR on DFS and OS occurred early with the majority of deaths within 2 years following surgery. Adjusted HRs for 5-year and 2-year outcomes in colon cancer per each additional 2-unit increase in NLR were 1.15 (95% CI 1.08–1.23) and 1.20 (95% CI 1.10–1.30), respectively. Addition of NLR enhanced prognostic utility of TNM (TNM alone vs. TNM + NLR: C-index 0. 60 vs. 0.68), and MSKCC (MSKCC alone vs MSKCC + NLR: C-index 0.71 vs. 0.73) models for colon cancer patients. NLR is an independent prognostic variable for non-metastatic colon cancer that enhances existing clinical staging systems.
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影响因子:
8.8
作者:
Schmidt, H;Bastholt, L;Geertsen, P;Christensen, I;Larsen, S;Gehl, J;von der Maase, H
通讯作者:
von der Maase, H
影响因子:
7.4
作者:
Galon J;Pagès F;Marincola FM;Angell HK;Thurin M;Lugli A;Zlobec I;Berger A;Bifulco C;Botti G;Tatangelo F;Britten CM;Kreiter S;Chouchane L;Delrio P;Arndt H;Asslaber M;Maio M;Masucci GV;Mihm M;Vidal-Vanaclocha F;Allison JP;Gnjatic S;Hakansson L;Huber C;Singh-Jasuja H;Ottensmeier C;Zwierzina H;Laghi L;Grizzi F;Ohashi PS;Shaw PA;Clarke BA;Wouters BG;Kawakami Y;Hazama S;Okuno K;Wang E;O'Donnell-Tormey J;Lagorce C;Pawelec G;Nishimura MI;Hawkins R;Lapointe R;Lundqvist A;Khleif SN;Ogino S;Gibbs P;Waring P;Sato N;Torigoe T;Itoh K;Patel PS;Shukla SN;Palmqvist R;Nagtegaal ID;Wang Y;D'Arrigo C;Kopetz S;Sinicrope FA;Trinchieri G;Gajewski TF;Ascierto PA;Fox BA
通讯作者:
Fox BA
影响因子:
50.5
作者:
Klingbiel, D.;Saridaki, Z.;Tejpar, S.
通讯作者:
Tejpar, S.
DOI:
10.1093/annonc/mds614
发表时间:
2013-05
期刊:
Annals of oncology : official journal of the European Society for Medical Oncology
影响因子:
--
作者:
Merok MA;Ahlquist T;Røyrvik EC;Tufteland KF;Hektoen M;Sjo OH;Mala T;Svindland A;Lothe RA;Nesbakken A
通讯作者:
Nesbakken A
影响因子:
3.7
作者:
Tohme, Samer;Sukato, Daniel;Tsung, Allan
通讯作者:
Tsung, Allan