Analytic lymph node number establishes staging accuracy by occult tumor burden in colorectal cancer

被引:8
作者
Hyslop, Terry [1 ]
Weinberg, David S. [2 ]
Schulz, Stephanie [1 ]
Barkun, Alan [3 ]
Waldman, Scott A. [1 ]
机构
[1] Thomas Jefferson Univ, Dept Pharmacol & Expt Therapeut, Philadelphia, PA 19107 USA
[2] Fox Chase Canc Ctr, Dept Med, Philadelphia, PA 19111 USA
[3] McGill Univ, Div Gastroenterol, Dept Med AB, Montreal, PQ, Canada
关键词
lymph node collection; colorectal cancer; molecular staging; occult tumor burden; guanylyl cyclase C; GUANYLYL CYCLASE-C; COLON-CANCER; SURVIVAL; MICROMETASTASES; DISPARITIES; RECURRENCE; EXPRESSION; CARCINOMA; DISEASE; MARKER;
D O I
10.1002/jso.23051
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Objectives Recurrence in lymph node-negative (pN0) colorectal cancer suggests the presence of undetected occult metastases. Occult tumor burden in nodes estimated by GUCY2C RT-qPCR predicts risk of disease recurrence. This study explored the impact of the number of nodes analyzed by RT-qPCR (analytic) on the prognostic utility of occult tumor burden. Methods Lymph nodes (range: 2-159) from 282 prospectively enrolled pN0 colorectal cancer patients, followed for a median of 24 months (range: 263), were analyzed by GUCY2C RT-qPCR. Prognostic risk categorization defined using occult tumor burden was the primary outcome measure. Association of prognostic variables and risk category were defined by multivariable polytomous and semi-parametric polytomous logistic regression. Results Occult tumor burden stratified this pN0 cohort into categories of low (60%; recurrence rate (RR)?=?2.3% [95% CI 0.14.5%]), intermediate (31%; RR?=?33.3% [23.744.1%]), and high (9%; RR?=?68.0% [46.585.1%], P?<?0.001) risk of recurrence. Beyond race and T stage, the number of analytic nodes was an independent marker of risk category (P?<?0.001). When >12 nodes were analyzed, occult tumor burden almost completely resolved prognostic risk classification of pN0 patients. Conclusions The prognostic utility of occult tumor burden assessed by GUCY2C RT-qPCR is dependent on the number of analytic lymph nodes. J. Surg. Oncol. 2012; 106:2430. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:24 / 30
页数:7
相关论文
共 40 条
[11]  
Edge SB., 2009, AJCC cancer staging manual, V7th
[12]  
Fielding LP, 1999, DIS COLON RECTUM, V42, P154
[13]   Adjuvant chemotherapy versus observation in patients with colorectal cancer: a randomised study [J].
Gray, Richard ;
Barnwell, Jennifer ;
McConkey, Christopher ;
Hills, Robert K. ;
Williams, Norman S. ;
Kerr, David J. .
LANCET, 2007, 370 (9604) :2020-2029
[14]   Does Stage II Colorectal Cancer Need to Be Redefined? [J].
Grothey, Axel .
CLINICAL CANCER RESEARCH, 2011, 17 (10) :3053-3055
[15]   Comparison of histopathology and RT-qPCR amplification of guanylyl cyclase C for detection of colon cancer metastases in lymph nodes [J].
Haince, Jean-Francois ;
Houde, Michel ;
Beaudry, Guillaume ;
L'Esperance, Sylvain ;
Garon, Genevieve ;
Desaulniers, Marie ;
Hafer, Laurie J. ;
Heald, James I. ;
Lyle, Stephen ;
Grossman, Steven R. ;
Tetu, Bernard ;
Sargent, Daniel J. ;
Fradet, Yves .
JOURNAL OF CLINICAL PATHOLOGY, 2010, 63 (06) :530-537
[16]   Limitations with light microscopy in the detection of colorectal cancer cells [J].
Hitchcock, CL ;
Sampsel, J ;
Young, DC ;
Martin, EW ;
Arnold, MW .
DISEASES OF THE COLON & RECTUM, 1999, 42 (08) :1046-1052
[17]  
Hyslop T, 2011, CANCER
[18]   Occult Tumor Burden Predicts Disease Recurrence in Lymph Node-Negative Colorectal Cancer [J].
Hyslop, Terry ;
Weinberg, David S. ;
Schulz, Stephanie ;
Barkun, Alan ;
Waldman, Scott A. .
CLINICAL CANCER RESEARCH, 2011, 17 (10) :3293-3303
[19]   The prognostic effect of micrometastases in previously staged lymph node negative (N0) colorectal carcinoma: A meta-analysis [J].
Iddings, Douglas ;
Ahmad, Aziz ;
Elashoff, David ;
Bilchik, Anton .
ANNALS OF SURGICAL ONCOLOGY, 2006, 13 (11) :1386-1392
[20]   Effects of socioeconomic status and treatment disparities in colorectal cancer survival [J].
Le, Hoa ;
Ziogas, Argyrios ;
Lipkin, Steven M. ;
Zell, Jason A. .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2008, 17 (08) :1950-1962