Craniocaudal Retroperitoneal Node Length as a Risk Factor for Relapse From Clinical Stage I Testicular Germ Cell Tumor

被引:14
作者
Howard, Stephanie A. [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Gray, Kathryn P. [7 ,8 ]
O'Donnell, Elizabeth K. [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Fennessy, Fiona M. [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Beard, Clair J. [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Sweeney, Christopher J. [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
机构
[1] Dana Farber Canc Inst, Dept Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Radiol, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Dept Radiat Oncol, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Oncol, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, Dept Radiat Oncol, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Boston, MA USA
[8] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
关键词
craniocaudal; craniocaudal lymph nodes; retroperitoneal; testicular cancer; testis cancer; ADJUVANT TREATMENT; CANCER; SEMINOMA; MANAGEMENT; DISSECTION;
D O I
10.2214/AJR.13.11615
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
OBJECTIVE. The purpose of this study was to investigate whether retroperitoneal craniocaudal nodal length or nodal volume predicts relapse risk in stage I testicular cancer. MATERIALS AND METHODS. We retrospectively reviewed 826 testicular cancer patients. Of these 826 patients, 118 had stage I disease and either less than 2 years of surveillance or retroperitoneal lymph node dissection with no adjuvant chemotherapy. These patients formed our analytic cohort, and 3D nodal volumes and craniocaudal nodal length were measured. Association between relapse risk and craniocaudal nodal length and nodal volume was evaluated using univariable or multivariable logistic regression models adjusted for known prognostic factors. RESULTS. Sixty-six (56%) of 118 patients had nonseminomatous germ cell tumor and 52 (44%) had seminomatous germ cell tumor. Craniocaudal nodal length proved to be an independent risk factor in nonseminomatous germ cell tumors using a multivariable logistic regression model adjusting for other potential known risk factors of embryonal predominance and lymphovascular invasion. For every 3-mm increase in craniocaudal nodal length, the risk of relapse increased by 52% (odds ratio [OR], 1.52; 95% CI, 1.03-2.25). For patients with seminomas, only primary tumor size was an independent risk factor for relapse (1.34, 1.02-1.75). CONCLUSION. In nonseminomatous germ cell tumors, craniocaudal nodal length was shown to be associated with increased risk of relapse independently of other known risk factors. If validated in an independent cohort, craniocaudal nodal length could provide important additional information to inform management decisions in these patients.
引用
收藏
页码:W415 / W420
页数:6
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