Craniocaudal retroperitoneal node length as a risk factor for relapse from clinical stage I testicular germ cell tumor.

2014 ◽  
Vol 32 (4_suppl) ◽  
pp. 363-363 ◽  
Author(s):  
Stephanie Anne Holler Howard ◽  
Kathryn P. Gray ◽  
Elizabeth O'Donnell ◽  
Fiona M. Fennessy ◽  
Clair Beard ◽  
...  

363 Background: To investigate if retroperitoneal craniocaudal nodal length (CCNL) or nodal volume (NV) predicts relapse risk in clinical stage I testicular cancer. Methods: This institutional review board-approved, Health Insurance Portability and Accountability Act (HIPAA)-compliant study retrospectively reviewed 826 patients with testicular cancer. One hundred eighteen out of 826 patients forming the analytic cohort had stage I disease and either more than or equal to 2 years surveillance or retroperitoneal lymph node dissection with no adjuvant chemotherapy. 3D NVs and CCNL were measured by two attending physicians in consensus. Association between relapse risk and CCNL/NV was evaluated using univariable/multivariable logistic regression analysis adjusted for known prognostic factors. Results: Sixty six out of 118 patients (56%) had nonseminomatous germ cell tumor (NSGCT) and 52 (44%) had seminomatous germ cell tumor (SGCT). Twenty one percent (25 out of 118) of patients relapsed: 24% (16 out of 66) for NSGCT and 17% (9 out of 52) for SGCT. Eighty percent of relapses were limited to the retroperitoneum; 90% of these were at the site of the largest lymph node. CCNL proved to be an independent risk factor in NSGCT using a multivariable logistic regression model adjusting for other potential known risk factors of embryonal predominance (EP) and lymphovascular invasion (LVI). For every 3 mm increase in CCNL, the risk of relapse increased by 52% (odds ratio [OR]=1.52; 95% CI=1.03- 2.25). For patients with SGCT, only the primary tumor size was an independent risk factor for relapse (OR=1.34; 95% CI=1.02-1.75). Conclusions: In NSGCT, CCNL was shown to be associated with increased risk of relapse independently of other known risk factors. If validated in a larger cohort, CCNL could provide important additional information used to inform management decisions in these patients.

2014 ◽  
Vol 203 (4) ◽  
pp. W415-W420 ◽  
Author(s):  
Stephanie A. Howard ◽  
Kathryn P. Gray ◽  
Elizabeth K. O'Donnell ◽  
Fiona M. Fennessy ◽  
Clair J. Beard ◽  
...  

1990 ◽  
Vol 13 (5) ◽  
pp. 379-381 ◽  
Author(s):  
Shreyaskumar R. Patel ◽  
Ronald L. Richardson ◽  
Larry Kvols ◽  
Horst Zincke

2020 ◽  
Vol 37 ◽  
Author(s):  
Carlos Eduardo Salazar-Mejía ◽  
Blanca Otilia Wimer-Castillo ◽  
Gisela Otilia García-Arellano ◽  
Raquel Garza-Guajardo ◽  
Oscar Vidal-Gutiérrez ◽  
...  

1984 ◽  
Vol 2 (4) ◽  
pp. 267-270 ◽  
Author(s):  
P C Sogani ◽  
W F Whitmore ◽  
H W Herr ◽  
G J Bosl ◽  
R B Golbey ◽  
...  

Forty-five patients with clinical stage I nonseminomatous germ cell tumor of the testis (NSGCTT) were entered in a prospective clinical trial to receive no treatment other than orchiectomy until clinical evidence of relapse. Of this group, 36 patients (80%) have been continuously free of disease for a median duration of 19.5 months after orchiectomy. Nine patients (20%) have relapsed, eight within seven months of orchiectomy. Seven of nine relapsing patients have been rendered free of disease with chemotherapy and/or surgery for a median duration of seven months (range, one to 33 months) after completion of treatment; the other two patients are presently under treatment although one has progressive disease. The relapse rate was higher in patients with embryonal carcinoma than in those with teratocarcinoma, 57% versus 17%. These preliminary results imply that the omission of routine lymphadenectomy or lymph-node irradiation in clinical stage I NSGCTT deserves further trial.


1998 ◽  
pp. 768-771 ◽  
Author(s):  
D. HAO ◽  
J. SEIDEL ◽  
R. BRANT ◽  
F. ALEXANDER ◽  
D. S. ERNST ◽  
...  

1995 ◽  
Vol 121 (S1) ◽  
pp. A38-A38
Author(s):  
C. W. Biermann ◽  
W. de Riese ◽  
T. M. Ulbright ◽  
R. Foster ◽  
L. Einhorn ◽  
...  

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