Risk factors for relapse in clinical stage I nonseminomatous testicular germ cell tumors: Results of the German Testicular Cancer Study Group Trial

被引:217
作者
Albers, P [1 ]
Siener, R
Kliesch, S
Weissbach, L
Krege, S
Sparwasser, C
Schulze, H
Heidenreich, A
de Riese, W
Loy, V
Bierhoff, E
Wittekind, C
Fimmers, R
Hartmann, M
机构
[1] Univ Bonn, Dept Urol, D-53105 Bonn, Germany
[2] Univ Bonn, Dept Med Biometry, D-53105 Bonn, Germany
[3] Univ Munster, Dept Urol, Munster, Germany
[4] Krankenhaus Urban, Inst Pathol, Berlin, Germany
[5] Krankenhaus Urban, Dept Urol, Berlin, Germany
[6] Univ Essen Gesamthsch, Dept Urol, Essen, Germany
[7] Inst Pathol Essen Mitte, Essen, Germany
[8] German Mil Hosp Ulm, Dept Urol, Ulm, Germany
[9] Stadt Kliniken, Dept Urol, Dortmund, Germany
[10] Univ Marburg, Dept Urol, Marburg, Germany
[11] Univ Leipzig, Inst Pathol, Leipzig, Germany
[12] Mil Hosp, Dept Urol, Hamburg, Germany
[13] Texas Tech Univ, Div Urol, Lubbock, TX 79409 USA
关键词
D O I
10.1200/JCO.2003.07.169
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To prospectively assess potential risk factors for relapse in clinical stage I nonseminomatous germ cell tumors of the testis (CS I NSGCT). Patients and Methods: From September 1996 to May 2002, 200 patients with CS I NSGCT were prospectively assigned to retroperitoneal lymph node dissection (RPLND), and risk factor assessment was performed within a multicenter protocol. One hundred sixty-five patients had an adequate minimum follow-up of 12 months (mean, 34.5 months) or had pathologic stage II. Results: Pathologic stage II disease was found in 27.9% of patients. Only 0.6% of patients relapsed in the retroperitoneum after confirmation of pathologic stage I disease. With reference pathology, vascular invasion (VI) was most predictive of stage in multifactorial analysis (accuracy, 65.1%). However, the positive predictive value (PPV) of VI to predict patients who have metastatic disease or relapse during follow-up was only 52.7%. With absent VI, low-risk patients had a negative predictive value (NPV) of 76.9%. With a combination of several risk factors, the PPV increased to 63.6% and the negative predictive value increased to 86.5%. Conclusion: Even with an optimal combination of prognostic factors and reference pathology, more than one third of patients predicted to have pathologic stage II or relapse during follow-up will not harbor metastatic disease and, therefore, would be overtreated with adjuvant therapy. However, patients at low risk may be predicted at an 86.5% level, and thus, surveillance in highly compliant patients would be a valuable option. For high-risk patients, further reduction of adjuvant treatment is necessary. (C) 2003 by American Society of Clinical Oncology.
引用
收藏
页码:1505 / 1512
页数:8
相关论文
共 41 条
[1]  
ALBERS P, 1995, CANCER, V75, P844, DOI 10.1002/1097-0142(19950201)75:3<844::AID-CNCR2820750316>3.0.CO
[2]  
2-C
[3]  
Albers P, 1997, CANCER, V79, P1710
[4]   Tumor proliferative activity is predictive of pathological stage in clinical stage A nonseminomatous testicular germ cell tumors - Reply [J].
Albers, P ;
Ulbright, TM ;
Albers, J ;
Miller, GA ;
Orazi, A ;
Crabtree, WN ;
Baniel, J ;
Reister, T ;
Sidner, RA ;
Foster, RS ;
Donohue, JP .
JOURNAL OF UROLOGY, 1996, 155 (02) :586-586
[5]  
Albers P, 1999, INT J CANCER, V83, P828, DOI 10.1002/(SICI)1097-0215(19991210)83:6<828::AID-IJC23>3.0.CO
[6]  
2-N
[7]   Positron emission tomography in the clinical staging of patients with stage I and II testicular germ cell tumors [J].
Albers, P ;
Bender, H ;
Yilmaz, H ;
Schoeneich, G ;
Biersack, HJ ;
Mueller, SC .
UROLOGY, 1999, 53 (04) :808-811
[8]  
[Anonymous], TNM CLASSIFICATION M
[9]   Long-term results following adjuvant chemotherapy in patients with clinical stage I testicular nonseminomatous malignant germ cell tumors with high risk factors [J].
Böhlen, D ;
Borner, M ;
Sonntag, RW ;
Fey, MF ;
Studer, UE .
JOURNAL OF UROLOGY, 1999, 161 (04) :1148-1152
[10]   SECONDARY NEOPLASMS FOLLOWING TREATMENT OF MALIGNANT GERM-CELL TUMORS [J].
BOKEMEYER, C ;
SCHMOLL, HJ .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (09) :1703-1709