Management of Low-stage Nonseminomatous Germ Cell Tumors of Testis: SIU/ICUD Consensus Meeting on Germ Cell Tumors (GCT), Shanghai 2009

被引:12
作者
Stephenson, Andrew J. [1 ]
Aprikian, Armen G.
Gilligan, Timothy D.
Oldenburg, Jan
Powles, Tom
Toner, Guy C.
Waters, W. Bedford
机构
[1] Cleveland Clin, Dept Urol Oncol, Glickman Urol & Kidney Inst, Cleveland, OH 44195 USA
关键词
LYMPH-NODE DISSECTION; RISK-ADAPTED TREATMENT; INDIANA-UNIVERSITY EXPERIENCE; CENTER 10-YEAR EXPERIENCE; I TESTICULAR TERATOMA; CANCER STUDY-GROUP; ADJUVANT CHEMOTHERAPY; RETROPERITONEAL LYMPHADENECTOMY; FOLLOW-UP; MULTICENTER TRIAL;
D O I
10.1016/j.urology.2011.02.030
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To advise urologists and other clinicians on the appropriate management of low-stage (clinical Stage [CS] I, IS, IIA, and IIB) nonseminomatous germ cell tumors of the testis. METHODS A panel was convened of experts from 5 countries. A literature search in MEDLINE was used to identify evidence from relevant studies on the outcome and toxicity of observational, surgical, and chemotherapeutic approaches for low-stage nonseminomatous germ cell tumors to form the basis of the panel's recommendations. RESULTS The panel has recommended the treatment of nonseminomatous germ cell tumors in centers with medical, surgical, and diagnostic expertise in testicular cancer. The cancer-specific survival rate for CS I and CS IIA-IIB should approach 100% and 95%-100%, respectively. Patients with CS I should be made aware of all treatments (ie, surveillance, primary chemotherapy, and retroperitoneal lymph node dissection) and the potential side effects. For patients with CS I at low risk of occult metastasis, surveillance is preferred. For patients at high risk of occult metastasis, all 3 options can be considered. For immediate treatment, the choice between primary chemotherapy and retroperitoneal lymph node dissection should be determined by patient preference and the specific expertise of the treating institution. Patients with increasing postorchiectomy serum alpha-fetoprotein or human choriogonadotropin levels (CS IS and CS IIA-IIB) should receive induction chemotherapy. Induction chemotherapy or retroperitoneal lymph node dissection can be considered for patients with CS IIA-IIB with normal postorchiectomy alpha-fetoprotein and human choriogonadotropin levels. Surveillance can be considered for patients with equivocal computed tomography retroperitoneal findings who are otherwise at low risk of metastatic disease. CONCLUSION These clinical practice guidelines are designed to improve clinical practice from the available evidence and the expert opinion of the panel. As such, deviation from these recommendations should be based on sound clinical judgment, considering the unique situation of the patient and the expertise of the treating physician and institution. UROLOGY 78: S444-S455, 2011. (C) 2011 Elsevier Inc.
引用
收藏
页码:S444 / S455
页数:12
相关论文
共 93 条
[61]   Prognostic factors in clinical stage I nonseminomatous germ cell testicular tumors:: Rationale for different risk-adapted treatment [J].
Ondrus, D ;
Matoska, J ;
Belan, V ;
Kausitz, J ;
Goncalves, F ;
Hornák, M .
EUROPEAN UROLOGY, 1998, 33 (06) :562-566
[62]   CLINICAL STAGE-II NONSEMINOTAMOUS GERM-CELL TESTICULAR-TUMORS - RESULTS OF MANAGEMENT BY PRIMARY CHEMOTHERAPY [J].
PECKHAM, MJ ;
HENDRY, WF .
BRITISH JOURNAL OF UROLOGY, 1985, 57 (06) :763-768
[63]   RETROPERITONEAL LYMPH-NODE DISSECTION IN CLINICAL STAGE-IIA AND STAGE-IIB NONSEMINOMATOUS GERM-CELL TUMORS OF THE TESTIS [J].
PIZZOCARO, G .
INTERNATIONAL JOURNAL OF ANDROLOGY, 1987, 10 (01) :269-275
[64]   Adjuvant chemotherapy for high-risk clinical stage I nonseminomatous testicular germ cell cancer: Long-term results of a prospective trial [J].
Pont, J ;
Albrecht, W ;
Postner, G ;
Sellner, F ;
Angel, K ;
Holtl, W .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (02) :441-448
[65]   Low-volume nodal metastases detected at retroperitoneal lymphadenectomy for testicular cancer: Pattern and prognostic factors for relapse [J].
Rabbani, F ;
Sheinfeld, J ;
Farivar-Mohseni, H ;
Leon, A ;
Rentzepis, MJ ;
Reuter, VE ;
Herr, HW ;
McCaffrey, JA ;
Motzer, RJ ;
Bajorin, DF ;
Bosl, GJ .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (07) :2020-2025
[66]   MEDICAL-RESEARCH-COUNCIL PROSPECTIVE-STUDY OF SURVEILLANCE FOR STAGE-I TESTICULAR TERATOMA [J].
READ, G ;
STENNING, SP ;
CULLEN, MH ;
PARKINSON, MC ;
HORWICH, A ;
KAYE, SB ;
COOK, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (11) :1762-1768
[67]   CLINICAL STAGE-1 TESTICULAR CANCER - THE ROLE OF MODIFIED RETROPERITONEAL LYMPHADENECTOMY [J].
RICHIE, JP .
JOURNAL OF UROLOGY, 1990, 144 (05) :1160-1163
[68]   IS ADJUVANT CHEMOTHERAPY NECESSARY FOR PATIENTS WITH STAGE B1 TESTICULAR CANCER [J].
RICHIE, JP ;
KANTOFF, PW .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (08) :1393-1396
[69]   Surveillance can be the standard of care for stage I nonseminomatous testicular tumors and even high risk patients [J].
Roeleveld, TA ;
Horenblas, S ;
Meinhardt, W ;
van de Vijver, M ;
Kooi, M ;
Huinink, WWTB .
JOURNAL OF UROLOGY, 2001, 166 (06) :2166-2170
[70]   Randomized trial of two or five computed tomography scans in the surveillance of patients with stage I nonseminomatous germ cell tumors of the testis: Medical Research Council Trial TE08, ISRCTN56475197 - The National Cancer Research Institute Testis Cancer Clinical Studies Group [J].
Rustin, Gordon J. ;
Mead, Graham M. ;
Stenning, Sally P. ;
Vasey, Paul A. ;
Aass, Nina ;
Huddart, Robert A. ;
Sokal, Michael P. ;
Joffe, Jonathan K. ;
Harland, Stephen J. ;
Kirk, Sarah J. .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (11) :1310-1315