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
[1]   PREDICTION OF LONG-TERM GONADAL TOXICITY AFTER STANDARD TREATMENT FOR TESTICULAR CANCER [J].
AASS, N ;
FOSSA, SD ;
THEODORSEN, L ;
NORMAN, N .
EUROPEAN JOURNAL OF CANCER, 1991, 27 (09) :1087-1091
[2]  
Abrams P, 2007, Prog Urol, V17, P681, DOI 10.1016/S1166-7087(07)92383-0
[3]  
ABRATT RP, 1994, S AFR MED J, V84, P605
[4]   Guidelines on testicular cancer [J].
Albers, P ;
Albrecht, W ;
Algaba, F ;
Bokemeyer, C ;
Cohn-Cedermark, G ;
Horwich, A ;
Klepp, O ;
Laguna, MP ;
Pizzocaro, G .
EUROPEAN UROLOGY, 2005, 48 (06) :885-894
[5]   Risk factors for relapse in clinical stage I nonseminomatous testicular germ cell tumors: Results of the German Testicular Cancer Study Group Trial [J].
Albers, P ;
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 .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (08) :1505-1512
[6]   Randomized phase III trial comparing retroperitoneal lymph node dissection with one course of bleomycin and etoposide plus cisplatin chemotherapy in the adjuvant treatment of clinical stage I nonseminomatous testicular germ cell tumors: AUO trial AH 01/94 by the German testicular cancer study group [J].
Albers, Peter ;
Siener, Roswitha ;
Krege, Susanne ;
Schmelz, Hans-Uwe ;
Dieckmann, Klaus-Peter ;
Heidenreich, Axel ;
Kwasny, Peter ;
Pechoel, Maik ;
Lehmann, Jan ;
Kliesch, Sabine ;
Koehrmann, Kai-Uwe ;
Fimmers, Rolf ;
Weissbach, Lothar ;
Loy, Volker ;
Wittekind, Christian ;
Hartmann, Michael .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (18) :2966-2972
[7]   Stage I non-seminomatous germ-cell tumours of the testis:: identification of a subgroup of patients with a very low risk of relapse [J].
Alexandre, J ;
Fizazi, K ;
Mahé, C ;
Culine, S ;
Droz, JP ;
Théodore, C ;
Terrier-Lacombe, MJ .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (05) :576-582
[8]   Risk-adapted treatment for patients with clinical stage I nonseminomatous germ cell tumor of the testis [J].
Amato, RJ ;
Ro, JY ;
Ayala, AG ;
Swanson, DA .
UROLOGY, 2004, 63 (01) :144-148
[9]   Adjuvant bleomycin, etoposide and cisplatin in pathological stage II non-seminomatous testicular cancer: the Indiana University experience [J].
Behnia, M ;
Foster, R ;
Einhorn, LH ;
Donohue, J ;
Nichols, CR .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (04) :472-475
[10]   Laparoscopic retroperitoneal lymph node dissection for clinical stage I nonseminomatous germ cell testicular cancer: A long-term update [J].
Bhayani, SB ;
Ong, A ;
Oh, WK ;
Kantoff, PW ;
Kavoussi, LR .
UROLOGY, 2003, 62 (02) :324-327