Subscribe to RSS
DOI: 10.1055/s-0034-1371840
Pretreatment for Bilateral Nephroblastomatosis is an Independent Risk Factor for Progressive Disease in Patients with Stage V Nephroblastoma
Vorbehandlung wegen einer Nephroblastomatose ist ein unabhängiger Risikofaktor für einen Erkrankungs Progress bei einer Stadium V NephroblastomatosePublication History
Publication Date:
12 May 2014 (online)
Abstract
Background: Treatment of stage V nephroblastoma is less established and more complex than in unilateral nephroblastoma.
Methods: Retrospective analysis of 121 consecutive patients with stage V nephroblastoma registered from January 1989 to May 2005. Registration, prospective data collection and treatment were carried out within the framework of 3 consecutive SIOP/GPOH-nephroblastoma-trials.
Results: 19 patients had metastasis and 29 syndromes at diagnosis. 13 patients had been pretreated for bilateral nephroblastomatosis. 1 patient was not treated and 17 patients had upfront surgery. Preoperative treatment duration ranged from 1–12 weeks (n=103). 1–3 preoperative treatment-cycles resulted in average tumor-volume-reduction of 45%. 1 patient underwent bilateral nephrectomy. 52% of the patients had 2 functioning kidneys after the end of treatment. 20 patients had died after mean follow-up of 8.6 years. 5y-Progression-Free (PFS) and Overall-Survival (OS) were excellent for patients having a localized disease without pretreatment for nephroblastomatosis (5yPFS/OS: 80±4%/93±3%). Metastasis at diagnosis (51±12%/56±12%; p=0.003) and pretreatment for nephroblastomatosis (37±14%/67±13%; p<0.001) were associated with significantly poorer outcome. Cox-regression analysis revealed an independent influence of pretreatment for nephroblastomatosis, metastasis and syndromes on PFS. The latter 2 as well as anaplasia and age (<2 years or >3 years) had an independent influence on OS.
Conclusions: Pretreatment for nephroblastomatosis, metastasis and syndromes are independent risk factors. 1–3 preoperative treatment-cycles are sufficient to achieve save nephron-sparing-surgery in most patients.
Zusammenfassung
Hintergrund: Die Behandlung von Patienten mit einem Stadium V Nephroblastom ist komplexer und variabler als bei Patienten mit unilateralem Nephroblastom.
Methoden: Retrospektive Analyse von 121 Patienten mit einem Stadium V Nephroblastom, die von Januar 1989 bis Mai 2005 im Rahmen dreier aufeinander folgenden SIOP/GPOH Studien registriert und behandelt wurden.
Resultate: 19 Patienten hatten Metastasen, 29 Patienten ein komplexes Syndrom bei Diagnose. 13 Patienten waren bereits wegen einer Nephroblastomatose behandelt worden. 17 Patienten wurden primär operiert. 1 Patient erhielt keine Behandlung. Die präoperative Behandlung von 103 Patienten dauerte 1–12 Wochen, entsprechend 1–3 präoperativen Zyklen. Es wurde eine Volumenreduktion von Ø 45% erzielt. 52% der Patienten hatte nach Operation 2 funktionierende Nieren, nur ein Patient erhielt eine bilaterale Nephrektomie. Nach einer Nachbeobachtungszeit von Ø 8,6 Jahren waren 20 Patienten verstorben. Patienten mit einer lokalisierten Erkrankung ohne Vorbehandlung haben ein 5y-PFS und OS von 80±4% respektive 93±3%. Metastasen bei Diagnose (51±12%/56±12%; p=0,003) und Vorbehandlung für eine Nephroblastomatose (37±14%/67±13%; p<0,001) gingen mit einem signifikant schlechterem Überleben einher. In der COX-Regressions-Analyse zeigten Vorbehandlung, Metastasen und Syndrome einen unabhängigen, signifikanten Einfluss auf das PFS. Die beiden Letzteren sowie Anaplasie und Alter (<2 Jahre oder >3 Jahre) hatten einen unabhängigen Einfluss auf das OS.
Schlussfolgerung: Vorbehandlung für Nephroblastomatose, Metastasen und Syndrome sind unabhängige Risikofaktoren. 1–3 präoperative Zyklen reichen in der Regel aus, um eine sichere, nierenerhaltende Operation zu ermöglichen.
-
References
- 1 Bergeron C, Iliescu C, Thiesse P et al. Does nephroblastomatosis influence the natural history and relapse rate in Wilms’ tumour? A single centre experience over 11 years. Eur J Cancer 2001; 37: 385-391
- 2 Blute ML, Kelalis PP, Offord KP et al. Bilateral Wilms tumor. J Urol 1987; 138(4 II): 968-973
- 3 Breslow NE, Collins AJ, Ritchey ML et al. End stage renal disease in patients with Wilms tumor: Results from the National Wilms Tumor Study Group and the United States Renal Data System. J Urol 2005; 174: 1972-1975
- 4 Coppes MJ, Arnold M, Beckwith JB et al. Factors affecting the risk of contralateral Wilms tumor development: A report from the national Wilms tumor study group. Cancer 1999; 85: 1616-1625
- 5 Coppes MJ, Kraker Jde, van Dijken PJ et al. Bilateral Wilms’ tumor: long-term survival and some epidemiological features. J Clin Oncol 1989; 7: 310-315
- 6 Hamilton TE, Green DM, Perlman EJ et al. Bilateral Wilms’ tumor with anaplasia: lessons from the National Wilms’. Tumor Study. J Pediatr Surg 2006; 41: 1641-1644
- 7 Hamilton TE, Ritchey ML, Argani P et al. Synchronous bilateral Wilm’s tumor with complete radiographic response managed without surgical resection: a report from the National Wilm’s Tumor Study 4. J Pediatr Surg 2008; 43: 1982-1984
- 8 Horwitz JR, Ritchey ML, Moksness J et al. Renal salvage procedures in patients with synchronous bilateral Wilms’ tumors: A report from the national Wilms’ tumor study group. J Pediatr Surg 1996; 31: 1020-1025
- 9 Indolfi P, Jenkner A, Terenziani M et al. Synchronous bilateral Wilms tumor: A report from the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP). Cancer. 2013
- 10 Kraker Jde, Graf N, van Tinteren H et al. Reduction of postoperative chemotherapy in children with stage I intermediate-risk and anaplastic Wilms’ tumour (SIOP 93-01 trial): A randomised controlled trial. Lancet 2004; 364: 1229-1235
- 11 Kumar R, Fitzgerald R, Breatnach F. Conservative surgical management of bilateral Wilms tumor: Results of the United Kingdom Children’s Cancer Study Group. J Urol 1998; 160: 1450-1453
- 12 Mitus A, Tefft M, Fellers FX. Long-term follow-up of renal functions of 108 children who underwent nephrectomy for malignant disease. Pediatrics 1969; 44: 912-921
- 13 Montgomery BT, Kelalis PP, Blute ML et al. Extended follow-up of bilateral Wilms tumor: results of the National Wilms Tumor Study. J Urol. 1991 146
- 14 Perlman EJ, Faria P, Soares A et al. Hyperplastic perilobar nephroblastomatosis: Long-term survival of 52 patients. Pediatric Blood and Cancer 2006; 46: 203-221
- 15 Reinhard H, Semler O, Bürger D et al. Results of the SIOP 93-01/GPOH trial and study for the treatment of patients with unilateral nonmetastatic wilms tumor. Klin Padiatr 2004; 216: 132-140
- 16 Royer-Pokora B. Genetics of pediatric renal tumors. Pediatric Nephrology 2013; 28: 13-23
- 17 Shamberger RC, Haase GM, Argani P et al. Bilateral Wilms’ tumors with progressive or nonresponsive disease. J Pediatr Surg 2006; 41: 652-657
- 18 Sudour H, Audry G, Schleimacher G et al. Bilateral wilms tumors (WT) treated with the SIOP 93 protocol in France: Epidemiological survey and patient outcome. Pediatr Blood Cancer. 2012
- 19 Tournade MF, Com-Nougué C, Kraker Jde et al. Optimal duration of preoperative therapy in unilateral and nonmetastatic Wilms’ tumor in children older than 6 months: Results of the Ninth International Society of Pediatric Oncology Wilms’ Tumor Trial and Study. Journal of Clinical Oncology 2001; 19: 488-500
- 20 Verschuur AC, Vujanic GM, van Tinteren H et al. Stromal and epithelial predominant Wilms tumours have an excellent outcome: the SIOP 93 01 experience. Pediatr Blood Cancer 2010; 55: 233-238
- 21 Vujanić GM, Sandstedt B, Harms D et al. Revised International Society of Paediatric Oncology (SIOP) working classification of renal tumors of childhood. Med Pediatr.Oncol 2002; 38: 79-82
- 22 Weirich A, Ludwig R, Graf N et al. Survival in nephroblastoma treated according to the trial and study SIOP-9/GPOH with respect to relapse and morbidity. Ann Oncol 2004; 15: 808-820
- 23 Zils K, Furtwängler R, Reinhard H et al. Consultation within the nephroblastoma trial SIOP 2001/GPOH as part of the workload in the trial office. Klin Padiatr. 2008 220. 183-188