Abstract
The outlook for children with newly diagnosed Wilms tumors (WT) has improved dramatically with the advent of multimodal therapy, which includes surgery, chemotherapy, and for some, radiation therapy, with survival rates currently approaching 90 % (Lemerle et al. 1983; D’Angio et al. 1981, 1976). Although the overall relapse rate for children with WT has decreased to less than 15 %, the overall long-term survival for patients with recurrent disease remains at approximately 50 % (Grundy et al. 1989; Pinkerton et al. 1991; Pein et al. 1998; Kremens et al. 2002; Tannous et al. 2000). Due to the small numbers of relapsed patients, advancements in the treatment of these patients have remained a challenge. Investigators from different cooperative groups have evaluated the role of different therapeutic strategies in an attempt to improve the outcomes of patients with recurrent WT. Therapy for these patients depends on characteristics of their primary disease, extent of previous therapy, and time from initial diagnosis to relapse.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Abu-Ghosh AM, Krailo MD, Goldman SC et al (2002) Ifosfamide, carboplatin and etoposide in children with poor-risk relapsed Wilms’ tumor: a Children’s Cancer Group report. Ann Oncol 13:460–469
Adamson PC, Matthay KK, O’Brien M, Reaman GH, Sato JK, Balis FM (2007) A phase 2 trial of all-trans-retinoic acid in combination with interferon-alpha2a in children with recurrent neuroblastoma or Wilms tumor: a Pediatric Oncology Branch, NCI and Children’s Oncology Group Study. Pediatr Blood Cancer 49:661–665
Bardeesy N, Beckwith JB, Pelletier J (1995) Clonal expansion and attenuated apoptosis in Wilms’ tumors are associated with p53 gene mutations. Cancer Res 55:215–219
Benesch M, Windelberg M, Sauseng W et al (2008) Compassionate use of bevacizumab (Avastin) in children and young adults with refractory or recurrent solid tumors. Ann Oncol 19:807–813
Bomgaars LR, Bernstein M, Krailo M et al (2007) Phase II trial of irinotecan in children with refractory solid tumors: a Children’s Oncology Group Study. J Clin Oncol 25:4622–4627
Campbell AD, Cohn SL, Reynolds M et al (2004) Treatment of relapsed Wilms’ tumor with high-dose therapy and autologous hematopoietic stem-cell rescue: the experience at Children’s Memorial Hospital. J Clin Oncol 22:2885–2890
Casey DA, Wexler LH, Merchant MS et al (2009) Irinotecan and temozolomide for Ewing sarcoma: the Memorial Sloan-Kettering experience. Pediatr Blood Cancer 53:1029–1034
D’Angio GJ, Evans AE, Breslow N et al (1976) The treatment of Wilms’ tumor: results of the national Wilms’ tumor study. Cancer 38:633–646
D’Angio GJ, Evans A, Breslow N et al (1981) The treatment of Wilms’ tumor: results of the Second National Wilms’ Tumor Study. Cancer 47:2302–2311
Dallorso S, Dini G, Faraci M, Spreafico F (2008) SCT for Wilms’ tumour. Bone Marrow Transplant 41(Suppl 2):S128–S130
Daw NC, Anderson JR, Hoffer FA et al (2014) A phase 2 study of vincristine and irinotecan in mestastatic diffuse anaplastic Wilms tumor: results from Children’s Oncology Group Study AREN0321. J Clin Oncol 32 (5s) suppl abstr 10032.
De Camargo B, Melarango R, Saba e Silva N et al (1994) Phase II study of carboplatin as a single drug for relapsed Wilms’ tumor: experience of the Brazilian Wilms’ Tumor Study Group. Med Pediatr Oncol 22:258–260
Dome JS, Liu T, Krasin M et al (2002) Improved survival for patients with recurrent Wilms tumor: the experience at St. Jude Children’s Research Hospital. J Pediatr Hematol Oncol 24:192–198
Dome JS, Neale G, Hill DA et al (2005) Anti-tumor activity of topotecan against Wilms’ tumor: translation of a xenograft model to phase II study. Pediatr Blood Cancer 45:432–433
Dome JS, Cotton CA, Perlman EJ et al (2006) Treatment of anaplastic histology Wilms’ tumor: results from the fifth National Wilms’ Tumor Study. J Clin Oncol 24:2352–2358
Fuchs J, Szavay P, Luithle T, Furtwangler R, Graf N (2008) Surgical implications for liver metastases in nephroblastoma–data from the SIOP/GPOH study. Surg Oncol 17:33–40
Garaventa A, Hartmann O, Bernard JL et al (1994) Autologous bone marrow transplantation for pediatric Wilms’ tumor: the experience of the European Bone Marrow Transplantation Solid Tumor Registry. Med Pediatr Oncol 22:11–14
Ghanem MA, van Steenbrugge GJ, Sudaryo MK, Mathoera RB, Nijman JM, van der Kwast TH (2003) Expression and prognostic relevance of vascular endothelial growth factor (VEGF) and its receptor (FLT-1) in nephroblastoma. J Clin Pathol 56:107–113
Green DM, Breslow NE, Ii Y et al (1991) The role of surgical excision in the management of relapsed Wilms’ tumor patients with pulmonary metastases: a report from the National Wilms’ Tumor Study. J Pediatr Surg 26:728–733
Green DM, Beckwith JB, Breslow NE et al (1994) Treatment of children with stages II to IV anaplastic Wilms’ tumor: a report from the National Wilms’ Tumor Study Group. J Clin Oncol 12:2126–2131
Green DM, Cotton CA, Malogolowkin M et al (2007) Treatment of Wilms tumor relapsing after initial treatment with vincristine and actinomycin D: a report from the National Wilms Tumor Study Group. Pediatr Blood Cancer 48:493–499
Gross RE, Neuhauser EB (1950) Treatment of mixed tumors of the kidney in childhood. Pediatrics 6:843–852
Grundy P, Breslow N, Green DM, Sharples K, Evans A, D’Angio GJ (1989) Prognostic factors for children with recurrent Wilms’ tumor: results from the Second and Third National Wilms’ Tumor Study. J Clin Oncol 7:638–647
Ha TC, Spreafico F, Graf N, Dallorso S, Dome JS, Malogolowkin M, Furtwängler R, Hale JP, Moroz V, Machin D, Pritchard-Jones K (2013) An international strategy to determine the role of high dose therapy in recurrent Wilms’ tumour. Eur J Cancer 49(1):194–210. doi:10.1016/j.ejca.2012.07.010
Hale J, Hobson R, Moroz V, Satori P (2008) Results of UK Children’s Cancer and Leukemia Group (CCLG) protocol for relapsed Wilms tumor (UKWR): unified relapse strategy improves outcome. In: 40th meeting of International Society of Paediatric Oncology, p 62
Italiano A, Sirvent N, Michiels JF, Peyrade F, Otto J, Thyss A (2005) Tumour response to paclitaxel in an adult with relapsed nephroblastoma. Lancet Oncol 6:252–253
Kremens B, Gruhn B, Klingebiel T et al (2002) High-dose chemotherapy with autologous stem cell rescue in children with nephroblastoma. Bone Marrow Transplant 30:893–898
Kung FH, Desai SJ, Dickerman JD et al (1995) Ifosfamide/carboplatin/etoposide (ICE) for recurrent malignant solid tumors of childhood: a Pediatric Oncology Group Phase I/II study. J Pediatr Hematol Oncol 17:265–269
Kushner BH, Kramer K, Modak S et al (2006) Irinotecan plus temozolomide for relapsed or refractory neuroblastoma. J Clin Oncol 24:5271–5276
Lemerle J, Voute PA, Tournade MF et al (1983) Effectiveness of preoperative chemotherapy in Wilms’ tumor: results of an International Society of Paediatric Oncology (SIOP) clinical trial. J Clin Oncol 1:604–609
Malogolowkin MH, Casak SJ, Feusner J et al (1994) Carboplatin and etoposide alternating with ifosfamide and doxorubicin for the treatment of children with recurrent Wilms’ tumors. Proc Am Soc Clin Oncol 13:424, (abstract no. 1453)
Malogolowkin M, Cotton CA, Green DM et al (2008) Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin. A report from the National Wilms Tumor Study Group. Pediatr Blood Cancer 50:236–241
Mascarenhas L, Lyden ER, Breitfel PP et al (2010) Randomized phase II window trial of two schedules of irinotecan with vincristine in patients with first relapse or progression of rhabdomyosarcoma: a report from the Children’s Oncology Group. J Clin Oncol 28:4658
McGregor LM, Spunt SL, Santana VM et al (2009) Phase 1 study of an oxaliplatin and etoposide regimen in pediatric patients with recurrent solid tumors. Cancer 115:655–664
Metzger ML, Stewart CF, Freeman BB 3rd et al (2007) Topotecan is active against Wilms’ tumor: results of a multi-institutional phase II study. J Clin Oncol 25:3130–3136
Natrajan R, Little SE, Sodha N et al (2007) Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms’ tumour. J Pathol 211:52–59
Nitschke R, Parkhurst J, Sullivan J, Harris MB, Bernstein M, Pratt C (1998) Topotecan in pediatric patients with recurrent and progressive solid tumors: a Pediatric Oncology Group phase II study. J Pediatr Hematol Oncol 20:315–318
Pappo AS, Lyden E, Breitfeld P et al (2007) Two consecutive phase II window trials of irinotecan alone or in combination with vincristine for the treatment of metastatic rhabdomyosarcoma: the Children’s Oncology Group. J Clin Oncol 25:362–9
Pein F, Pinkerton R, Tournade MF et al (1993) Etoposide in relapsed or refractory Wilms’ tumor: a phase II study by the French Society of Pediatric Oncology and the United Kingdom Children’s Cancer Study Group. J Clin Oncol 11:1478–1481
Pein F, Tournade MF, Zucker JM et al (1994) Etoposide and carboplatin: a highly effective combination in relapsed or refractory Wilms’ tumor–a phase II study by the French Society of Pediatric Oncology. J Clin Oncol 12:931–936
Pein F, Michon J, Valteau-Couanet D et al (1998) High-dose melphalan, etoposide, and carboplatin followed by autologous stem-cell rescue in pediatric high-risk recurrent Wilms’ tumor: a French Society of Pediatric Oncology study. J Clin Oncol 16:3295–3301
Pein F, Rey A, de Kraker J et al (1999) Multivariate analysis of adverse prognostic factors (APF) in children with recurrent (Rec) Wilms’ tumor (WT) after initial treatment according to SIOP-6 or SIOP-9 strategies. Med Pediatr Oncol 33:170, (abstract no. 11)
Perlman EJ (2005) Pediatric renal tumors: practical updates for the pathologist. Pediatr Dev Pathol 8:320–338
Pinkerton CR, Groot-Loonen JJ, Morris-Jones PH, Pritchard J (1991) Response rates in relapsed Wilms’ tumor. A need for new effective agents. Cancer 67:567–571
Ramanathan RK, Rubin JT, Ohori NP, Belani CP (2000) Dramatic response of adult wilms tumor to paclitaxel and cisplatin. Med Pediatr Oncol 34:296–298
Reinhard H, Schmidt A, Furtwangler R et al (2008) Outcome of relapses of nephroblastoma in patients registered in the SIOP/GPOH trials and studies. Oncol Rep 20:463–467
Spreafico F, Bisogno G, Collini P et al (2008) Treatment of high-risk relapsed Wilms tumor with dose-intensive chemotherapy, marrow-ablative chemotherapy, and autologous hematopoietic stem cell support: experience by the Italian Association of Pediatric Hematology and Oncology. Pediatr Blood Cancer 51:23–28
Spunt SL, Freeman BB 3rd, Billups CA et al (2007) Phase I clinical trial of oxaliplatin in children and adolescents with refractory solid tumors. J Clin Oncol 25:2274–2280
Tannous R, Giller R, Holmes E et al (2000) Intensive therapy for high risk (HR) relapsed Wilms’ tumor (WT). A CCG-4921/POG-9445 study report. In: Proceeding of ASCO, p 588a, (abstract no. 2315)
Tournade MF, Lemerle J, Brunat-Mentigny M et al (1988) Ifosfamide is an active drug in Wilms’ tumor: a phase II study conducted by the French Society of Pediatric Oncology. J Clin Oncol 6:793–796
Tubergen DG, Stewart CF, Pratt CB et al (1996) Phase I trial and pharmacokinetic (PK) and pharmacodynamics (PD) study of topotecan using a five-day course in children with refractory solid tumors: a pediatric oncology group study. J Pediatr Hematol Oncol 18:352–361
Turner CD, Gururangan S, Eastwood J et al (2002) Phase II study of irinotecan (CPT-11) in children with high-risk malignant brain tumors: the Duke experience. Neuro Oncol 4:102–108
Vassal G, Giammarile F, Brooks M et al (2008) A phase II study of irinotecan in children with relapsed or refractory neuroblastoma: a European cooperation of the Société Française d’Oncologie Pédiatrique (SFOP) and the United Kingdom Children Cancer Study Group (UKCCSG). Eur J Cancer 44:2453–2460
Venkatramani R, Malogolowkin MH, Mascarenhas L (2014) Treatment of multiply relapsed wilms tumor with vincristine, irinotecan, temozolomide and bevacizumab. Pediatr Blood Cancer 61:756–9
Vujanic GM, Sandstedt B, Harms D, Kelsey A, Leuschner I, de Kraker J (2002) Revised International Society of Paediatric Oncology (SIOP) working classification of renal tumors of childhood. Med Pediatr Oncol 38:79–82
Wagner LM, McAllister N, Goldsby RE et al (2007) Temozolomide and intravenous irinotecan for treatment of advanced Ewing sarcoma. Pediatr Blood Cancer 48:132–139
Witt O, Hammerling S, Stockklausner C et al (2009) 13-cis retinoic acid treatment of a patient with chemotherapy refractory nephroblastomatosis. J Pediatr Hematol Oncol 31:296–299
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2014 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Spreafico, F., Malogolowkin, M.H. (2014). Treatment of Relapsed Wilms Tumor. In: Pritchard-Jones, K., Dome, J. (eds) Renal Tumors of Childhood. Pediatric Oncology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-44003-2_7
Download citation
DOI: https://doi.org/10.1007/978-3-662-44003-2_7
Published:
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-662-44002-5
Online ISBN: 978-3-662-44003-2
eBook Packages: MedicineMedicine (R0)