Surgical Treatment Results in Unilateral Wilms Tumor: Experience from a High-Volume Pediatric Oncology Center in Turkey


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DOI:

https://doi.org/10.5152/EurJTher.2018.506

Keywords:

Child, preoperative chemotherapy, survival, Wilms tumor

Abstract

Objective: The aim of the present study was to evaluate the clinical characteristics, factors affecting treatment approach, and longterm outcome of patients with Wilms tumor.
Methods: We identified the demographic features, mode of presentation, applied treatments, and long-term outcomes of 88 patients treated between 1990 and 2011 at Hacettepe University İhsan Doğramacı Children’s Hospital according to the Turkish Pediatric Oncology Group protocol. Data were analyzed using SPSS program, and chi-square test was used for statistical analysis.
Results: The study included 88 patients (50 females and 38 males) with a mean age at presentation of 3±2.48 years. Patients were classified as stage 1 (n=35, 39.8%), stage 2 (n=16, 18.2%), stage 3 (n=17, 19.3%), and stage 4 (n=20, 22.7%). Pathological examination of tumors revealed favorable histology in 76 (86.4%) patients and unfavorable histology in 10 (11.4%) patients. Forty-nine (55.6%) patients received preoperative chemotherapy, and patient’s age at diagnosis and physical examination findings influenced the decision of the administration of preoperative chemotherapy (p<0.05). Of the 88 patients, 25% aged <1 year and 75% aged between 3 and 5 years received preoperative chemotherapy. The palpated mass was crossing the midline in 20.5% of patients who were subjected to primary surgery. Tumor ruptured in 5.6% of patients intraoperatively. Long-term prognosis of patients was as follows: 68 (83.9%) children were cured and 13 (16%) children died due to recurrences and metastases. Survival rates reached 100% in stage 1 and 2 patients but decreased to 75% and 50% in stage 3 and 4 patients, respectively.
Conclusion: Age at presentation and physical examination findings are significant in surgical planning. Stage is the most important prognostic factor. Patients with Wilms tumor are treated with low complication and high survival rates due to multidisciplinary treatment approach at our institution.

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References

Ehrlich PF. Wilms tumor: progress and considerations for the surgeon. Surg Oncol 2007; 16: 157-71.

Sarin YK, Bhatnagar SN. Wilms’ tumor- roadmaps of management. Indian J Pediatr 2012; 79: 776-86.

Hamilton TE, Shamberger RC. Wilms tumor: recent advances in clinical care and biology. Semin Pediatr Surg 2012; 21: 15-20.

Akyuz C, Yalcin B, Yildiz I, Hazar V, Yoruk A, Tokuc G, et al. Treatment of Wilms tumor: a report from the Turkish Pediatric Oncology Group (TPOG). Pediatr Hematol Oncol 2010; 27: 161-78.

Suita S, Kinoshita Y, Tajiri T, Hara T, Tsuneyoshi M, Mizote H, et al. Clinical characteristics and outcome of Wilms tumors with a favorable histology in Japan: a report from the Study Group for Pediatric Solid Malignant Tumors in the Kyushu area, Japan. J Pediatr Surg 2006; 41: 1501-5.

Pritchard-Jones K, Moroz V, Vujanic G, Powis M, Walker J, Messahel B, et al. Treatment and outcome of Wilms’ tumor patients: an analysis of all cases registered in the UKW3 trial. Ann Oncol 2012; 23: 2457-63.

Kalapurakal JA, Dome JS, Perlman EJ, Malogolowkin M, Haase GM, Grundy P, et al. Management of Wilms’ tumour: current practice and future goals. Lancet Oncol 2004; 5: 37-46.

Ng A, Griffiths A, Cole T, Davison V, Griffiths M, Larkin S, et al. Congenital abnormalities and clinical features associated with Wilms’ tumour: a comprehensive study from a centre serving a large population. Eur J Cancer 2007; 43: 1422-9.

Ahmed HU, Arya M, Tsiouris A, Sellaturay SV, Shergill IS, Duffy PG, et al. An update on the management of Wilms’ tumour. Eur J Surg Oncol 2007; 33: 824-31.

Lamb MG, Aldrink JH, O’Brien SH, Yin H, Arnold MA, Ranalli MA. Renal tumors in children younger than 12 months of age: a 65-year single institution review. J Pediatr Hematol Oncol 2017; 39: 103-7.

Green DM. Controversies in the management of Wilms tumour- immediate nephrectomy or delayed nephrectomy? Eur J Cancer 2007; 43: 2453-6.

Ehrlich PF, Ritchey ML, Hamilton TE, Haase GM, Ou S, Breslow N, et al. Quality assessment for Wilms’ tumor: a report from the National Wilms’ Tumor Study-5. J Pediatr Surg 2005; 40: 208-12.

Ko EY, Ritchey ML. Current management of Wilms’ tumor in children. J Pediatr Urol 2009; 5: 56-65.

Kieran K, Anderson JR, Dome JS, Ehrlich PF, Ritchey ML, Shamberger RC, et al. Lymph node involvement in Wilms tumor: results from National Wilms Tumor Studies 4 and 5. J Pediatr Surg 2012; 47: 700-6.

Hall G, Grant R, Weitzman S, Maze R, Greenberg M, Gerstle JT. Predictors of surgical outcome in Wilms’ tumor: a single-institution comparative experience. J Pediatr Surg 2006; 41: 966-71.

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Published

2019-03-11

How to Cite

User, İdil R., Ekinci, S., Karnak, İbrahim, Çiftçi, A. Özden, Büyükpamukçu, M., Tanyel, F. C., & Şenocak, M. E. (2019). Surgical Treatment Results in Unilateral Wilms Tumor: Experience from a High-Volume Pediatric Oncology Center in Turkey. European Journal of Therapeutics, 25(1), 19–22. https://doi.org/10.5152/EurJTher.2018.506

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Original Articles