Advances in Clinical and Experimental Medicine

Title abbreviation: Adv Clin Exp Med
JCR Impact Factor (IF) – 1.736
5-Year Impact Factor – 2.135
Index Copernicus  – 168.52
MEiN – 70 pts

ISSN 1899–5276 (print)
ISSN 2451-2680 (online)
Periodicity – monthly

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Advances in Clinical and Experimental Medicine

2015, vol. 24, nr 3, May-June, p. 497–504

doi: 10.17219/acem/43768

Publication type: original article

Language: English

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Evaluation of Renal Function in Pediatric Patients After Treatment for Wilms’ Tumor

Małgorzata Janeczko1,A,B,C,D, Ewa Niedzielska1,A,C,E, Wojciech Pietras1,E,F

1 Department and Clinic of Pediatric Hematology, Oncology and Bone Marrow Transplantation, Wroclaw Medical University, Poland

Abstract

Background. Wilms’ tumor is the most common kidney cancer in children. Treatment consists of preand post-operative chemotherapy, surgery and in some cases radiotherapy. The treatment of nephroblastomas is very effective. Hence, the population of adult patients cured of this cancer in their childhood is steadily growing, generating a need for longterm health assessment, including renal function, due to the specifications of the therapy and the location of the tumor.
Objectives. The aim of the study was to evaluate nephrological complications after treatment for nephroblastoma.
Material and Methods. The study group consisted of 50 children treated in the Department of Pediatric Hematology, Oncology and Bone Marrow Transplantation at Wroclaw Medical University (Poland) from 2002 to 2012. An analysis of the patients’ medical histories was carried out. The glomerular filtration rate estimated by the Schwartz formula (GFR by Schwartz), serum creatinine levels, urea and electrolyte concentrations; the results of urinalysis and blood pressure were assessed. Each of these analyses was performed at the time of diagnosis, at the end of therapy, as well as 6 months, one year and two years after its completion.
Results. The study showed that, in most cases, implemented therapy had no significant impact on the deterioration of renal parameters in the two-year period following treatment for Wilms’ tumor. However, the group of patients treated with cyclophosphamide and carboplatin required more careful monitoring, due to a higher risk of renal function deterioration.
Conclusion. The study shows that the problem of nephrotoxicity after treatment for Wilms’ tumor is more frequent than indicated in other studies; however, the deterioration of kidney function in most cases is not serious. Additional attention should be paid to patients treated with cyclophosphamide and carboplatin. Assessment of the early and late effects of the treatment is a key element in improving the quality of the patients’ life.

Key words

Wilms’ tumor, renal tubular dysfunction, renal glomerulus dysfunction, GFR by Schwartz.

References (16)

  1. Pietras W: Advances and changes in the treatment of children with nephroblastoma. Adv Clin Exp Med 2012, 21, 809–820.
  2. Amirian ES: The Role of Hispanic Ethnicity in Pediatric Wilms’ Tumor Survival. Pediatr Hematol Oncol 2013, 30, 317–327.
  3. Green DM: The evolution of treatment for Wilms tumor. J Pediatr Surg 2013, 48, 14–19.
  4. Ziółkowska H: Przewlekła choroba nerek u dzieci. Nowa Pediatr 2010, 2, 50–66.
  5. Kwiecień J, Gładysz P, Dudek S, Szczepańska M, Ziora K: Ocena czynności nerek u dzieci hospitalizowanych z powodu ostrego nieżytu żołądkowo-jelitowego. Pediatr Współcz Gastroenterol Hepatol Żyw Dziec 2011, 13, 213–217.
  6. Opracowanie norm ciśnienia tętniczego dzieci i młodzieży w Polsce. http://olaf.czd.pl OLAF (PL0080).
  7. Millar AJW, Davidson A, Rode H, Numanoglu H, Hartley PS, Farieda D: Nephron-sparing surgery for bilateral Wilms’ tumours: A single-centre experience with 23 cases. Afr J Paediatr Surg 2011, 8, 49–56.
  8. Romão RL, Pippi Salle JL, Shuman C, Weksberg R, Figueroa V, Weber B, Bägli DJ, Farhat WA, Grant R, Gerstle JT, Lorenzo AJ: Nephron sparing surgery for unilateral Wilms tumor in children with predisposing syndromes: single center experience over 10 years. J Urol 2012, 188, 1493–1498.
  9. Daw NC, Gregornik D, Rodman J, Marina N, Wu J, Kun LE, Jenkins JJ, McPherson V, Wilimas J, Jones DP: Renal Function After Ifosfamide, Carboplatin and Etoposide (ICE) Chemotherapy, Nephrectomy, and Radiotherapy in Children With Wilms Tumour. Eur J Cancer 2009, 45, 99–106.
  10. Bailey S, Roberts A, Brock C, Price L, Craft AW, Kilkarni R, Lee REJ, Skillen AW, Skinner R: Nephrotoxicity in survivors of Wilms’ tumours in the North of England. Br J Cancer 2002, 87, 1092–1098.
  11. De Graaf SSN, van Gent H, Reitsma-Bierens WCC, van Luyk WHJ, Dolsma WV, Potsma A: Renal Function after Unilateral Nephrectomy for Wilms’ Tumour: the Influence of Radiation Therapy. Eur J Cancer 1996, 32A, 465–469.
  12. Di Tullio MT, Casale F, Indolfi P, Polito C, Giuliano M, Martini A, Cimmaruta E, Morgera C, Cioce F, Greco N: Compensatory Hypertrophy and Progressive Renal Damage in Children Nephrectomized for Wilms’ Tumour. Med Paediatr Oncol 1996, 26, 325–328.
  13. Levitt GA, Yeomans E, Dicks Mireaux C, Breatnach F, Kingston J, Pritchard J: Renal size and function after cure of Wilms’ tumour. Br J Cancer 1992, 66, 877–882.
  14. Finkelstein JZ, Norkool P, Green DM, Breslow N, d’Angio GJ: Diastolic hypertension in Wilms tumour survivors: a late effect of treatment? A report from the National Wilms’ Tumor Study Group. Am J Clin Oncol 1993, 16, 201–205.
  15. Janda J, Lukes M, Lukesova M: Morphology and function of the single kidney (SK) after nephrectomy due to Wilms tumour. Paediatr Nephrol 1993, 5, 44.
  16. Wright KD, Green DM, Daw NC: Late Effects of Treatment for Wilms Tumor. Pediatr Hematol Oncol 2009, 26, 407–413.