Management of bilateral Wilms tumor over three decades: The perspective of a single center.

INTRODUCTION Outcomes of Wilms tumor improved in last 50 years and excellent survival rates can be achieved especially in case of non-metastatic disease and favorable histology. Nevertheless, bilateral cases still stand as a therapeutic challenge. Prognosis of bilateral Wilms tumor (BWT) is not as good as the unilateral tumors of similar stage and histology in terms of survival and renal function. OBJECTIVE Management of BWT is constantly evolving and still stands as a therapeutic challenge. This study is designed to review and share our experiences on this topic from a surgical standpoint. STUDY DESIGN The records of patients treated in our clinic between 1980 and 2013 according to Turkish Pediatric Group of Oncology protocol were analyzed retrospectively and clinical data, surgical details, pathology results, long term outcomes were analyzed. RESULTS Thirteen girls and 7 boys with a mean age of 2,5 years were treated. There were 2 patients with Wilms tumor-Aniridia-Growth Retardation complex and one with isolated hemihypertrophy. Metastasis were detected in lungs of 4 patients; liver of 2 and in the cranium of one. All patients except one with the presumptive diagnosis of unilateral Wilms tumor were given preoperative chemotherapy. To sum up; 19 nephroureterectomies, 8 partial nephrectomies and 13 enucleations were performed to 36 kidneys without any major early or late postoperative complications. Pathologic results revealed positive surgical margins in 2 lesions with enucleation and in 2 with partial nephrectomies and anaplasia in 4 patients. Two patients were not operated due to parental disapproval. Two patients had the need of dialysis; one was anephric and the others' renal functions recovered over a year. Seven patients received radiotherapy for pulmonary metastasis, positive surgical margins or local recurrences. Overall, 13 patients survived and 7 died due to metastasis, recurrences, and complication of dialysis and refusal of surgical treatment. Survival among all patients was 65% and 72.2% among operated ones. Of the 7 patients with the partial nephrectomy, 2 died and 5 survived. Among enucleation group, 8 out of 10 survived and 2 died. Survival was slightly higher among enucleation group (80% vs 71.4%). Median time of follow-up for survivors of disease is 5.8 years (min: 6 months and max: 14 years). DISCUSSION Outcomes of BWT management have changed dramatically during the last few decades from only survival, to a long life expectancy without the need of renal replacement therapy owing to improvements in treatment options. We argue that positive surgical margins do not necessarily lead to local recurrence. For this reason it may be wiser to favor on more nephron sparing surgery than to achieve negative surgical margins. Adjuvant chemotherapy and radiotherapy may be adequate to prevent local recurrence. Also, survival did not differ significantly between different ways of nephron sparing surgeries, so it may be wiser to choose enucleation over partial nephrectomy which preserves more nephrons. Nephron-sparing surgery should have utmost importance despite the risk of positive margins. On the other hand, there is not enough data to interpret if positive surgical margins have role on distant metastases or not. Presence of metastasis and recurrence seems to be an important determinant of prognosis given the fact that none of the survivors had any metastasis or recurrence. CONCLUSION Nephron preservation should be the aim while taking positive surgical margin risk on nephron sparing surgery side relying on postoperative chemotherapy and carefully planned radiotherapy to avoid recurrence. However, there is significant diversity on the management BWT in different centers and a certain validated guideline or protocol to provide the optimal treatment is still lacking.

[1]  P. Ehrlich Bilateral Wilms’ tumor: the need to improve outcomes , 2009, Expert review of anticancer therapy.

[2]  A. Davidoff,et al.  The feasibility and outcome of nephron‐sparing surgery for children with bilateral Wilms tumor , 2008, Cancer.

[3]  H. Brisse,et al.  Bilateral disease and new trends in Wilms tumour , 2007, Pediatric Radiology.

[4]  M. Ritchey,et al.  Current management of Wilms' tumor in children. , 2009, Journal of pediatric urology.

[5]  P. Argani,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. , 2008, Journal of pediatric surgery.

[6]  H. Rode,et al.  Bilateral Wilms' tumors: a single-center experience with 19 cases. , 2005, Journal of pediatric surgery.

[7]  R. Kubiak,et al.  Renal function and outcome following salvage surgery for bilateral Wilms' tumor. , 2004, Journal of pediatric surgery.

[8]  N. Olgun,et al.  TREATMENT OF WILMS TUMOR: A Report from the Turkish Pediatric Oncology Group (TPOG) , 2010, Pediatric hematology and oncology.

[9]  P. Ramdial,et al.  Bilateral Wilms’ tumour in a developing country: a descriptive study , 2013, Pediatric surgery international (Print).

[10]  T. Kolon,et al.  Nephron-sparing partial nephrectomy for bilateral Wilms' tumor. , 2012, Journal of pediatric surgery.

[11]  M. Ghoneim,et al.  Bilateral Wilms' tumors: single-center experience with 22 cases and literature review. , 2010, Urology.

[12]  P. Argani,et al.  Bilateral Wilms' tumors with progressive or nonresponsive disease. , 2006, Journal of pediatric surgery.

[13]  H. Heij,et al.  Long‐term outcome of bilateral Wilms tumors (BWT) , 2011, Pediatric blood & cancer.