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Repeat nephron-sparing surgery for children with bilateral Wilms tumor
Kathleen Kieran1, Mark A Williams2, Lisa M McGregor3
1Department of Urology, University of Iowa Hospitals and Clinics, Iowa City, IA.
Journal of Pediatric Surgery
|January 21, 2014
Summary
Repeat nephron-sparing surgery (NSS) for recurrent Wilms tumor is feasible. This approach offers good oncologic outcomes and preserves kidney function in most cases, but blastemal histology warrants caution.
Area of Science:
- Pediatric Oncology
- Surgical Oncology
- Nephrology
Background:
- Wilms tumor recurrence impacts renal function, especially in bilateral cases.
- Nephron-sparing surgery (NSS) is standard for initial treatment but its role in recurrence is unclear.
- Assessing repeat NSS for recurrent Wilms tumor is crucial for preserving renal function.
Purpose of the Study:
- To evaluate the feasibility of repeat NSS for recurrent Wilms tumor.
- To assess oncologic and renal function outcomes after repeat NSS.
- To determine survival rates and identify prognostic factors in recurrent Wilms tumor.
Main Methods:
- Retrospective review of children with bilateral, favorable histology Wilms tumor.
- Identification of patients undergoing repeat NSS for local recurrence.
- Evaluation of tumor recurrence, renal function, and patient survival.
Main Results:
- Eight of 36 patients (22%) with bilateral Wilms tumor underwent repeat NSS for recurrence.
- Six patients (75%) survived without disease after repeat NSS, with preserved renal function.
- Two deaths occurred in patients with blastemal-predominant histology at repeat NSS.
Conclusions:
- Repeat NSS is a feasible option for local recurrence of favorable histology bilateral Wilms tumor.
- This approach can achieve acceptable oncologic outcomes and preserve renal function.
- Aggressive therapy may be needed for recurrences with blastemal-predominant histology.
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