Comparing oncologic outcomes after minimally invasive and open surgery for pediatric neuroblastoma and Wilms tumor

Pediatr Blood Cancer. 2018 Jan;65(1). doi: 10.1002/pbc.26755. Epub 2017 Aug 9.

Abstract

Background: Minimally invasive surgery (MIS) has been widely adopted for common operations in pediatric surgery; however, its role in childhood tumors is limited by concerns about oncologic outcomes. We compared open and MIS approaches for pediatric neuroblastoma and Wilms tumor (WT) using a national database.

Methods: The National Cancer Data Base from 2010 to 2012 was queried for cases of neuroblastoma and WT in children ≤21 years old. Children were classified as receiving open or MIS surgery for definitive resection, with clinical outcomes compared using a propensity matching methodology (two open:one MIS).

Results: For children with neuroblastoma, 17% (98 of 579) underwent MIS, while only 5% of children with WT (35 of 695) had an MIS approach for tumor resection. After propensity matching, there was no difference between open and MIS surgery for either tumor for 30-day mortality, readmissions, surgical margin status, and 1- and 3-year survival. However, in both tumors, open surgery more often evaluated lymph nodes and had larger lymph node harvest.

Conclusion: Our retrospective review suggests that the use of MIS appears to be a safe method of oncologic resection for select children with neuroblastoma and WT. Further research should clarify which children are the optimal candidates for this approach.

Keywords: Wilms tumor; laparoscopy; minimally invasive surgery; neuroblastoma; outcomes.

Publication types

  • Comparative Study

MeSH terms

  • Child
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Kidney Neoplasms / mortality
  • Kidney Neoplasms / surgery*
  • Male
  • Minimally Invasive Surgical Procedures
  • Neuroblastoma / mortality
  • Neuroblastoma / surgery*
  • Registries
  • Retrospective Studies
  • Wilms Tumor / mortality
  • Wilms Tumor / surgery*