Abstract
Outcome for the vast majority of high-risk neuroblastoma patients with refractory or relapsed disease is dismal. We report two high-risk patients who remain progression-free for more than 113 and 18 months following the diagnosis of refractory/relapsed disease who were treated with surgery alone. Complete resolution of a refractory thoracic mass and relapsed liver nodules was observed in one patient. The refractory/relapsed disease in the second patient has remained stable. In both cases, the tumor showed histologic evidence of neuroblastoma maturation. These cases demonstrate that refractory/relapsed neuroblastoma is clinically heterogeneous and highlight the need for better biomarkers to optimize patient care.
Original language | English (US) |
---|---|
Pages (from-to) | 512-514 |
Number of pages | 3 |
Journal | Pediatric Blood and Cancer |
Volume | 60 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2013 |
Keywords
- Neuroblastoma
- Pathology
- Refractory neuroblastoma
- Relapsed neuroblastoma
ASJC Scopus subject areas
- Hematology
- Oncology
- Pediatrics, Perinatology, and Child Health