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The ganglioside GD2 as a circulating tumor biomarker for neuroblastoma.
Balis, Frank Milton; Busch, Christine Maria; Desai, Ami Vijay; Hibbitts, Emily; Naranjo, Arlene; Bagatell, Rochelle; Irwin, Meredith; Fox, Elizabeth.
Afiliación
  • Balis FM; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Busch CM; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Desai AV; Comer Children's Hospital, Chicago, Illinois.
  • Hibbitts E; Children's Oncology Group Statistics and Data Center, University of Florida, Gainesville, Florida.
  • Naranjo A; Children's Oncology Group Statistics and Data Center, University of Florida, Gainesville, Florida.
  • Bagatell R; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Irwin M; Hospital for Sick Children, Toronto, Canada.
  • Fox E; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Pediatr Blood Cancer ; 67(1): e28031, 2020 01.
Article en En | MEDLINE | ID: mdl-31612589
ABSTRACT

BACKGROUND:

GD2 is a ganglioside that is ubiquitously expressed in the plasma membrane of neuroblastoma and is shed into the circulation. PROCEDURE GD2 was measured with a high-pressure liquid chromatography/tandem mass spectrometry assay in serum or plasma from 40 children without cancer (controls) and in biobanked samples from 128 (73 high-risk) children with neuroblastic tumors at diagnosis, 56 children with relapsed neuroblastoma, 14 children with high-risk neuroblastoma after treatment, and 8 to 12 children each with 10 other common childhood cancers at diagnosis.

RESULTS:

The C18 (18 carbon fatty acid) lipoform was the predominant circulating form of GD2 in controls and in patients with neuroblastoma. The median concentration of GD2 in children with high-risk neuroblastoma at diagnosis was 167 nM (range, 16.1-1060 nM), which was 30-fold higher than the median concentration (5.6 nM) in controls. GD2 was not elevated in serum from children with the differentiated neuroblastic tumors, ganglioneuroma (n = 10) and ganglioneuroblastoma-intermixed subtype (n = 12), and in children with 10 other childhood cancers. GD2 concentrations were significantly higher in serum from children with MYCN-amplified tumors (P = 0.0088), high-risk tumors (P < 0.00001), International Neuroblastoma Staging System (INSS) stage 4 tumors (P < 0.00001), and in children who died (P = 0.034).

CONCLUSIONS:

Circulating GD2 appears to be a specific and sensitive tumor biomarker for high-risk/high-stage neuroblastoma and may prove to be clinically useful as a diagnostic or prognostic circulating tumor biomarker. GD2 will be measured prospectively and longitudinally in children enrolled on a high-risk neuroblastoma treatment trial to assess its ability to measure response to treatment and predict survival.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biomarcadores de Tumor / Gangliósidos / Neuroblastoma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Humans Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Biomarcadores de Tumor / Gangliósidos / Neuroblastoma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Humans Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2020 Tipo del documento: Article