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Diffuse Midline H3K27-Altered Gliomas in the Spinal Cord: A Systematic Review.
Watanabe, Gina; Wong, Jennifer Manyu; Estes, Bradley; Khan, Mohammad Faizan; Ogasawara, Christian; Umana, Giuseppe E; Martin, Allan R; Bloch, Orin; Palmisciano, Paolo.
Afiliación
  • Watanabe G; John A. Burns School of Medicine, University of Hawai'i, Honolulu, HI, USA.
  • Wong JM; John A. Burns School of Medicine, University of Hawai'i, Honolulu, HI, USA.
  • Estes B; University of Kansas School of Medicine, Kansas City, KS, USA.
  • Khan MF; Indiana University School of Medicine, Indianapolis, IN, USA.
  • Ogasawara C; Department of Neurosurgery, University of Texas Medical Branch, Galveston, TX, USA.
  • Umana GE; Department of Neurosurgery, Trauma Center, Gamma Knife Center, Cannizzaro Hospital, Catania, Italy.
  • Martin AR; Department of Neurological Surgery, University of California, Davis, Sacramento, CA, USA.
  • Bloch O; Department of Neurological Surgery, University of California, Davis, Sacramento, CA, USA.
  • Palmisciano P; Department of Neurological Surgery, University of California, Davis, Sacramento, CA, USA. paolo.palmisciano94@gmail.com.
J Neurooncol ; 166(3): 379-394, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38342826
ABSTRACT

PURPOSE:

To systematically review the clinical features, management, and outcomes of diffuse midline H3K27-altered gliomas of the spinal cord (DMG-SCs).

METHODS:

PubMed, Ovid EMBASE, Scopus, and Web of Science were searched from database inception to 23 September 2023 for histologically confirmed cases of DMG-SC. Patient demographics, tumor characteristics, management information, and survival outcomes were extracted and analyzed.

RESULTS:

A total of 279 patients from 39 studies were collected. Patients were mostly male (61%), with an average age of 32 years. Patients were treated with surgery, radiotherapy, and chemotherapy combined (31%) or surgery only (24%), and extent of resection was most often subtotal (38%). Temozolomide was the most common chemotherapeutic agent (81%). Radiation therapy was delivered with mean dose of 47 Gy in 23 fractions. At mean follow-up time of 21 months, 13% of patients were alive. Average median overall survival was 24 months (range of 13 to 40 months) with a median progression-free survival of 14 months. Historical WHO grades of 2 or 3 appeared to exhibit a longer average median overall survival time than that of grade 4 DMG-SCs (32 vs. 23 months, p = 0.009).

CONCLUSIONS:

Outcomes for DMG-SCs are poor overall but appear to be favorable compared to intracranial DMGs. Despite the recent WHO 2021 grade 4 classification for all DMGs, given the differences in overall survival reported based on historical grading systems, future studies on DMG-SCs are needed to further define if DMG-SCs may represent a heterogeneous group of tumors with different prognoses.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Systematic_reviews Idioma: En Revista: J Neurooncol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Systematic_reviews Idioma: En Revista: J Neurooncol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos