Evidence map›Paper›PMID 38342826›Full record

SynthesisJournal of neuro-oncology2024

Diffuse Midline H3K27-Altered Gliomas in the Spinal Cord: A Systematic Review.

Gina Watanabe, Jennifer Manyu Wong, Bradley Estes, Mohammad Faizan Khan, Christian Ogasawara, Giuseppe E Umana, Allan R Martin, Orin Bloch, Paolo Palmisciano

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Journal of neuro-oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.6field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Adult spinal cord diffuse midline gliomas with piloid features have a better prognosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  4. Article
  5. H3Journal of clinical medicine · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 7 institutions in 2 countries.

Gina WatanabeJohn A. Burns School of Medicine, University of Hawai'i, Honolulu, HI, USA.
Jennifer Manyu WongJohn A. Burns School of Medicine, University of Hawai'i, Honolulu, HI, USA.
Bradley EstesUniversity of Kansas School of Medicine, Kansas City, KS, USA.
Mohammad Faizan KhanIndiana University School of Medicine, Indianapolis, IN, USA.
Christian OgasawaraDepartment of Neurosurgery, University of Texas Medical Branch, Galveston, TX, USA.
Giuseppe E UmanaDepartment of Neurosurgery, Trauma Center, Gamma Knife Center, Cannizzaro Hospital, Catania, Italy.
Allan R MartinDepartment of Neurological Surgery, University of California, Davis, Sacramento, CA, USA.
Orin BlochDepartment of Neurological Surgery, University of California, Davis, Sacramento, CA, USA.
Paolo PalmiscianoDepartment of Neurological Surgery, University of California, Davis, Sacramento, CA, USA. paolo.palmisciano94@gmail.com.
Neurological Surgery · USUniversity of Hawaiʻi at Mānoa · USIndiana University School of MedicineOspedale Cannizzaro · ITThe University of Texas Medical Branch at Galveston · USUniversity of California, Davis · USUniversity of Kansas · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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

methodsPubMed, 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.

resultsA 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).

conclusionsOutcomes 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.

Indexed as

GliomaSpinal Cord NeoplasmsHistonesHumansPrognosisHistonesDiffuse midline gliomaIntramedullarySpinal cordSystematic reviewTumor

Identifiers

PMID38342826
OpenAlexW4391750876

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.