Evidence map›Paper›PMID 40064706›Full record

ArticleJournal of cancer research and clinical oncology2025

Bone mineral density as potential individual prognostic biomarker in patients with neurosurgically treated spinal metastasis.

H Asoglu, T Lampmann, M Jaber, L Khalafov, J Dittmer, I Ilic, G H Gielen, M Toma, H Vatter, Z Bendella and 4 more

Abstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

H AsogluDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany. harun.asoglu@ukbonn.de.
T LampmannDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany.
M JaberDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany.
L KhalafovDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany.
J DittmerDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany.
I IlicDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany.
G H GielenDepartment of Neuropathology, University Hospital Bonn, Bonn, Germany.
M TomaDepartment of Pathology, University Hospital Bonn, Bonn, Germany.
H VatterDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany.
Z BendellaDepartment of Neuroradiology, University Hospital Bonn, Bonn, Germany.
M SchneiderDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany.
C SchmeelDepartment of Neuroradiology, University Hospital Bonn, Bonn, Germany.
M HamedDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany.
M BanatDepartment of Neurosurgery, University Hospital Bonn, Bonn / Venusberg-Campus 1, 53127, Bonn, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBone mineral density (BMD) plays a crucial role in diagnosing and treating various systemic chronic diseases. Patients with multiple or singular spinal metastasis (SM) are typically in advanced stages of systemic cancer, often leading to significant alterations in BMD. The present study investigated the prognostic value of perioperative Hounsfield units (HU) as a surrogate independent marker for estimated BMD in patients with SM after surgical treatment (ST).

methodsHU values, serving as a surrogate for estimated BMD, were measured from circular regions of interest (ROIs) in the spine -first lumbar vertebra (L1)- from routine preoperative staging computed tomography (CT) scans in 187 patients after ST. The estimated BMD was stratified into pathologic and physiologic values and correlated with survival parameters in our cohorts.

resultsMedian L1 BMD of 92 patients (49%) with pathologic BMD was 79.5 HU (IQR 67.25-93.5) compared to 145 HU (IQR 123-166) for 95 patients (51%) with physiologic BMD (p ≤ 0.001). Patients with pathological BMD exhibited a median overall survival of 8 months compared to 12.2 months in patients with physiologic BMD (p = 0.006). Multivariable analysis revealed pathologic BMD as an independent negative prognostic predictor for increased 1 year mortality (AUC: 0.637, 95% CI: 0.556-0.718; p = 0.001).

conclusionsThe present study demonstrates that decreased perioperative BMD values, as derived from HU measurements, may represent a previously unrecognized negative prognostic factor in patients of SM after ST. The estimated perioperative BMD could emerge as an individualized, readily available potential biomarker for prognostic, treatment, and discussion of affected patients with SM.

Indexed as

Bone DensitySpinal NeoplasmsAdultAgedAged, 80 and overBiomarkers, TumorFemaleHumansLumbar VertebraeMaleMiddle AgedNeurosurgical ProceduresPrognosisRetrospective StudiesTomography, X-Ray ComputedBiomarkers, TumorBone mineral densityOverall survivalSpinal metastasis

Identifiers

PMID40064706
PMCPMC11893684

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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.