Evidence map›Paper›PMID 39659302›Full record

ArticleCureus2024

Risk Factors and Impact on Survival of Pathological Fractures in Patients With Humeral Metastasis.

Shiro Saito, Hiroaki Kimura, Hisaki Aiba, Yohei Kawaguchi, Hideki Murakami

Abstract read
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Shiro SaitoDepartment of Orthopaedic Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya, JPN.
Hiroaki KimuraDepartment of Orthopaedic Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya, JPN.
Hisaki AibaDepartment of Orthopaedic Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya, JPN.
Yohei KawaguchiDepartment of Orthopaedic Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya, JPN.
Hideki MurakamiDepartment of Orthopaedic Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Bone metastases often cause pathological fractures and impair patients' quality of life and survival. Although several studies have been conducted on pathological fractures in the femur and spine, limited research has been done on the upper limbs. This study aimed to reveal the risk factors and determine how pathological fractures impact survival in patients with humeral metastasis. Methods This retrospective study was based on patients with humerus metastasis treated in the Nagoya-City University Hospital from 2010 to 2020. Patient characteristics, including sex, age at diagnosis of humeral metastasis, primary cancer, prior treatment, anatomical location, and metastatic lesion size, were retrieved from medical records. The patients were divided into pathological fracture and non-fracture groups, and their backgrounds and survival rates were compared. Results Of the 31 patients with 32 metastatic lesions included in this study, 19 had pathological fractures (one patient had bilateral fractures) and 12 had no fractures. Our analysis revealed that the risk factors for pathological fracture were treatment without bone-modifying agents, treatment without radiotherapy, and larger circumferential cortical involvement. The median overall survival was 21 months; 1-year survival was 56% in the non-fracture group and 59% in the fracture group. There was no significant difference in survival rates between the two groups and only chemotherapy correlated with longer survival in multivariate analysis. Conclusions Bone-modifying agents have the benefit of preventing pathological fractures due to humeral metastases. The humeral pathological fracture did not affect the patient's survival, and chemotherapy was the only prognostic factor that prolonged survival.

Indexed as

bone modifying agentschemotherapyhumeral metastasisoverall survivalpathological fracture

Identifiers

PMID39659302
PMCPMC11630055

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