Axial cortical involvement of metastatic lesions to identify impending femoral fractures; a clinical validation study.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
03 2020
Historique:
received: 24 05 2019
revised: 11 10 2019
accepted: 14 10 2019
pubmed: 17 11 2019
medline: 15 4 2021
entrez: 17 11 2019
Statut: ppublish

Résumé

Patients with advanced cancer may develop painful bone metastases, potentially resulting in pathological fractures. Adequate fracture risk assessment is of key importance to prevent fracturing and maintain mobility. This study aims to validate the clinical reliability of axial cortical involvement with a 30 mm threshold on conventional radiographs to assess fracture risk in femoral bone metastases. All patients with bone metastases who received radiotherapy for pain included in two multicentre prospective studies were selected. Conventional radiographs obtained at a maximum of two months prior to radiotherapy were collected. Three experts independently measured lesions and scored radiographic characteristics. Sensitivity, specificity, positive (PPV) and negative predictive value (NPV) were calculated. Hundred patients were included with a median follow-up of 23.0 months (95%CI: 10.6-35.5). Two fractures occurred in lesions with axial cortical involvement <30 mm, and 12 in lesions ≥30 mm. Sensitivity, specificity, PPV and NPV of axial cortical involvement for predicting femoral fractures were 86%, 50%, 20% and 96%, respectively. Patients with lesions ≥30 mm had a 5.3 times higher fracture risk than patients with smaller lesions. Our validation study confirmed the use of 30 mm axial cortical involvement to assess fracture risk in femoral bone metastases. Until a more accurate and practically feasible method has been developed, this clinical parameter remains an easy method to assess femoral fracture risk to aid patients and clinicians to choose the optimal individual treatment modality.

Sections du résumé

BACKGROUND AND PURPOSE
Patients with advanced cancer may develop painful bone metastases, potentially resulting in pathological fractures. Adequate fracture risk assessment is of key importance to prevent fracturing and maintain mobility. This study aims to validate the clinical reliability of axial cortical involvement with a 30 mm threshold on conventional radiographs to assess fracture risk in femoral bone metastases.
MATERIALS AND METHODS
All patients with bone metastases who received radiotherapy for pain included in two multicentre prospective studies were selected. Conventional radiographs obtained at a maximum of two months prior to radiotherapy were collected. Three experts independently measured lesions and scored radiographic characteristics. Sensitivity, specificity, positive (PPV) and negative predictive value (NPV) were calculated.
RESULTS
Hundred patients were included with a median follow-up of 23.0 months (95%CI: 10.6-35.5). Two fractures occurred in lesions with axial cortical involvement <30 mm, and 12 in lesions ≥30 mm. Sensitivity, specificity, PPV and NPV of axial cortical involvement for predicting femoral fractures were 86%, 50%, 20% and 96%, respectively. Patients with lesions ≥30 mm had a 5.3 times higher fracture risk than patients with smaller lesions.
CONCLUSION
Our validation study confirmed the use of 30 mm axial cortical involvement to assess fracture risk in femoral bone metastases. Until a more accurate and practically feasible method has been developed, this clinical parameter remains an easy method to assess femoral fracture risk to aid patients and clinicians to choose the optimal individual treatment modality.

Identifiants

pubmed: 31733489
pii: S0167-8140(19)33143-3
doi: 10.1016/j.radonc.2019.10.007
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

59-64

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

C W P G van der Wal (CWPG)

Department of Orthopaedic Surgery, Leiden University Medical Center, The Netherlands. Electronic address: c.w.p.g.van_der_wal@lumc.nl.

F Eggermont (F)

Orthopedic Research Laboratory, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.

M Fiocco (M)

Medical Statistics Department of Biomedical Data Sciences, Leiden University Medical Center, The Netherlands; Mathematical Institute, Leiden University, The Netherlands.

H M Kroon (HM)

Department of Radiology, Leiden University Medical Center, The Netherlands.

O Ayu (O)

Department of Orthopaedic Surgery, Leiden University Medical Center, The Netherlands.

A Slot (A)

Department of Radiotherapy, Radiotherapy Institute Friesland, Leeuwarden, The Netherlands.

A Snyers (A)

Department of Radiotherapy, Radboud University Medical Center, Nijmegen, The Netherlands.

T Rozema (T)

Department of Radiotherapy, Bernard Verbeeten Institute, Tilburg, The Netherlands.

N J J Verdonschot (NJJ)

Orthopedic Research Laboratory, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands; Laboratory of Biomechanical Engineering, University of Twente, Enschede, The Netherlands.

P D S Dijkstra (PDS)

Department of Orthopaedic Surgery, Leiden University Medical Center, The Netherlands.

E Tanck (E)

Orthopedic Research Laboratory, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.

Y M van der Linden (YM)

Department of Radiotherapy, Leiden University Medical Center, The Netherlands.

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