Evidence map›Paper›PMID 41338597›Full record

ArticleBMJ open respiratory research2025

Denosumab usage is associated with better overall survival of patients with lung cancer and bone metastases: a retrospective cohort study.

Chung Chi Yu, Ho-Shen Lee, Jiun-Ting Wu, Chia-Chen Huang, Jung Yueh Chen

Abstract read
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Article in BMJ open respiratory research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

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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.

Chung Chi YuChest Medicine, E-Da Hospital, Yanchao District, Taiwan.ORCID http://orcid.org/0009-0001-0458-4109
Ho-Shen LeeChest Medicine, E-Da Hospital, Yanchao District, Taiwan.
Jiun-Ting WuChest Medicine, E-Da Cancer Hospital, Kaohsiung, Taiwan.
Chia-Chen HuangPharmacology, E-Da Hospital, Yanchao District, Taiwan.
Jung Yueh ChenChest Medicine, E-Da Hospital, Yanchao District, Taiwan ethmoid0716@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer with progressive bone metastases usually leads to skeletal-related events (SREs) and a reduced quality of life. Denosumab delays the onset of SREs and is associated with improved overall survival. However, other factors associated with overall survival in patients with lung cancer and bone metastases remain unclear. This study aimed to evaluate the survival benefit of denosumab use in patients with lung cancer and bone metastases and how other factors affect overall survival in these patients.

methodsThis retrospective cohort study included 622 patients with lung cancer treated at a southern Taiwan Medical Center between 2018 and 2022. The overall survival of patients with lung cancer and bone metastases treated with denosumab (n=90) was compared with that of patients who did not receive denosumab (n=212). Kaplan-Meier survival analysis and Cox proportional hazards models were used to evaluate the factors associated with the overall survival of these patients.

resultsDenosumab use was associated with improved overall survival among patients with lung cancer and bone metastases compared with untreated patients (HR 0.61, 95% CI 0.47 to 0.80, p<0.001, overall survival 455 days vs 172 days), particularly in patients who had received more than five cycles of treatment (HR 0.31, 95% CI 0.19 to 0.50, p<0.001). Systemic cancer treatments, such as tyrosine kinase inhibitors, chemotherapy and immunotherapy, were also associated with improved overall survival in these patients.

conclusionsDenosumab usage, especially good compliance, for over five cycles in patients with lung cancer and bone metastases was associated with improved overall survival. Future studies should focus on strategies to improve adherence to denosumab treatment and maximise its clinical benefits.

Indexed as

Bone Density Conservation AgentsBone NeoplasmsDenosumabLung NeoplasmsAgedAged, 80 and overFemaleHumansKaplan-Meier EstimateMaleMiddle AgedRetrospective StudiesTaiwanBone Density Conservation AgentsDenosumabComplianceLung Cancer

Identifiers

PMID41338597
PMCPMC12673539

What Socratic holds

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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 Socratic graph.