Evidence map›Paper›PMID 41732250›Full record

ArticleJournal of bone oncology2026

Post-operative survival and use of systemic therapy in metastatic long-bone disease: 12 years of institutional experience.

Tom M de Groot, Joris R H Hendriks, Michelle R Shimizu, Jens P Te Velde, Olivier Q Groot, Erik T Newman, Kevin Raskin, Job N Doornberg, Paul C Jutte, Santiago Lozano-Calderón and 1 more

Abstract read
In one paragraph

Article in Journal of bone oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Tom M de GrootDepartment of Orthopedic Surgery, Massachusetts General Hospital, Boston, MA, USA.
Joris R H HendriksDepartment of Orthopedic Surgery, Massachusetts General Hospital, Boston, MA, USA.
Michelle R ShimizuLoyola University School of Medicine, Chicago, IL, USA.
Jens P Te VeldeDepartment of Orthopedic Surgery, Massachusetts General Hospital, Boston, MA, USA.
Olivier Q GrootDepartment of Orthopedic Surgery, Massachusetts General Hospital, Boston, MA, USA.
Erik T NewmanDepartment of Orthopedic Surgery, Massachusetts General Hospital, Boston, MA, USA.
Kevin RaskinDepartment of Orthopedic Surgery, Massachusetts General Hospital, Boston, MA, USA.
Job N DoornbergDepartment of Orthopedic Surgery, University Medical Center Groningen, Groningen, the Netherlands.
Paul C JutteDepartment of Orthopedic Surgery, University Medical Center Groningen, Groningen, the Netherlands.
Santiago Lozano-CalderónDepartment of Orthopedic Surgery, Massachusetts General Hospital, Boston, MA, USA.
Joseph H SchwabDepartment of Orthopedic Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Survival prediction in metastatic long-bone disease is essential for surgical decision-making, yet the performance of legacy prognostic models has declined in the era of immunotherapy and molecularly targeted agents. As these systemic therapies become routine, treatment patterns themselves may influence survival in ways not captured by earlier models. We, therefore, quantified preoperative systemic therapy use over the last decade and evaluated its association with postoperative overall survival in patients undergoing surgery for long-bone metastases. Methods: We conducted a retrospective cohort study of 975 consecutive adults who underwent surgery for long-bone metastases at two affiliated tertiary centers between January 2010 and June 2022. Preoperative systemic therapy was categorized into four groups: chemotherapy only, targeted therapy only, combined chemotherapy and targeted therapy, or neither. Postoperative was defined as time from surgery to death from any cause. We described temporal uptake of therapies by calendar year and assessed associations with postoperative survival using multivariable Cox regression adjusting for demographics, ECOG performance status, Katagiri primary tumor grouping, visceral/brain metastases, and laboratory variables. Adjusted survival over calendar time was summarized via marginal standardization at fixed horizons (1, 3, 12, and 24 months). Results: Use of targeted agents including checkpoint inhibitors rose markedly, from 2% in 2015 to 43% in 2022. In multivariable Cox models, preoperative chemotherapy alone was associated with worse survival versus no preoperative systemic therapy (HR 1.41, 95% CI 1.21-1.65; p < 0.01), as was combined chemotherapy plus targeted therapy (HR 1.24, 95% CI 1.05-1.47; p = 0.01). In contrast, targeted therapy alone before surgery was associated with better survival (HR 0.76, 95% CI 0.58-0.99; p = 0.04). Adjusted survival appeared to increase modestly across calendar years, but the pre-specified joint Wald test for the calendar year spline terms was not significant (p = 0.17), indicating a non-significant trend over time. Conclusion: This study found that preoperative systemic therapy patterns are strongly associated with post-operative survival in metastatic long-bone disease: targeted therapy alone correlates with improved survival whereas preoperative use of chemotherapy-alone or combined with targeted agents-was associated with worse survival. These findings support incorporating contemporary treatment exposure into prognostic models and suggest that model recalibration to the immunotherapy era may be warranted.

Indexed as

ImmunotherapyMetastatic bone diseaseSurvival predictionTargeted treatment

Identifiers

PMID41732250
PMCPMC12925594

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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.