Evidence map›Paper›PMID 40479555›Full record

ArticleThe Journal of the American Academy of Orthopaedic Surgeons2025

Orthopaedic Implant-Associated Rhabdomyosarcoma.

Danielle E Brown, Carla Saoud, Cristina R Antonescu, Leonard H Wexler, Edmund K Bartlett, Carol D Morris

Abstract readCase Reports
In one paragraph

Article in The Journal of the American Academy of Orthopaedic Surgeons, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Danielle E BrownFrom the Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY (Brown, Bartlett, and Morris), the Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY (Saoud and Antonescu), and the Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY (Wexler).
Carla Saoud
Cristina R Antonescu
Leonard H Wexler
Edmund K Bartlett
Carol D Morris

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundMetallic implants are widely used in orthopaedic surgery. These implants may have carcinogenic properties, but the incidence of associated malignancies appears to be low, and to date, only case reports and small case series have been reported. We describe a series of patients with soft-tissue sarcoma adjacent to orthopaedic implant.

methodsCases of soft-tissue sarcomas treated at our institution were reviewed to identify tumors arising next to orthopaedic implant. We collected diagnostic, therapeutic, surgical, and outcome data and conducted genetic testing on the implant-associated tumors and control tumors.

resultsWe identified 4 cases, all of which were high-grade sclerosing rhabdomyosarcoma. Median age at diagnosis was 50 years (range: 35 to 58 years). Three tumors were in the lower extremity following internal fixation of the tibia and/or fibula, whereas the fourth was posterior to spinal implant. Mean time from implant placement to diagnosis was 19.0 years (range: 10.9 to 24.3 years). Three patients underwent wide surgical resection, whereas one had metastatic disease at diagnosis and declined surgery. All were treated with chemotherapy and radiation. Genetic testing revealed a MYOD1 mutation in all four tumors. The tumor mutational burden and fraction of genome altered were slightly higher in the control tumors than in the implant-adjacent tumors, although the differences were not statistically significant. Median follow-up was 1.7 years (range: 0.8 to 2.6 years). Of the three patients with localized disease, two had no evidence of disease at latest follow-up and one died of unknown cause at 2.6 years. The patient with metastatic disease died of disease at 0.8 years.

conclusionsWe found no genetic differences between implant-associated and non-implant-associated rhabdomyosarcomas. Further investigation is needed to understand the contribution of metallic implants to tumorigenesis. Physicians should be aware of this diagnosis when a new mass arises in a patient with long-standing orthopaedic implants.

Indexed as

Prostheses and ImplantsRhabdomyosarcomaSoft Tissue NeoplasmsAdultFemaleHumansMaleMiddle AgedMutationMyoD ProteinMyoD1 myogenic differentiation proteinMyoD Protein

Identifiers

PMID40479555
PMCPMC12259143

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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.