Evidence map›Paper›PMID 39675926›Full record

ArticleCancer reports (Hoboken, N.J.)2024

Demographic and Treatment Analysis of Periosteal Osteosarcoma.

Michael C Larkins

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
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

1 author.

Michael C LarkinsBrody School of Medicine (BSOM), East Carolina University (ECU), Greenville, North Carolina, USA.ORCID 0000-0002-2322-8345

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsPeriosteal osteosarcoma (PO) is a rare bone cancer that makes up between 1% and 6% of osteosarcomas. No epidemiological survey of the United States has been conducted to study this disease, and most of the literature is limited to single-center analyses and case reports. We seek to perform the first such assessment.

methodsThe Surveillance, Epidemiology, and End Results (SEER) Program was queried for patients with primary PO (ICD-O-3 code 9193/3). Analysis of demographic, disease, and treatment variables was conducted via Fisher's exact test and 20-year cause-specific survival (20y CSS) was assessed via logrank analysis.

resultsFifty-four patients with PO were identified; median age was 20-24 years at diagnosis. Multivariate analysis demonstrated surgery provided 20y CSS benefit (hazard ratio [HR] = 0.08, p = 0.040) while chemotherapy (CTX) did not (p = 0.29); however, given the limited number of events (n = 11), recalculation of Cox regression for each variable demonstrated significance only with race (p = 0.026). Younger patients were more likely to be diagnosed with PO of the appendicular skeleton compared to the axial skeleton (p = 0.038). Mean survival time was greater among patients diagnosed with appendicular PO (16.0 years [14.2, 17.9]) compared to axial PO (10.9 years [9.5, 12.4]). Stage-stratified survival analysis demonstrated surgery alone was non-inferior to surgery with the addition of CTX (local disease: p = 0.37; regional disease: p = 0.85).

conclusionAxial PO is associated with decreased mean 20y CSS compared to appendicular PO, though in general, appendicular PO is more common than axial PO. In keeping with current literature, treatment of PO with CTX in addition to surgery should be reserved for high-risk patients, though its use in the treatment of PO is questionable.

Indexed as

Bone NeoplasmsOsteosarcomaPeriosteumSEER ProgramAdolescentAdultChildFemaleHumansMaleMiddle AgedRetrospective StudiesUnited StatesYoung Adultcancer epidemiologychemotherapyperiosteal osteosarcomasurgical oncology

Identifiers

PMID39675926
PMCPMC11646689

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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.