Evidence map›Paper›PMID 36937397›Full record

ArticleFrontiers in oncology2023

Prognostic factors and treatment outcomes of spinal osteosarcoma: Surveillance, epidemiology, and end results database analysis.

Jing Wang, Xiang-Zhi Ni, Ming-Lei Yang, Xing Huang, Shu-Ming Hou, Cheng Peng, Jia-Shi Cao, Tie-Long Liu

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Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Primary spinal bone sarcomas in Japan: a nationwide comparative analysis of demographic and pathologic features, treatment patterns, and survival.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2026
    Article
  2. Is survival in primary spinal osteosarcoma determined by surgical margins or tumour biology? A systematic review.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2026
    Review
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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

8 authors.

Jing WangDepartment of Orthopaedic Oncology, Spinal Tumor Center, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Xiang-Zhi NiDepartment of Orthopaedic Oncology, Spinal Tumor Center, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Ming-Lei YangDepartment of Orthopaedic Oncology, Spinal Tumor Center, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Xing HuangDepartment of Orthopaedic Oncology, Spinal Tumor Center, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Shu-Ming HouDepartment of Orthopaedic Oncology, Spinal Tumor Center, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Cheng PengDepartment of Orthopaedic Oncology, Spinal Tumor Center, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Jia-Shi CaoDepartment of Orthopaedic Oncology, Spinal Tumor Center, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.
Tie-Long LiuDepartment of Orthopaedic Oncology, Spinal Tumor Center, Shanghai Changzheng Hospital, Naval Medical University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Spinal osteosarcoma is a rare osseous neoplasm. The aim of this study is to make a comprehensive analysis of the demographic features, clinicopathologic characteristics and factors affecting prognosis of spinal osteosarcoma using the Surveillance, Epidemiology and End Results (SEER) database. Methods: SEER data were reviewed to identify patients diagnosed with spinal osteosarcoma between 1975 and 2016 and determine their overall survival (OS) and disease-specifc survival (DSS). Univariate and multivariate analyses were performed using the Cox-regression proportional hazards model and Kaplan-Meier method. Results: A total of 668 patients (53.1% males) with spinal osteosarcoma were identified. The mean age at diagnosis was 45.2 years, including 67.5% patients younger than 60 years. The median OS of these patients was 15 months, and the 5-year OS was 16.8%. Multivariate analysis showed that age ≥60 year (HR=2.271, p = 0.008), high grade (HR=1.323, p = 0.008), regional stage (HR=1.658, p = 0.017), metastasis stage (HR=3.045, p < 0.001) and no-surgery treatment (HR=1.761, p < 0.001) were adversely associated with OS; gender (HR=0.657, p = 0.044), tumor grade (HR=1.616, p = 0.006), tumor stage (HR=3.329, p = 0.011; HR=7.983, p < 0.001) and radiotherapy (HR=0.606, p = 0.031) were independent prognostic factors affecting DSS. Conclusion: Based on SEER data analysis, male, high tumor grade, regional stage, metastasis stage and radiotherapy are independent predictors of poor survival of patients with spinal osteosarcoma. The clinical treatment of spinal osteosarcoma still faces serious challenges. Future research should focus on the clinical impact and survival outcomes of the emerging targeted and immune therapies for the sake of improving the survival stalemate of spinal osteosarcoma.

Indexed as

epidemiologyprognosisSEERspinal osteosarcomasurvival

Identifiers

PMID36937397
PMCPMC10014918

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