Skip to content

Infantile Versus Adult-type Fibrosarcoma and the Risk of Multiple Primary Malignancies

Infantile Versus Adult-type Fibrosarcoma and the Risk of Multiple Primary Malignancies: a Retrospective Cohort Based on SEER Database

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06662734
Enrollment
12783
Registered
2024-10-29
Start date
2000-01-01
Completion date
2021-12-30
Last updated
2024-10-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fibrosarcoma

Keywords

infantile fibrosarcoma, Fibrosarcoma, SEER

Brief summary

Fibrosarcoma is a malignant tumor originating from mesenchymal tissues and consists of fibroblasts with various types of collagen production. It represents 10% of musculoskeletal sarcomas and less than 5% of all primary bone tumors. It affects middle-aged patients with the most common location in the femur and 70% long tubular bones. Studies reported that fibrosarcoma patients tend to develop a subsequent primary malignancy, the analysis showed a higher risk of SPMs even a decade following the initial diagnosis of fibrosarcoma. SPMs affect the long-term survival of patients with soft tissue tumors, and since there are no available studies analyzing the risk of second primary malignancies in different types of fibrosarcomas, especially the infantile and adult-type. Therefore, the purpose of this study was to assess the risk of second primary malignancies following primary fibrosarcoma diagnosis for a better understanding of the nature of this rare neoplasm. The investigators used the Surveillance, Epidemiology and End Results (SEER) database to extract the data and calculate the standardized incidence ratio as Observed/Expected and the Excess risk for second primary malignancies with 95% Confidence Interval. Significance was achieved at 0.05.

Interventions

None listed

Sponsors

asmaa salama ibrahim
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with fibrosarcoma from 2000 to 2021. * Sequence 0 or 1. * Histological types: Infantile fibrosarcoma, Fibromyxosarcoma, Periosteal fibrosarcoma, Facial fibrosarcoma, Dermatofibrosarcoma, Central odontogenic fibrosarcoma, Ameloblastic fibrosarcoma

Exclusion criteria

* Patients with unknown histology type

Design outcomes

Primary

MeasureTime frameDescription
The standardized incidence ratio and excess risk of developing multiple primary malignancies following fibrosarcoma diagnosisfrom Jan, 2000 till Dec, 2021The surveillance, epidemiology and End Results (SEER) database was used to calculate the standardized incidence ratio (SIR) as Observed/Expected (O/E) and calculated the Excess absolute risk for Multiple primary malignancies for fibrosarcoma patients
The standardized incidence ratio and excess risk of developing second primary malignancies for different subtypes of fibrosarcomafrom Jan, 2000 till Dec, 2021

Secondary

MeasureTime frame
The standardized incidence ratio and excess risk of multiple primary malignancies in fibrosarcoma patients across different racial groupsfrom Jan, 2000 till Dec, 2021
The standardized incidence ratio and excess risk of multiple primary malignancies in both males and females in fibrosarcoma patientsfrom Jan, 2000 till Dec, 2021

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026