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Predictive Models of Treatment Responses and Survival Outcomes in Patients With Osteosarcoma

Predictive Models of Treatment Responses and Survival Outcomes in Patients With Osteosarcoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05194605
Enrollment
800
Registered
2022-01-18
Start date
2021-01-01
Completion date
2024-12-31
Last updated
2022-01-31

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

Conditions

Osteosarcoma

Brief summary

The aim of this study was to developed and validated models to predict therapeutic responses and patients' survivals in patients with osteosarcoma and compared these models with currently available models.

Detailed description

The investigator performed a retrospective-prospective cohort study with the aim of developing and validating comprehensive models to predict treatment responses and survival outcomes in patients with biopsy-proven osteosarcoma. Secondly, the investigator aimed to compare the predictive accuracy with currently available noninvasive model.

Interventions

OTHERPrediction model

We develop and validate clinical models to predict treatment responses and survival outcomes in patients with biopsy-proven with osteosarcoma.

Sponsors

West China Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Receiving no treatment before diagnosis * With written informed consent

Exclusion criteria

* Clinical data missing * Without written informed consent

Design outcomes

Primary

MeasureTime frameDescription
Treatment responseAt least 1-year follow upThe primary outcome was the evaluation of treatment response to individualized therapy in patients with osteosarcoma.
Progression-free survival outcomesAt least 5-year follow upThe endpoint was defined as the occurrence of progression or recurrence, or the last follow-up. Patients were followed from the day of histological diagnosis until the occurrence of progression or recurrence, or last visit. The outcome was evaluated by an experienced oncologist in each center every 3-6 months. At each visit, a medical history, physical examination, and standard laboratory tests were performed.
Overall survival outcomesAt least 5-year follow upThe endpoint was defined as the occurrence of death or the last follow-up. Patients were followed from the day of histological diagnosis until the occurrence of progression or recurrence or last visit. The outcome was evaluated by an experienced oncologist in each center every 3-6 months. At each visit, a medical history, physical examination, and standard laboratory tests were performed.

Countries

China

Contacts

Primary ContactYuhan Yang, MD
yyh_1023@163.com8613258389785

Outcome results

None listed

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