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Study on Clinical Features, Treatment Mode and Survival of Sarcoma

A Single-center Retrospective Study of Clinical Features, Treatment Patterns, and Survival of Sarcomas

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05453409
Enrollment
6000
Registered
2022-07-12
Start date
2022-06-07
Completion date
2024-12-31
Last updated
2024-02-07

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

Conditions

Sarcoma

Brief summary

The clinical data of all eligible patients who received chemotherapy, radiotherapy, targeted therapy, immunotherapy, interventional therapy and surgery in Henan Tumor Hospital from June 1, 2012 to May 30, 2022 were retrospectively collected.

Detailed description

This study was a single-center retrospective clinical study, which retrospectively collected the clinical data of all eligible patients receiving chemotherapy, radiotherapy, targeted therapy, immunotherapy, interventional therapy and surgical treatment in Henan Tumor Hospital from June 1, 2012 to May 30, 2022. The efficacy, recurrence and survival of various treatments were collected.

Interventions

OTHERNo intervention

No intervention

Sponsors

Henan Cancer Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

No age limit, male or female. A certain subtype of sarcoma was diagnosed by pathology in our hospital. Has received at least one hospitalization in this hospital. Target lesions can be evaluated according to solid tumor efficacy evaluation criteria (RECIST; Version 1.1) Measure diameter changes. Complete follow-up data.

Exclusion criteria

No clear pathology. Incomplete follow-up data.

Design outcomes

Primary

MeasureTime frameDescription
Progression-free survivalUp to approximately 24monthsProgression-free survival is defined as time from enrollment to the first occurrence of progression of disease or death from any cause within 63 days of last response assessment.
Overall survivalUp to approximately 120monthsTime from pathological diagnosis to death

Countries

China

Contacts

Primary ContactWang Jiaqiang, Dr.
wjqwtj@126.com13592413731

Outcome results

None listed

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