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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04191252
Other study ID # EOC-TMB
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 19, 2019
Est. completion date January 1, 2023

Study information

Verified date December 2019
Source Peking Union Medical College Hospital
Contact Lei Li, M.D.
Phone +8613911988831
Email lileigh@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Little is known about the characteristics of genetic mutation in a large multi-gene panel in epithelial ovarian cancer. This study is to explore the targeted genetic mutations via a multi-gene panel, which consists of more than 500 hundred genes. The mutation characteristics are to be revealed in single nucleotide variants, copy number variations, insertion-deletion variations, and genomic structural variations. The total mutation burden (TMB) will be calculated. The status of microsatellite instability, expression of PD-1 and PD-L1 antibodies are also tested. These findings will be studies in association with the patients' prognosis and sensitivity to platinum-based chemotherapy.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date January 1, 2023
Est. primary completion date January 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Aged 18 years or older

- Pathology confirmed of recurrent cervical adenocarcinoma, squamous carcinoma or adenosquamous carcinoma

- With available materials for analysis

- With detailed clinicopathological information

- Given consent to participate the trial

Exclusion Criteria:

- Not meeting all of the inclusion criteria

Study Design


Intervention

Diagnostic Test:
A multi-gene panel testing
A multi-gene panel, which consists of more than 500 hundred genes will be provided for mutation analysis

Locations

Country Name City State
China Lei Li Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Lei Li

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Frequency of genetic mutations Frequency of various genetic mutations among recruited patients Two years
Secondary Total mutation burden Total mutation burden calculated in definite patient Two years
Secondary Frequency of microsatellite Instability Microsatellite Instability in definite patient Two years
Secondary Expression rates of PD-1 and PD-L1 antibodies Expression rates of PD-1 and PD-L1 antibodies among recruited patients Two years
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