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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02987777
Other study ID # ICL_2016_0001
Secondary ID
Status Completed
Phase N/A
First received November 28, 2016
Last updated December 6, 2016
Start date January 2016
Est. completion date August 2016

Study information

Verified date December 2016
Source Institut de Cancérologie de Lorraine
Contact n/a
Is FDA regulated No
Health authority France: Commission nationale de l'informatique et des libertés
Study type Observational

Clinical Trial Summary

The aim of this study was to assess the frequency of PD-L1 expression in stage III-IV ECs and to investigate its correlation impact with progression-free survival (PFS), and clinicopathological features including microsatellite instability and quantified stromal and intraepithelial tumor-infiltrating CD8+ lymphocytes (TILs)


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date August 2016
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All patients consecutively enrolled from January 2004 to December 2014 treated for Endometrial cancer

- Stage III-IV endometrial cancer with available tissue blocks, including biopsies, hysterectomy specimens and resections of metastatic foci

Exclusion Criteria:

- A patient record captured outside the time frame from January 2004 to December 2014

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Institut de Cancérologie de Lorraine

Outcome

Type Measure Description Time frame Safety issue
Primary progression-free survival 84 months No
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