PD-L1 Expression in Japanese Renal Cell Carcinoma Patients

Sponsor
Chugai Pharmaceutical (Industry)
Overall Status
Completed
CT.gov ID
NCT03748901
Collaborator
(none)
830
1
31.1
26.6

Study Details

Study Description

Brief Summary

This is a multicenter retrospective study designed to compare overall survival (OS) by PD-L1 expression status in patients with RCC who have received systemic chemotherapy for recurrent or metastatic RCC, to determine whether the prognosis is worse in PD-L1-positive than in PD-L1-negative RCC.

Total 600 RCC surgical specimens will be collected from patients who started systemic chemotherapy for recurrent or metastatic RCC between January 1, 2010 and December 31, 2015 at about 30 participating study sites in Japan.

PD-L1 expression status (IC; immune cell) on tumor-infiltrating immune cells will be evaluated by IHC, and classified by score: IC0 (PD-L1-negative) and IC1, IC2, IC3 (PD-L1-positive). Unless otherwise specified, between-group comparisons will be performed between IC0 and IC1/2/3.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    830 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    A Retrospective Multicenter Analysis of PD-L1 Expression in Japanese Renal Cell Carcinoma Patients
    Actual Study Start Date :
    Dec 16, 2018
    Actual Primary Completion Date :
    Jul 21, 2021
    Actual Study Completion Date :
    Jul 21, 2021

    Arms and Interventions

    Arm Intervention/Treatment
    Full analysis set

    Patients with recurrent or metastatic RCC who have initiated first line treatment between 1 January 2010 and 31 December 2015, with representative FFPE of nephrectomy surgical specimen which are suitable for assessment of PD-L1 expression

    Outcome Measures

    Primary Outcome Measures

    1. Overall survival in PD-L1 negative (IC0) and positive (IC1/2/3) patients. [Baseline]

      Overall survival is defined as the time from the initiation date of first line treatment to death due to any cause.

    Secondary Outcome Measures

    1. Overall survival by PD-L1 expression status (IC0, IC1, IC2, IC3) [Baseline]

      Overall survival is defined as the time from the initiation date of first line treatment to death due to any cause.

    2. Overall survival after nephrectomy (including cytoreductive nephrectomy) [Baseline]

      Overall survival is defined the time from nephrectomy (including cytoreductive nephrectomy) to death due to any cause.

    3. Time to recurrence after radical nephrectomy [Baseline]

      Time to recurrence after radical nephrectomy is the duration from the day of surgery to diagnosis of recurrent.

    4. Treatment duration (first-line and second-line therapy) [Baseline]

      Treatment duration is the duration from the day1 of systemic therapy for mRCC to the end of the treatment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
      1. Written informed consent for this study. In the case obtaining written informed consent is difficult due to death, change of address, and so on, the opt-out consent is accepted by giving patients or their relatives notification regarding the usage of their clinical information and surgical samples for the research.
      1. Age at nephrectomy≧20 years
    • 3.Patients with recurrent or metastatic RCC who have initiated first line treatment between 1 January 2010 and 31 December 2015, with representative FFPE of nephrectomy surgical specimen which are suitable for assessment of PD-L1 expression

    Exclusion Criteria:
      1. Malignancies other than RCC is co-existed from the time of nephrectomy and death.
      1. Treatment with anti-CTLA-4 antibody, anti-PD-1/PD-L1 antibodies as first-line therapy for recurrent or metastatic RCC.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Aichi Medical University Nagoya-city Aichi Japan 480-1103

    Sponsors and Collaborators

    • Chugai Pharmaceutical

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Chugai Pharmaceutical
    ClinicalTrials.gov Identifier:
    NCT03748901
    Other Study ID Numbers:
    • CMA-Ate004
    First Posted:
    Nov 21, 2018
    Last Update Posted:
    Aug 30, 2021
    Last Verified:
    Aug 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 30, 2021