FLPOD24: Clinical Outcomes of Early-progressed Follicular Lymphoma in Korea

Sponsor
Samsung Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT04048395
Collaborator
(none)
80
1
9.8
8.2

Study Details

Study Description

Brief Summary

This retrospective study was proposed by the investigators to analyze treatment status and outcome in patients with early relapsed follicular lymphoma. In patients with follicular lymphoma who experienced disease progression within 24 months after initiation of treatment, the second-line therapy, stem cell transplantation, tumor response, progression free survival, and overall survival will be analyzed.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Follicular lymphoma is the second most common non-Hodgkin's lymphoma in Western countries, but it is relatively less frequent in Asia. As a result, the prognosis and treatment status in Korean patients with follicular lymphoma have been rarely studied.

    With the recent addition of monoclonal antibodies targeting CD20 into existing cytotoxic chemotherapy, the overall life expectancy of patients with follicular lymphoma has improved a lot. However, nearly 20% of these patients experience early worsening of disease within the first 24 months of treatment, followed by poor prognosis. Since patients with early relapse within 24 months usually experience worsening of disease during treatment with rituximab combined with chemotherapy or during rituximab maintenance therapy, optimal treatment for such patients is unknown, but remission induction therapy followed by stem cell transplantation, bendamustine combined with obinutuzumab, PI3K inhibitors, and lenalidomide are possible options. However, most of these drugs are limited for use in Korea, and there is little information with regard to treatment guidelines for patients with early relapsed follicular lymphoma or their treatment outcome in Korea.

    This retrospective study was proposed by the investigators to analyze treatment status and outcome in patients with early relapsed follicular lymphoma. This study will provide basic data for follicular lymphoma study in Korea and for future clinical trial design.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    80 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Clinical Outcomes of Early-progressed Follicular Lymphoma in Korea : A Multicenter, Retrospective Analysis
    Actual Study Start Date :
    Jul 8, 2019
    Anticipated Primary Completion Date :
    Apr 30, 2020
    Anticipated Study Completion Date :
    Apr 30, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Follicular lymphoma arm

    The analysis will involve patients diagnosed with follicular lymphoma who received induction chemotherapy and then experienced a worsening of disease within 24 months from the start date of the treatment.

    Outcome Measures

    Primary Outcome Measures

    1. Overall survival [from the date of the IRB approval until 12 month]

      Overall survival is defined as the time from the diagnosis to death or last follow-up.

    Secondary Outcome Measures

    1. Progression free survival [from the date of the IRB approval until 12 month]

      Progression free survival is defined as the time from diagnosis to relapse, disease progression, or last follow-up

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Patients histologically diagnosed with follicular lymphoma (ICD-10 C82.0 to C82.9)

    2. Radiologically confirmed disease progression within 24 months from the start date of an induction chemotherapy

    3. All of the following should be available for retrospective analysis.

    • Pathologic findings report

    • Medical records containing age, sex, date of diagnosis, clinical symptoms, laboratory findings, treatment methods, progression, survival, death, etc.

    Exclusion Criteria:
    1. Known histologic transformation to aggressive lymphoma

    2. Follicular lymphoma grade 3B

    3. Patients whose pathologic findings report and appropriate medical records are not available

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 81, Irwon-ro, Gangnam-gu, Seoul, Republic of Korea Seoul Korea, Republic of 06351

    Sponsors and Collaborators

    • Samsung Medical Center

    Investigators

    • Principal Investigator: Wonseog Kim, Professor, Samsung Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Won Seog Kim, Principal Investigator, Samsung Medical Center
    ClinicalTrials.gov Identifier:
    NCT04048395
    Other Study ID Numbers:
    • 2019-04-027
    First Posted:
    Aug 7, 2019
    Last Update Posted:
    Aug 7, 2019
    Last Verified:
    Aug 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    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 7, 2019