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Switched Memory B-cells as a Marker for Humoral Immune System Recovery in Patients With Secondary Antibody Deficiency Due to Hematological Malignancies (SAD)

Primary Purpose

Secondary Antibody Deficiency

Status
Not yet recruiting
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Immunoglobulin replacement therapy (IGRT)
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Secondary Antibody Deficiency

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: History of leukemia, lymphoma, or plasma cell disease Receiving IGRT for SAD for at least 12 months Over 18 years of age Able to provide informed consent Able to speak English or French Available for ongoing follow-up as required Exclusion Criteria: Receiving chemotherapy or immune-oncology treatment during the study period Severe infection within the last 6 months Pregnancy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Other

    Arm Label

    IGRT discontinuation

    Arm Description

    Participants will be tested to determine Switched memory B cells (SMB) levels. If SMB cells are ≥ 2%, IGRT will be discontinued. If SMB cells are < 2%, the patient will remain on IGRT and a maximum of 40 mL of blood will be drawn again in 3-6 months to reassess SMB levels and eligibility for IGRT discontinuation.

    Outcomes

    Primary Outcome Measures

    IGRT discontinuation sucess rate
    IGRT discontinuation success rate defined as the proportion of patients with normal SMB levels who stop IGRT and experience less than or equal to 1 moderate infection and no severe infection within 12 months of IGRT discontinuation. Moderate infection will be defined as an infection that requires outpatient oral antimicrobial treatment. Severe infection will be defined as an infection that requires intravenous antimicrobial treatment and/or hospitalization.
    IGRT discontinuation rate
    IGRT discontinuation rate defined as the proportion of recruited adult patients with SAD who discontinue IGRT during the study period.

    Secondary Outcome Measures

    Change in Health-Related Quality of Life
    Change in Health-Related Quality of Life (HRQoL) before and after IGRT discontinuation. The 36-item Short Form Survey (SF-36, RAND Corporation) will be used to obtain HRQoL data.
    Change in Health-Related Quality of Life
    Change in Health-Related Quality of Life (HRQoL) before and after IGRT discontinuation. The Euroqol 5-dimension 5-level (EQ-5D-5L) questionnaire will be used to obtain HRQoL data.
    Cost saving potential
    Calculated potential cost saving based on the study IGRT discontinuation rate using SMB as a marker for discontinuation.
    Receiver operating curve (ROC)
    We will estimate a receiver operating curve (ROC) of SMB proportion as a predictor of successful discontinuation.

    Full Information

    First Posted
    October 1, 2022
    Last Updated
    November 4, 2022
    Sponsor
    Ottawa Hospital Research Institute
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05612607
    Brief Title
    Switched Memory B-cells as a Marker for Humoral Immune System Recovery in Patients With Secondary Antibody Deficiency Due to Hematological Malignancies
    Acronym
    SAD
    Official Title
    Switched Memory B-cells as a Marker for Humoral Immune System Recovery in Patients With Secondary Antibody Deficiency Due to Hematological Malignancies
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    November 10, 2022 (Anticipated)
    Primary Completion Date
    October 10, 2023 (Anticipated)
    Study Completion Date
    December 31, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Ottawa Hospital Research Institute

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    Current treatment for patients with secondary antibody deficiency (SAD) is Immunoglobulin replacement therapy (IGRT). There are currently no clinical guidelines for IGRT discontinuation in patients with SAD. This study will examine the IGRT discontinuation success rate and IGRT discontinuation rate in patients.
    Detailed Description
    Immunoglobulin replacement therapy (IGRT) is a mainstay treatment for SAD and has been shown to reduce the risk of infection and increase quality of life in patients with SAD. Current guidelines recommend that patients with severe hypogammaglobulinemia (IgG <4 g/L) or patients with a history of recurrent or severe infections should be offered IGRT, which can be administered intravenously on a monthly basis or more frequently by subcutaneous infusions. There are currently no clinical guidelines for IGRT discontinuation. Although research conducted at the Ottawa Hospital indicates successful discontinuation of IGRT, clinicians need a tool to predict the recovery of humoral immunity and the risk of infection in these patients in order to determine whether IGRT may be safely discontinued.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Secondary Antibody Deficiency

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Phase 4
    Interventional Study Model
    Single Group Assignment
    Model Description
    Patients will be tested to determine SMB cell proportion/SMB cell levels for eligibility for IGRT discontinuation. If SMB cells are ≥ 2%, IGRT will be discontinued. If SMB cells are < 2%, the patient will remain on IGRT and a maximum of 40 mL of blood will be drawn again in 3-6 months to reassess SMB levels and eligibility for IGRT discontinuation.
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    100 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    IGRT discontinuation
    Arm Type
    Other
    Arm Description
    Participants will be tested to determine Switched memory B cells (SMB) levels. If SMB cells are ≥ 2%, IGRT will be discontinued. If SMB cells are < 2%, the patient will remain on IGRT and a maximum of 40 mL of blood will be drawn again in 3-6 months to reassess SMB levels and eligibility for IGRT discontinuation.
    Intervention Type
    Drug
    Intervention Name(s)
    Immunoglobulin replacement therapy (IGRT)
    Intervention Description
    IGRT discontinuation will be dependent on participant's SMB levels. If SMB cells are ≥ 2%, IGRT will be discontinued. If SMB cells are < 2%, the patient will remain on IGRT and a maximum of 40 mL of blood will be drawn again in 3-6 months to reassess SMB levels and eligibility for IGRT discontinuation.
    Primary Outcome Measure Information:
    Title
    IGRT discontinuation sucess rate
    Description
    IGRT discontinuation success rate defined as the proportion of patients with normal SMB levels who stop IGRT and experience less than or equal to 1 moderate infection and no severe infection within 12 months of IGRT discontinuation. Moderate infection will be defined as an infection that requires outpatient oral antimicrobial treatment. Severe infection will be defined as an infection that requires intravenous antimicrobial treatment and/or hospitalization.
    Time Frame
    12 months post discontinuation
    Title
    IGRT discontinuation rate
    Description
    IGRT discontinuation rate defined as the proportion of recruited adult patients with SAD who discontinue IGRT during the study period.
    Time Frame
    12 months post discontinuation
    Secondary Outcome Measure Information:
    Title
    Change in Health-Related Quality of Life
    Description
    Change in Health-Related Quality of Life (HRQoL) before and after IGRT discontinuation. The 36-item Short Form Survey (SF-36, RAND Corporation) will be used to obtain HRQoL data.
    Time Frame
    Through study completion, an average of 1 year
    Title
    Change in Health-Related Quality of Life
    Description
    Change in Health-Related Quality of Life (HRQoL) before and after IGRT discontinuation. The Euroqol 5-dimension 5-level (EQ-5D-5L) questionnaire will be used to obtain HRQoL data.
    Time Frame
    Through study completion, an average of 1 year
    Title
    Cost saving potential
    Description
    Calculated potential cost saving based on the study IGRT discontinuation rate using SMB as a marker for discontinuation.
    Time Frame
    Through study completion, an average of 1 year
    Title
    Receiver operating curve (ROC)
    Description
    We will estimate a receiver operating curve (ROC) of SMB proportion as a predictor of successful discontinuation.
    Time Frame
    Through study completion, an average of 1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: History of leukemia, lymphoma, or plasma cell disease Receiving IGRT for SAD for at least 12 months Over 18 years of age Able to provide informed consent Able to speak English or French Available for ongoing follow-up as required Exclusion Criteria: Receiving chemotherapy or immune-oncology treatment during the study period Severe infection within the last 6 months Pregnancy
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Juthaporn Cowan, MD, PhD, FRCPC, FAPC
    Phone
    6137378899
    Ext
    79617
    Email
    jcowan@toh.ca

    12. IPD Sharing Statement

    Learn more about this trial

    Switched Memory B-cells as a Marker for Humoral Immune System Recovery in Patients With Secondary Antibody Deficiency Due to Hematological Malignancies

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