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Red Blood Cell Transfusion Thresholds and QOL in MDS (EnhanceRBC)

Primary Purpose

Myelodysplastic Syndromes (MDS), Quality of Life, Red Blood Cell (RBC) Transfusions

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Red Blood Cell Transfusions
Sponsored by
Sunnybrook Health Sciences Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myelodysplastic Syndromes (MDS)

Eligibility Criteria

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

Inclusion Criteria:

  • All patients with MDS ≥18 years of age
  • Transfusion dependent: at least 1 transfusion per month in the last 8 weeks
  • Hb <100g/L pre transfusion
  • Life expectancy > 6 months

Exclusion Criteria:

  • Unstable cardiac disease (Canadian Cardiovascular Society (CCS) III/IV angina or New York Heart Association (NYHA) III/IV congestive heart failure) requiring the transfusion target range to remain >85-100 g/L at all times
  • ECOG ≥3
  • Patients with red cell antibodies against high frequency antigens or multiple antibodies (would potentially delay finding blood)
  • Patients on ESA's or disease modifying agents (like azacitidine) for their MDS

Sites / Locations

  • Juravinski Cancer CentreRecruiting
  • Princess Margaret HospitalRecruiting
  • Sunnybrook Health Sciences Centre/Odette Cancer CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Liberal transfusion strategy

Restrictive transfusion strategy

Arm Description

Intervention: Red Blood Cell transfusions. Transfuse pRBC at a higher threshold- maintain Hb level between 110 and 120 g/L: to achieve this, 2 units of pRBCs are transfused when Hb level is < 105 g/L and 1 unit of RBCs when Hb level is 105-110 g/L. Transfusions administered more frequently.

Intervention: Red Blood Cell transfusions. Transfuse pRBC at standard of care thresholds- maintain Hb level between 85 and 100 g/L: to achieve this, 2 units of packed red blood cells (pRBCs) will be transfused when the Hb level is < 80 g/L and 1 unit of pRBCs when Hb level is 80-85 g/L: standard administration

Outcomes

Primary Outcome Measures

Percentage compliance of q2weekly hemoglobins
The percentage compliance of q2weekly hemoglobins being within or above the target range of the RBC transfusion threshold assigned (after the 4 week run-in at study start as defined above). We will consider this study feasible and worthy of future development into a larger randomized trial (powered for QOL difference) if compliance is ≥70%. A compliance rate of 50-70%, would not exclude going forward with such an RCT but only after careful discussion and statistical planning

Secondary Outcome Measures

Measures of feasibility
Number of patients ineligible due to screen failure Enrolment rates defined by the number of enrolled patients/month Percentage compliance with QOL questionnaire completion at least 3 serial times Other logistical issues related to protocol implementation, recruitment rates, randomization implementation strategy, data collection, patient tolerability of study schedule
Quality of life
• The magnitude of change in physical functioning, fatigue, dyspnea and global health scores on the EORTC QLQ-C30, calculated health utility on the EQ-5D and fatigue score on FACT-F comparing the 2 RBC transfusion thresholds above.
Adverse events
The rate of transfusion reactions (as defined by TTISS (Transfusion Transmitted Injuries Surveillance System by Public Health Agency of Canada)) Rate of adverse events such as cardiac events and thromboembolic events as per NCI CTCAE version 4.0 criteria
Alloimmunization rates
Rate of alloimmunization to significant blood group antigens
Hemosiderosis
• The impact on transfusion associated hemosiderosis rates and burdens (as measured by changes in ferritin levels and iron chelating medications)
Overall utilization of blood
How many units of blood are required to maintain the hemoglobin threshold chosen
Time commitment
• The overall time commitment per group, measured as the time spent in transfusion medicine clinic

Full Information

First Posted
March 26, 2014
Last Updated
April 24, 2018
Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Princess Margaret Hospital, Canada, Juravinski Cancer Center
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1. Study Identification

Unique Protocol Identification Number
NCT02099669
Brief Title
Red Blood Cell Transfusion Thresholds and QOL in MDS
Acronym
EnhanceRBC
Official Title
Red Blood Cell Transfusion Thresholds and QOL in MDS (EnhanceRBC): a Pilot, Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 2014 (undefined)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
January 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Princess Margaret Hospital, Canada, Juravinski Cancer Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Myelodysplastic syndromes (MDS) are bone marrow malignancies characterized by poor bone marrow function that may progress to acute myeloid leukemia. Many patients become red blood cell transfusion-dependent. Transfusion dependence is associated with inferior quality of life (QOL). However, the relationship between the degree of anemia and QOL is less clear. A commonly used transfusion strategy is to target the hemoglobin (Hb) in the range of 80-90 g/L (normal hemoglobin > 120-130g/L). The question is: would a higher hemoglobin target lead to improvement in QOL despite the negative impact transfusion dependence may have on QOL (due to associated time commitments, expense, transfusion reactions etc). Several groups have prospectively shown that targeting hemoglobin levels of greater than 120 g/L (with hematopoietic growth factors (HGFs) and/or blood transfusions) or incremental increases of 15-20 g/L (with HGFs alone) were associated with improved QOL. The investigators MDS program has been conducting prospective assessments of QOL since 2007 in all registered and consented patients using a variety of validated questionnaires. Preliminary analysis (in 236 patients) revealed that, compared with an age-matched healthy general population, MDS patients have inferior QOL. Transfusion dependence and anemia were independently predictive of poor functioning, fatigue and decreased health utility. Furthermore, a hemoglobin level of ≥100 g/L seemed to be the key threshold for improvement in function and symptom scores. The investigators hypothesize that the target hemoglobins in transfusion dependent MDS patients are too low and this may account for their inferior quality of life. Our goal is to compare the effect on QOL of a restrictive strategy (which is the current standard of care), with a liberal transfusion strategy in a large randomized controlled trial of transfusion dependent MDS outpatients. Before embarking on such an endeavor, the investigators must first prove feasibility in a smaller pilot randomized controlled trial.
Detailed Description
Myelodysplastic syndromes (MDS) are bone marrow malignancies characterized by poor bone marrow function that may progress to acute myeloid leukemia. Many patients become red blood cell transfusion-dependent. Transfusion dependence is associated with inferior quality of life (QOL). However, the relationship between the degree of anemia and QOL is less clear. A commonly used transfusion strategy is to target the hemoglobin (Hb) in the range of 80-90 g/L (normal hemoglobin > 120-130g/L). The question is: would a higher hemoglobin target lead to improvement in QOL despite the negative impact transfusion dependence may have on QOL (due to associated time commitments, expense, transfusion reactions etc). Several groups have prospectively shown that targeting hemoglobin levels of greater than 120 g/L (with hematopoietic growth factors (HGFs) and/or blood transfusions) or incremental increases of 15-20 g/L (with HGFs alone) were associated with improved QOL. The investigators MDS program has been conducting prospective assessments of QOL since 2007 in all registered and consented patients using a variety of validated questionnaires. Preliminary analysis (in 236 patients) revealed that, compared with an age-matched healthy general population, MDS patients have inferior QOL. Transfusion dependence and anemia were independently predictive of poor functioning, fatigue and decreased health utility. Furthermore, a hemoglobin level of ≥100 g/L seemed to be the key threshold for improvement in function and symptom scores. The investigators hypothesize that the target hemoglobins in transfusion dependent MDS patients are too low and this may account for their inferior quality of life. Our goal is to compare the effect on QOL of a restrictive strategy (which is the current standard of care), with a liberal transfusion strategy in a large randomized controlled trial of transfusion dependent MDS outpatients. Before embarking on such an endeavor, the investigators must first prove feasibility in a smaller pilot randomized controlled trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myelodysplastic Syndromes (MDS), Quality of Life, Red Blood Cell (RBC) Transfusions

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Liberal transfusion strategy
Arm Type
Experimental
Arm Description
Intervention: Red Blood Cell transfusions. Transfuse pRBC at a higher threshold- maintain Hb level between 110 and 120 g/L: to achieve this, 2 units of pRBCs are transfused when Hb level is < 105 g/L and 1 unit of RBCs when Hb level is 105-110 g/L. Transfusions administered more frequently.
Arm Title
Restrictive transfusion strategy
Arm Type
Active Comparator
Arm Description
Intervention: Red Blood Cell transfusions. Transfuse pRBC at standard of care thresholds- maintain Hb level between 85 and 100 g/L: to achieve this, 2 units of packed red blood cells (pRBCs) will be transfused when the Hb level is < 80 g/L and 1 unit of pRBCs when Hb level is 80-85 g/L: standard administration
Intervention Type
Other
Intervention Name(s)
Red Blood Cell Transfusions
Primary Outcome Measure Information:
Title
Percentage compliance of q2weekly hemoglobins
Description
The percentage compliance of q2weekly hemoglobins being within or above the target range of the RBC transfusion threshold assigned (after the 4 week run-in at study start as defined above). We will consider this study feasible and worthy of future development into a larger randomized trial (powered for QOL difference) if compliance is ≥70%. A compliance rate of 50-70%, would not exclude going forward with such an RCT but only after careful discussion and statistical planning
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Measures of feasibility
Description
Number of patients ineligible due to screen failure Enrolment rates defined by the number of enrolled patients/month Percentage compliance with QOL questionnaire completion at least 3 serial times Other logistical issues related to protocol implementation, recruitment rates, randomization implementation strategy, data collection, patient tolerability of study schedule
Time Frame
3 months
Title
Quality of life
Description
• The magnitude of change in physical functioning, fatigue, dyspnea and global health scores on the EORTC QLQ-C30, calculated health utility on the EQ-5D and fatigue score on FACT-F comparing the 2 RBC transfusion thresholds above.
Time Frame
3 months
Title
Adverse events
Description
The rate of transfusion reactions (as defined by TTISS (Transfusion Transmitted Injuries Surveillance System by Public Health Agency of Canada)) Rate of adverse events such as cardiac events and thromboembolic events as per NCI CTCAE version 4.0 criteria
Time Frame
3 months
Title
Alloimmunization rates
Description
Rate of alloimmunization to significant blood group antigens
Time Frame
3 months
Title
Hemosiderosis
Description
• The impact on transfusion associated hemosiderosis rates and burdens (as measured by changes in ferritin levels and iron chelating medications)
Time Frame
3 months
Title
Overall utilization of blood
Description
How many units of blood are required to maintain the hemoglobin threshold chosen
Time Frame
3 months
Title
Time commitment
Description
• The overall time commitment per group, measured as the time spent in transfusion medicine clinic
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients with MDS ≥18 years of age Transfusion dependent: at least 1 transfusion per month in the last 8 weeks Hb <100g/L pre transfusion Life expectancy > 6 months Exclusion Criteria: Unstable cardiac disease (Canadian Cardiovascular Society (CCS) III/IV angina or New York Heart Association (NYHA) III/IV congestive heart failure) requiring the transfusion target range to remain >85-100 g/L at all times ECOG ≥3 Patients with red cell antibodies against high frequency antigens or multiple antibodies (would potentially delay finding blood) Patients on ESA's or disease modifying agents (like azacitidine) for their MDS
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jennifer Gallagher
Email
jennifer.gallagher@sunnybrook.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Geetha Yogendron
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rena Buckstein, MD
Organizational Affiliation
Sunnybrook Health Sciences Centre/Odette Cancer Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Juravinski Cancer Centre
City
Hamilton
State/Province
Ontario
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Erin Jamula, MSc
Phone
905-521-2100
Ext
76461
Email
jamulae@mcmaster.ca
First Name & Middle Initial & Last Name & Degree
Brian Leber, MD
Facility Name
Princess Margaret Hospital
City
Toronto
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karen Yee, MD
First Name & Middle Initial & Last Name & Degree
Karen Yee, MD
Facility Name
Sunnybrook Health Sciences Centre/Odette Cancer Centre
City
Toronto
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jennifer Gallagher
Email
jennifer.gallagher@sunnybrook.ca
First Name & Middle Initial & Last Name & Degree
Rena Buckstein

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34932836
Citation
Carson JL, Stanworth SJ, Dennis JA, Trivella M, Roubinian N, Fergusson DA, Triulzi D, Doree C, Hebert PC. Transfusion thresholds for guiding red blood cell transfusion. Cochrane Database Syst Rev. 2021 Dec 21;12(12):CD002042. doi: 10.1002/14651858.CD002042.pub5.
Results Reference
derived

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Red Blood Cell Transfusion Thresholds and QOL in MDS

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