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Safety and Effectiveness of Granulocyte Transfusions in Resolving Infection in People With Neutropenia (The RING Study)

Phase 3
Completed
Conditions
Infection
Neutropenia
Interventions
Drug: Standard antimicrobial therapy
Drug: G-CSF/dexamethasone
Biological: Granulocyte transfusions
Device: Apheresis machine
Registration Number
NCT00627393
Lead Sponsor
Carelon Research
Brief Summary

Neutropenia, a condition characterized by an abnormally low number of infection-fighting white blood cells called neutrophils, commonly develops in people who have undergone chemotherapy or hematopoietic stem cell (HSC) transplantation. The severely reduced immunity of those with neutropenia can put them at risk of entry of life-threatening infections, making the implementation of treatments that increase white blood cell numbers important. Several studies have shown that the transfusion of donor granulocytes, a type of white blood cell that includes neutrophils, is effective in promoting the recovery of adequate numbers of granulocytes. However, granulocyte transfusions can cause side effects, and it is not known whether the success of the therapy outweighs the health risks of the side effects. This study will evaluate the safety and effectiveness of granulocyte transfusions in treating people with a bacterial or fungal infection during neutropenia.

Detailed Description

Thousands of people each year are hospitalized for neutropenia, which continues to cause substantial morbidity and mortality for those affected. Neutropenia is primarily caused by chemotherapy and various other cancer treatments, such as radiation therapy, biotherapy, and HSC transplantation. Signs and symptoms of neutropenia may include high fever, chills, sore throat, and diarrhea. In neutropenia, the number of neutrophils, a type of granulocyte, is greatly reduced, weakening the body's immune system and increasing the risk of infection. Therefore, a method to provide adequate numbers of functional granulocytes to people with neutropenia could be of greatest benefit for recovery. Administration of a combination of two drugs, granulocyte colony-stimulating factor (G-CSF) and dexamethasone, has been show to stimulate the body to produce a large number of granulocytes. Granulocyte transfusions obtained from donors who have received these two drugs may help people with low white blood cell counts fight infections until their own white blood cell counts recover. However, it is not clear whether the benefits of granulocyte transfusions outweigh the risks of side effects. This study will compare the safety and effectiveness of granulocyte transfusions with standard antimicrobial therapy versus the safety and effectiveness of standard antimicrobial therapy alone in increasing granulocyte numbers and in improving survival rates in people with bacterial or fungal infection during neutropenia.

Participation in the research portion of this study will last about 3 months. All participants who were not previously receiving treatment with standard antimicrobial therapy will begin therapy immediately upon study entry. Participants will then be assigned randomly to receive either granulocyte transfusion plus continued antimicrobial therapy or continued antimicrobial therapy alone. All participants will be monitored for a maximum of 42 days, during which they will provide information on medical history and ongoing status of antimicrobial therapy. Daily blood samples to measure white blood cell count will be obtained from participants until samples show that participants are making their own granulocytes. Samples will then be collected weekly until Day 42. There may be additional blood draws depending on the type of infection present in participants.

Granulocyte transfusions will be given daily during the 42-day treatment period, depending on granulocyte donor availability. Blood counts will be checked immediately before and after each transfusion to measure granulocyte levels. Transfusions will be stopped if participants start making their own granulocytes, experience serious side effects, or show a reduction in infection. At Month 3 after study entry, follow-up information will be collected about all participants' health status through reviewing their medical records and contacting their physicians.

Participation for granulocyte donors will last 1 week from the time of donation. Community donors may provide more than one granulocyte donation, but no more than one donation every 3 days. Frequency of donation from a family member will be according to local blood bank criteria with approval from a blood bank physician. Both community donors and family donors are limited to eight donations each year. Twelve hours before each donation, participants will be injected with Neupogen, which contains G-CSF, and they will take one dose of dexamethasone by mouth. Participants will then undergo a blood draw, followed by a procedure using an apheresis machine for granulocyte collection. The procedure will last 3 to 4 hours and will involve the drawing of blood from each arm, the separation of granulocytes from the red blood cells and plasma in the machine, and the return of the red blood cells and plasma to the participants.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
114
Inclusion Criteria
  • Severe neutropenia (Absolute Neutrophil Count < 500/mm^3) due to marrow failure caused by underlying disease or therapy
  • Must have one of the following: fungemia; bacteremia; proven or presumptive invasive tissue bacterial infection; or proven, probable, or presumptive invasive fungal infection
Exclusion Criteria
  • Unlikely to survive 5 days
  • Evidence that patient will not be neutropenic at least 5 days
  • Previously enrolled in this study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1Standard antimicrobial therapyParticipants will receive granulocyte transfusions in addition to standard antimicrobial therapy
1Granulocyte transfusionsParticipants will receive granulocyte transfusions in addition to standard antimicrobial therapy
2Standard antimicrobial therapyParticipants will receive standard antimicrobial therapy alone
3G-CSF/dexamethasoneParticipants will donate granulocytes after receiving a combination of two drugs, G-CSF and dexamethasone
3Apheresis machineParticipants will donate granulocytes after receiving a combination of two drugs, G-CSF and dexamethasone
Primary Outcome Measures
NameTimeMethod
Percentage of Participants Who Are Alive at 42 Days After Treatment and Have Had Microbial ResponseMeasured at Day 42

Microbial response was defined as follows:

* A negative blood culture test at 42 days after randomization for subjects with fungemia (candidemia or fusariosis) or bacteremia.

* Improvement of signs and symptoms of infectious disease (complete or partial response) at 42 days after randomization.

Secondary Outcome Measures
NameTimeMethod
Overall Incidence of Adverse EffectsMeasured through Day 42
Graft Versus Host Disease Among Recipients of Allogeneic Stem Cell TransplantationMeasured at Day 42

Time to GVHD incidence between the two treatment groups was compared using Gray's model that takes into account death as a competing risk.

Alloimmunization, Defined as the Appearance of Anti-human Leukocyte Antigen (HLA) or Antineutrophil AntibodiesMeasured at Days 14 and 42
Time to Negative Blood Culture for Participants With Positive Blood Culture at BaselineMeasured through Day 42
Donor Availability (Proportion of Scheduled Granulocyte Transfusion Days on Which Granulocytes Were Available)Measured through study completion
Discontinuation of Granulocyte Transfusions Due to Toxicity or IntoleranceMeasured through Day 42
Serious Granulocyte Transfusion Reactions, Including Febrile, Allergic, and Pulmonary Reactions (Transfusion Arm Only)Measured within 6 hours after end of transfusion
Fever ResolutionMeasured through Day 42

Fever resolution between the two treatment groups was compared using Gray's model that takes into account death as a competing risk.

Time to Negative Test for Fungal Antigenemia (e.g., Galactomannan Antigenemia Among Participants With Invasive Aspergillosis)Measured at Days 7, 14, and 42
Long-term SurvivalMeasured at Month 3
Serious Adverse Events in Granulocyte DonorsMeasured at Week 1 after G-CSF administration
Evaluation of Granulocyte YieldMeasured immediately after each granulocyte donation

Trial Locations

Locations (13)

Chlidren's Hospital of Philadelphia

🇺🇸

Philadelphia, Pennsylvania, United States

Johns Hopkins Hospital

🇺🇸

Baltimore, Maryland, United States

University of Iowa Hospitals and Clinics

🇺🇸

Iowa City, Iowa, United States

University of Pittsburgh Presbyterian and Shadyside

🇺🇸

Pittsburgh, Pennsylvania, United States

University of Washington Medical Center

🇺🇸

Seattle, Washington, United States

University of Wisconsin at Madison

🇺🇸

Madison, Wisconsin, United States

University of Oklahoma Health Sciences Center

🇺🇸

Oklahoma City, Oklahoma, United States

Children's Hospital Boston

🇺🇸

Boston, Massachusetts, United States

Froedtert Memorial Lutheran Hospital

🇺🇸

Milwaukee, Wisconsin, United States

University of Pennsylvania

🇺🇸

Philadelphia, Pennsylvania, United States

Weill Medical College, Cornell University

🇺🇸

New York, New York, United States

University of Minnesota

🇺🇸

Minneapolis, Minnesota, United States

Montefiore Medical Center

🇺🇸

Bronx, New York, United States

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