A Trial to Treat Polyomavirus Infections (BKPyV) in Kidney and Simultaneous Kidney Pancreas Transplant Recipients
- Conditions
- BK ViremiaKidney Transplant InfectionKidney Transplant Failure and Rejection
- Interventions
- Drug: Immunosuppression reduction/modification + intravenous immunoglobulinOther: Immunosuppression reduction/modification
- Registration Number
- NCT05325008
- Lead Sponsor
- The University of Queensland
- Brief Summary
BEAT-BK will see the effect of immunosuppression reduction/modification with and without IVIG on BKPyV infection, allograft function, allograft loss, acute transplant rejection, immunosuppression load and death in kidney and simultaneous kidney pancreas transplant recipients with polyomavirus infections (BKPyV).
- Detailed Description
BKPyV infection is a rare but also devastating disease in kidney and SPK transplant recipients. Immunosuppression used in transplantation minimises the risk of acute rejection and eventual graft loss, but suppression of the immune system increases the risk of opportunistic infections and reactivation of latent viruses causing disease, such as BKPyV infection. Therefore, balancing the complications of excessive versus inadequate immunosuppression is a key priority for patients and health professionals. The BEAT-BK trial is designed through a structured, consensus process, and informed by the pilot observational data generated by the investigators. The conventional immunosuppression reduction approach may include judicious reduction in the doses of calcineurin inhibitors and anti-proliferative agents, or conversion to less potent immunosuppression therapy such as a switch from tacrolimus to cyclosporine, or mycophenolate to azathioprine. While adjuvant therapy is not commonly used, 63% of participants would consider IVIG as a 'rescue', when conventional therapy has failed, or the graft function is deteriorating rapidly. IVIG is a nondepleting agent containing natural antibodies with potential antiviral and immunomodulatory properties. It is used against some chronic infections (Epstein-Barr virus) and the treatment of antibody-mediated rejection in kidney transplantation. In BKPyV infection, the certainty of the evidence for IVIG is very low due to imprecision, and high risk of bias (small, case series, retrospective cohorts), but it holds promise based on findings from our observational data (n = 50). Recipients with BKPyV-DNAemia who received IVIG as adjuvant therapy were more likely to achieve complete viral clearance at 12 months (77.3% vs. 33.3%, p \< 0.01) and less likely to relapse (11% vs. 27.3%, p=0.01) compared to recipients who received conventional therapy alone.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 280
- Aged 2 years or above
- Have received a kidney or simultaneous pancreas-kidney transplant
- Have BKPyV-Viremia (detected by RT-PCR) with a viral count ≥ 5,000 copies per mL, or histological confirmation of BKPyVAN, within 3 weeks prior to randomisation.
- Be able to provide informed consent or consent given by a parent or guardian (if age <18 years) or other authorised person
- Contraindications to receiving IVIG as a treatment
- Current active acute rejection (≤ 3 months prior)
- Treating clinicians would regard as unsafe to be enrolled
- Limited life expectancy (< 12 months)
- Receiving Belatacept as part of their immunosuppression protocol
- Currently undergoing or who have previously received, viral-specific T-cell therapy for BK viremia
- Prior infection and treatment for BKPyV-Viremia
- Received IVIG treatment in the past with last IVIG treatment < 4 weeks prior to randomisation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Immunosuppression reduction/modification + Intravenous Immunoglobulin Immunosuppression reduction/modification + intravenous immunoglobulin Receives Immunosuppression reduction/modification + Intravenous Immunoglobulin Immunosuppression reduction/modification Immunosuppression reduction/modification Receives Immunosuppression reduction/modification as part of standard of care.
- Primary Outcome Measures
Name Time Method Composite ordinal outcome based on all cause death, allograft loss, eGFR decline, acute allograft rejection or BKV load > 1000 copies/mL, and immunosuppression load. 11 - 13 weeks All participants will be allocated a rank at 12 weeks between rank 5 (worst) and rank 1 (best). The primary comparison of interest is between participants randomised to intravenous immunoglobulin (IVIG) and participants randomised to the control arm.
Outcome measures include: Rank 5 - all cause death, allograft loss, eGFR decline ≥10mls/min 1.73². Rank 4 - acute allograft rejection or BK viral load to \>1000 copies/mL. Ranks 3, 2, and 1 - the degree of immunosuppression reduction relative to baseline immunosuppression.
- Secondary Outcome Measures
Name Time Method All cause death 12, 24 & 48 weeks Compare the mortality rate in the intervention and control groups.
Graft loss 12, 24 & 48 weeks Compare the number of graft survival and death-censored graft survival participants in the intervention and control groups.
Acute rejection of kidney and/or pancreas allografts 12 & 48 weeks Compare the number of acute rejections (cellular and antibody mediated) episodes between the intervention and control groups.
Infusion reactions and/ or venous thromboembolism events 12 weeks Compare the incidence rate (number) of infusion reactions and venous thromboembolism between the intervention and control groups
BKPyV final viral load 12 weeks Compare the number of participants in the intervention and control groups with a BK Polyomavirus viral load to \<1000 copies/mL
eGFR decline 12, 24 & 48 weeks Compare the number of participants in the intervention and control groups with an estimated glomerular filtration rate (eGFR) decline ≥ 10 ml/min/1.73 m2
Donor Specific Anti-HLA Antibody 12 & 48 weeks Compare the number of participants that develop de novo donor-specific antibodies between the intervention and control groups
Hospitalisations due to infection events Baseline,1,2,3,4,5,6,7,8,10,12,24,48 weeks Compare the number of hospitalisation due to infection between the intervention and control groups.
Number of infectious events requiring antimicrobial (antibacterial, antiviral, antifungal, antiprotozoal) therapy. Baseline,1,2,3,4,5,6,7,8,10,12,24,48 weeks Compare the number of infectious events requiring antimicrobial therapy between the intervention and control groups
EuroQol-5 Dimension-5 Level for adults/ Health Utilities Index-3 for children Baseline, 12, 24 & 48 weeks Compare the outcomes of health-related quality of life between the intervention and control groups.
BK polyomavirus associated nephropathy events 12 & 48 weeks Compare the number of participants that develop BK polyomavirus associated nephropathy between the intervention and control groups
Any cancer diagnosis or cancer related death 24 & 48 weeks Compare the incidence rate (number) of cancer outcomes between the intervention and control groups.
Composite ranked outcome 24 & 48 weeks Compare the long-term composite ranked outcome between the intervention and control groups
Adverse events of special interest and serious adverse events Baseline,1,2,3,4,5,6,7,8,10,12,24,48 weeks Compare the incidence rate (number) of safety related events between intervention and control group.
Trial Locations
- Locations (13)
Royal Prince Alfred Hospital
🇦🇺Sydney, New South Wales, Australia
Royal North Shore Hospital
🇦🇺Sydney, New South Wales, Australia
The Childrens Hospital Westmead
🇦🇺Sydney, New South Wales, Australia
Perth Children's Hospital
🇦🇺Perth, Western Australia, Australia
Sir Charles Gairdner Hospital
🇦🇺Perth, Western Australia, Australia
Canberra Hospital
🇦🇺Canberra, Australian Capital Territory, Australia
John Hunter Hospital
🇦🇺New Lambton Heights, New South Wales, Australia
Prince of Wales Hospital
🇦🇺Randwick, New South Wales, Australia
Western Sydney Local Health District (Westmead Hospital)
🇦🇺Westmead, New South Wales, Australia
Queensland Children's Hospital
🇦🇺Brisbane, Queensland, Australia
Princess Alexandra Hospital
🇦🇺Woolloongabba, Queensland, Australia
Flinders Medical Centre
🇦🇺Adelaide, South Australia, Australia
Monash Health
🇦🇺Melbourne, Victoria, Australia