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Идёт набор NCT05325008

A Trial to Treat Polyomavirus Infections (BKPyV) in Kidney and Simultaneous Kidney Pancreas Transplant Recipients

Фаза III С лечением BK Viremia Kidney Transplant Infection Kidney Transplant Failure and Rejection

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Immunosuppression reduction/modification + intravenous immunoglobulin, Immunosuppression reduction/modification.
Кому может быть актуально
Состояния в реестре: BK Viremia, Kidney Transplant Infection, Kidney Transplant Failure and Rejection. Базовые параметры: от 2 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Австралия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

An Adaptive Randomised Controlled Trial to Treat Polyomavirus Infections (BKPyV) in Kidney and Kidney Pancreas Transplant Recipients

Обзор

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).

Подробное описание

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.

Вмешательства

  • Препарат Immunosuppression reduction/modification + intravenous immunoglobulin
    Participants will receive intravenous immunoglobulin along with immunosuppression reduction/modification.
  • Другое Immunosuppression reduction/modification
    Participants will receive immunosuppression reduction/modification.

Первичные конечные точки

  • Composite ordinal outcome based on all cause death, allograft loss, eGFR decline, acute allograft rejection or BKV load > 1000 copies/mL, and immunosuppression load. [Срок оценки: 11 - 13 weeks]
Вторичные конечные точки (12)
  • BKPyV final viral load [Срок оценки: 12 weeks]
  • eGFR decline [Срок оценки: 12, 24 & 48 weeks]
  • All cause death [Срок оценки: 12, 24 & 48 weeks]
  • Graft loss [Срок оценки: 12, 24 & 48 weeks]
  • Acute rejection of kidney and/or pancreas allografts [Срок оценки: 12 & 48 weeks]
  • Donor Specific Anti-HLA Antibody [Срок оценки: 12 & 48 weeks]
  • Infusion reactions and/ or venous thromboembolism events [Срок оценки: 12 weeks]
  • Hospitalisations due to infection events [Срок оценки: Baseline,1,2,3,4,5,6,7,8,10,12,24,48 weeks]
  • Number of infectious events requiring antimicrobial (antibacterial, antiviral, antifungal, antiprotozoal) therapy. [Срок оценки: Baseline,1,2,3,4,5,6,7,8,10,12,24,48 weeks]
  • EuroQol-5 Dimension-5 Level for adults/ Health Utilities Index-3 for children [Срок оценки: Baseline, 12, 24 & 48 weeks]
  • BK polyomavirus associated nephropathy events [Срок оценки: 12 & 48 weeks]
  • Any cancer diagnosis or cancer related death [Срок оценки: 24 & 48 weeks]

Критерии участия

Критерии включения

  • 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

Критерии исключения

  • 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

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Простое слепое
Основная цель
Лечение

Центры проведения

Австралия · 13 центров
  • Canberra Hospital — Canberra
  • John Hunter Hospital — New Lambton Heights
  • Prince of Wales Hospital — Randwick
  • Royal Prince Alfred Hospital — Sydney
  • The Childrens Hospital Westmead — Sydney
  • Western Sydney Local Health District (Westmead Hospital) — Westmead
  • Queensland Children's Hospital — Brisbane
  • Townsville University Hospital — Townsville
  • … и ещё 5 центров

Публикации

  • Helle F, Aubry A, Morel V, Descamps V, Demey B, Brochot E. Neutralizing Antibodies Targeting BK Polyomavirus: Clinical Importance and Therapeutic Potential for Kidney Transplant Recipients. J Am Soc Nephrol. 2024 Oct 1;35(10):1425-1433. doi: 10.1681/ASN.0000000000000457. Epub 2024 Jul 9. PMID 39352862

Идентификаторы

NCT: NCT05325008 · AKTN 20.07

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗