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Идёт набор NCT05192122

Free From Maintenance Drug Therapy in Multiple Myeloma (The FREEDMM Trial) for Minimal Residual Disease (MRD

Фаза I С лечением Multiple Myeloma

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: Discontinue maintenance therapy SOC.
Кому может быть актуально
Состояния в реестре: Multiple Myeloma. Базовые параметры: от 18 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
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Free From Maintenance Drug Therapy in Multiple Myeloma (The FREEDMM Trial): A Pilot Study of Minimal Residual Disease (MRD)-Driven Discontinuation of Maintenance (HEME-20)

Обзор

A pilot study to assess the risk of progression after stopping post-autologous stem cell transplant (ASCT) maintenance therapy in Minimal Residual Disease (MRD)-negative MM patients.

Подробное описание

This is a pilot study to assess the risk of progression after stopping post-autologous stem cell transplant (ASCT) maintenance therapy in Minimal Residual Disease (MRD)-negative Multiple Myeloma (MM) patients. Patients will be eligible if they have a diagnosis of active MM, have completed at least 2 years of maintenance therapy post-ASCT, and meet International Myeloma Working Group (IMWG) criteria for very good partial response (VGPR) or complete response (CR). Once eligibility is confirmed and informed consent is signed, MRD testing will be performed on routine bone marrow aspirate using standard of care next-generation sequencing (NGS) testing and will be defined at a threshold of 10-6. Patients who are in VGPR or CR and sustained MRD (defined as MRD-negative at two time points that are at least 1 year apart) will go on to discontinue maintenance therapy. MRD-positive patients will continue to be treated as per standard of care (i.e., continue maintenance). Both MRD-positive and MRD-negative patients will be followed as per standard of care for progression using IMWG criteria and for MRD. Quality of life will be assessed at baseline and at 3 months after discontinuing maintenance therapy in MRD-negative patients and at baseline and at the time of next follow-up after MRD testing in MRD-positive patients. In patients who stop maintenance therapy, MRD status will be re-assessed by yearly bone marrow aspirate as per standard of care. Treatment for relapsed/ refractory myeloma will be instituted at the treating physician's discretion for documented clinical and/or biochemical progression. For all patients, a 5-mL peripheral blood and bone marrow sample will be collected and stored at the time of each standard of care bone marrow biopsy and at time of documented disease progression for correlative testing.

Вмешательства

  • Другое Discontinue maintenance therapy SOC
    MRD testing through NGS Clonoseq will be performed as standard of care on all bone marrow samples. MRD negativity will be defined as observation of no templates at a sensitivity of 1 in a 1,000,000 (10-6) cells assessed, with a minimum of 1 million cells undergoing assessment. In addition, patients must be in VGPR/CR/PR as defined previously.

Первичные конечные точки

  • Number of participants that have a sustained MRD-negative VGPR or CR measured by a bone marrow biopsy [Срок оценки: 12 months after stopping maintenance therapy]
Вторичные конечные точки (12)
  • Number of participants that have a sustained MRD-negative VGPR or CR measured by a bone marrow biopsy [Срок оценки: 2 years after stopping maintenance therapy]
  • Number of participants that relapse per IMWG at 1 year after stopping maintenance therapy [Срок оценки: 1 year after stopping maintenance therapy]
  • Number of participants that relapse per IMWG at 2 years after stopping maintenance therapy [Срок оценки: 2 years after stopping maintenance therapy]
  • Progression-free survival (PFS) in multiple myeloma patients [Срок оценки: I year]
  • Progression-free survival (PFS) in multiple myeloma patients [Срок оценки: 2 years]
  • Progression-free survival (PFS) in multiple myeloma patients [Срок оценки: 3 years]
  • Compare health-related quality of life (HRQoL) between MM patients stopping versus continuing maintenance therapy [Срок оценки: Baseline]
  • Compare health-related quality of life (HRQoL) between MM patients stopping versus continuing maintenance therapy [Срок оценки: 3 months]
  • Correlate peripheral blood circulating myeloma cell numbers (CELLSEARCH) with conventional IMWG response [Срок оценки: 1 year]
  • Correlate peripheral blood circulating myeloma cell numbers (CELLSEARCH) with conventional IMWG response [Срок оценки: 2 years]
  • Correlate peripheral blood circulating myeloma cell numbers (CELLSEARCH) with conventional IMWG response [Срок оценки: 3 years]
  • Correlate peripheral blood circulating myeloma cell numbers (CELLSEARCH) with conventional IMWG response [Срок оценки: 1 year]

Критерии участия

Критерии включения

  • ECOG Performance Status equal to or less than 2 within 30 days prior to registration
  • Revised International Staging System (R-ISS) I,2 or 3
  • Patients with multiple myeloma as defined by IMWG
  • Received at least 2 years of post ASCT maintenance (patients may have received any number of prior lines of therapy).
  • Maintenance therapy is defined as any anti-myeloma therapy initiated after ASCT to prevent disease recurrence and prolong time in remission (i.e., lenalidomide, bortezomib, RVD, etc.)
  • Disease response is VGPR or CR at the time of enrollment as defined by IMWG criteria.
  • Patients or their legally authorized representative must be able to understand and be willing to sign a voluntary informed consent form and agree to compliance with the protocol schedule; with the knowledge that they may withdraw consent at any time without impact on future medical care

Критерии исключения

  • Patients with plasma cell leukemia, AL amyloidosis or Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal protein, Skin (POEMS) syndrome
  • Prior organ transplant or condition requiring immunosuppressive therapy
  • Prior allogeneic hematopoietic cell transplant
  • Treatment with any investigational drug within 30 days prior to enrollment
  • Unable to sign an informed consent or their legally authorized represnetative

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Нерандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

США · 1 центр
  • University of Illinois Cancer Center — Chicago

Идентификаторы

NCT: NCT05192122 · 2021-1196

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗