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Идёт набор NCT06720727

Craniospinal Irradiation in Histone AlteRed Midline Glioma

Без фазы С лечением Glioma

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: craniospinal irradiation.
Кому может быть актуально
Состояния в реестре: Glioma. Базовые параметры: 3 лет — 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
Индия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Craniospinal Irradiation in Histone AlteRed Midline Glioma (CHARM) - A Phase II Open Label Prospective Study

Обзор

Paediatric H3K27/H3G34 mutant diffuse midline gliomas are high grade gliomas that arise in midline structures/cerebral hemispheres and are known to have dismal outcomes. Standard treatment includes definitive radiation therapy to primary site along with concurrent temozolomide chemotherapy following histological confirmation with a biopsy. Studies have shown poorer outcomes in the paediatric age group compared to that of adults and an increased risk to fail/recur in the leptomeninges(covering of brain and spinal cord). The following study is planned in order to assess the benefit of craniospinal irradiation(delivering radiotherapy to brain, spinal cord and its covering membrane in this high risk population. Thereby the investigator aim to improve survival in newly diagnosed histone mutant pediatric midline gliomas in the upfront setting. Patterns of disease failure, treatment related toxicities and quality of life will also be assessed as a part of this study. If proven beneficial, this study will influence how patients with this diagnosis will be treated in the future.

Подробное описание

Introduction: Paediatric H3K27/H3G34 mutant diffuse midline gliomas (DMGs) are aggressive high-grade gliomas predominantly affecting midline structures and cerebral hemispheres. Despite aggressive therapy including radiation and chemotherapy, these tumors carry a poor prognosis, particularly in children, with frequent recurrence and high risk of leptomeningeal spread. Current standard treatment involves definitive radiation therapy to the primary site and concurrent temozolomide chemotherapy following histological confirmation via biopsy. However, outcomes remain suboptimal, prompting exploration of more intensive therapeutic strategies.

Primary objective:

To study if the addition of craniospinal irradiation to standard practice improves outcomes in pediatric diffuse midline glioma.

Secondary objectives:

* Estimate median time to leptomeningeal dissemination and compare with historical control * Study patterns of failure * Early and late toxicities * Study quality of life indices * To estimate QTWiST (Quality of life without symptoms or toxicity)

Primary endpoint: Overall survival at 12 months

Secondary endpoints:

* Time to leptomeningeal dissemination in months * Incidence of different failure patterns from clinico-radiological assessment * Toxicity assessment with the NCI Common Terminology Criteria for Adverse Events version 5 (CTCAE v5) during CSI(weekly), at conclusion of radiotherapy , post completion of 6 cycles adjuvant temozolomide, and in subsequent follow-ups at 3, 6, 9 and 12 months. * Quality of life indices using the EORTC QLQC- 30 and its BN -20 module at baseline, after completion of radiotherapy, post completion of 6 cycles adjuvant temozolomide and in subsequent follow-up visits at 3, 6, 9 and 12 months. * Quality of life without symptoms or toxicity in three health states TOX (toxicity), TWIST (time without symptoms) and REL (relapse) at baseline, after completion of radiotherapy, post completion of 6 cycles adjuvant temozolomide and in subsequent follow-up visits at 3, 6, 9 and 12 months.

Study setting: The study will be conducted in the department of Radiation Oncology, Neuro Oncology Disease management group

Вмешательства

  • Лучевая терапия craniospinal irradiation
    Delivering radiotherapy to brain, spinal cord and its covering membrane.

Первичные конечные точки

  • Survival Outcomes [Срок оценки: at 12 months]
Вторичные конечные точки (6)
  • Leptomeningeal Dissemination [Срок оценки: at 12 months]
  • Patterns of failure [Срок оценки: at 12 months]
  • Any treatment emergent acute toxicity recording [Срок оценки: Baseline , week 1 , week 2 , week 3 , week 4 , week 5 ,week 6 , conclusion of RT]
  • Quality of life indices [Срок оценки: will be done at 3 months]
  • QTWiST (Quality of life Without Symptoms or Toxicity) calculation [Срок оценки: will be done at 3 months]
  • Any treatment emergent late toxicity recording [Срок оценки: After completion of 6 cycles of adjuvant chemotherapy, at 3months, 6months, 9months and 12months follow up]

Критерии участия

Критерии включения

  • Newly diagnosed biopsy proven histone altered diffuse midline glioma
  • Age- ≥3 to <18 years at time of diagnosis
  • Karnofsky/Lansky Performance Score more than or equal to 70
  • Has provided written informed consent/ assent form
  • No prior therapy except debulking surgery or biopsy

Критерии исключения

  • Recurrent or progressive disease
  • Clinical features or family history suggestive of Inherited Cancer Predisposition such as Constitutional Mismatch Repair Deficiency (CMMRD)
  • Previous history of malignancy
  • Not willing /unlikely to comply with proposed therapy and follow up

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Лечение

Центры проведения

Индия · 1 центр
  • Tata Memorial Hospital — Mumbai

Идентификаторы

NCT: NCT06720727 · 4481

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗