Geriatric Assessment-Guided Treatment Selection in Older Adults With Acute Myeloid Leukemia
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: GA-directed treatment regimens.
- Кому может быть актуально
- Состояния в реестре: Acute Myeloid Leukemia. Базовые параметры: от 60 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 →
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Официальное название
Geriatric Assessment-Guided Treatment Selection in Older Adults With Acute Myeloid Leukemia (The ALIGN-AML Trial)
Обзор
This is a phase 2 randomized controlled trial to evaluate whether a geriatric assessment (GA)-guided treatment strategy reduces treatment-related toxicity and improves patient-centered outcomes compared with usual oncologist-directed care in adults aged 60 years and older with newly diagnosed AML.
Подробное описание
Acute myeloid leukemia (AML) primarily affects older adults, yet treatment decision-making in this population remains largely inconsistent. Older adults with AML are highly heterogeneous with respect to physiologic reserve, functional status, cognition, and comorbidities, all of which strongly influence treatment tolerance and outcomes. Despite this heterogeneity, treatment decisions are often made rapidly and rely heavily on chronological age and clinician judgment, approaches that have been repeatedly shown to inadequately predict toxicity, early mortality, and functional decline. The proposed trial addresses a critical scientific question: whether a structured geriatric assessment (GA)-guided treatment strategy improves clinically meaningful outcomes compared with usual oncologist-directed care in older adults with AML. Although GA has been extensively validated as a prognostic and risk stratification tool in oncology and has improved care delivery in solid tumors, it has not been tested in a randomized controlled trial in AML, where treatment urgency, toxicity burden, and early adverse events are especially pronounced. This study therefore fills a major evidence gap at the intersection of geriatric oncology and hematologic malignancies.
This multicenter, prospective, randomized controlled trial is designed to evaluate whether a geriatric assessment (GA)-guided treatment strategy improves clinically meaningful outcomes compared with usual oncologist-directed care in older adults with newly diagnosed acute myeloid leukemia (AML). Approximately 120 adults aged 60 years and older will be enrolled across 3 academic and community institutions affiliated with the Cancer and Aging Research Group (CARG). Patients will be randomized in a 1:1 ratio to either a GA-guided treatment arm or a usual-care arm, with randomization stratified by study site and GA-defined fitness category (fit, vulnerable, frail). All patients will undergo a structured GA using the Practical Geriatric Assessment recommended by the American Society of Clinical Oncology and adapted for hematologic malignancies. However, GA results will be used to guide treatment selection only for participants assigned to the intervention arm.
Вмешательства
- Препарат GA-directed treatment regimens
Fit, vulnerable, and frail patients will receive predefined regimens based on their GA results.
Первичные конечные точки
- Treatment failure rate at 3 months [Срок оценки: 3 months after treatment initiation]
Вторичные конечные точки (12)
- Treatment failure rate at 6 months [Срок оценки: 6 months after treatment initiation]
- Overall Response Rate [Срок оценки: 6 months after treatment initiation]
- Overall survival [Срок оценки: Up to 2 years after randomization]
- Event-free survival [Срок оценки: Up to 2 years after randomization]
- Grade 3-5 toxicities [Срок оценки: 6 months after treatment initiation]
- Unplanned hospitalizations [Срок оценки: 6 months after treatment initiation]
- Activities of Daily Living (ADL) [Срок оценки: Collected baseline, start of cycle 2 or consolidation (28 day cycle), day 90]
- Instrumental Activities of Daily Living (IADL) [Срок оценки: Collected baseline, start of cycle 2 or consolidation (28 day cycle), day 90]
- Fall History [Срок оценки: Collected baseline, start of cycle 2 or consolidation (28 day cycle), day 90]
- Short Physical Performance Battery (SPPB) [Срок оценки: Collected baseline, start of cycle 2 or consolidation (28 day cycle), day 90]
- Montreal Cognitive Assessment (MoCA) [Срок оценки: Collected baseline, start of cycle 2 or consolidation (28 day cycle), day 90]
- Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety [Срок оценки: Collected baseline, start of cycle 2 or consolidation (28 day cycle), day 90]
Критерии участия
Критерии включения
- Age 60 and above
- A diagnosis of de novo, secondary or treatment-related acute myeloid leukemia (AML), other AML equivalent such as myeloid sarcoma, myelodysplastic syndrome in transformation to AML
- AML diagnosis can be based on the World Health Organization (WHO) 2022 criteria or International Consensus Classification (ICC) 2022 criteria
- The use of hydroxyurea, cytarabine (up to 1 gm total dose), or leukapheresis for cytoreduction is allowed
- Patients with brief exposure to all-trans retinoic acid (ATRA), arsenic trioxide (ATO) or similar product for suspected acute promyelocytic leukemia (APL), who later turn out not to have APL, are eligible
- The use of other cancer-directed treatments (e.g., hormonal treatment, targeted treatment, immunotherapy, radiation) other than chemotherapy for other concurrent malignancies is allowed
- Able to provide informed consent
Критерии исключения
- Acute promyelocytic leukemia
- Unwilling to complete study procedures
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
- Открытое
- Основная цель
- Лечение
Центры проведения
США · 1 центр
- University of Rochester Medicine — Rochester
Публикации
- Bhatt VR, Wichman CS, Koll TT, Fisher AL, Wildes TM, Haddadin M, Berger AM, Armitage JO, Holstein SA, Maness LJ, Gundabolu K. A Phase II Trial of Geriatric Assessment-Guided Selection of Treatment Intensity in Older Adults With AML. Am J Hematol. 2025 Jul;100(7):1163-1172. doi: 10.1002/ajh.27694. Epub 2025 Apr 29. PMID 40298352
Идентификаторы
NCT: NCT07735208 · UMLEU26044