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Идёт набор NCT06151080

Lenalidomide Combined With G-CHOP in the Treatment of Newly Diagnosed DLBCL With FL

Фаза II С лечением DLBCL - Diffuse Large B Cell Lymphoma Follicular Lymphoma

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: Lenalidomide combined with G-CHOP (LO CHOP).
Кому может быть актуально
Состояния в реестре: DLBCL - Diffuse Large B Cell Lymphoma, Follicular Lymphoma. Базовые параметры: 18 лет — 70 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
Китай
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

An Open, Single-arm Clinical Study of Lenalidomide Combined With G-CHOP(LO-CHOP) in the Treatment of Newly Diagnosed Diffuse Large B-cell Lymphoma With Follicular Lymphoma (CDLBCL-FL).

Обзор

To evaluate the efficacy and adverse effects of lenalidomide combined with G-CHOP(LO-CHOP) in the treatment of newly diagnosed diffuse large B-cell lymphoma with follicular lymphoma (CDLBCL-FL).

Подробное описание

This is a Phase 2, open-label clinical trial study that aims to evaluate the efficacy (Complete response, Overall Survival, Progression Free Survival) and adverse effects of lenalidomide combined with G-CHOP(LO-CHOP) in the treatment of newly diagnosed diffuse large B-cell lymphoma with follicular lymphoma (CDLBCL-FL).

Вмешательства

  • Препарат Lenalidomide combined with G-CHOP (LO CHOP)
    Lenalidomide combined with G-CHOP to treat newly diagnosed diffuse large B-cell lymphoma with follicular lymphoma (CDLBCL-FL)

Первичные конечные точки

  • Complete remission rate [Срок оценки: Up to 28 months]
Вторичные конечные точки (2)
  • Progression-free survival [Срок оценки: From the randomization until the first documentation of PD or death whichever occurs first or up to 28 months]
  • Overall survival [Срок оценки: Up to 28 months]

Критерии участия

Критерии включения

  • Age: 18-70 years old, gender is not limited;
  • According to the REAL/WHO classification, the newly diagnosed diffuse large b-cell lymphoma with follicular lymphoma (CDLBCL-FL): the same lymph node specimen showed diffuse large b-cell lymphoma and follicular lymphoma, or the tissue specimen showed diffuse large b-cell lymphoma and indolent lymphoma in bone marrow pathology; or the different group specimens suggested diffuse large b-cell lymphoma and/or follicular lymphoma, respectively, with stage II-IV.
  • Using the Lugano 2014 lymphoma response evaluation criteria, there must be at least one measurable or evaluable lesion: PET/CT can evaluate the lesion, CT or MRI can evaluate the lesion in the node with a diameter greater than 1.5 cm, a short diameter greater than 1.0 cm, or an extranodal lesion with a diameter greater than or equal to 1.0 cm
  • ECOG 0-2
  • Left ventricular ejection fraction (LVEF) was less than 45%
  • HBV-positive serology (occult carriers: anti-HBeAg +, anti-HBsAg-, anti-HBsAg +/-) can only be enrolled if the HBV-dna test is negative.
  • Normal major organ function: liver function: serum bilirubin ≤2.0 × ULN, serum ALT and AST ≤2.5 × ULN, renal function: serum CR ≤2.0 × ULN; (unless caused by lymphoma)
  • Absolute neutrophil count (ANC)≥1.0 × 109 l, platelet count (PLT)≥100 × 109 L, hemoglobin content (HGB)≥80 g L, if myeloma was involved, ANC ≥0.75 × 109 L, platelet count (PLT)≥50 × 109 L, HGB content (HGB) was not required.
  • Life expectancy ≥6 months
  • Informed consent (all studies had to sign a patient's informed consent form)

Критерии исключения

  • DLBCL of primary and secondary centers;
  • HIV-positive patients and/or HCV-active infections (recorded through HCV-RNA-positive testing)
  • Clinically evident secondary cardiovascular diseases such as uncontrollable hypertension (resting diastolic pressure>115 mmHG), uncontrolled arrhythmias, symptomatic angina pectoris, or NYHA III-IV congestive heart failure.
  • Severe chronic obstructive pulmonary disease complicated with hypoxemia.
  • Active bacterial, fungal, and/or viral infections beyond the control of systemic therapy
  • Except for cured skin basal cell carcinoma or cervical carcinoma in situ, or early prostate cancer that does not require systemic treatment or early breast cancer only requires surgery. Other malignant tumors have occurred within the past 3 years or at the same time

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

Китай · 1 центр
  • Bing Xu — Xiamen

Идентификаторы

NCT: NCT06151080 · XMDYYYXYK-01

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗