EBUS-TBNA vs Transbronchial Mediastinal Cryobiopsy for Adequacy of Next Generation Sequencing

Официальное название

A Multicenter Randomized Trial of EBUS-TBNA Versus Transbronchial Mediastinal Cryobiopsy for Adequacy of Next Generation Sequencing

Обзор

This is a multi-center clinical trial evaluating the effect of transbronchial mediastinal cryobiopsy for its ability to improve the likelihood of obtaining tissue sufficient for molecular analysis. Patients in outpatient clinics or pre-operative holding areas planning to undergo a bronchoscopic biopsy of a suspected malignant lesion (peripheral or mediastinal) for initial diagnosis, staging, or tissue acquisition for molecular analysis will be considered for enrollment and consented. Patients will only be enrolled if intraoperative ROSE suggests malignancy. Patients will be randomized to continue with the operator's initial EBUS-TBNA needle or switch to a cryoprobe to perform a sampling.

Подробное описание

Primary Objective:

\- To evaluate the utility of transbronchial mediastinal cryobiopsy on its ability to improve the likelihood of acquiring tissue sufficient for next-generation sequencing (NGS).

Safety Endpoints:

* Pneumothorax within 7 days of procedure * Moderate bleeding defined as controlled with bronchoscope, saline, or epinephrine * Serious bleeding is defined as uncontrolled, leading to respiratory failure, need for transfusion, or cardiovascular instability * Respiratory failure is defined as a new oxygen requirement or escalation in oxygen delivery within 7 days of procedure * Unplanned hospitalization related to the procedure within 7 days of procedure * Death

Exploratory Endpoints:

* The proportion of samples adequate for NGS testing * The proportion of samples with adequate PD-1 / PD-L1 immunohistochemical staining * Proportion of samples that are adequate for complete NGS library sequencing * Estimated total number of tumor cells per H\&E-stained slide * Histological disease subtyping

Вмешательства

• Процедура Endobronchial ultrasound with transbronchial needle aspiration
  Participants will undergo Endobronchial ultrasound with transbronchial needle aspiration
• Процедура Bronchoscopy
  Participants will undergo Bronchoscopy
• Процедура Cryobiopsy
  Participants will undergo Cryobiopsy

Первичные конечные точки

• Proportion of samples sufficient for next-generation sequencing testing [Срок оценки: Up to 12 months]

Вторичные конечные точки (4)

• Proportion of samples with adequate PD-1 / PD-L1 immunohistochemical staining [Срок оценки: Up to 12 months]
• Proportion of samples that are adequate for complete NGS library sequencing [Срок оценки: Up to 12 months]
• Estimated total number of tumor cells per H&E-stained slide [Срок оценки: Up to 12 Months]
• Histological disease subtyping [Срок оценки: Up to 12 Months]

Критерии участия

Критерии включения

• Lesions on PET or CT concerning for primary or metastatic malignancy that are amenable to biopsy by linear EBUS
• Malignant cells present on rapid on-site cytological evaluation (ROSE)

Критерии исключения

• Patient is known to be less than 18 years old
• Patient is known to be pregnant
• Patient is known to be a prisoner
• Operator deems lesion is not safe to biopsy

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

Диагностика

Центры проведения

США · 1 центр

• Vanderbilt University/Ingram Cancer Center — Nashville

Идентификаторы

NCT: NCT06105801 · VICC-VDTHO23177 · NCI-2023-08954

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗