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Feasibility Study on the Contribution of Guided Puncture With Echoendoscopy (APOGEE)

Primary Purpose

Hypermetabolic Lymphadenopathy Mediastinum Lower, Posterior and Middle, Detected by PET-CT With 18F-FDG (PET)

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Guided punction of mediastinal lymphadenopathy by echoendoscopy
PET scan
Sponsored by
Institut Bergonié
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Hypermetabolic Lymphadenopathy Mediastinum Lower, Posterior and Middle, Detected by PET-CT With 18F-FDG (PET) focused on measuring Mediastinal lymphadenopathy, PET CT to 18FDG, EUS

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Any patients who have had PET showing one or more hypermetabolic lymphadenopathy in middle mediastinum and/or lower and/or posterior, and requiring diagnostic certainty for support.
  2. PET scans performed in these particulars :

    • Pre-treatment assessment of thoracic or extra-thoracic malignancies (patients without a history of cancer).
    • Evaluation of response to treatment referred to oncological.
    • Suspicion of relapse in patients with a personal history of thoracic or extra-thoracic malignancies.
  3. PET, the result is positive :

    • For above-centimeter lymph node short axis: greater result than or equal to the background hepatic noise.
    • For sub-centimeter lymph node small axis : greater result than the background hepatic noise
  4. Patient with indication of diagnostic procedure surgically (whether realized or not)
  5. Lymph node(s) available(s) puncture by EUS esophageal, so for a technically feasible for esophageal puncture (without vascular recusants structures)
  6. Age ≥ 18 years.
  7. PET scan performed within 6 weeks before EUS
  8. Platelets ≥ 70 000/mm3; TP ≥ 60%.
  9. Patient of childbearing age with negative pregnancy test and / or a contraception.
  10. Patient gave informed consent signed.
  11. Patient affiliated to a social security scheme.

Exclusion Criteria:

  • Contra-indication (s) Director (s) to achieve a EUS.
  • Balance adverse anesthetic (not allowing a general anesthetic).
  • Esophageal stenosis.
  • Coagulation disorders.
  • Pregnant or lactating women.
  • Unable to undergo medical monitoring test for geographical, social or psychological reasons.
  • Private patient freedom and major subject of a measure of legal protection or unable to consent.

Sites / Locations

  • Insitut Bergonie

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

hypermetabolic mediastinal lymph nodes in PET,

Arm Description

hypermetabolic mediastinal lymph nodes in PET,in a context of New cancer or cancer recurrence.

Outcomes

Primary Outcome Measures

Sensitivity of Endoscopic Ultrasound-guided (EUS-guided) Puncture
The performance of EUS-guided biopsy has been evaluated in terms of sensitivity. EUS-guided was performed after detection of lymph nodes with positron emission tomography (PET). In most cases, only one lymph node is taken and performance analysis will be done by patient and not by injury. PET, the reference technique (gold standard), is followed for 12 months. Sensitivity is the rate of subjects with a diagnosis of malignancy (excluding the results atypical / suspicious or non-contributory) according the results of EUS among all subjects with a neoplastic disease by the gold reference. To sum up , the sensitivity corresponds to the rate of patients detected as "malignant" with the new technique (EUS-guided), among the patients detected as "malignant" at the reference PET examination (12 months assessment).

Secondary Outcome Measures

Negative Predictive Value
The negative predictive value of EUS-guided biopsy has been evaluated by the rate of subjects with a diagnosis of benign pathology according the gold standard (PET) among all subjects for wich EUS reveal a benign pathology (excluding atypical/suspects findings or non contributory)
Matching Between Therapeutic Strategies RCP1/RCP2
Impact of the management of patient : Concordance between therapeutic strategies before the results of the endoscopy (Multidisciplinary consultation meeting 1 (RCP1) in absence of documentation) and after the results of endoscopy (Multidisciplinary consultation meeting 2 (RCP2) post-documentation) for the eligible and evaluable population
Clinical Utility (Avoid More Invasive Procedure)
The clinical utility of puncture under echo-endoscopy puncture has been considered to have a clinical utility, if it allows the patient to avoid more invasive diagnostic procedures (mediastinoscopy or thoracoscopy) or if it allows the patient to benefit from appropriate treatment (result of the malignant biopsy) or to avoid receiving unjustified treatment (result of the benign biopsy): case of patients well classified as malignant/benign by puncture under echo-endoscopy. The puncture will be considered to have no clinical utility if the result of the puncture under echo-endoscopy is invalidated by the reference examination, or if the result of the puncture does not allow a diagnosis to be made.

Full Information

First Posted
June 26, 2013
Last Updated
April 26, 2021
Sponsor
Institut Bergonié
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1. Study Identification

Unique Protocol Identification Number
NCT01892501
Brief Title
Feasibility Study on the Contribution of Guided Puncture With Echoendoscopy
Acronym
APOGEE
Official Title
Feasibility Study on the Contribution of Guided Puncture With Echoendoscopy in Evaluation of Hypermetabolic Lymphadenopathy Mediastinum Lower, Rear and Middle, Detected in PET-CT to 18 FDG (PET)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
January 8, 2013 (Actual)
Primary Completion Date
October 10, 2019 (Actual)
Study Completion Date
October 10, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Bergonié

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Impact of screening nodes mediastinal by PET, at different times of the management of cancer disease, remain unclear. Benefits of combined PET and puncture with echoendoscopy for the diagnosis subsequent therapeutic management should be evaluated in these different contexts. We would like to demonstrate the clinical utility of this association to replace more invasive diagnostic procedures and to assess the impact of the puncture on a possible modification of the therapeutic management. It is a single center prospective diagnostic assessment
Detailed Description
Main objective : Assess the performance (in terms of sensitivity) of guided punction by echoendoscopy in the characterization of hypermetabolic mediastinal lymph nodes in PET, in a context of New cancer or cancer recurrence. Conduct of the study : When a patient has had a PET scan showing a hypermetabolic or mediastinal lymph nodes in the lower, middle or posterior, his case is presented in a multidisciplinary meeting (PCR # 1), with definition of diagnostic strategy: Approved indication is achieve a biopsy surgically to have a histological documentation of mediastinal lymph nodes with obvious impact on treatment decisions. We distinguish two groups of patients based on the feasibility of the surgical procedure: Group A biopsy is surgically feasible Group B: biopsy by surgery can not be performed (against medical contraindications or anesthetics) at that moment, definition of therapeutic strategy that was decided in the absence of histological documentation: Surgery outset Chemotherapy or other oncological treatment Supports non-oncological if benign disease suspected No treatment. EUS is performed by oesophageal for two patient groups for the two groups of patients (within a maximum period of six weeks after the PET scan), under general anesthesia and endoscopic control. According the pathological findings, the therapeutic strategy is defined in a second PCR (PCR # 2), to assess the impact of the puncture: Surgery outset Chemotherapy or other oncological treatment Supports non-oncological when benign pathology documented No treatment Selecting another surgical diagnostic procedure (non-contributory income). A patient monitoring will be conducted for 12 months. The clinical and radiological data carried over the standard of care of the patient will be collected. Achieving a thoracoabdominopelvic scanner (TAP) at 1 year to characterize the evolution of the disease marks the end of the study for the patient. For the patients who have had a negative biopsy, monitoring will involve a scanner TAP 6 month and 12 month then consultation with the oncologist.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypermetabolic Lymphadenopathy Mediastinum Lower, Posterior and Middle, Detected by PET-CT With 18F-FDG (PET)
Keywords
Mediastinal lymphadenopathy, PET CT to 18FDG, EUS

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
hypermetabolic mediastinal lymph nodes in PET,
Arm Type
Other
Arm Description
hypermetabolic mediastinal lymph nodes in PET,in a context of New cancer or cancer recurrence.
Intervention Type
Procedure
Intervention Name(s)
Guided punction of mediastinal lymphadenopathy by echoendoscopy
Intervention Description
EUS (by oesophageal) is performed within a maximum period of six weeks after the PET scan, under general anesthesia and endoscopic control, with a disposable 19-gauge needle (EchoTip, Cook Endoscopy) and 3 passes of the needle ganglion. Pathological samples are taken : 3 tubes collected by node (one tube per needle pass), in most cases, only one node will be taken.
Intervention Type
Device
Intervention Name(s)
PET scan
Intervention Description
The benefits of combined PET and punction EUS for the diagnosis and subsequent therapeutic management should be evaluated in these different contexts
Primary Outcome Measure Information:
Title
Sensitivity of Endoscopic Ultrasound-guided (EUS-guided) Puncture
Description
The performance of EUS-guided biopsy has been evaluated in terms of sensitivity. EUS-guided was performed after detection of lymph nodes with positron emission tomography (PET). In most cases, only one lymph node is taken and performance analysis will be done by patient and not by injury. PET, the reference technique (gold standard), is followed for 12 months. Sensitivity is the rate of subjects with a diagnosis of malignancy (excluding the results atypical / suspicious or non-contributory) according the results of EUS among all subjects with a neoplastic disease by the gold reference. To sum up , the sensitivity corresponds to the rate of patients detected as "malignant" with the new technique (EUS-guided), among the patients detected as "malignant" at the reference PET examination (12 months assessment).
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Negative Predictive Value
Description
The negative predictive value of EUS-guided biopsy has been evaluated by the rate of subjects with a diagnosis of benign pathology according the gold standard (PET) among all subjects for wich EUS reveal a benign pathology (excluding atypical/suspects findings or non contributory)
Time Frame
12 months
Title
Matching Between Therapeutic Strategies RCP1/RCP2
Description
Impact of the management of patient : Concordance between therapeutic strategies before the results of the endoscopy (Multidisciplinary consultation meeting 1 (RCP1) in absence of documentation) and after the results of endoscopy (Multidisciplinary consultation meeting 2 (RCP2) post-documentation) for the eligible and evaluable population
Time Frame
12 months
Title
Clinical Utility (Avoid More Invasive Procedure)
Description
The clinical utility of puncture under echo-endoscopy puncture has been considered to have a clinical utility, if it allows the patient to avoid more invasive diagnostic procedures (mediastinoscopy or thoracoscopy) or if it allows the patient to benefit from appropriate treatment (result of the malignant biopsy) or to avoid receiving unjustified treatment (result of the benign biopsy): case of patients well classified as malignant/benign by puncture under echo-endoscopy. The puncture will be considered to have no clinical utility if the result of the puncture under echo-endoscopy is invalidated by the reference examination, or if the result of the puncture does not allow a diagnosis to be made.
Time Frame
12 months
Other Pre-specified Outcome Measures:
Title
Side Effects - Number of Adverse Event Declared According to DINDO Classification
Description
In all cases the side effects associated with the implementation of the guided puncture EUS has been collected and classified according to the classification of surgical complications of Clavien-Dindo [P Clavien and al. Ann Surg 2009, 250: 187-96]. Classification of surgical complications of Clavien-Dindo ranges from grade 1 (any deviation from the normal postoperative course) to grade 5 (death of patient)
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Any patients who have had PET showing one or more hypermetabolic lymphadenopathy in middle mediastinum and/or lower and/or posterior, and requiring diagnostic certainty for support. PET scans performed in these particulars : Pre-treatment assessment of thoracic or extra-thoracic malignancies (patients without a history of cancer). Evaluation of response to treatment referred to oncological. Suspicion of relapse in patients with a personal history of thoracic or extra-thoracic malignancies. PET, the result is positive : For above-centimeter lymph node short axis: greater result than or equal to the background hepatic noise. For sub-centimeter lymph node small axis : greater result than the background hepatic noise Patient with indication of diagnostic procedure surgically (whether realized or not) Lymph node(s) available(s) puncture by EUS esophageal, so for a technically feasible for esophageal puncture (without vascular recusants structures) Age ≥ 18 years. PET scan performed within 6 weeks before EUS Platelets ≥ 70 000/mm3; TP ≥ 60%. Patient of childbearing age with negative pregnancy test and / or a contraception. Patient gave informed consent signed. Patient affiliated to a social security scheme. Exclusion Criteria: Contra-indication (s) Director (s) to achieve a EUS. Balance adverse anesthetic (not allowing a general anesthetic). Esophageal stenosis. Coagulation disorders. Pregnant or lactating women. Unable to undergo medical monitoring test for geographical, social or psychological reasons. Private patient freedom and major subject of a measure of legal protection or unable to consent.
Facility Information:
Facility Name
Insitut Bergonie
City
Bordeaux
State/Province
Grionde
ZIP/Postal Code
33076
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
35341993
Citation
Bechade D, Bellera C, Gauquelin L, Soubeyran I, McKelvie-Sebileau P, Debled M, Chomy F, Roubaud G, Fonck M, Pernot S, Roch A, Cazeau AL. Diagnostic accuracy and clinical impact of endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) in Positron Emission Tomography - Computed Tomography (PET-CT)-positive mediastinal lymphadenopathies in patients with thoracic or extra-thoracic malignancies. Clin Res Hepatol Gastroenterol. 2022 May;46(5):101912. doi: 10.1016/j.clinre.2022.101912. Epub 2022 Mar 25.
Results Reference
derived
Links:
URL
https://www.e-cancer.fr/Professionnels-de-sante/Le-registre-des-essais-cliniques/Le-registre-des-essais-cliniques
Description
National Cancer Institut
URL
https://www.bergonie.fr/essais_cliniques/
Description
Official site Bergonie

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Feasibility Study on the Contribution of Guided Puncture With Echoendoscopy

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