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Trial Title:
HSI for Intersegmental Plane Identification During Sublobar Pulmonary Resections
NCT ID:
NCT05676788
Condition:
Lung Neoplasm
Pulmonary Metastasis
Conditions: Official terms:
Lung Neoplasms
Conditions: Keywords:
Hyperspectral Imaging
Lung cancer
Segmentectomy
Indocyanine green
Intersegmental plane
Machine learning strategies
Study type:
Interventional
Study phase:
N/A
Overall status:
Not yet recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Primary purpose:
Diagnostic
Masking:
None (Open Label)
Intervention:
Intervention type:
Device
Intervention name:
Hyperspectral Imaging
Description:
Identification of the intersegmental plane
Arm group label:
Intersegmental plane identification by HSI and ICG
Summary:
The purpose of this study is the identification of the intersegmental plane and
navigation during sublobar pulmonary resections in lung cancer using Hyperspectral
Imaging, the comparison with ICG fluorescence intersegmental plane identification, and
the establishment of automatic intersegmental plane navigation using machine learning
strategies for intraoperative navigation.
Detailed description:
Lung cancer is the leading cause of cancer-related death worldwide. Due to the
generalization of screening strategies, especially for risk populations, an increasing
number of lung cancer cases are detected in an early stage. In this regard, lung cancer
is also increasingly diagnosed in patients with impaired pulmonary function. For
preserving lung function and reducing complication incidence, pulmonary segmentectomies
are currently evaluated in this cohort. Thus, the latest version of the German guideline
for the prevention, diagnosis, treatment and follow-up of lung cancer recommends
segmentectomy for patients with impaired pulmonary function in tumor stage I/II. However,
the identification of the intersegmental plane - the key step of segmentectomy - remains
challenging. Inaccurate recognition of the intersegmental plane may lead to dysfunction
of the remaining lung tissue, mismatching of ventilation or blood flow, or long-term air
leakage after surgery, which even requires unplanned secondary surgery. Indocyanine green
(ICG) is one the latest evaluated identification methods and is considered as gold
standard. Hyperspectral Imaging (HSI) - a newly established intraoperative imaging
technique - enables a non-invasive evaluation of tissue perfusion and the discrimination
of pulmonary tissue with different tissue perfusion during segmentectomies.
The purpose of this prospective, single-center, non-inferiority IDEAL Stage 2b study is
the identification of the intersegmental plane and navigation during sublobar pulmonary
resections in lung cancer using Hyperspectral Imaging, the comparison with ICG
fluorescence intersegmental plane identification, and the establishment of automatic
intersegmental plane navigation using machine learning strategies for intraoperative
navigation.
To address this, the intersegmental plane will be detected by both HSI and
ICG-fluorescence during pulmonary segmentectomies and the correspondence of the two
identification methods will be compared with one another. Using machine learning
strategies, the detection of perfused and non-perfused pulmonary tissue and
intersegmental plane will be analyzed. Finally, the investigators will study motion
tracking for the improvement of future HSI illustrations during surgery.
The hypothesis of this study is that HSI could improve the intraoperative navigation
during pulmonary segmentectomies providing as reliable intersegmental plane
identification as the gold standard of indocyanine green fluorescence. In this case, an
intravenous application of fluorescent dye would not be required anymore for the
intersegmental plane identification.
In the case of complex segment resection, a large amount or repeated use of ICG is
necessary due to its short pulmonary circulation time. Multiple use of ICG may result in
ICG entering the target lung tissue through the bronchial circulation and increases the
risk of adverse drug reactions of ICG. In contrast, the advantages of HSI would be a
faster and repetitive measurement during surgery. There will be a potential for reducing
the total measurement time during intersegmental plane dissection (10 seconds vs. 3
minutes / measurement) and consequently patient's burden. In this context, several
studies of HSI-based perfusion measurement during esophageal or colorectal surgery showed
already an improved patients' outcome. Furthermore, HSI can be used for surgery on
patients with hyperthyroidism or impaired renal or hepatic function.
In order to support this hypothesis, a prospective non-inferiority trial design will be
used in this study. To ensure the quality of data acquisition and reporting, the study
will be conducted in accordance with the IDEAL reporting guidelines. During pulmonary
segmentectomies, the intersegmental plane will be identified by both HSI and ICG
fluorescence. The determined HSI intersegmental margin will be benchmarked against the
ground truth ICG fluorescence and the feasibility and reproducibility of HSI and ICG
mapping will be studied.
Machine learning methods have greatly improved the interpretation of subtle patterns in
medical image data. Convolutional neural networks (CNNs) can be considered
state-of-the-art for classification and segmentation of medical images. The investigators
will extend CNN-based methods for HSI classification and particularly study patch-based
differentiation between perfused and non-perfused tissue using ICG and HSI data acquired
at the same position. A further challenge is the relatively slow acquisition of HSI (10
seconds/measurement), which makes it prone to motion artifacts, e.g., due to pulsatile
motion. To address this, the investigators will study motion tracking, which is also
relevant for the future illustration of the segment boundary during surgery.
Machine learning approaches and particularly CNNs allow to directly optimize classifiers
based on actual clinical data and the spectral dimension can be handled in a
straightforward fashion. Moreover, as a versatile method for image processing, CNNs can
also be used for localization and motion compensation during intraoperative imaging,
e.g., they can be trained to detect image features and their motion in red/green/blue
image streams. This is interesting for the proposed HSI data acquisition, which is based
on a sequence of measurements which are sensitive to tissue motion.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
1. Histologically confirmed lung cancer stage I/II or malignancy suspicious nodules
2. Segmentectomy is oncologically indicated or impaired pulmonary and/or cardiac
function prevent anatomical resection
3. Male or female patients aged ≥ 18 years without upper age limit
4. Serum creatinine ≤ 1.5 x upper limit of normal or creatinine clearance (CrCl ≥ 50
mL/min, Cockcroft-Gault formula)
5. Total bilirubin ≤ 1.5 x upper limit of normal (except patients with Gilbert Syndrome
(Morbus Meulengracht) in whom total bilirubin < 3.0 mg/dL is allowed)
6. Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase)/alanine
aminotransferase (ALT) (serum glutamate pyruvate transaminase) ≤ 2.5 x upper limit
of normal
7. Full legal capacity
8. Written informed consent obtained according to international guidelines and local
laws
9. Ability to understand the nature of the trial and the trial related procedures and
to comply with them
Exclusion Criteria:
1. Requirement of a lobectomy or pneumonectomy to achieve complete resection
2. Allergy to indocyanine green or iodine
3. Hyperthyroidism
4. Current or planned pregnancy, nursing period (if defined as requirement of clinical
routine treatment)
5. Medical condition which poses a high risk to undergo surgery as defined by the
investigator
6. Covid19 / SARS-CoV2-infection at time of screening
7. Participation in any other interventional clinical trial within the last 30 days
before the start of this trial
8. Simultaneous participation in other interventional trials which could interfere with
this trial; simultaneous participation in registry and diagnostic trials is allowed
9. Known or persistent abuse of medication, drugs or alcohol
10. Person who is in a relationship of dependence/employment with the coordinating
investigator or the investigator
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
LungenClinic Großhansdorf
Address:
City:
Großhansdorf
Zip:
22927
Country:
Germany
Start date:
April 2023
Completion date:
June 2027
Lead sponsor:
Agency:
LungenClinic Grosshansdorf
Agency class:
Other
Collaborator:
Agency:
Institute of Medical Technology and Intelligent Systems, Hamburg University of Technology, Germany
Agency class:
Other
Source:
LungenClinic Grosshansdorf
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05676788