Haematopoietic Stem Cell Transplantation Clinical Trial
Official title:
Diagnosis of Acute Gastrointestinal Graft-versus-Host Disease by Early Endomicroscopic Features of the Small Intestine
Early diagnosis of acute Gastrointestinal Graft-versus-Host disease (aGI-GvHD) has a strong impact on morbidity and mortality of patients who underwent haematopoietic stem cell transplantation (HSCT). Recent results at the investigators department showed that mucosal biopsies from the small intestine have a high diagnostic yield for aGI-GvHD specific changes. By performing an enteroscopic examination, aGI-GvHD suspected patients can be prevented from colonoscopy and prior bowel preparation which is clinically important, considering the rather bad general condition of this patient group. To further reduce invasive procedures the investigators want to evaluate the in vivo histological features of aGI-GvHD in the small bowel. Therefore aGI-GvHD suspected patients will undergo confocal laser endomicroscopy of the upper GI-tract, including duodenum and jejunum, in the context of a prospective clinical pilot trial. The histological evaluation of biopsy samples taken from these sites will be used as comparable gold standard. Endomicroscopic aspects of patients with celiac disease, infectious enteritis, inflammatory bowel disease and healthy subjects should serve as controls. If it is possible to diagnose aGI-GvHD from endomicroscopic features of the small bowel alone, this could be another important step to improve the diagnostic management of post HSCT patients, especially when taking of biopsy samples is difficult because of a bad coagulation status. Additionally, an accurate diagnosis in vivo could lead to immediate treatment to prevent progression and site spreading of the disease.
Graft-versus-host disease (GvHD) represents a major cause for morbidity and mortality in
patients who underwent haematopoietic stem cell transplantation (HSCT) [1]. In the
gastrointestinal tract as one of the main target organs of GvHD diagnosis may be difficult
because of many similar presenting differential diagnoses, most notable, infections by
cytomegalovirus [2]. Experts disagree about the best diagnostic approach for patients
suspected of acute gastrointestinal GvHD (aGI-GvHD). There have been many studies supporting
the endoscopic evaluation of either the lower [3, 4, 5], the upper [6, 7] or both parts of
the GI-tract [8, 9]. In either case, the histological evaluation of biopsy samples serves as
standard tool to establish the final diagnosis [10].
Considering the rather bad general condition of patients after HSCT as a limiting factor for
endoscopic and histological evaluation, some new approaches have been introduced into the
diagnostic manual of aGI-GvHD in order to reduce the amount of invasive examinations.
Conventional imaging techniques like magnetic resonance imaging [11], computer tomography
[12] and high-resolution ultrasonography with Doppler Imaging [13] reported bowel wall
thickening in GvHD patients. But as such findings are only unspecific signs of
gastrointestinal pathology, conventional imaging techniques cannot replace endoscopy with
biopsies [14]. The same holds for video capsule endoscopy which was indeed found to have a
high negative predictive value for the detection of aGI-GvHD, but shares the important
shortcoming of missing biopsy samples for histological evaluation [15, 16, 17].
At least this method shifted the focus of interest onto the small bowel. Biopsies deriving
from this former neglected GI part had shown a high sensitivity for GvHD-related changes in
previous studies [18]. As similar results were seen at the study site, the investigators
prospectively compared enteroscopy with biopsies to the present gold standard in the
diagnostic aGI-GvHD management, colonoscopy with biopsies. In the context of this
investigation the large intestine showed much stronger affection by aGI-GvHD than all other
locations, although there was no pair of examinations, in which colonoscopy revealed
aGI-GvHD without the presence of such findings at enteroscopy. Quite the opposite,
enteroscopy even revealed GvHD related pathologies in one case where the respective
colonoscopy remained inconspicuous. Consequently, they postulated that enteroscopic findings
may replace the need for colonoscopy [19], wherefore post-HSCT patients could remain without
stressful bowel preparation, often limited by their rather bad general condition.
One of the latest developments in the endoscopic management of the gastrointestinal tract is
the so called confocal laser endomicroscope (CLE). Confocal microscopy was developed by
Marvin Minsky in the late 1950s. Its principle is the microscopic scanning of focal points
below the surface of an object. In comparison to conventional light microscopy it uses a
special filter system to avoid image overlapping by surrounding tissue. In detail, a light
source (normally a laser) is focused by a microscope objective lens to a diffraction limited
spot on or inside the object. Light that is scattered, or fluorescence excited (achieved
through fluorescein staining, for example) and emitted, at the focus in the sample will
partially return back through the optics along the path from which it arrived. A
beam-splitter placed into the path reflects the return light towards a detector. The optics
will focus the light from the focal point in the specimen to its conjugate focus near the
detector (hence the technology is termed "con-focal"). Here a spatial filter ("pinhole") is
used to extinguish all light deriving from areas outside the focal point. Light reflections
from the focal point itself will be forwarded to the detector which is connected to a
computer system that digitalises the optical signal and creates the in vivo histological
image [20].
Focusing on its clinical impact, confocal microscopy is the first technique to allow in vivo
evaluation of tissue structures beneath their surface. Because of many breakthroughs in
miniaturisation (mostly in the 1990s) this technology could be applied for intraluminal use
in gastroenterology, integrated into a otherwise standard endoscope. It allows the in vivo
histological visualisation of the upper 250 micrometers of all walls within the
gastrointestinal tract, additionally to the normal function of white light endoscopy
(provided by two separate screens on top of the workstation) [20].
The first clinical use of CLE in a prospective pilot trial including 35 patients after HSCT
was reported by Bojarski et al. in 2009. CLE of the colonic mucosa could predict the
positive diagnosis of aGI-GvHD in 14 of 19 patients, later confirmed by histological
evaluation. The in vivo findings of aGI-GvHD, varying from single crypt apoptosis to
complete crypt loss, were clearly distinguishable from pathologies of other origin like
infectious colitis or ulcerative colitis, both used as comparative control [21].
Study Aims
In this clinical investigation the investigators intend to continue the diagnostic approach
for acute Gastrointestinal Graft-versus-Host Disease (aGI-GvHD). Based on the recent results
at the study institution (explained above, [19]) that showed a remarkable diagnostic yield
for aGI-GvHD associated pathologies in the small intestine the investigators intend to
evaluate confocal laser endomicroscopy (CLE) of the small intestine as primary diagnostic
procedure in patients with suspected aGI-GvHD after haematopoietic stem cell transplantation
(HSCT).
- The investigators aim to examine whether early diagnosis of aGI-GvHD in the duodenum
and jejunum can be achieved by evaluating endomicroscopic features.
- In comparison with conventional biopsies from the mentioned GI-parts as gold standard
the investigators want to test whether the markers described by Bojarski et al. for the
colon also hold true for the small intestine.
- Including endomicroscopic results of patients with celiac disease, enteral infections,
inflammatory bowel disease and healthy subjects as controls the investigators aim to
establish aGI-GvHD specific markers that can be used for a "biopsy-free" in vivo
diagnosis of aGI-GvHD.
Study Design
Prospective clinical pilot trial without randomisation or blinding
Study Population
Patients after haematopoietic stem cell transplantation (HSCT) who are referred to the study
site for clarification of one of the following symptoms:
- anorexia
- nausea
- vomiting
- abdominal pain
- diarrhea
- intestinal bleeding
To exclude possible side effects of the conditioning therapy, GI symptoms must have occurred
or persisted 20 days after the respective transplantation date [22].
Exclusion criteria:
- infection with CMV or HSV
- bacterial infection of the GI tract
- medication related symptoms
- patients allergic to one of the drug components (including drugs used for conscious
sedation like propofol or midazolam as well as fluorescein, the fluorescent dye used
for CLE )
- refusal to participate in the study
- patient's age below 18 years.
Methods
This investigation will be performed at the Medical University of Vienna, Department of
Internal Medicine III, Division of Gastroenterology and Hepatology. Patient recruitment will
be achieved in close cooperation with the Department of Internal Medicine I, Division of
Oncology, Bone Marrow Transplantation Unit.
As this study has been planned as a pilot trial, it mainly focuses on the qualitative
endomicroscopic features of the small intestine in GvHD-patients to yield reference
pathologies for accurate diagnosis in the future. Nevertheless, a quantitative analysis will
be performed by comparing CLE-derived diagnoses with histological results to calculate
sensitivity and specificity of CLE-based aGI-GvHD diagnosis in the small intestine.
Considering the current diagnostic yield of 62% for the detection of aGI-GvHD in symptomatic
post-HSCT-patients by conventional histology [19], the investigators estimated to include 40
patients with suspected aGI-GvHD in order to discover a meaningful sample of patients
affected by aGI-GvHD for qualitative and quantitative analysis. In comparison, Bojarski et
al included 35 patients of whom 19 finally turned out to suffer from aGI-GvHD by
conventional histology. They could then calculate a sensitivity of 74% and specificity of
100% for the prediction of the histological diagnosis by CLE [21]. On the basis of the
current frequency of post-HSCT-patients at the study site the investigators estimate to
include the aimed amount of 40 patients within a time period of 2 years.
All patients who fulfill the listed inclusion criteria, will receive the patient information
form of this study together with the usual informed consent form of the respective
endoscopic examination they are about to undergo. Patient information will be done at least
24 hours before the intervention, as practiced at our unit. If the patient agrees to
participate in the study he/she will be prepared for endoscopy by administration of
intravenous propofol and/or midazolam as routinely used for conscious sedation during
endoscopic procedures at our department. Additionally, 5-10 ml of a 10% solution of
fluorescein sodium will be administered intravenously to enhance tissue fluorescence during
endomicroscopy. As so far no specific CLE-enteroscope is available, we will use the
CLE-colonoscope (Pentax EC-3870 CIFK with the ISC-1000 confocal endomicroscopy processor -
Pentax, Tokyo, Japan and Optiscan Pty Ltd, Notting Hill, Victoria, Australia) to reach the
small intestine, comparable to an enteroscopic procedure (oral access).
All drugs will be administered by medical specialists, assistant doctors or registered
nurses, as routinely practiced at our institution.
CLE picture capturing will start at the deepest point reachable in the jejunum. During
withdrawal of the scope CLE pictures will be taken every 10 centimetres in the small bowel,
then from the antrum and body of the stomach and from the esophagus. Furthermore, CLE will
be applied for distinct looking areas, suspicious of pathologic origin. Wherever CLE
pictures are obtained, a conventional biopsy will be taken from the same localisation.
CLE pictures will be captured and stored routinely using our standard data management
system. They will be evaluated immediately after the endoscopic procedure together with a
board certified GI-pathologist, who will establish an initial diagnosis.
Conventional biopsies will be stained with Haematoxylin & Eosin, as well as PAS stain.
In-situ hybridization for CMV and HSV will be performed to exclude viral infection.
Classification of GvHD will be done according to McDonald and Sale in 4 grades,
appropriately modified for the small intestine [23]:
- Grade I: individual cell necrosis
- Grade II: crypt abscess
- Grade III: drop out of one ore more whole crypts in a biopsy
- Grade IV: total denudation of epithelium
Endomicroscopic controls (patients with celiac disease, enteral infections, inflammatory
bowel disease and healthy subjects) will be collected from present data of endomicroscopic
procedures already performed within routine examinations.
At the end of the study all CLE pictures and histological cuts will be evaluated separately
by two blinded board certified pathologists. In case of discordant diagnoses they will
analyse the respective cases together to reach an agreement on the final diagnosis. All
cases where the initial and the final diagnosis are deviating from each other will be
re-evaluated together by all specialists involved.
Risk/Benefit assessment
GvHD represents a major cause of morbidity and mortality after allogeneic HSCT.
Approximately 10-40% of patients who undergo HSCT develop significant GvHD, and about half
of these patients die from this disease or from therapy resulting complications [1].
Endoscopic procedures in patients with suspected aGI-GvHD are well established. Until now
the histological evaluation of GI deriving biopsies is the gold standard tool to set an
accurate aGI-GvHD diagnosis. Endoscopy of the upper GI-tract is more comfortable than the
endoscopic assessment of the lower GI-tract as there is no need for bowel preparation.
Therefore it is the primary technique to assess post HSCT patients at our department.
Supported by recent results at the study institution [19] these upper GI endoscopies are
routinely performed as enteroscopies instead of gastroscopies in order to include the small
intestine in the diagnostic evaluation. The safety of enteroscopy has not been studied
systematically but reported experience is substantial and complications have been rare [24].
Confocal laser endomicroscopy is a safe new technique that has already been studied in
clinical trials [25, 26]. Its safety is being guaranteed by the use of low intensity laser
light that can at worst cause local bleaching of fluorescein containing cells, which is
harmless, reversible and even used as diagnostic sign in experimental conditions [20].
Ethical implications
This study protocol was approved by the ethics commission of the Medical University of
Vienna.
All procedures in the context of this study will be performed in accordance to the
Declaration of Helsinki as well as to the guidelines for Good Scientific Practice (GSP) of
the Medical University of Vienna.
Expected impact and Outlook
If the investigators find aGI-GvHD specific markers that can be used for a "biopsy-free" in
vivo diagnosis of aGI-GvHD this could lead to another reduction of invasive procedures for
patients after HSCT. This would have a big clinical impact, as biopsy assessment is often
limited by the bad coagulation status of this patient group.
In case they cannot clearly determine specific markers of aGI-GvHD, CLE should at least
reduce the amount of conventional biopsies needed for diagnosis by taking them under CLE
guidance.
Despite from the expected reduction of invasive procedures, aGI-GvHD diagnosis in vivo could
lead to immediate initiation of immunosuppressive treatment in order to reduce progression
and site spreading of the disease.
In case the study aims will be supported by the results of this pilot trial, a randomized
controlled trial comparing in vivo diagnosis to conventional histological assessment in
matters of hospitalisation and survival will be performed.
;
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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