SINGAPORE, March 17,
2025 /PRNewswire/ -- HistoIndex, a global leader in
stain-free digital pathology solutions for managing fibrotic
diseases, has announced the launch of their first Laboratory
Developed Test (LDT) FibroSIGHT™ – now available in the United States. This marks a significant milestone
for HistoIndex as the company enters clinical care for
patients with Metabolic Dysfunction-Associated Steatohepatitis
(MASH). "I am excited to see how our core expertise in clinical
trial assessments is now transcending into the realm of precise and
personalized patient care," said
Dr. Gideon Ho, Chief Executive
Officer of HistoIndex." With FibroSIGHT, we aim to empower
clinicians with a more definitive and accurate assessment of liver
fibrosis."
MASH has long been a challenging and progressive liver disease,
characterized by fat build-up and inflammation that, if left
untreated, leads to fibrosis and, ultimately, cirrhosis. After
decades of research and therapeutic development, the field reached
a pivotal moment in 2024 with the approval of Rezdiffra®
- the first drug for the treatment of MASH with moderate to
advanced fibrosis[1,2*]. As treatment options
expand, accurate fibrosis assessment becomes even more critical in
guiding clinical decisions and optimizing patient outcomes.
HistoIndex has been playing a key role in the development of MASH
treatments and is now leading the way in this next phase of patient
care with FibroSIGHT.
FibroSIGHT seamlessly integrates into routine clinical
workflows, leveraging on HistoIndex's proprietary stain-free
imaging technology to enhance the sensitivity of fibrillar
collagens detection — key in evaluating fibrosis severity in liver
biopsy samples (see Figure 1). By eliminating variability
associated with traditional staining techniques, FibroSIGHT
delivers reliable and precise fibrosis assessment for MASH
patients.
Clinicians can now order FibroSIGHT for MASH patients, on whom
liver biopsies were performed, whenever definitive and accurate
assessments of fibrosis are needed[2,3]. This includes use at the time
of diagnosis to determine treatment decisions, when non-invasive
assessments of degree of fibrosis are either inconclusive or
discordant. Additionally, FibroSIGHT can be ordered post treatment
to evaluate patients' response, especially in cases where there are
no apparent improvement.
"By providing more accurate and objective evaluation of
fibrosis, FibroSIGHT will enable more personalized treatment
strategies and better evaluations of effectiveness of treatment
leading to overall better care for patients," commented Dr Naim Alkhouri, MD,
Chief Medical Officer of Arizona Liver Health. "Where biopsy
evaluation is needed for a MASH patient, I can see incorporating
FibroSIGHT in the workup, and in doing so, benefiting the entire
MASH clinical care community."
FibroSIGHT testing is
performed in HistoIndex's CAP/CLIA accredited laboratory in
Irvine, California. With the
launch of FibroSIGHT, HistoIndex reaffirms its long-standing
commitment in advancing fibrosis assessment and personalized
treatment for MASH. By bridging research with clinical care,
FibroSIGHT empowers informed treatment decisions, driving better
patient care in the evolving landscape of liver disease
management.
About MASH
Metabolic dysfunction-associated steatohepatitis (MASH) is a
progressive form of Metabolic dysfunction-associated steatotic
liver disease (MASLD) characterized by steatosis and inflammation,
which can lead to fibrosis (scarring), cirrhosis, liver failure,
and an increased risk of liver cancer. The presence of ballooned
hepatocytes (enlarged and damaged liver cells) is a key feature
distinguishing MASH from simple steatosis. Pathologist assessments
of liver biopsy remain the gold standard for diagnosing and
assessing the severity of MASH. Histological categorial scoring
systems are often used as surrogate endpoints to evaluate drug
efficacy in clinical trials. These endpoints are limited in
capturing the complex and heterogeneous nature of the disease. As a
result, there is a growing need for more accurate and reliable
tools, such as AI-based digital pathology solutions, to improve the
assessment of treatment response and disease severity in MASH.
About HistoIndex
Founded in 2010, HistoIndex pioneers in stain-free, fully
automated imaging solutions for visualizing and quantifying
fibrosis in biological tissues. By combining cutting-edge
biophotonic technology with AI-based analysis, HistoIndex provides
innovative tools to improve the assessment of fibrosis changes and
drug efficacy. HistoIndex's breakthrough digital pathology
solutions are currently used in accelerating clinical research,
expediting pharmaceutical drug development, and transforming
medical standards.
References:
|
1. U.S. Food and Drug
Administration. (2024, Mar 14).
https://www.fda.gov/news-events/press-announcements/fda-approves-first-treatment-patients-liver-scarring-due-fatty-liver-disease
|
2. Noureddin et al.
(2024). Clin Gastroenterol Hepatol, 22(12), 2367-2377. (*consistent
with stages F2 to F3 fibrosis, also referred to in the literature
as "MASH with significant fibrosis," "MASH and moderate fibrosis,"
or "at-risk MASH.")
|
3. EASL; EASD; EASO
(2024). J Hepatol. 81(3):492-542.
|
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SOURCE Histoindex Pte. Ltd.