Landmark Study Shows CareDx’s HeartCare Outperforms dd-cfDNA Alone in Identifying Rejection and Patients Experienced Excellent Outcomes with Fewer Biopsies
16 Maggio 2024 - 10:05PM
Business Wire
HeartCare Results Effectively Stratified
Patients at Highest Risk for Acute Cellular Rejection
Cardiologists Performed the Fewest Biopsies
After Dual Negative HeartCare Results Compared to Single or Dual
Positive Results
Two-Year Clinical Outcomes Data Demonstrate
Excellent Survival and Allograft Function
CareDx, Inc. (Nasdaq: CDNA) – The Transplant Company™ – a
leading precision medicine company focused on the discovery,
development, and commercialization of clinically differentiated,
high-value healthcare solutions for transplant patients and
caregivers – today announced findings from the SHORE (Surveillance
HeartCare Outcomes Registry) study, one of the largest heart
transplant studies of its kind, published in The Journal of Heart
and Lung Transplantation.
The prospective observational study demonstrates that HeartCare®
which combines AlloSure® Heart donor-derived cell-free DNA
(dd-cfDNA) and AlloMap® Heart gene-expression profiling (GEP),
identifies acute cellular rejection in heart transplant patients
better than dd-cfDNA testing alone and is associated with fewer
biopsies and excellent clinical outcomes.1
Key Findings from the SHORE Study Publication1:
- Dual-positive HeartCare results are associated with the highest
incidence (9.2%) of acute cellular rejection (ACR), whereas
dual-negative HeartCare results are associated with the lowest
incidence (1.5%) of ACR.
- Follow-up endomyocardial biopsies (EMB) are performed at the
lowest rate (8.8%) following a dual-negative HeartCare result, and
at the highest rate (35.4%) following a dual positive HeartCare
result.
- The rate of biopsies performed in response to a single positive
result is 56% lower than dual-positive HeartCare results.
- Clinician behavior to HeartCare results changed over time as
centers gained experience with the testing. By the end of the study
cardiologists performed 10% fewer biopsies in the first year
post-transplant and 40% fewer in the second year post-transplant
despite an increase in follow-up biopsy rates for dual
positives.
- Excellent clinical outcomes were observed in patients managed
with HeartCare including fewer follow-up endomyocardial biopsies,
95% survival and 97% with normal allograft function at two years
post-transplantation.
“This large, prospective, multicenter study demonstrates that
HeartCare significantly improves clinicians’ ability to assess
acute cellular rejection risk and its use is associated with lower
biopsy rates and excellent clinical outcomes two-years
post-transplant,” said John W. Hanna, CareDx President and CEO.
“The SHORE study confirms the superior performance of dual
molecular testing, combining donor-derived cell-free DNA and
gene-expression profiling for acute cellular rejection surveillance
in optimizing care for heart transplant patients. This approach
allows for refined patient selection for surveillance biopsies,
leading to fewer invasive procedures over time while maintaining
vigilant ACR monitoring, and achieving excellent clinical
outcomes,” said Kiran Khush, MD, MAS, Cardiologist, Professor of
Cardiovascular Medicine, Stanford Medicine.
One of the largest heart transplant studies of its kind, SHORE
is a prospective 67-center, observational study of over 2,700 heart
transplant patients in the United States receiving non-invasive
molecular testing with AlloSure Heart dd-cfDNA and AlloMap Heart
GEP or HeartCare. Together, these different molecular tests offer a
more comprehensive evaluation of a patient’s heart transplant
status by assessing both allograft health and immune system
activity. The published study was designed to evaluate the utility
of combined molecular testing using HeartCare for acute cellular
rejection (ACR) surveillance.
To read the publication, go here.
About CareDx – The Transplant Company
CareDx, Inc., headquartered in Brisbane, California, is a
leading precision medicine solutions company focused on the
discovery, development, and commercialization of clinically
differentiated, high-value healthcare solutions for transplant
patients and caregivers. CareDx offers testing services, products,
and digital healthcare solutions along the pre- and post-transplant
patient journey and is the leading provider of genomics-based
information for transplant patients. For more information, please
visit: www.CareDx.com.
Forward-Looking Statements
This press release includes forward-looking statements related
to CareDx, Inc., including statements regarding the potential
benefits and results that may be achieved with HeartCare, which
combines AlloSure Heart donor-derived cell-free DNA (dd-cfDNA) and
AlloMap Heart gene-expression profiling (GEP). These
forward-looking statements are based upon information that is
currently available to CareDx and its current expectations, speak
only as of the date hereof, and are subject to risks and
uncertainties that could cause actual results to differ materially
from those projected, including risks that CareDx does not realize
the expected benefits of HeartCare, which combines AlloSure Heart
donor-derived cell-free DNA (dd-cfDNA) and AlloMap Heart
gene-expression profiling (GEP); risks that the findings in the
SHORE study supporting the data may be inaccurate, general economic
and market factors; and other risks discussed in CareDx’s filings
with the Securities and Exchange Commission (the “SEC”), including,
but not limited to, the Annual Report on Form 10-K for the fiscal
year ended December 31, 2023 filed by CareDx with the SEC on
February 28, 2024, the quarterly report on Form 10-Q for the
quarter ended March 31, 2024 filed by CareDx with the SEC on May 9,
2024 and other reports that CareDx has filed with the SEC. Any of
these may cause CareDx’s actual results, performance, or
achievements to differ materially and adversely from those
anticipated or implied by CareDx’s forward-looking statements.
CareDx expressly disclaims any obligation, except as required by
law, or undertaking to update or revise any such forward-looking
statements.
References:
1. Khush K, Hall S, Kao A, et al. Surveillance with Dual
Non-invasive Testing for Acute Cellular Rejection After Heart
Transplantation: Outcomes from the Surveillance HeartCare Outcomes
Registry (SHORE). The Journal of Heart and Lung Transplantation.
Published online May 15, 2024. DOI:
https://doi.org/10.1016/j.healun.2024.05.003
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version on businesswire.com: https://www.businesswire.com/news/home/20240516103531/en/
CareDx, Inc. Media Relations Anna Czene 818-731-2203
aczene@caredx.com
Investor Relations Greg Chodaczek investor@caredx.com
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