 |
 |
Abstract:
ASN Annual Meeting 2020 -- Digital Meeting
|
Hogan J, Diva U, Murphy E, et al.
Complete Remission of Proteinuria in Patients with Focal Segmental
Glomerulosclerosis Treated with Sparsentan, a Dual Endothelin and
Angiotensin Receptor Antagonist, in the DUET Trial
ASN Annual Meeting 2020 -- Digital Meeting
J Am Soc Nephrol
(Oct) 31:55A 2020

BACKGROUNDIn FSGS, partial remission (FSGS partial remission
endpoint [FPRE]: 40% proteinuria reduction and urine protein/creatinine ratio
(UP/C) <1.5 g/g) and complete remission (CR) of proteinuria are strong
predictors of kidney survival. In the DUET trial, sparsentan (SPAR) resulted
in greater reductions in proteinuria and a higher rate of FPRE vs irbesartan
(IRB) over the 8-week double-blind (DB) period. This antiproteinuric effect
of SPAR was sustained during the open-label extension (OLE) period of DUET.
Here we analyze patients who achieved CR (UP/C <0.3 g/g) in
DUET. METHODSDUET randomized patients age 8-75 years with
biopsy-proven FSGS, UP/C>1 g/g, and eGFR>30 mL/min to SPAR or IRB for 8
weeks, followed by OLE with all patients receiving SPAR. UP/C and other
parameters were measured every 12 weeks during OLE. This post-hoc analysis
included all patients on SPAR treatment regardless of original
randomization. RESULTSMedian follow-up on SPAR was 42.5
months. Of 108 subjects dosed with SPAR, 44 (41%) reached CR at least once
and 30 (28%) patients reached CR in ≥2 visits (68% of CR patients). CR was
achieved by 28 patients within the 1st year on SPAR (Kaplan-Meier estimate:
29%). A history of, or nephrotic syndrome at baseline, was documented in 8
(18%) of CR patients. Of subjects with CR, 14%, 41%, and 45% were originally
assigned to 200, 400, and 800 mg/day of SPAR dose cohorts, respectively. No
patient achieved CR while on IRB during the DB period. Compared to the
overall DUET population, CR patients had similar age, sex, and baseline eGFR,
but lower baseline mean UP/C (1.67 g/g vs 2.65 g/g), and higher proportion of
baseline immunosuppression (45% vs 35%), in particular with mycophenolate
mofetil (18% vs 12%). Achieving CR was associated with better preservation of
kidney function compared to not achieving CR. In 6 patients (14%), occurrence
of CR followed the initiation of new steroid
treatment. CONCLUSIONIn the DUET trial, a high proportion of
patients achieved CR on at least one occasion. These observations support the
long-term nephroprotective potential of SPAR in FSGS. 
c Copyright 2020 -2021 American Society of Nephrology.
Reproduced with permission. All ASN abstracts from the 2020 Annual
Meeting are available at this
link and also are archived in .pdf form at ASN-Online.org
Disclaimer: Abstracts often have errors, both
typographical and otherwise. This posting is an electronic translation of
submitted abstracts which has not been verified against the original
submitted abstract nor with the authors for accuracy. As a result, there
may be errors, especially with regard to drug doses, but not limited to
these. Abstracts undergo only limited review, and data often are changed
as a result of the peer review process, so their reliability is less than
manuscripts published in peer-reviewed journals. In using these
summaries, you are agreeing that you are aware of these limitations.
The materials are provided on an as-is basis without any warranty of
any kind, either express or implied. In addition to errors, the
information presented may be incomplete or outdated.
The information contained is not intended nor recommended as a substitute
for professional medical advice. You are advised to check the appropriate
medical literature and the product information currently provided by the
manufacturer of each device to be used or drug to be administered to
verify the dosage, the method and duration of administration, or
contraindications. It is the responsibility of the treating physician or
other health care professional, relying on independent experience and
knowledge of the patient, to determine drug, disease, and the best
treatment for the patient.
To the fullest extent permitted by law, HDCN, ASN and their affiliates and
suppliers disclaim all
warranties, express or implied, including, but not limited to, any
warranty of merchantability, non- infringement or fitness for a
particular purpose.
In no event shall HDCN, ASN, or their affiliates or suppliers be
liable for any damages whatsoever (including, but not limited to,
direct, indirect, incidental, consequential, punitive or exemplary
damages, or any damages for loss of profits, use, data, goodwill or
other intangibles) arising from or in any way relating to these terms,
the materials, or any information, goods or services obtained from or
referred to in the materials, whether based on warranty, contract, tort
(including, but not limited to, negligence), or any other legal theory,
and whether or not any or all of the limited entities is advised of the
possibility of such damages.
|
Related Folders: |
 |
|
|
|
|