Groundbreaking Data Demonstrate Superiority of EARLY TAVR in Asymptomatic Severe Aortic Stenosis Patients
Edwards Lifesciences (NYSE: EW) announced groundbreaking results from the EARLY TAVR Trial, demonstrating superior outcomes for asymptomatic severe aortic stenosis patients treated with TAVR compared to clinical surveillance. The trial, involving 901 patients across 75 sites in the US and Canada, showed that 26.8% of TAVR patients experienced death, stroke, or unplanned cardiovascular hospitalization versus 45.3% in the surveillance group over a 3.8-year median follow-up. Early TAVR intervention prevented rapid symptom progression and quality of life decline, with lower stroke rates (4.2% vs 6.7%). Notably, 26.2% of surveillance patients required valve replacement within six months, rising to 47.2% at 12 months.
Edwards Lifesciences (NYSE: EW) ha annunciato risultati innovativi dal Trial EARLY TAVR, dimostrando risultati superiori per i pazienti asintomatici con stenosi aortica severa trattati con TAVR rispetto alla sorveglianza clinica. Lo studio, che ha coinvolto 901 pazienti in 75 sedi negli Stati Uniti e in Canada, ha mostrato che il 26,8% dei pazienti TAVR ha sperimentato morte, ictus o ospedalizzazione cardiovascolare non programmata rispetto al 45,3% nel gruppo di sorveglianza dopo un follow-up mediano di 3,8 anni. L'intervento precoce con TAVR ha prevenuto una rapida progressione dei sintomi e un deterioramento della qualità della vita, con tassi di ictus più bassi (4,2% contro 6,7%). In particolare, il 26,2% dei pazienti in sorveglianza ha richiesto la sostituzione della valvola entro sei mesi, salendo a 47,2% a 12 mesi.
Edwards Lifesciences (NYSE: EW) anunció resultados innovadores del Ensayo EARLY TAVR, demostrando resultados superiores para pacientes asintomáticos con estenosis aórtica severa tratados con TAVR en comparación con la vigilancia clínica. El ensayo, que involucró a 901 pacientes en 75 sitios en EE. UU. y Canadá, mostró que el 26,8% de los pacientes TAVR experimentaron muerte, accidente cerebrovascular o hospitalización cardiovascular no planificada frente a el 45,3% en el grupo de vigilancia durante un seguimiento mediano de 3,8 años. La intervención temprana con TAVR previno la rápida progresión de los síntomas y el deterioro de la calidad de vida, con tasas de accidente cerebrovascular más bajas (4,2% frente a 6,7%). Notablemente, el 26,2% de los pacientes en vigilancia requirieron un reemplazo de válvula dentro de seis meses, aumentando al 47,2% a los 12 meses.
에드워즈 라이프사이언스 (NYSE: EW)는 EARLY TAVR 시험의 혁신적인 결과를 발표하며, TAVR로 치료받은 무증상 심각한 대동맥 협착증 환자가 임상 감시에 비해 우수한 결과를 보였다고 밝혔습니다. 이 시험은 미국과 캐나다의 75개 사이트에서 901명의 환자를 포함했으며, 26.8%의 TAVR 환자가 3.8년의 중간 추적 관찰 기간 동안 사망, 뇌졸중 또는 계획되지 않은 심혈관 입원 경험을 했던 반면, 감시 그룹에서는 45.3%였습니다. 조기 TAVR 중재는 증상의 급격한 진행과 삶의 질 저하를 예방하였으며, 뇌졸중 비율이 낮았습니다 (4.2% 대 6.7%). 특히, 감시 환자의 26.2%가 6개월 이내에 판막 교체가 필요하였고, 12개월에는 47.2%로 증가했습니다.
Edwards Lifesciences (NYSE: EW) a annoncé des résultats révolutionnaires de l'Essai EARLY TAVR, démontrant des résultats supérieurs pour les patients asymptomatiques atteints de sténose aortique sévère traités par TAVR par rapport à la surveillance clinique. L'essai a impliqué 901 patients dans 75 sites aux États-Unis et au Canada, montrant que 26,8% des patients TAVR ont connu décès, AVC ou hospitalisation cardiovasculaire non planifiée contre 45,3% dans le groupe de surveillance sur une période de suivi médiane de 3,8 ans. L'intervention précoce TAVR a empêché une progression rapide des symptômes et une détérioration de la qualité de vie, avec des taux d'AVC plus bas (4,2% contre 6,7%). Notamment, 26,2% des patients sous surveillance ont nécessité un remplacement valvulaire dans les six mois, passant à 47,2% à 12 mois.
Edwards Lifesciences (NYSE: EW) hat bahnbrechende Ergebnisse aus der EARLY TAVR-Studie vorgestellt, die überlegene Ergebnisse für asymptomatische Patienten mit schwerer Aortenstenose zeigen, die mit TAVR behandelt wurden, im Vergleich zur klinischen Überwachung. Die Studie, die 901 Patienten an 75 Standorten in den USA und Kanada einbezog, ergab, dass 26,8% der TAVR-Patienten im Vergleich zu 45,3% in der Überwachungsgruppe innerhalb eines medianen Nachbeobachtungszeitraums von 3,8 Jahren Tod, Schlaganfall oder ungeplante kardiovaskuläre Krankenhausaufenthalte erlebten. Die frühe TAVR-Intervention verhinderte eine rasche Symptomprogression und einen Rückgang der Lebensqualität, mit niedrigeren Schlaganfallraten (4,2% gegenüber 6,7%). Bemerkenswerterweise benötigten 26,2% der Patienten in der Überwachung innerhalb von sechs Monaten einen Klappenersatz, der bei 12 Monaten auf 47,2% anstieg.
- Superior clinical outcomes with 26.8% vs 45.3% composite endpoint in TAVR vs surveillance groups
- Lower stroke rates in TAVR group (4.2% vs 6.7%)
- First randomized controlled trial showing benefits of early intervention
- Results support potential changes to current treatment guidelines
- None.
Insights
The EARLY TAVR trial results represent a paradigm shift in treating severe aortic stenosis. The data shows significantly superior outcomes with early TAVR intervention, reducing the composite endpoint of death, stroke, or unplanned cardiovascular hospitalization by
The rapid conversion rate to AVR in the surveillance arm (
This evidence will likely prompt updates to clinical guidelines, expanding TAVR indications to include asymptomatic severe AS patients, potentially growing Edwards' addressable market substantially.
This groundbreaking trial significantly expands Edwards' TAVR market opportunity. With asymptomatic severe AS patients now showing superior outcomes with early intervention, the addressable patient population could increase by
The robust evidence supporting early intervention should drive faster insurance coverage decisions and help overcome reimbursement barriers. This could translate to accelerated revenue growth in Edwards' TAVR segment, which represents over
With a median follow up of 3.8 years, the data demonstrated superiority of early TAVR, with
- Prevented unpredictable and rapid progression of symptoms, which sometimes resulted in emergent intervention and/or hospitalization;
- Prevented clinically meaningful and rapid decline in quality of life; and
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Resulted in numerically lower rate of stroke for patients with early TAVR (
4.2% vs.6.7% at a median follow-up time of 3.8 years).
“What we learned in this trial is that without intervention, patients rigorously confirmed as asymptomatic experienced unpredictable and rapid decline with numerous adverse outcomes. These results shatter 60 years of ingrained belief on the treatment for severe aortic stenosis, with guidelines that currently recommend ‘watchful waiting’ for intervention until symptoms develop,” said Philippe Genereux, MD, director of the structural heart program at Gagnon Cardiovascular Institute, Morristown Medical Center,
The EARLY TAVR Trial enrolled 901 patients – with an average age of 76 and average KCCQ-OS score of 92.7 – at 75 sites across the US and
“This is the first pivotal trial to generate evidence about the best strategy for disease management of severe aortic stenosis,” said Larry Wood, Edwards’ corporate vice president and group president, transcatheter aortic valve replacement and surgical structural heart. “EARLY TAVR challenges the current standard of care by definitively showing that patients who don’t have symptoms of severe aortic stenosis have a deadly disease that requires urgent treatment.”
About Edwards Lifesciences
Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most. Discover more at www.edwards.com and follow us on LinkedIn, Facebook, Instagram and YouTube.
This news release includes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. We intend the forward-looking statements contained in this release to be covered by the safe harbor provisions of such Acts. These forward-looking statements can sometimes be identified by the use of forward-looking words, such as “may,” “might,” “believe,” “will,” “expect,” “project,” “estimate,” “should,” “anticipate,” “plan,” “goal,” “continue,” “seek,” “intend,” “optimistic,” “aspire,” “confident” and other forms of these words and include, but are not limited to, statements made by Mr. Wood and statements regarding expected product benefits, patient outcomes, objectives and expectations and other statements that are not historical facts. Forward-looking statements are based on estimates and assumptions made by management of the company and are believed to be reasonable, though they are inherently uncertain and difficult to predict. Our forward-looking statements speak only as of the date on which they are made, and we do not undertake any obligation to update any forward-looking statement to reflect events or circumstances after the date of the statement. Investors are cautioned not to unduly rely on such forward-looking statements.
Forward-looking statements involve risks and uncertainties that could cause results to differ materially from those expressed or implied by the forward-looking statements based on a number of factors as detailed in the company's filings with the Securities and Exchange Commission. These filings, along with important safety information about our products, may be found at Edwards.com.
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Source: Edwards Lifesciences Corporation
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