NeoGenomics to Present New Data at ESMO 2024, Highlighting the Value of ctDNA and NGS for Advancing Cancer Diagnostics and Personalized Treatment
NeoGenomics (NASDAQ: NEO) will present three studies at the ESMO Congress 2024 in Barcelona, showcasing advancements in cancer diagnostics using ctDNA and NGS. Key findings include:
1. NGS testing for 19 drug-targetable fusions can identify up to 4x more patients for matched therapies compared to testing.
2. A large-scale study on ctDNA in early-stage NSCLC identifies high-risk patients who may benefit from aggressive treatment.
3. A Phase II trial evaluating ctDNA as a marker for treatment decisions in high-risk melanoma patients.
These studies highlight the potential of advanced molecular diagnostics to improve early cancer detection and personalized treatment strategies.
NeoGenomics (NASDAQ: NEO) presenterà tre studi al Congresso ESMO 2024 a Barcellona, evidenziando i progressi nella diagnostica oncologica utilizzando ctDNA e NGS. I risultati principali includono:
1. Il test NGS per 19 fusioni trattabili con farmaci può identificare fino a 4 volte più pazienti per terapie mirate rispetto ai test tradizionali.
2. Uno studio su larga scala sul ctDNA nei pazienti con NSCLC in stadio iniziale identifica quelli ad alto rischio che potrebbero beneficiare di trattamenti aggressivi.
3. Uno studio di Fase II che valuta il ctDNA come marcatore per decisioni terapeutiche nei pazienti con melanoma ad alto rischio.
Questi studi evidenziano il potenziale della diagnostica molecolare avanzata per migliorare la rilevazione precoce del cancro e le strategie di trattamento personalizzate.
NeoGenomics (NASDAQ: NEO) presentará tres estudios en el Congreso ESMO 2024 en Barcelona, destacando los avances en el diagnóstico del cáncer utilizando ctDNA y NGS. Los hallazgos clave incluyen:
1. Las pruebas de NGS para 19 fusiones tratables con medicamentos pueden identificar hasta 4 veces más pacientes para terapias seleccionadas en comparación con las pruebas convencionales.
2. Un estudio a gran escala sobre ctDNA en pacientes con NSCLC en estadio inicial identifica a los pacientes de alto riesgo que podrían beneficiarse de un tratamiento agresivo.
3. Un ensayo de Fase II que evalúa el ctDNA como marcador para decisiones de tratamiento en pacientes con melanoma de alto riesgo.
Estos estudios subrayan el potencial de la diagnóstica molecular avanzada para mejorar la detección temprana del cáncer y las estrategias de tratamiento personalizadas.
NeoGenomics (NASDAQ: NEO)는 바르셀로나에서 열리는 ESMO Congress 2024에서 ctDNA와 NGS를 활용한 암 진단의 발전을 보여주는 세 가지 연구를 발표할 예정입니다. 주요 발견 사항은 다음과 같습니다:
1. 19개의 약물 타겟화 융합에 대한 NGS 테스트는 기존의 테스트에 비해 최대 4배 더 많은 환자를 일치하는 치료법으로 식별할 수 있습니다.
2. 초기 단계 NSCLC에서 ctDNA에 대한 대규모 연구가 공격적인 치료를 통해 혜택을 받을 수 있는 고위험 환자를 식별합니다.
3. 고위험 멜라노마 환자의 치료 결정을 위한 마커로서 ctDNA를 평가하는 2상 시험입니다.
이 연구들은 조기 암 발견과 개인화된 치료 전략을 개선하기 위한 고급 분자 진단의 잠재력을 강조합니다.
NeoGenomics (NASDAQ: NEO) présentera trois études lors du Congrès ESMO 2024 à Barcelone, mettant en avant des avancées dans le diagnostic du cancer utilisant ctDNA et NGS. Les résultats clés incluent :
1. Les tests NGS pour 19 fusions ciblables par des médicaments peuvent identifier jusqu'à 4 fois plus de patients pour les thérapies assorties par rapport aux tests traditionnels.
2. Une étude à grande échelle sur le ctDNA dans le NSCLC à un stade précoce identifie les patients à haut risque qui pourraient bénéficier d'un traitement agressif.
3. Un essai de Phase II évaluant le ctDNA comme marqueur pour les décisions thérapeutiques chez les patients atteints de mélanome à haut risque.
Ces études soulignent le potentiel des diagnostics moléculaires avancés pour améliorer la détection précoce du cancer et les stratégies de traitement personnalisées.
NeoGenomics (NASDAQ: NEO) wird auf dem ESMO-Kongress 2024 in Barcelona drei Studien präsentieren, die Fortschritte in der Krebsdiagnostik mithilfe von ctDNA und NGS zeigen. Die wichtigsten Ergebnisse umfassen:
1. NGS-Tests für 19 medikamenten-targetierbare Fusionsgene können bis zu 4-mal mehr Patienten für passende Therapien identifizieren als herkömmliche Tests.
2. Eine groß angelegte Studie über ctDNA bei frühen NSCLC-Patienten identifiziert Hochrisikopatienten, die von aggressiven Behandlungen profitieren könnten.
3. Eine Phase-II-Studie zur Bewertung von ctDNA als Marker für Behandlungsentscheidungen bei Hochrisiko-Melanom-Patienten.
Diese Studien heben das Potenzial fortschrittlicher molekularer Diagnostik zur Verbesserung der frühen Krebsdiagnose und personalisierten Behandlungsstrategien hervor.
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“Emerging technologies leveraging ctDNA and NGS are increasing our ability to identify cancers in high-risk patients, which was previously beyond reach,” said Dr. Nathan Montgomery, Vice President of Medical Services at NeoGenomics. “Collectively, our findings demonstrate the potential of advanced molecular diagnostics to detect cancer earlier, guide more personalized treatments, and ultimately improve patient outcomes worldwide.”
NeoGenomics’ poster presentations include:
-
Real-World Analysis of Actionable Gene Fusions Identified by NGS and Correlation with IHC in 422 Patients from the Community (78P)
- Presentation Date: Sunday, September 15, 2024
- Results show that testing for 19 drug-targetable fusions can identify up to four times more patients for matched therapies compared to testing only for NTRK fusions or using IHC, suggesting that NGS testing for multiple fusions could greatly expand treatment options for cancer patients.
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ctDNA-Lung-Detect: Profiling of Non-Shedding ctDNA Early Stage Resected Non-Small Cell Lung Cancers (1236P)
- Presentation Date: Saturday, September 14, 2024
- This study represents one of the largest prospective cohorts of ctDNA assessments in early-stage non-small cell lung cancer (NSCLC), identifying patients at high risk of relapse who may benefit from more aggressive treatment.
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CLEAR-Me: Interception Trial to Detect and Clear Molecular Residual Disease in Patients with High-Risk Melanoma (226TiP)
- Presentation Date: Sunday, September 15, 2024
- This Phase II trial evaluated ctDNA as a marker to guide treatment decisions in high-risk melanoma patients. It compares the effectiveness of combining anti-LAG-3 with anti-PD-1 therapy versus anti-PD-1 inhibition alone.
For more details on NeoGenomics’ presentations, visit ESMO 2024.
About NeoGenomics, Inc.
NeoGenomics, Inc. specializes in cancer genetics testing and information services, providing one of the most comprehensive oncology-focused testing menus for physicians to help them diagnose and treat cancer. The Company's Advanced Diagnostic Division also serves pharmaceutical clients in clinical trials and drug development.
Headquartered in
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Source: NeoGenomics, Inc.
FAQ
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