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	<title>Nieuws &#8211; Cell Free DNA</title>
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	<link>https://cfdna.nl</link>
	<description>Grensverleggende innovatie in oncologische biomarker diagnostiek</description>
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		<title>cfDNA-dag 2026 • 26 juni 2026</title>
		<link>https://cfdna.nl/cfdna-dag-2026-26-juni-2026/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Sat, 11 Apr 2026 09:47:29 +0000</pubDate>
				<category><![CDATA[Agenda home]]></category>
		<category><![CDATA[CMBD Themadag]]></category>
		<category><![CDATA[Nieuws]]></category>
		<category><![CDATA[Recent Events]]></category>
		<guid isPermaLink="false">https://cfdna.nl/?p=21630</guid>

					<description><![CDATA[Nederlandse Cell Free DNA, 26 juni 2026. Deze CMBD Themadag is toegankelijk voor alle disciplines die zich bezig houden met cell free DNA. ]]></description>
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			<p class="p1"><span class="s1"><span class="dropcap insignia-dropcap dropcap-square  dropcap-normal">D</span>eze CMBD Themadag is toegangelijk voor alle disciplines die zich bezig houden met cell free DNA.</span></p>
<p class="p1"><span class="s1"><i>Het achtste Nederlandse Cell Free DNA Symposium: Grensverleggende innovaties in de moleculaire diagnostiek</i></span></p>
<p><strong>&gt; <a href="https://pathologie.nl/cfdna-dag/">Direct aanmelden</a></strong></p>

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<blockquote id="ins-blockquotes-69dff053a7400" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">Cell free DNA: grensverleggende innovatie in de moleculaire diagnostiek</q></blockquote><script type="text/javascript">
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<p class="p1"><span class="s1">Het veld van de moleculaire diagnostiek ontwikkelt zich razendsnel. Nieuwe technieken maken het mogelijk om steeds sneller en goedkoper deze vorm van diagnostiek uit te voeren. Daarnaast creëren deze ontwikkelingen ook nieuwe samenwerkingsverbanden. </span></p>
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		<title>7e Nederlandse cfDNA-dag • 4 juli 2025</title>
		<link>https://cfdna.nl/4-juli-2025-zevende-nederlandse-cfdna-dag/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Fri, 18 Apr 2025 07:28:55 +0000</pubDate>
				<category><![CDATA[CMBD Themadag]]></category>
		<category><![CDATA[Nieuws]]></category>
		<category><![CDATA[Recent Events]]></category>
		<guid isPermaLink="false">https://cfdna.nl/?p=21530</guid>

					<description><![CDATA[Het zevende Nederlandse Cell Free DNA, 4 juli  2025. Deze CMBD Themadag is toegangelijk voor alle disciplines die zich bezig houden met cell free DNA. ]]></description>
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			<p class="p1"><span class="s1"><span class="dropcap insignia-dropcap dropcap-square  dropcap-normal">D</span>eze CMBD Themadag is toegangelijk voor alle disciplines die zich bezig houden met cell free DNA.</span></p>
<p class="p1"><span class="s1"><i>Het zevende Nederlandse Cell Free DNA Symposium: Grensverleggende innovaties in de moleculaire diagnostiek</i></span></p>
<p><strong>&gt; <a href="https://www.nvkc.nl/actueel/agenda/7de-nederlands-cfdna-symposium">Direct aanmelden</a></strong></p>

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<blockquote id="ins-blockquotes-69dff053ac593" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">Cell free DNA: grensverleggende innovatie in de moleculaire diagnostiek</q></blockquote><script type="text/javascript">
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<p class="p1"><span class="s1">Het veld van de moleculaire diagnostiek ontwikkelt zich razendsnel. Nieuwe technieken maken het mogelijk om steeds sneller en goedkoper deze vorm van diagnostiek uit te voeren. Daarnaast creëren deze ontwikkelingen ook nieuwe samenwerkingsverbanden. </span></p>
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		<title>Subsidie voor DNA paspoort in de eerste lijn</title>
		<link>https://cfdna.nl/subsidie-voor-dna-paspoort-in-de-eerste-lijn/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Thu, 10 Apr 2025 15:07:08 +0000</pubDate>
				<category><![CDATA[CMBD Themadag]]></category>
		<category><![CDATA[Nieuws]]></category>
		<category><![CDATA[Past Events]]></category>
		<category><![CDATA[Recent Events]]></category>
		<guid isPermaLink="false">https://cfdna.nl/?p=21586</guid>

					<description><![CDATA[Subsidie voor DNA paspoort in de eerste lijn]]></description>
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			<p class="p1"><span class="s1"><span class="dropcap insignia-dropcap dropcap-square  dropcap-normal">S</span></span><span class="s1">ubsidie voor DNA paspoort in de eerste lijn toegekend door <a href="https://www.linkedin.com/company/zonmw-geneesmiddelen/"><span class="s2"><b>ZonMw: Geneesmiddelen</b></span></a>.</span></p>
<p class="p1">Op 24 maart 2025 is bekend geworden dat het P4CARE consortium de subsidie voor dit project toegewezen heeft gekregen!</p>
<p class="p1"><span class="s1">Eind 2025 zal de officiële start zijn van het project. Tot die tijd wordt er hard gewerkt aan de voorbereidingen. Houd deze website en onze<a href="https://www.linkedin.com/company/p4care-consortium-nl/posts/"><span class="s3"> LinkedInpagina</span></a> in de gaten voor updates.</span></p>
<p><strong>&gt; <a href="https://www.p4care.com/">Meer info</a></strong></p>

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<blockquote id="ins-blockquotes-69dff053ad6f6" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">P4CARE - A Pharmacogenetic-passport for optimizing drug treatment before the first Pharmacological treatment for Psychiatric conditions in Primary CARE</q></blockquote><script type="text/javascript">
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			<p class="p1"><span class="s1"><a href="https://www.linkedin.com/search/results/all/?keywords=%23p4care&amp;origin=HASH_TAG_FROM_FEED"><b>#P4CARE</b></a></span><span class="s2"> staat voor 𝙋𝘩𝘢𝘳𝘮𝘢𝘤𝘰𝘨𝘦𝘯𝘦𝘵𝘪𝘤-𝘱𝘢𝘴𝘴𝘱𝘰𝘳𝘵 𝘧𝘰𝘳 𝘰𝘱𝘵𝘪𝘮𝘪𝘻𝘪𝘯𝘨 𝘥𝘳𝘶𝘨 𝘵𝘳𝘦𝘢𝘵𝘮𝘦𝘯𝘵 𝘣𝘦𝘧𝘰𝘳𝘦 𝘵𝘩𝘦 𝘧𝘪𝘳𝘴𝘵 𝙋𝘩𝘢𝘳𝘮𝘢𝘤𝘰𝘭𝘰𝘨𝘪𝘤𝘢𝘭 𝘵𝘳𝘦𝘢𝘵𝘮𝘦𝘯𝘵 𝘧𝘰𝘳 𝙋𝘴𝘺𝘤𝘩𝘪𝘢𝘵𝘳𝘪𝘤 𝘤𝘰𝘯𝘥𝘪𝘵𝘪𝘰𝘯𝘴 𝘪𝘯 𝘗𝘳𝘪𝘮𝘢𝘳𝘺 𝘊𝘈𝘙𝘌</span></p>
<p class="p1"><span class="s2">👉 Doelen van het P4CARE onderzoek zijn:</span></p>
<p class="p1"><span class="s2">1. Aantonen 𝗸𝗹𝗶𝗻𝗶𝘀𝗰𝗵𝗲- en 𝗸𝗼𝘀𝘁𝗲𝗻𝗲𝗳𝗳𝗲𝗰𝘁𝗶𝘃𝗶𝘁𝗲𝗶𝘁 DNA-paspoort voor de behandeling van depressie en angststoornissen in de eerstelijnszorg</span></p>
<p class="p1"><span class="s2">2. Creëren 𝗶𝗻𝗳𝗿𝗮𝘀𝘁𝗿𝘂𝗰𝘁𝘂𝘂𝗿 en 𝗿𝗼𝘂𝘁𝗲𝗸𝗮𝗮𝗿𝘁 voor een doelmatige implementatie</span></p>
<p class="p1"><span class="s2">👉 Het onderzoek wordt uitgevoerd door een multidisciplinair team met een </span>𝐠𝐫𝐨𝐭𝐞 𝐫𝐨𝐥 𝐯𝐨𝐨𝐫 𝐝𝐞 𝐞𝐞𝐫𝐬𝐭𝐞𝐥𝐢𝐣𝐧𝐬𝐳𝐨𝐫𝐠 waarvoor al 63 (FTO) groepen van huisartsen en apothekers uit heel NL zich hebben aangemeld.</p>

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		<title>Klinische ctDNA-test voor alvleesklierkanker</title>
		<link>https://cfdna.nl/klinische-ctdna-test-voor-alvleesklierkanker/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Fri, 01 Nov 2019 14:47:46 +0000</pubDate>
				<category><![CDATA[Nieuws]]></category>
		<guid isPermaLink="false">https://cfdna.nl/2019/?p=17577</guid>

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			<p class="p1"><span class="s1"><span class="dropcap insignia-dropcap dropcap-square  dropcap-normal">E</span><strong>en nieuwe bloedtest onthult alvleesklierkanker twee maanden voordat de tumor zichtbaar is op een scan. Het gaat om een zogeheten ctDNA-test, een test die circulerend tumor-DNA detecteert. Dankzij promotieonderzoek van Vincent Groot is de test nu beschikbaar voor patiënten van Johns Hopkins Hospital. </strong></span></p>
<p>Je zou het een doorbraak kunnen noemen, zelf noemt Vincent Groot het liever een eerste stap. Voor het UMC Utrecht en het Johns Hopkins Hospital in Baltimore verrichtte hij promotieonderzoek naar een nieuwe bloedtest voor patiënten met alvleesklierkanker (pancreaskanker). Met de test wordt in het bloed gezocht naar afbraakproducten van de tumor, circulerend tumor DNA genoemd (ctDNA). Specifiek wordt met de test gezocht naar een mutatie die 95 procent van de patiënten met pancreaskanker heeft: KRAS.</p>

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<blockquote id="ins-blockquotes-69dff053b01f6" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">We gaan een nieuw tijdperk in waarin we kankerpatiënten niet als groep zien, maar naar een gepersonaliseerde behandeling streven.</q></blockquote><script type="text/javascript">
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<p class="p1"><span class="s1">Vincent volgde patiënten bij wie een tumor in de alvleesklier chirurgisch was verwijderd. Alvleesklierkanker (2500 patiënten per jaar in Nederland, 500.000 wereldwijd) is een van de kankersoorten die de slechtste behandelresultaten laten zien en de tumor keert in de meeste gevallen dan ook terug. </span></p>
<p class="p1"><span class="s1"><strong>Verhoogd KRAS ctDNA</strong><br />
</span><span class="s1">Uit <a href="https://surfdrive.surf.nl/files/index.php/s/wOZoF626dAnT3Gr" target="_blank" rel="noopener noreferrer">zijn promotieonderzoek</a> bleek dat de bloedtest twee maanden voordat een terugkerende tumor op scans te zien is, al een verhoogd KRAS ctDNA vindt. Vincent: “Van 60 patiënten hebben we voor en na de operatie bloed afgenomen en geanalyseerd hoe de bloedwaarden veranderen en wat er in het lichaam gebeurt. Wij zagen hoe de kanker terugkeerde, terwijl er op de scan nog niets te zien was.” De test biedt 99 procent zekerheid en wordt nu aangeboden in het Johns Hopkins Hospital. Daarmee is het ’s werelds eerste ctDNA-test die de overstap maakt van het lab naar de kliniek.  </span></p>
<p><a href="https://www.umcutrecht.nl/nl/Nieuws/Klinische-ctDNA-test-voor-alvleesklierkanker">Lees meer</a></p>
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		<title>ZonMw financiert gezondheidsonderzoek</title>
		<link>https://cfdna.nl/zonmw-financiert-gezondheidsonderzoek/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Wed, 05 Dec 2018 07:40:44 +0000</pubDate>
				<category><![CDATA[Nieuws]]></category>
		<guid isPermaLink="false">https://insigniathemes.com/laboratory/?p=915</guid>

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			<p><span class="dropcap insignia-dropcap dropcap-square pc-bg dropcap-normal">Z</span>onMw stimuleert gezondheidsonderzoek en zorginnovatie. Vooruitgang vraagt om onderzoek en ontwikkeling.</p>
<p>ZonMw financiert gezondheidsonderzoek én stimuleert het gebruik van de ontwikkelde kennis. Daarmee dragen we bij aan het verbeteren van de zorg en gezondheid.</p>

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<blockquote id="ins-blockquotes-69dff053b194b" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">Twee dingen zijn nodig om de zorg en gezondheid te verbeteren: kennis en het daadwerkelijk gebruiken van die kennis.</q></blockquote><script type="text/javascript">
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			<p>ZonMw stimuleert met allerlei subsidieprogramma’s de totale innovatiecyclus. Van fundamenteel onderzoek tot implementatie van nieuwe behandelingen, preventieve interventies of verbeteringen in de structuur van de gezondheidszorg.</p>
<p>Bij de selectie van subsidievoorstellen zoekt ZonMw altijd de vernieuwing in combinatie met kwaliteit. Alleen zo doen ze recht aan de complexiteit van de uitdagingen in de huidige samenleving en krijgen cliënten betaalbare zorg van hoog niveau.</p>
<p>https://www.zonmw.nl/nl/over-zonmw/</p>

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		<title>12-13 June 2018 &#124;  1st Annual Benelux Precision Medicine Forum</title>
		<link>https://cfdna.nl/12-13-june-2018-1st-annual-benelux-precision-medicine-forum/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Tue, 12 Jun 2018 15:17:19 +0000</pubDate>
				<category><![CDATA[Nieuws]]></category>
		<guid isPermaLink="false">https://cfdna.nl/2019/?p=17126</guid>

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			<p class="p1"><span class="s1"><span class="dropcap insignia-dropcap dropcap-square  dropcap-normal">T</span></span>he Benelux region represent a unique opportunity when it comes to healthcare; boasting a wealth of data, being host to world leading universities and a plethora of technology companies.</p>
<p>As such it is little surprise that the precision medicine revolution is creating such a buzz; disruptive technology, a strong economic setting and decades of social and health data collection are coming together to create the perfect storm for the future of healthcare in the region.</p>
<p>It is widely accepted that for the promise of precision medicine to become a reality we must work together; sharing data and research via a multi-disciplinary approach as well as cross border collaboration.</p>

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<blockquote id="ins-blockquotes-69dff053b30a0" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">Create the perfect storm for the future of healthcare</q></blockquote><script type="text/javascript">
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		<title>May 30th – June 1st 2018 &#124;  First Nordic conference on Personalized Medicine</title>
		<link>https://cfdna.nl/may-30th-june-1st-2018-first-nordic-conference-on-personalized-medicine/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Wed, 30 May 2018 18:25:46 +0000</pubDate>
				<category><![CDATA[Nieuws]]></category>
		<guid isPermaLink="false">https://cfdna.nl/2019/?p=17136</guid>

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			<p class="p1"><span class="s1"><span class="dropcap insignia-dropcap dropcap-square  dropcap-normal">T</span></span>his 3-day conference will focus on both basic and clinical aspects of research regarding personalized medicine. The program will consist of talks and workshops within pharmacogenetics, drug interactions, epigenetics and other factors that may cause variation in drug response among individuals. Furthermore, there will be focus on methods available across the participating researchers.</p>
<p>This conference will be an excellent opportunity to network with colleagues and possibly establish international collaborations.</p>

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<blockquote id="ins-blockquotes-69dff053b418d" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">Focus on both basic and clinical aspects of research regarding personalized medicine.</q></blockquote><script type="text/javascript">
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<p><a href="https://www.farmacogenetica.nl/First%20Nordic%20conference.pdf" target="_blank" rel="noopener noreferrer">Program</a></p>
<p><a href="http://www.norpm2018.com/" target="_blank" rel="noopener noreferrer">More info</a></p>
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		<title>April 30-May 2 &#124; AMP Europe 2018</title>
		<link>https://cfdna.nl/april-30-may-2-amp-europe-2018/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Mon, 30 Apr 2018 21:46:19 +0000</pubDate>
				<category><![CDATA[Nieuws]]></category>
		<guid isPermaLink="false">https://cfdna.nl/2019/?p=17091</guid>

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			<p class="p1"><span class="s1"><span class="dropcap insignia-dropcap dropcap-square  dropcap-normal">T</span></span>he emerging field of precision cancer medicine, in which the use of molecular data at the point of care directly impacts patient treatment and clinical decision-making, has already had a substantial, direct clinical impact on many aspects of medical oncology.</p>
<p>The introduction of large-scale genomic technologies at the point of care has catalyzed discoveries in translational oncology and is driving new research that aims to dissect selective responses to targeted, immune-driven therapies and to chemotherapies, as well as identifying novel targets for which therapies are now in development. However, precision cancer medicine remains a promise rather than a solid and robust reality.</p>
<p>Although the molecular landscapes of many cancers have been revealed using precision oncology approaches, many of the alterations observed in patients remain undruggable, and viable targets are incompletely characterized. In this conference we will discuss and address current advances, challenges and ignite solutions for the advancement of precision medicine.</p>

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<blockquote id="ins-blockquotes-69dff053b52f0" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">The theme of this meeting is: Achieving Dramatic Insights into Molecular Oncology &amp; Precision Medicine.</q></blockquote><script type="text/javascript">
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			<p>Rotterdam, April 30-May 2, The Netherlands</p>
<p><a href="http://amp-europe-congress.com/registration/" target="_blank" rel="noopener noreferrer">Registration </a></p>
<p><a href="http://amp-europe-congress.com/wp-content/uploads/2018/04/AMP2018_Final_Program-1.pdf" target="_blank" rel="noopener noreferrer">Program</a></p>
<p><a href="http://amp-europe-congress.com/" target="_blank" rel="noopener noreferrer">More info</a></p>

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		<title>4-7 Oct 2017 &#124; ESPT Annual Meeting Catania</title>
		<link>https://cfdna.nl/4-7-oct-2017-espt-annual-meeting-catania/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Wed, 04 Oct 2017 21:35:15 +0000</pubDate>
				<category><![CDATA[Nieuws]]></category>
		<guid isPermaLink="false">https://cfdna.nl/2019/?p=17083</guid>

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			<p class="p1"><span class="s1"><span class="dropcap insignia-dropcap dropcap-square  dropcap-normal">E</span>uropean Society for Pharmacogenomics and Personalized Therapy, 4th Conference.</span></p>
<p>Pictures: https://www.abomics.fi/en/news/132-espt-2017-conference</p>

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<blockquote id="ins-blockquotes-69dff053b64e0" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">IFCC – EuroMedLab 2017 | European Congress of the International Federation of Clinical Chemistry and Laboratory Medicine</q></blockquote><script type="text/javascript">
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<p><a href="http://www.esptnet.eu" target="_blank" rel="noopener noreferrer">Info and registration.</a></p>
<p>ESPT Annual Meeting 2017</p>
<p>Oct 4-7</p>
<p>Catania</p>
<p>Sicily</p>
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		<title>October 4-5-6-7 &#124; 2017 &#124;  4th ESPT Conference</title>
		<link>https://cfdna.nl/october-4-5-6-7-2017-4th-espt-conference/</link>
		
		<dc:creator><![CDATA[ronald]]></dc:creator>
		<pubDate>Wed, 04 Oct 2017 18:45:02 +0000</pubDate>
				<category><![CDATA[Nieuws]]></category>
		<guid isPermaLink="false">https://cfdna.nl/2019/?p=17150</guid>

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			<p class="p1"><span class="s1"><span class="dropcap insignia-dropcap dropcap-square  dropcap-normal">T</span>The Fourth European Society of Pharmacogenomics and Personalized Therapy biennial conference was organized in collaboration with the Italian Society of Personalized Medicine (SIMeP) and was held at Benedictine Monastery of San Nicolò l&#8217;Arena in Catania, Sicily (Italy) on 4-7 October 2017. </span></p>
<p class="p1"><span class="s1">The congress addressed the research progress and clinical implementation in pharmacogenomics and personalized medicine. </span></p>
<p class="p1"><span class="s1">The Fourth European Society of Pharmacogenomics and Personalized Therapy congress brought together leading international scientists and healthcare professionals actively working in the fields of pharmacogenomics and personalized therapy. Altogether, 25 speakers in 15 session comprehensively covered broad spectrum of pharmacogenetics and pharmacogenomics research, clinical applications in different clinical disciplines attended by 270 delegates.</span></p>

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<blockquote id="ins-blockquotes-69dff053b798c" class="ins-blockquotes ins-blockquotes text-left pc-border " ><q style="color: #074575">Pharmacogenomics and personalized medicine - research progress and clinical implementation.</q></blockquote><script type="text/javascript">
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			<p>https://www.ncbi.nlm.nih.gov/pubmed/31588876</p>

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