{"id":9525,"date":"2025-04-25T16:00:46","date_gmt":"2025-04-25T14:00:46","guid":{"rendered":"https:\/\/www.hartwigmedicalfoundation.nl\/?p=9525"},"modified":"2025-04-25T16:33:50","modified_gmt":"2025-04-25T14:33:50","slug":"automatically-the-right-trial-and-treatment-with-actin-a-new-step-in-cancer-care","status":"publish","type":"post","link":"https:\/\/www.hartwigmedicalfoundation.nl\/en\/automatically-the-right-trial-and-treatment-with-actin-a-new-step-in-cancer-care\/","title":{"rendered":"Automatically the right trial and treatment with ACTIN: A new step in cancer care \u00a0"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\"><strong>Imagine you have a patient with cancer sitting across from you: can\u2019t be cured, but he is determined to try everything. You consider an early-phase clinical trial and begin sifting through a long list of inclusion and exclusion criteria. But what if selecting an appropriate study based on clinical, tumor, and genomic characteristics could be done automatically? And imagine you see a patient with a new cancer diagnosis next. What if, for this patient and based on those same characteristics, it could also be determined automatically which standard treatment is most appropriate and which clinical trial options are available? This may sound like something from the distant future, but with ACTIN, this approach is closer than you think, say medical oncologist and principal investigator Debbie Robbrecht, MD, PhD, nurse practitioner and PhD candidate Andrea van Puffelen, MSc, PhD candidate Jesse Wolters, MSc, (all from Erasmus MC in Rotterdam), and pulmonologist Joop de Langen, MD, PhD, (Antoni van Leeuwenhoek in Amsterdam).<\/strong>&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><em>Photo: Andrea van Puffelen, Jesse Wolters, Debbie Robbrecht, Joop de Langen<\/em><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><em>Bianca Hagenaars, MSc, science journalist<\/em>&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">The development of the Algorithmic Cancer Treatment Initiative (ACTIN) began several years ago with ACTIN 1.0. Andrea van Puffelen explains the motivation behind the initiative: \u201cTo determine whether patients with metastatic solid tumors are eligible for clinical trials, physicians must check numerous factors and variables. And each study has unique inclusion and exclusion criteria \u2013 on average about fifty. So, in practice, physicians often screen in broad terms whether a patient is eligible. If that looks promising, the remaining criteria are then reviewed. This process takes time \u2013 time many cancer patients do not have. This led to the idea of linking patient data from medical records to clinical trials using an algorithm: ACTIN 1.0.\u201d&nbsp;<\/p>\n\n\n\n<figure class=\"wp-block-pullquote\"><blockquote><p>Andrea van Puffelen<\/p><cite>\u201cThe treating oncologist receives a report with an overview of the identified mutations, as well as a list of potential trials the patient may participate in. The report also lists trials the patient does not qualify for, along with the reasons why. This spares patients from unnecessary screening.\u201d <\/cite><\/blockquote><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Overview of studies<\/strong><br>The algorithm, developed by Hartwig Medical Foundation, is fed with clinical characteristics, tumor features, and genomic information (obtained through whole genome sequencing or another broad panel), as well as the inclusion and exclusion criteria of clinical trials. Van Puffelen: \u201cThe treating oncologist receives a report with an overview of the identified mutations, as well as a list of potential trials the patient may participate in. The report also lists trials the patient does not qualify for, along with the reasons why. This spares patients from unnecessary screening.\u201d ACTIN 1.0 is currently running as a research project at Erasmus MC for all tumor types and at Antoni van Leeuwenhoek for lung cancer.&nbsp;<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p class=\"wp-block-paragraph\"><em>The algorithm, developed by Hartwig Medical Foundation, is fed with clinical characteristics, tumor features, and genomic information , as well as the inclusion and exclusion criteria of clinical trials.<\/em><\/p>\n<\/blockquote>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Accurate study matching<\/strong>&nbsp;<br>\u201cAt Antoni van Leeuwenhoek, we have many ongoing trials related to lung cancer, usually about thirty, for different mutations,\u201d says Joop de Langen. \u201cWhen discussing patients in the molecular tumor board, we do not always have all these trials top of mind. ACTIN really helps in this regard. And it does not just look at mutations for eligibility. Factors like kidney and liver function, previous treatments, measurable disease or not, et cetera, are also included in the algorithm. This gives us very accurate study matching.\u201d&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Ideally for every patient<\/strong><br>The algorithm is already working very well, according to those involved. De Langen: \u201cA small part of the information still must be entered manually, but that is minimal. Ideally, this will become available for every patient in the future.\u201d&nbsp;&nbsp;&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">To make this possible, a significant step has already been taken for lung cancer trials. Not only can patients with lung cancer be matched to studies ongoing at Erasmus MC or Antoni van Leeuwenhoek, but a link has also been made between ACTIN and the study platform <em>longkankeronderzoek.nl<\/em>. Any hospital can submit its lung cancer trials here, allowing ACTIN to match patients to appropriate studies nationwide, regardless of where the trial is being conducted. Every patient is entitled to an ACTIN report prior to the start of first-line or subsequent treatment. The options for treatment within and outside trial settings can then be discussed by the treating specialist with the patient to make the best choice.&nbsp;&nbsp;&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">De Langen: \u201cMy ideal is that it should not matter which hospital a patient visits \u2013 they should receive the same care and access to the same studies everywhere.\u201d Robbrecht adds: \u201cWe have a similar ideal for standard treatments offered to patients. We want to be able to offer every patient the best standard of care. That is why we continued developing ACTIN for personalized treatment, known as ACTIN 2.0. Whereas ACTIN 1.0 focused on building the algorithm and automating the process, we are now further developing and extending the algorithm for patients with a new cancer diagnosis. ACTIN 2.0 will initially focus on colorectal cancer and non-small cell lung cancer.\u201d&nbsp;<\/p>\n\n\n\n<figure class=\"wp-block-pullquote\"><blockquote><p>Joop de Langen<\/p><cite>\u201cMy ideal is that it should not matter which hospital a patient visits \u2013 they should receive the same care and access to the same studies everywhere.\u201d <\/cite><\/blockquote><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>ACTIN 2.0<\/strong><br>Whereas Van Puffelen\u2019s PhD focuses mainly on ACTIN 1.0, Jesse Wolters\u2019 doctoral research centers on ACTIN 2.0. He says: \u201cThe main question behind ACTIN 2.0 is: can we, based on data and treatment outcomes from a large number of previous patients, predict the treatment outcome for a new patient?\u201d To answer this, three major steps need to be taken. Wolters: \u201cStep one is analyzing data from previous patients and building a large database. What data do we actually have at our disposal? For this, we use data from the Dutch Cancer Registry, as well as from randomized controlled trials, and we investigate whether we can extract information from electronic health records (EHRs). That leads to step two: can we automatically extract a new patient\u2019s data from the EHR and match it to our database? In the third step we want to identify, based on the database consisting of previous patients, which characteristics are relevant for determining the best standard treatment for a new patient and what benefits that treatment might offer. The medical oncologist and patient can then consider whether, with this expected treatment benefit, the treatment is worth trying.\u201d&nbsp;<\/p>\n\n\n\n<figure class=\"wp-block-pullquote\"><blockquote><p>Jesse Wolters<\/p><cite>\u201cThe main question behind ACTIN 2.0 is: can we, based on data and treatment outcomes from a large number of previous patients, predict the treatment outcome for a new patient?\u201d <\/cite><\/blockquote><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Major challenges<\/strong>&nbsp;<br>Work is currently underway to build the algorithm for ACTIN 2.0. \u201cWe are approaching this from two angles,\u201d says Wolters. \u201cOn one hand, Hartwig Medical Foundation is investigating which characteristics are needed to answer our main question. On the other, I\u2019m focusing on how to automatically extract information from EHRs \u2013 starting with free text. This needs to be pseudonymized and converted from text that we as humans can read into data the algorithm can use.\u201d&nbsp;&nbsp;&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">These two key points are also the two biggest challenges Robbrecht adds. \u201cWe must safeguard patient privacy and strive for an automated system with minimal manual input. By focusing on efficiency and user-friendliness right from the start, we want to ensure that future clinical implementation will go smoothly \u2013 and avoid building a brilliant system that no one ends up using.\u201d&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Dot on horizon<\/strong>&nbsp;<br>It will therefore take some time before the ACTIN algorithm becomes standard practice. The goal, however, is to roll out ACTIN 2.0 nationally and for more tumor types. Robbrecht: \u201cIf ACTIN proves effective in identifying the best treatment for our patients, it will be a powerful support tool in the consultation room. It could lead to more personalized and effective treatments and better outcomes for cancer patients. That is our dot on the horizon.\u201d&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">This interview was originally posted on <a href=\"https:\/\/www.oncologie.nu\/nieuws\/automatisch-de-juiste-studie-en-behandeling-met-actin-een-nieuwe-stap-in-kankerzorg\/\">Oncologie.nu<\/a>.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a href=\"https:\/\/www.hartwigmedicalfoundation.nl\/en\/actin\/\"><strong>More information about ACTIN<\/strong><\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Imagine you have a patient with cancer sitting across from you: can\u2019t be cured, but he is determined to try &hellip;<\/p>\n","protected":false},"author":3,"featured_media":9518,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[90,87,93,85,76,79,81,73,82,80],"tags":[],"class_list":["post-9525","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-algorithms","category-end-of-treatment","category-hartwig-medical-foundation","category-learning-healthcare-system","category-molecular-diagnostics","category-onco-act","category-participating-hospitals","category-personalized-treatment","category-research","category-whole-genome-sequencing"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - 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