{"id":46413,"date":"2023-12-05T14:00:00","date_gmt":"2023-12-05T14:00:00","guid":{"rendered":"https:\/\/ogkologos.com\/how-joining-a-clinical-trial-helped-me-find-hope-while-living-with-a-genetic-cancer-condition\/"},"modified":"2024-11-03T15:12:20","modified_gmt":"2024-11-03T15:12:20","slug":"how-joining-a-clinical-trial-helped-me-find-hope-while-living-with-a-genetic-cancer-condition","status":"publish","type":"post","link":"https:\/\/ogkologos.com\/en\/how-joining-a-clinical-trial-helped-me-find-hope-while-living-with-a-genetic-cancer-condition\/","title":{"rendered":"How Joining a Clinical Trial Helped Me Find Hope While Living With a Genetic Cancer Condition"},"content":{"rendered":"<p><i>This post was first published on\u202f<\/i><a href=\"https:\/\/ascopost.com\/issues\/march-25-2023\/i-haven-t-known-a-life-without-von-hippel-lindau-disease\/\" target=\"_blank\" rel=\"noopener\"><i>The ASCO Post<\/i><\/a><i>, March 25, 2023. It has been edited for content.\u202fThe\u202fASCO Post, in partnership with the American Society of Clinical Oncology (ASCO), communicates news of evidence-based multidisciplinary cancer care to a broad audience of oncology professionals and ASCO members.\u202f\u202f<\/i><\/p>\n<p><i>Alexandra Vitale is a von Hippel-Lindau syndrome survivor living in Townsend, Delaware.<\/i><i>&nbsp;<\/i><\/p>\n<p><a href=\"https:\/\/www.cancer.net\/cancer-types\/von-hippel-lindau-syndrome\">Von Hippel-Lindau (VHL) disease<\/a> has been with me since I was 5 years old, when a benign tumor was found on the optic nerve of my left eye, leaving me blind in that eye. But I didn\u2019t get an official diagnosis of the disease until 2011, when I was 20. By then, it was like a light switch had turned on, and I began developing tumors in my central nervous system, endocrine system, kidneys, and brain. The pace of the growth of new tumors was relentless. Each time I went in for an imaging scan every 3 to 6 months, another new tumor was detected.<\/p>\n<p>By 2011, I was having surgeries in quick succession. The most intense surgery by then was an adrenalectomy to remove benign growths on my adrenal glands. Then, in 2015, I was diagnosed with renal cell carcinoma, a type of <a href=\"https:\/\/www.cancer.net\/cancer-types\/kidney-cancer\/introduction\">kidney cancer<\/a>, and in 2016, I was diagnosed with <a href=\"https:\/\/www.cancer.net\/cancer-types\/neuroendocrine-tumor-pancreas\">pancreatic neuroendocrine carcinoma<\/a>.<\/p>\n<p>These years were probably the hardest for me emotionally because it was the first time the word \u201ccancer\u201d was used to describe the tumors. The surgeries to extract the cancers, a <a href=\"https:\/\/www.cancer.net\/blog\/2021-09\/whipple-procedure-pancreatic-cancer-how-prepare-and-what-expect\">Whipple procedure<\/a> to remove the neuroendocrine tumors, and a partial nephrectomy to remove the tumors in my kidney, were also extremely difficult to recover from physically.<\/p>\n<h3>Rolling with the punches<\/h3>\n<p>Prior to undergoing these surgeries, an imaging scan detected yet another tumor. This time, it was on my cerebellum, the lower back part of the brain. \u201cI wouldn\u2019t be surprised if we have to do something about that tumor in the coming year,\u201d my surgeon said. To avoid becoming overwhelmed by the seemingly endless development of tumors throughout my body, I decided to focus on the surgeries in front of me and deal with the others later. In December 2016, I had the Whipple and nephrectomy procedures. Then, 8 months later, I had brain surgery to remove the tumor in my cerebellum, which had begun pushing against my spinal cord, affecting my coordination. Fortunately, that tumor was benign.<\/p>\n<p>Although these tumors were found and removed before they could become life-threatening, the toll they were taking on my mental health was crushing. Every time I had to have a new <a href=\"https:\/\/www.cancer.net\/navigating-cancer-care\/diagnosing-cancer\/tests-and-procedures\/magnetic-resonance-imaging-mri\">magnetic resonance imaging (MRI) scan<\/a> or a meeting with my physician, I was filled with fear. But I decided to just roll with the punches. What else could I do?<\/p>\n<h3>Staying free of new tumors<\/h3>\n<p>In 2018, another tumor cropped up on one of my kidneys. This made me eligible to participate in a clinical trial investigating belzutifan (Welireg), a medication that targets hypoxia-inducible factor-2 alpha (HIF2a) in people with VHL-associated renal cell carcinoma. In people with VHL, HIF2a activates more than 100 critical targets that contribute to tumor growth. The drug has been successful in shrinking my tumor and stabilizing it, so I most likely will not have to have additional surgery to remove it.<\/p>\n<p>Remarkably, I haven\u2019t had any new tumors develop since I\u2019ve been on belzutifan. I\u2019m still enrolled in the clinical trial and most likely will have to remain on this therapy indefinitely.<\/p>\n<div class=\"highlight\" readability=\"13.830584707646\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/www.cancer.net\/sites\/cancer.net\/files\/shuch-circle.png\" alt width=\"100\" height=\"100\"><\/p>\n<p><i>\u201cVHL disease is a challenging condition that impacts a wide range of organs with manifestations that include both benign and malignant tumors. Both the disease and the associated morbidity from effective treatment can impact patients\u2019 quality and quantity of life. Belzutifan, a well-tolerated systemic treatment,&nbsp;is a major addition to the field, as it may help delay or avoid surgery when a tumor is present but does not need immediate treatment.\u201d<\/i> \u2013 Brian Shuch, MD, director of the Kidney Cancer Program and the Alvin &amp; Carrie Meinhardt Endowed Chair in Kidney Cancer Research at UCLA Health and a 2023 <a href=\"https:\/\/www.cancer.net\/about-us\/cancernet-editorial-board\/specialty-editors\/brian-shuch-md\">Cancer.Net Specialty Editor for Genitourinary Cancer<\/a><\/p>\n<\/div>\n<h3>Remaining hopeful about the future<\/h3>\n<p>I haven\u2019t known a life without VHL, and I\u2019ve learned to live with that fact. But it has definitely colored how I approach each day. Cancer has a way of making you prioritize your goals in life and helping you figure out what is most important to you. I stave off depression by telling myself that tomorrow is not a promised day, and I don\u2019t want to waste time ruminating over circumstances I can\u2019t change. I have to fight every day for my life and keep moving forward. There is no other way to survive this disease. Pain and stress are just reminders to me that I\u2019m still alive.<\/p>\n<p>Since the development of belzutifan, I have never had so much hope for myself and for other survivors of VHL. I\u2019m only 31, and although I know I will never be rid of the effects of the disease, I\u2019m optimistic that research advances will bring us closer to more effective therapies\u2014and maybe even a cure\u2014by the time I\u2019m in my 40s or 50s.<\/p>\n<p>And I\u2019m willing to do my part. Being enrolled in this clinical trial has given me a strong appreciation for research, and I am willing to dedicate myself if it will help others with this disease or help to find cures for other cancers. I want oncologists and researchers to know that what they do every day to help people like me is making a difference in our lives.<\/p>\n<p>For my entire life, my mantra has been to stay positive and continue to move forward. Honestly, it\u2019s a message everyone can benefit from, whether you have cancer or not.&nbsp;<\/p>\n<p><a href=\"https:\/\/www.cancer.net\/blog\/2023-12\/how-joining-clinical-trial-helped-me-find-hope-while-living-with-genetic-cancer-condition\">Source<\/a><\/p>","protected":false},"excerpt":{"rendered":"<p>This post was first published on\u202fThe ASCO Post, March 25, 2023. It has been edited for content.\u202fThe\u202fASCO Post, in partnership with the American Society of Clinical Oncology (ASCO), communicates news of evidence-based multidisciplinary cancer care to a broad audience of oncology professionals and ASCO members.\u202f\u202f Alexandra Vitale is a von Hippel-Lindau syndrome survivor living in [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"footnotes":""},"categories":[5137],"tags":[],"class_list":["post-46413","post","type-post","status-publish","format-standard","hentry","category-world-news"],"_links":{"self":[{"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/posts\/46413","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/comments?post=46413"}],"version-history":[{"count":1,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/posts\/46413\/revisions"}],"predecessor-version":[{"id":46869,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/posts\/46413\/revisions\/46869"}],"wp:attachment":[{"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/media?parent=46413"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/categories?post=46413"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/ogkologos.com\/en\/wp-json\/wp\/v2\/tags?post=46413"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}