DiscoverCOR2ED - Oncology Medical Conversation VideoUnderstanding Rare NSCLC Mutations: Insights, access and support
Understanding Rare NSCLC Mutations: Insights, access and support

Understanding Rare NSCLC Mutations: Insights, access and support

Update: 2025-05-14
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Listen to a revealing conversation between Dr Joshua Sabari, a Medical Oncologist specialising in the treatment of rare alternations of NSCLC and Debra Montague, President of Lung Cancer Europe (LuCE) and founder of ALK Positive UK.   


As a patient advocate as well as a patient herself, Debra brings a wealth of experience and depth of insight into the discussion with Dr Sabari.   


Dr Sabari shares his clinical knowledge regarding diagnosis, biomarker testing and treatment of such alterations, together with his own first-hand experience of treating and empowerig patients like Debra in their own treatment journey. 


What does the patient pathway look like from both perspectives?  What are the needs of Medical Oncologists and patients when navigating the treatment journey?  What do patients need from their oncologists?  What do oncologists think their patients need from them?  Are these needs matched by the support currently available?   


You can also watch a video of the experts in conversation and download the transcript on our website: https://cor2ed.com/lung-connect/programmes/understanding-rare-nsclc-mutations/?media=0 


Or watch on YouTube: https://www.youtube.com/watch?v=Z57cUtQx1BE&t 


 


Follow LUNG CONNECT on social media: 


X – https://x.com/lung_connect  


LinkedIn – https://www.linkedin.com/company/lungconnect/  


This content is intended for healthcare professionals only. 


The experts in this podcast are expressing their own views and not those of COR2ED, Supporters or their institution.  This podcast is supported by an Independent Education Grant from Boehringer Ingelheim. 


 


This podcast is developed by cor2ed.com 


Published on May 2025 


 


Subscribe to this channel to stay up to date with new Independent Education programmes as they’re released. 

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Understanding Rare NSCLC Mutations: Insights, access and support

Understanding Rare NSCLC Mutations: Insights, access and support

COR2ED Medical Education