Royal Marsden NHS Foundation Trust
Dr Khan research-active consultant in the Gastrointestinal Unit who contributed significantly to the development and business approval of a new Acute Oncology Service (AOS) at the Sutton site.
His clinical training at the Northern Ireland Cancer Centre and Royal Marsden Hospital provided him with broad exposure to a wide range of clinical problems, therapeutic clinical trials of chemotherapy, targeted agents and immunotherapy in both common and rare cancers.
He gained significant experience in the set-up and running of large multicentre academic and translational studies from the time that he spent in full-time research, which included working as trial physician for phase II/III studies in early and advanced Colorectal Cancer sponsored by the industry and the Royal Marsden Hospital and led to an MD (Res). In collaboration with Professor Cunningham, he secured grant funding from Industry to run an academic phase II study of regorafenib in metastatic refractory colorectal cancer that completed recruitment in 2017. He also wrote a successful application for NIHR portfolio adoption of this study. The findings from this study were published in GUT last year. The other important component of my thesis defining the role of ctDNA in metastatic colorectal cancer was considered practice changing and was published in Cancer Discovery earlier this year.
Within the Royal Marsden Drug Development Unit he also gained useful experience of early phase trials. He has been a member of the Royal Marsden Research Ethics Committee and Drugs and Therapeutics Committee since 2018. He also serves as expert member of Surrey Borders National Research and Ethics Committee since 2016.
He enjoys teaching and has played an active role in improving the educational experience of the junior doctors. He writes questions for MRCP (UK) and Medical Oncology exams since 2014, to ensure his positive contribution towards national teaching.
Biomarkers of response and/or resistance to targeted therapies in refractory mCRC
Liquid biopsies capture spatial and temporal heterogeneity underpinning resistance to targeted therapies in various cancers. Dense serial sampling is however needed to predict the time to treatment failure and generate a window of opportunity for intervention.
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