Tony Ng
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Recent Grants
Grant: Close
Integrated multi-modal tissue state mapping of TNBC progression
Open Date: 2021-09-01
Close Date: 2024-08-01
Grant: Close
GSK - KCL Translational Oncology Research Hub
Open Date: 2021-08-01
Close Date: 2026-08-01
Grant: Close
Multimodality Early Detection of Head and Neck Cancer Recurrence
Open Date: 2021-03-01
Close Date: 2026-02-01
Grant: Close
Next generation molecular imaging and therapy with radionuclides
Open Date: 2019-10-01
Close Date: 2024-09-01
Grant: Close
A multiuser radioanalytical facility for molecular imaging and radiouclide therapy re-search.
Open Date: 2019-07-01
Close Date: 2024-06-01
Articles (15)
Year:
2025
Year:
2024
Year:
2023
Year:
2023
Year:
2023
Year:
2023
Year:
2022
Background: Advanced head and neck squamous cell carcinoma (HNSCC) is associated with a poor prognosis, and biomarkers that predict response to treatment are highly desirable. The primary aim was to predict progression-free survival (PFS) with a multivariate risk prediction model. Methods: Experimental covariates were derived from blood samples of 56 HNSCC patients which were prospectively obtained within a Phase 2 clinical trial (NCT02633800) at baseline and after the first treatment cycle of combined platinum-based chemotherapy with cetuximab treatment. Clinical and experimental covariates were selected by Bayesian multivariate regression to form risk scores to predict PFS. Results: A ‘baseline’ and a ‘combined’ risk prediction model were generated, each of which featuring clinical and experimental covariates. The baseline risk signature has three covariates and was strongly driven by baseline percentage of CD33 + CD14 + HLADR high monocytes. The combined signature has six covariates, also featuring baseline CD33 + CD14 + HLADR high monocytes but is strongly driven by on-treatment relative change of CD8 + central memory T cells percentages. The combined model has a higher predictive power than the baseline model and was successfully validated to predict therapeutic response in an independent cohort of nine patients from an additional Phase 2 trial (NCT03494322) assessing the addition of avelumab to cetuximab treatment in HNSCC. We identified tissue counterparts for the immune cells driving the models, using imaging mass cytometry, that specifically colocalized at the tissue level and correlated with outcome. Conclusions: This immune-based combined multimodality signature, obtained through longitudinal peripheral blood monitoring and validated in an independent cohort, presents a novel means of predicting response early on during the treatment course. Funding: Daiichi Sankyo Inc, Cancer Research UK, EU IMI2 IMMUCAN, UK Medical Research Council, European Research Council (335326), Merck Serono. Cancer Research Institute, National Institute for Health Research, Guy’s and St Thomas’ NHS Foundation Trust and The Institute of Cancer Research. Clinical trial number: NCT02633800 .
Year:
2022
Year:
2022
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2021
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2021
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2021
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2021
Year:
2021
Year:
2021
Collaborators (21)
Daniel Alexander
University College London
anna barnes
King's College London
Rafał Matkowski
Wroclaw Medical University
Philip Blower
King’s College London
Sheeba Irshad
King’s College London
Richard Beatson
University College London
Radhouene Neji
Senior Lecturer in MR Physics and Computing
King's College London
Daniel McGowan
Oxford University Hospitals NHS Foundation Trust
Kevin M. Brindle
University of Cambridge
Susan Heavey
University College London
James Arnold
Reader
King’s College London
James O'Connor
Professor and Team Leader
Institute of Cancer Research
Francesco Dazzi
King’s College London
Hayley Whitaker
University College London
Toby Lawrence
King’s College London
Khuloud T. Al‐Jamal
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Joseph M. Norris
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Manuel Rodriguez-Justo
Consultant & Professor Research Pathology
University College London
Geoff Higgins
University of Oxford
Gary Cook
King’s College London
Balaji Ganeshan
University College London
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