Paediatric Solid Tumour Biology and Therapeutics Group

Professor Louis Chesler’s group is investigating the genetic causes for the childhood cancers, neuroblastoma, medulloblastoma and rhabdomyosarcoma. 

Research, projects and publications in this group

Our group's aim is to improve the treatment and survival of children with neuroblastoma, medulloblastoma and rhabdomyosarcoma.

The goal of our laboratory is to improve the treatment and survival of children with neuroblastoma, medulloblastoma and rhabdomyosarcoma, three paediatric solid tumours in which high-risk patient cohorts can be defined by alterations in a single oncogene. We focus on the role of the MYCN oncogene, since aberrant expression of MYCNis very significantly associated with high-risk in all three diseases and implies that they may have a common cell-of-origin.

Elucidating the molecular signalling pathways that control expression of the MYCN oncoprotein and targeting these pathways with novel therapeutics is a major goal of the laboratory. We use a variety of innovative preclinical drug development platforms for this purpose.

Technologically, we focus on genetically engineered cancer models incorporating novel imaging (optical and fluorescent) modalities that can be used as markers to monitor disease progression and therapeutic response.

Our group has several key objectives:

  • Mechanistically dissect the role of the MYCN oncogene, and other key oncogenic driver genes in poor-outcome paediatric solid tumours (neuroblastoma, medulloblastoma, rhabdomyosarcoma).
  • Develop novel therapeutics targeting MYCN oncoproteins and other key oncogenic drivers
  • Develop improved genetic cancer models dually useful for studies of oncogenesis and preclinical development of novel therapeutics.
  • Use such models to develop and functionally validate optical imaging modalities useful as surrogate markers of tumour progression in paediatric cancer.

Professor Louis Chesler

Clinical Senior Lecturer/Group Leader:

Paediatric Solid Tumour Biology and Therapeutics Professor Louis Chesler (Profile pic)

Professor Louis Chesler is working to understand the biology of children’s cancers and use that information to discover and develop new personalised approaches to cancer treatment. His work focuses on improving the understanding of the role of the MYCN oncogene.

Researchers in this group

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Email: [email protected]

Location: Sutton

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Phone: +44 20 3437 6124

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OrcID: 0000-0003-3977-7020

Phone: +44 20 3437 6109

Email: [email protected]

Location: Sutton

I obtained an MSci in Biochemistry from the University of Glasgow in 2018. In October 2018 I joined the labs of Dr Michael Hubank and Professor Andrea Sottoriva to investigate the use of liquid biopsy to monitor clonal frequency and emergence of resistance mutations in paediatric cancers.

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Email: [email protected]

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Location: Sutton

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Email: [email protected]

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Professor Louis Chesler's group have written 113 publications

Most recent new publication 4/2025

See all their publications

Vacancies in this group

Working in this group

Postdoctoral Training Fellow

  • Chelsea
  • Structural Biology
  • Salary Range: £45,600 - £55,000 per annum
  • Fixed term

Under the leadership of Claudio Alfieri, we are seeking to appoint a Postdoctoral Training Fellow to join the Molecular Mechanisms of Cell Cycle Regulation Group at the Chester Beatty Laboratories, Fulham Road in London. This project aims to investigate the molecular mechanisms of cell cycle regulation by macromolecular complexes involved in cell proliferation decisions, by combining genome engineering, proteomics and in situ structural biology. For general information on Post Doc's at The ICR can be found here. Key Requirements The successful candidate must have a PhD in cellular biochemistry and experience in Cryo-EM and CLEM is desirable. The ICR has a workforce agreement stating that Postdoctoral Training Fellows can only be employed for up to 7 years as PDTF at the ICR, providing total postdoctoral experience (including previous employment at this level elsewhere) does not exceed 7 years Department/Directorate Information: The candidate will work in the Molecular Mechanisms of Cell Cycle Regulation Group within the ICR Division of Structural Biology headed by Prof. Laurence Pearl and Prof. Sebastian Guettler. The division has state-of-the-art facilities for protein expression and biophysics/x-ray crystallography, in particular the Electron Microscopy Facility is equipped with a Glacios 200kV with Falcon 4i detector with Selectris energy filter and the ICR has access to Krios microscopes via eBIC and the LonCEM consortium. We encourage all applicants to access the job pack attached for more detailed information regarding this role. For an informal discussion regarding the role, please contact Claudio Alfieri via Email on [email protected]

Postdoctoral Training Fellow - Computational Single Cell Biology (Dr Stephen-John Sammut)

  • Chelsea
  • Cancer Dynamics
  • Salary Range: £45,600 - £51,450 per annum
  • Fixed term

Under the leadership of Dr Stephen-John Sammut, we are seeking a highly motivated and ambitious postdoctoral researcher to apply existing and develop cutting-edge single-cell computational methods for modelling breast tumour evolution during chemotherapy and immunotherapy. Your work will contribute to the development of predictive frameworks that can be deployed in breast clinical trials to guide treatment decisions. This role offers an outstanding opportunity to drive innovation at the interface of computational biology and clinical research, shaping the future of precision oncology. For general information on Post Doc's at The ICR can be found here. The ICR has a workforce agreement stating that there is a maximum duration of employment of 7 years including pre-ICR PDTF experience. Key Requirements The successful candidate must have a PhD in a computational biology or other numerical subject, have extensive programming experience, and possess a basic knowledge of cancer biology. A background in the analysis and interpretation of molecular data is essential. If available, please include a link to your online, publicly-available source code repository in your application. Department/Directorate Information: The Cancer Dynamics Laboratory headed by Dr Stephen John Sammut, focuses on developing computational and experimental frameworks that model changes in breast cancer biology during treatment to develop personalised precision cancer therapies. The Breast Cancer Now Toby Robins Research Centre at the ICR is the first centre in the UK entirely devoted to breast cancer research. Our goal is to advance research into the causes, diagnosis and treatment of breast cancer. It is located in state-of-the-art laboratory space, with excellent core facilities and is funded through a long term renewable programme grant from Breast Cancer Now. The Centre is directed by Clinician Scientist Professor Andrew Tutt. We encourage all applicants to access the job pack attached for more detailed information regarding this role. What we offer A dynamic and supportive research environment Access to state-of-the-art facilities and professional development opportunities Collaboration with leading researchers in the field Competitive salary and pension We encourage all applicants to access the job pack attached for more detailed information regarding this role.

Industrial partnership opportunities with this group

Opportunity: A novel test for predicting future cancer risk in patients with inflammatory bowel disease

Commissioner: Professor Trevor Graham

Recent discoveries from this group

02/06/25

A one-time immunotherapy treatment using a patient’s own immune cells has shown long-lasting benefit for people with advanced melanoma, a serious form of skin cancer, according to new five-year follow-up data from a pivotal clinical trial.

 Results from the C-144-01 clinical trial, a global, multicentre Phase 2 study involving 153 patients across Europe and the U.S. were presented today at the 2025 American Society for Clinical Oncology (ASCO) annual meeting. The Royal Marsden NHS Foundation Trust was the lead UK centre for the international trial.

Harnessing the immune system

 The trial explored the use of lifileucel, a type of immunotherapy, called TIL therapy, which harnesses the patient’s own immune system to fight cancer. The therapy involves isolating T cells from a site of cancer, expanding and activating these in a lab, before reinfusing back into the patient; these cells are then better able to recognise and attack cancer cells.

 Patients involved in the trial had metastatic melanoma refractory to standard approaches, meaning that the patient’s cancer had not responded to other treatment options, including targeted therapies and checkpoint inhibitors, which are drugs that block checkpoint molecules and reactivate the immune system so it can better recognise and destroy cancer cells.  

 Before immunotherapy, advanced melanoma was almost always fatal within a year. For patients on the trial, tumour shrinkage was seen in nearly four in five (79.3 per cent) of patients overall. Among those who responded, almost a third (31.4 per cent) remained in response at five years and one in 20 patients (5.9 per cent) had a complete response, meaning they had no evidence of cancer.

Nearly one in five alive after five years

Some patients saw their responses deepen over time, improving from partial to complete response, even a year after treatment. The median overall survival was 13.9 months.

 Nearly one in five patients (19.7 per cent) were still alive at five years and no new or delayed side effects related to the therapy were reported over the five-year follow-up.

The results, now representing the longest follow-up of a TIL therapy in this patient population, highlight the potential of lifileucel to provide hope for people who previously had few, if any, treatment options.

 Building on these results, lifileucel is now being tested in combination with pembrolizumab, a standard checkpoint inhibitor, for use as a first-line treatment in newly diagnosed patients with advanced melanoma in the TILVANCE-301 Phase 3 trial.

Lifileucel was approved by the U.S. Food and Drug Administration (FDA) for the treatment of advanced melanoma last year and is the first cellular therapy to be approved for solid tumours. Regulatory review on the therapy is now taking place in Europe and the UK, which also paves the way for earlier use of TIL therapy in a patient’s treatment journey.

‘Six weeks after my TIL therapy the tumours had disappeared’

 Zoe Phillips, 46, from Dorset was diagnosed with stage 4 metastatic melanoma in 2023 after previously being treated for skin cancer on her neck two years earlier. She was referred to The Royal Marsden where she able to join a first-line TIL therapy trial.

 Zoe says: “Six weeks after my first TIL therapy treatment my scans showed that the tumours had completely disappeared. Before coming to The Royal Marsden I was told that I would probably die, so hearing that my treatment had been successful was amazing, I was over the moon.  

 “I come back to the hospital regularly for pembrolizumab immunotherapy treatment and currently still have no evidence of cancer. I can’t thank The Royal Marsden enough, this trial has saved my life and enabled me to continue making memories with my husband and daughter.”

Dr Andrew Furness, Consultant Medical Oncologist who led the trial at The Royal Marsden NHS Foundation Trust, said: “While current forms of immunotherapy have revolutionised the treatment of cancer in recent years, overall these benefit a minority rather than majority of treated patients. Results from this trial have shown that TIL therapy may change the outlook for people with advanced melanoma.

“We’re continuing our research into the use of TIL therapy, as well as other forms of cellular therapy, across a broader spectrum of cancers including advanced lung, liver, ovary, skin and testicular subtypes as well as soft tissue sarcoma.”

‘A transformative option in melanoma care’

Co-author of the study, Professor James Larkin, Consultant Medical Oncologist at The Royal Marsden and Professor at The Institute of Cancer Research, London, said:

“These significant results offer a compelling case for TIL therapy as a transformative option in melanoma care. The study demonstrates that for patients with few options left, a single infusion of lifileucel can provide a deep and lasting response and even complete remission in some cases. This marks a major advance in how we think about treating solid tumours.”

The C-144-01 clinical trial was funded by Iovance Biotherapeutics. Solid tumour cellular therapy research at The Royal Marsden is funded by supporters of The Royal Marsden Cancer Charity including a generous donation from Nationwide Building Society, and funding from The National Institute for Health and Care Research (NIHR) Biomedical Research Centre at The Royal Marsden NHS Foundation Trust and The Institute of Cancer Research, London.