Close-up of an the ICR logo on a research centre

Centre for In Vivo Modelling

The Centre for In Vivo Modelling is a newly established research centre within the Division of Cancer Biology at the ICR. Our scientists and clinical researchers use state-of-the-art in vivo models to address fundamental questions in cancer biology, with the ultimate aim of identifying curative treatments. We also serve as a collaborative hub across the ICR and The Royal Marsden, providing cutting-edge expertise in advanced mouse genetics and humanised in vivo models of cancer.

Professor Kamil R Kranc, Chair of Haemato-Oncology, serves as the Centre's Director, while Fabiana Muzzonigro is the Centre Administrator.

 

How we conduct research at this centre

Solid tumours and blood cancers are highly complex ecosystems, with many composed of varying cell types including rare cancer stem cells at the apex of a hierarchical organisation, more differentiated malignant progeny, and a dynamic microenvironment that nurtures tumour growth and survival. At our Centre, we seek to elucidate the fundamental principles that govern this malignant ecosystem. We employ advanced mouse genetics (including barcoding and lineage tracing) and PDX models to dissect how tumour cells function, evolve under selective pressures, evade therapy, and engage with their microenvironment to sustain disease progression. By decoding these intricate cellular and molecular interactions, we aim to identify transformative therapeutic strategies capable of eradicating cancer at its origin - achieving durable remission while preserving normal tissue integrity.

A particular strength of our Centre lies in the generation and application of in vivo models, which are essential for uncovering novel aspects of cancer biology and evaluating emerging therapies. We work in close collaboration with ICR researchers and clinicians at The Royal Marsden to develop patient-derived xenograft (PDX) models of leukaemias and solid tumours by transplanting human cancer tissue into immunocompromised mice. In parallel, we generate and utilise genetically engineered mouse models (GEMMs) to interrogate cancer biology in a physiologically relevant context. By leveraging these sophisticated in vivo systems, the Centre aims to:

  • Uncover new facets of cancer biology in a complex in vivo ecosystem
  • Discover and validate novel therapeutic targets allowing for elimination of cancer stem cells and their malignant progeny in blood cancers and solid tumours
  • Collaborate closely with drug discovery teams at the ICR to develop inhibitors of these targets
  • Evaluate new anti-cancer drugs in pre-clinical in vivo models, paving the way for clinical trials.

In addition to our academic focus, CIVM serves as a collaborative hub across the ICR and The Royal Marsden, providing the ICR community with cutting-edge expertise in advanced mouse genetics and humanised mouse models of cancer.

Join us

We are recruiting two exceptional Group Leaders to join the Division of Cancer Biology and the Centre for In Vivo Modelling (CIVM). This is a unique opportunity to shape the future of cancer biology research, lead innovative programmes, and make discoveries that transform patient outcomes.

These new Group Leaders will investigate fundamental mechanisms of tumour initiation, progression, and treatment resistance, and develop cutting-edge preclinical models to advance understanding of cancer biology. Working in close collaboration across the ICR and The Royal Marsden Hospital, the postholders will translate discovery science into new therapeutic opportunities, contributing to the ICR’s mission to make the discoveries that defeat cancer.

Find out more about the vacancies

Members of this Centre

Pipettes and well plates

In Vivo Modelling core

We provide cutting-edge expertise in advanced mouse genetics and humanized mouse models of cancer.

CIVM Service Core

Other staff:

Driving discovery through collaboration 

At CIVM, our collaborative spirit drives our mission to advance cancer cures. We actively partner with basic science, translational, and clinical research groups across the ICR and The Royal Marsden. Our collaborations also extend beyond, working closely with distinguished academic teams at the Universities of Oxford, Cambridge, Edinburgh, Cardiff, London, Glasgow, and the Francis Crick Institute.

 

News from the Centre

We are recruiting a Group Leader in In Vivo Cancer Modelling. We welcome applications at both the Career Development Faculty and Career Faculty levels. Competitive start up package is available. For further particulars please contact [email protected].

 

 

Current vacancies

There are currently no vacancies available in this group or area.

News from the ICR

18/06/26

Thousands of men with prostate cancer in England will be offered a more precise form of radiotherapy that cuts treatment time by up to 75 per cent, based on the results of a trial led by The Institute of Cancer Research, London and The Royal Marsden NHS Foundation Trust.

The PACE-B trial showed that stereotactic body radiotherapy (SBRT) – also known as stereotactic ablative radiotherapy (SABR) – which is more powerful and targeted than standard external radiotherapy, can effectively treat many small, low-risk prostate cancers in just five hospital visits, rather than 20. 

Now, all 48 NHS radiotherapy centres in England will begin offering this five-session SBRT treatment to eligible men within the next three months. 

Who is SABR for?

NHS England has approved SBRT for men in England with early-stage prostate cancer that hasn’t grown outside the prostate, and that has a low or medium risk of growing or spreading.

NHS England’s modelling suggests that around 3,500 men with this type of early-stage low or medium-risk prostate cancer will choose the new treatment over standard radiotherapy each year.

Power and precision

SBRT combines the power of multiple tiny, intense energy beams aimed at a tumour from different angles. These beams converge over the tumour, delivering a very high dose of radiation to cancer cells while minimising the impact on healthy cells.

Because of its pinpoint accuracy, SBRT is especially suitable for treating small, well-defined cancers. If a cancer has begun to grow or spread, standard radiotherapy is usually a better option, as its wider beams can kill cancer cells outside the tumour.

The PACE-B trial, which was managed by the Clinical Trials and Statistics Unit at the ICR, tested whether five sessions of SBRT radiotherapy in a fortnight are as effective for treating low-risk, localised prostate cancer as 20 sessions of standard intensity-modulated radiotherapy (IMRT) delivered Monday to Friday for four weeks.

The phase III international randomised trial found that both treatments worked equally well, keeping cancer under control in moth patients.

Keeping cancer under control

 Five years after entering the study, cancer remained under control, with no recurrence or worsening, in 96 per cent of patients who had SBRT compared to 95 per cent of patients who had conventional radiation.

Side effects were low in both groups. At five years post-treatment, 5.5 per cent of patients who received SBRT experienced grade 2 or higher side effects affecting the genital or urinary organs, compared to 3.2 per cent in the conventional group. Only one person in each group experienced grade 2 or higher gastrointestinal side effects. Grade 2 side effects can be bothersome, and may affect daily activity, but they require little to no medical treatment.

Because it only takes a quarter of the sessions required for standard radiotherapy, SBRT puts much less strain on people and the health service. If, as NHS England estimates, 1 in 5 eligible men choose it over standard radiotherapy, an extra 50,000 prostate cancer treatment appointments could be made available each year.

'A game-changer'

Professor Emma Hall, Director of the Clinical Trials and Statistics Unit at The Institute of Cancer Research, London, which managed the PACE-B trial, said:

“I am delighted to see that SBRT, offering patients treatment in just five doses rather than 20, is now being recommended by the NHS. Treating patients in a fraction of the time is a game-changer – they can spend less time in hospital and travelling to appointments, whilst still receiving highly effective treatment.”

Professor Nicholas van As, Consultant Clinical Oncologist at The Royal Marsden NHS Foundation Trust, Professor in Precision Prostate Radiotherapy at The Institute of Cancer Research, London, and Chief Investigator of the PACE-B trial, said:

“We are delighted that eligible prostate cancer patients across England will now be able to benefit from this treatment following NHS England's announcement.

“The news demonstrates the value of clinical research in improving cancer care. At The Royal Marsden and the ICR, we are focused on developing smarter, better and kinder treatments for patients across the UK and around the world.

“The PACE-B trial was designed to answer an important question: can we safely deliver prostate radiotherapy in far fewer treatment sessions without compromising outcomes? The results showed that we can. Delivering treatment in just five sessions was as safe and effective as conventional radiotherapy, while significantly reducing the burden of treatment for patients. The findings helped establish the evidence base for wider adoption of the treatment and have informed clinical practice internationally.”

Professor Peter Johnson, NHS National Clinical Director for Cancer, said:

“This technology lets us focus a powerful and precise beam of radiotherapy directly onto the cancer, limiting the damage to healthy cells. And the fact it can be delivered in 15 fewer doses will help men get back to living their lives far more quickly.” 

Banner image: IMRT radiotherapy machine. SBRT can be delivered on a Cyberknife or standard radiotherapy machines.