Discovered more cancer drugs than any other academic institution, including abiraterone and the clinical use of PARP inhibitors.
The Institute of Cancer Research in London has discovered more cancer drugs than any other academic institution, including abiraterone through Johann de Bono and the clinical use of PARP inhibitors through Andrew Tutt and Alan Ashworth's synthetic lethality work, and it is the research partner of The Royal Marsden. Its Cancer Therapeutics Unit is also the origin of capivasertib, and its people include Christopher Lord, Kristian Helin, Mel Greaves, Mitch Dowsett and Judith M. Bliss. OnCo links it to olaparib, capivasertib, abiraterone and STAMPEDE, to the DNA replication stress pathway, and to ideas including a non-profit phase 1b combination unit. The valley of death between lab and product is the bottleneck it exists to cross. Its drug discovery, prostate and synthetic lethality programmes are listed below.
From OpenAlex, oncology works in the last five years (2022 to 2026, current year in progress); counted on 2026-09-24.
Matched to Institute of Cancer Research, including child institutions. 637 works · 10,594 citations · 76% open access · 13% clinical trials · 1% reviews.
Led OlympiA, the trial that showed a year of olaparib after surgery improves survival in BRCA-mutated breast cancer.
Cancer biologist who directs the Cancer Research UK Convergence Science Centre, the joint Institute of Cancer Research and Imperial College London programme bringing engineering and physical sciences into cancer research.
Co-discovered the synthetic lethality between PARP inhibition and BRCA loss that underlies PARP inhibitor therapy.
British radiation oncologist who led CHHiP, the trial that showed prostate cancer can be treated in 20 radiotherapy sessions rather than 37 with the same results, changing practice worldwide.
Medical oncologist who leads cancer services at Cork University Hospital as Clinical Director, with a focus on gynaecological and thoracic cancers and early-phase trials.
A Royal Marsden gastrointestinal oncologist who has shaped UK colorectal and upper gastrointestinal trials and who works on the blood test for residual disease after bowel surgery.
Melanoma and kidney cancer trialist who co-led CheckMate 067, the trial with 10-year immunotherapy survival data.
Johann de Bono led the trials that brought abiraterone and olaparib to prostate cancer patients.
Statistician who ran the START, FAST-Forward and POETIC trials that reshaped breast cancer radiotherapy and endocrine therapy.
Kevin Harrington is a head and neck oncologist and oncolytic virus pioneer who led the OPTiM trial of T-VEC.
Epigenetics researcher who leads the ICR, the academic institution with the most cancer drug discoveries.
Showed that childhood leukaemia begins before birth and framed cancer as an evolutionary process.
The translational scientist behind the aromatase inhibitor era and the Ki67 response test used in POETIC.
The Royal Marsden oncologist who runs the UK trial testing whether a blood test for leftover tumour DNA can decide who needs chemotherapy after bowel cancer surgery.
Nicholas James is chief investigator of STAMPEDE, the platform trial that reshaped treatment of advanced prostate cancer.
Breast cancer researcher who turned ctDNA into a tool for choosing treatment, leading SERENA-6 and CAPItello-291.
The Royal Marsden oncologist who ran the trial that cut a four-week course of prostate radiotherapy to five treatments, and published the higher urinary side-effect rate alongside the good news.
Drug-discovery pioneer who built the ICR's Cancer Therapeutics Unit and championed the 'pharmacological audit trail'.
The oncogeneticist who found most of the common genetic variants that raise a man's risk of prostate cancer, and whose work is the reason the UK's first prostate screening programme is defined by a gene rather than by an age.
The Royal Marsden thoracic oncologist, now its chief medical officer, who has been an investigator on most of the UK trials that put targeted drugs into lung cancer practice.
Chief investigator of monarchE, the trial that added abemaciclib to adjuvant endocrine therapy for high-risk early breast cancer.
Uwe Oelfke is the radiotherapy physicist behind the Marsden's pioneering MR-linac programme.
The first prospective test of acting on ctDNA in triple-negative disease, and a negative one: with a quarterly, single-mutation assay the window between detectable DNA and visible metastasis was too short to intervene. Later designs use tumour-informed assays, earlier sampling and drugs with more single-agent activity.
For TNBC, where brain metastases are common, the blind spot matters: a negative ctDNA test does not exclude intracranial relapse.
Patients with head and neck squamous cell cancer that has recurred or spread should be treated first with pembrolizumab: alone if their tumour is strongly PD-L1 positive and they can wait for a slower response, or with chemotherapy if the tumour is bulky or PD-L1 low. Cetuximab-based chemotherapy is no longer the default. Long-term follow-up shows a small but real group of patients alive at four to five years, which was almost unheard of before.
Men diagnosed with prostate cancer that has already spread, or that is locally advanced and high risk, should start abiraterone (or another androgen-receptor pathway inhibitor) at the same time as testosterone suppression rather than waiting for resistance. This roughly halves the risk of death over several years. The same platform later showed that docetaxel chemotherapy and, in high-volume metastatic disease, triple therapy also help, and that abiraterone benefits men with high-risk disease treated with radiotherapy.
The proof-of-principle paper for molecular residual disease in breast cancer, and the origin of the personalised digital PCR approach that c-TRAK TN later tested prospectively in TNBC.
The first molecularly stratified treatment in prostate cancer, and the proof that the synthetic lethality that works in ovarian and breast cancer works here too. Every PARP inhibitor now licensed in prostate cancer traces back to this trial.
The proof, in people, that castration-resistant prostate cancer is usually still androgen-driven. It renamed the disease (hormone-refractory became castration-resistant) and it opened the line of drugs that now dominate treatment at every stage from first diagnosis of metastatic disease onwards.
Shares FAST (5-fraction whole-breast radiotherapy), IMPORT LOW, START-A (UK Standardisation of Breast Radiotherapy, trial A), START-B (UK Standardisation of Breast Radiotherapy).
Shares FAST (5-fraction whole-breast radiotherapy), START-A (UK Standardisation of Breast Radiotherapy, trial A), START-B (UK Standardisation of Breast Radiotherapy), CHHiP.
Shares FAST (5-fraction whole-breast radiotherapy), START-A (UK Standardisation of Breast Radiotherapy, trial A), START-B (UK Standardisation of Breast Radiotherapy), CHHiP.
Shares Paul Workman, Scale up public drug development that takes academic assets to phase 1, The valley of death between lab and product, Cancer Research UK.
Shares Ian Chau, Naureen Starling, The Royal Marsden.
Open-source projects that this organisation maintains, from OnCo's own catalogue: licence and last activity as the repository reported them on the day of the fetch. Listing is not endorsement; check the licence before reuse and the validation before clinical use.
Expert reviews of chemical probes for protein targets so researchers pick well-validated tools, from the Institute of Cancer Research and partners.