The world's top-ranked cancer hospital, home of MSK-IMPACT sequencing, the dostarlimab rectal cancer study, and CAR-T pioneers.
Memorial Sloan Kettering Cancer Center is a New York cancer centre founded in 1884, NCI-designated as comprehensive and ranked first in the Newsweek/Statista World's Best Specialized Hospitals list for oncology, which makes it the reference point against which other cancer hospitals are measured. Its firsts include MSK-IMPACT, an FDA-authorised tumour sequencing panel that feeds OncoKB and cBioPortal, co-development of CD19 CAR-T cell therapy with Sadelain's group, the dostarlimab study in mismatch-repair-deficient rectal cancer led by Andrea Cercek, and the Paige AI digital pathology spin-out. It runs one of the largest oncology trial portfolios in the United States. The open question for a centre this large is how quickly its knowledge reaches practice elsewhere, a bottleneck OnCo tracks explicitly. Its people and trials pages are the best way into the detail.
From OpenAlex, oncology works in the last five years (2022 to 2026, current year in progress); counted on 2026-09-24.
Matched to Memorial Sloan Kettering Cancer Center, including child institutions. 5,120 works · 95,936 citations · 69% open access · 15% clinical trials · 1% reviews.
Led the trials of larotrectinib, entrectinib, repotrectinib and selpercatinib that turned rare gene fusions into treatable targets.
In the 1940s the General Motors chairman joined engineer Charles Kettering to establish the Sloan Kettering Institute, dedicated in 1948, which gave Memorial Hospital a research arm and its modern name.
Led the study in which every patient with mismatch-repair-deficient rectal cancer had a complete response to dostarlimab, without surgery or radiation.
Ran the trials that made trastuzumab deruxtecan the first HER2-directed drug for lung cancer.
The inventor of the electric car starter and head of General Motors research joined Alfred Sloan in the 1940s to establish the Sloan Kettering Institute for cancer research.
Co-developed imatinib's successor dasatinib and the prostate drug enzalutamide, and explained how cancers resist targeted drugs.
Defined the molecular subtypes of small-cell lung cancer and led early trials of DLL3-targeted therapy.
Clifford Hudis is a breast oncologist who has run ASCO since 2016.
In 1971 he put nearly all of his international holdings into a cancer research institute that carries his name reluctantly; it has since spent more than $1.8 billion of its own money on cancer science.
Built MSK-IMPACT, the first FDA-authorised tumour sequencing panel, and the clinical genomics programme behind OncoKB and cBioPortal.
Treated for prostate cancer from 1992, he gave MIT $100 million in 2007 to build an institute that puts engineers and cancer biologists under one roof, and MSK $150 million in 2015 for a new outpatient cancer building.
Led CheckMate 274, which established adjuvant nivolumab after bladder cancer surgery.
Led PATHFINDER, the first prospective study of a multi-cancer blood test in practice, and the PROSPECT rectal cancer trial.
Leading pancreatic cancer trialist, including the maintenance PARP-inhibitor and germline-BRCA studies.
A breast cancer survivor and Estée Lauder executive who co-created the pink ribbon in 1992 and founded the Breast Cancer Research Foundation in 1993, now one of the largest private funders of breast cancer research.
Led the enasidenib and revumenib trials that brought IDH2 and menin inhibitors to acute leukaemia.
Led HIMALAYA and ClarIDHy, which gave liver cancer a dual-immunotherapy option and biliary cancer its first targeted drug.
Led PRIMA, which established rituximab maintenance in follicular lymphoma, and co-chaired POLARIX in DLBCL.
Lung cancer doctor who led PHAROS, the trial that brought the encorafenib and binimetinib pair to BRAF V600E-mutant lung cancer.
Mapped how EGFR-mutant lung cancers resist osimertinib and led the HER3-directed ADC trials that followed.
Defined how prostate cancer trials are run and read, from PSA working-group criteria to circulating tumour cell biomarkers.
Led INDIGO, the trial that made vorasidenib the first targeted therapy for low-grade IDH-mutant glioma.
Ran the long-term CD19 CAR-T studies in adult leukaemia that showed durable remissions and defined toxicity risk.
Radiochemist who built the zirconium-89 immuno-PET platform and MSKCC's radiopharmaceutical pipeline.
A psychiatrist who set up the first full-time psychiatry service in a cancer hospital at Memorial Sloan Kettering in 1977, founded the field's societies and journal, and made distress a vital sign in cancer care.
In 1936 he donated the land on York Avenue to which Memorial Hospital moved; Memorial Sloan Kettering has been there ever since.
In 1884 he and his wife Charlotte were among the group who founded New York Cancer Hospital, the institution that became Memorial Sloan Kettering Cancer Center.
Led the early enfortumab vedotin trials and the atezolizumab study that first brought immunotherapy to bladder cancer.
Surgeon who led OPRA, showing half of rectal cancer patients can keep their rectum with total neoadjuvant therapy and watch-and-wait.
Leads the next wave of endocrine therapy: oral SERDs like imlunestrant and the PI3K inhibitor inavolisib.
Co-led the work that made pembrolizumab the first tumour-agnostic cancer drug approval, for mismatch-repair-deficient tumours.
New York breast oncologist and cancer geneticist who led OlympiAD, the trial that made olaparib the first PARP inhibitor approved for BRCA-mutated breast cancer.
Led CheckMate 069, the first randomised trial of nivolumab plus ipilimumab, and defines how to manage immunotherapy side effects.
Built MSK-IMPACT, the tumour sequencing test used on more than 100,000 patients and the first FDA-authorised hospital panel.
Principal investigator of the VISION trial that made lutetium-PSMA a standard prostate cancer treatment.
Breast surgeon whose margin and axillary guidelines cut unnecessary re-excisions and lymph node surgery worldwide.
His 2006 pledge of $100 million, then the largest individual commitment in MSK's history, built a 23-storey laboratory tower that nearly doubled the centre's research space.
Developed the anti-GD2 antibodies 3F8 and naxitamab that treat relapsed neuroblastoma.
New York melanoma doctor who was lead author of BRIM-3, the trial that showed vemurafenib lengthens survival in BRAF-mutant melanoma and launched targeted therapy for the disease.
Lung cancer doctor who was lead author of VISION, the trial that established tepotinib for lung cancers with MET exon 14 skipping mutations.
New York haematologist who led MANIFEST-2, the trial testing whether adding the BET inhibitor pelabresib to ruxolitinib helps people with myelofibrosis more than ruxolitinib alone.
The kidney cancer trialist behind sunitinib, CheckMate 214 and CLEAR, three shifts in first-line standard of care.
New York oncologist who was lead author of the KRYSTAL-1 colorectal report, which showed adagrasib with cetuximab shrinks KRAS G12C-mutant colorectal cancer and led to the combination's approval.
Discovered the JAK2 mutation behind most myeloproliferative neoplasms and defined the genetics of clonal haematopoiesis.
Saad Usmani led the pivotal teclistamab study, the first bispecific antibody approved for myeloma.
Led SPEARHEAD-1, the trial that made afami-cel the first engineered TCR T-cell therapy approved for a solid tumour.
In 2016 he founded and funded an institute that runs cancer immunotherapy research as one network across a dozen leading cancer centres, sharing data, samples and patents rather than competing for them.
Selwyn Vickers is a surgeon-scientist who leads the world's top-ranked cancer hospital.
Led DESTINY-Breast01 and DESTINY-Breast04, the trials that created the HER2-low category and opened T-DXd to most breast cancers.
Diagnosed with metastatic melanoma at 22, she received the anti-CTLA-4 antibody ipilimumab in an early trial at Memorial Sloan Kettering and has been cancer-free since. Her meeting with James Allison in 2006 is part of immunotherapy's history.
Led ECHELON-2, the first trial to improve survival in peripheral T-cell lymphoma, using brentuximab vedotin.
Thoracic surgeon who led the IASLC staging projects that define how lung cancer and mesothelioma are staged.
New York oncologist who led KEYNOTE-775, the trial that established lenvatinib plus pembrolizumab for advanced endometrial cancer after chemotherapy.
Surgeon-scientist whose personalised mRNA vaccine trial showed pancreatic cancer can provoke lasting T-cell immunity.
Sarcoma oncologist who led ANNOUNCE and the pexidartinib trial that produced the first drug for tenosynovial giant cell tumour.
Led CheckMate 649, which made immunotherapy plus chemotherapy the first-line standard for gastric cancer, and the pembrolizumab-trastuzumab combination in HER2-positive disease.
For gallbladder cancer the points that matter are that HER2 can disappear under HER2-directed pressure, that SMAD4 co-mutation predicts a worse response, and that sequencing at progression, not just at diagnosis, may be needed to guide the next line.
For patients with advanced melanoma, immunotherapy offers a realistic chance of long-term survival and probably cure, and the ten-year data show that patients who are alive and progression-free at three years rarely die of melanoma afterwards. Nivolumab plus ipilimumab gives the best long-term results but at a high price in serious side effects; nivolumab alone or nivolumab plus relatlimab are alternatives for patients at lower risk or with autoimmune concerns. The trial is also a caution about surrogate endpoints: the survival plateau took years to become visible.
For mismatch repair-deficient rectal cancer, six months of a single antibody now replaces chemotherapy, radiotherapy and an operation, and the same appears to be true for early-stage mismatch repair-deficient cancers of other organs.
The strongest human evidence that a cancer vaccine can make durable T cells in a tumour with few mutations; the randomised phase 2 IMCODE003 (260 patients, primary completion listed for January 2031) is the test of whether that translates into fewer relapses.
The cleanest split of HER2 alterations in gallbladder cancer into amplification and mutation, which matters because IHC and ISH only see the amplified tumours. It also shows the high-incidence Chilean population has not been sequenced at scale.
Young adults with a grade 2 IDH-mutant glioma who have had surgery can now take a daily tablet that slows or reverses tumour growth and defers radiotherapy and chemotherapy, both of which carry long-term cognitive costs, by years. It confirms that the IDH mutation is a driver that can be targeted, not just a marker. Whether it improves survival or cognition over the long term, and whether it helps in higher-grade or previously treated tumours, is unknown.
Pancreatic cancer was thought to be immunologically inert because of its low mutation burden; this study showed that with the right vaccine platform its few neoantigens can still be targeted. It is the strongest human evidence so far that personalised cancer vaccines can generate durable, tumour-specific immunity, and it justifies the randomised trials now running in pancreatic cancer and melanoma. Benefit is not yet proven, because responders may simply have had more immunogenic tumours.
It is the strongest case that mutation burden is real biology in lung cancer and, at the same time, the clearest demonstration that its threshold is not fixed, which is why it never became a reliable selector.
Shares Break Through Cancer, Damon Runyon Cancer Research Foundation, National Comprehensive Cancer Network (NCCN), Sean Parker.
Shares Newsweek/Statista World's Best Specialized Hospitals: Oncology, Break Through Cancer, Cut the nerve supply to tumours with old drugs, David H. Koch.
Shares Cut the nerve supply to tumours with old drugs, Damon Runyon Cancer Research Foundation, Daniel K. Ludwig, Ludwig Cancer Research.
Shares Mortimer Zuckerman, Evelyn Lauder, John Jacob Astor III, Alfred P. Sloan Jr..
Shares Dean F. Bajorin, Michael A. Postow, Yelena Y. Janjigian, Regionally delivered mesothelin CAR-T with PD-1 blockade.
Shares Durvalumab with or without tremelimumab for patients with metastatic pancreatic ductal adenocarcinoma: a phase 2 randomized clinical trial, Circadian control, What actually holds T cells at the tumour border?, Association of high tumor mutation burden in non-small cell lung cancers with increased immune infiltration and improved clinical outcomes of PD-L1 blockade across PD-L1 expression levels.
Shares Break Through Cancer, A revised classification system and recommendations from the Baltimore consensus meeting for neoplastic precursor lesions in the pancreas, Limited heterogeneity of known driver gene mutations among the metastases of individual patients with pancreatic cancer, Precancerous neoplastic cells can move through the pancreatic ductal system.
Shares What makes a neoantigen actually immunogenic?, Identification of unique neoantigen qualities in long-term survivors of pancreatic cancer, Shared splice-derived neoantigens as off-the-shelf vaccine targets, Association of high tumor mutation burden in non-small cell lung cancers with increased immune infiltration and improved clinical outcomes of PD-L1 blockade across PD-L1 expression levels.
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.
The open platform for exploring multidimensional cancer genomics data, hosting TCGA, GENIE and hundreds of studies and installed at cancer centres worldwide.
Converts VCF variant calls into the MAF format used by cBioPortal and TCGA, running Ensembl VEP for annotation.
The Computational Environment for Radiological Research, a MATLAB platform for radiotherapy plan analysis, radiomics and outcomes modelling from MSK.
Planning and Optimization for Radiation Therapy: an open Python platform with benchmark patient data for planning research, from MSK.
Allele-specific copy-number and clonal heterogeneity analysis for tumour sequencing, from Memorial Sloan Kettering; the method behind many MSK-IMPACT copy-number calls.
The React front end of cBioPortal: OncoPrints, mutation mappers, survival plots and cohort comparison.
Scripts that annotate MAF, copy-number and fusion files with OncoKB levels of evidence through its API token.
Memorial Sloan Kettering's open classification of cancer types used by cBioPortal, GENIE and OncoKB.
Commercial and regulated products that this organisation sells. Each card says what is behind it: a regulator's database, the literature, a public body's list, or only the company's own words. Listing is not endorsement, and a clearance is a regulatory fact, not a clinical one.
A hospital's own targeted sequencing test and its analysis pipeline, authorised in the United States and the source of one of the largest public clinical sequencing cohorts.