Consistently the top-ranked US hospital overall, with strong proton therapy and the first US carbon-ion centre under construction.
Mayo Clinic, headquartered in Rochester, Minnesota, is consistently the top-ranked US hospital overall and holds NCI comprehensive designation through the Mayo Clinic Comprehensive Cancer Center, which spans Rochester, Phoenix and Jacksonville; it sits fifth in the Newsweek/Statista oncology ranking. Its cancer strengths are multiple myeloma, lymphoma and individualised medicine, with proton therapy and the first US carbon-ion facility under construction in Jacksonville. OnCo links it to the Atlas pathology model built with Aignostics and Charité, to liver transplantation for cancer, to senescence and JAK-STAT pathway work, and to people including S. Vincent Rajkumar, Shaji K. Kumar and Matthew P. Goetz. Whether carbon-ion therapy earns its cost against protons is the open question its new centre will help answer. The Arizona and Florida campuses have their own OnCo pages.
From OpenAlex, oncology works in the last five years (2022 to 2026, current year in progress); counted on 2026-09-24.
Matched to Mayo Clinic, including child institutions. 4,572 works · 48,202 citations · 60% open access · 13% clinical trials · 3% reviews.
Led VISION, the trial that made lutetium-PSMA the first radioligand therapy for prostate cancer.
Cheryl Willman is a leukaemia genomics pioneer who leads Mayo Clinic's cancer centre across its three sites.
Evanthia Galanis is a brain tumour specialist who chairs one of the largest US clinical trial networks.
Mayo Clinic neuro-oncologist who was lead author of the long-term RTOG 9802 results, which showed that adding PCV chemotherapy to radiotherapy roughly doubles survival in high-risk low-grade glioma.
Mayo Clinic oncologist who chaired the American Thyroid Association guidelines for anaplastic thyroid cancer, one of the fastest-growing human cancers.
Leukaemia specialist who led E1910, the trial that put blinatumomab into frontline treatment for adults in remission.
Breast oncologist who led MONARCH 3 and studies how genetics shapes response to endocrine therapy.
Mayo Clinic radiation oncologist whose trials showed that focused radiosurgery preserves thinking and memory better than whole-brain radiotherapy for brain metastases, and that sparing the hippocampus reduces cognitive harm when whole-brain treatment is needed.
Myeloma expert who wrote the diagnostic criteria the field uses and a persistent critic of drug prices.
Myeloma trialist who led venetoclax and quadruplet studies and helped define MRD response criteria.
Mayo Clinic urologist who led the trial of nadofaragene firadenovec, the first gene therapy approved for bladder cancer that no longer responds to BCG.
Stephen Russell built the engineered measles viruses used against cancer and reported the case in which one intravenous dose put a patient's myeloma into complete remission.
GI oncologist behind trials of KRAS, HER2, and FGFR-directed therapy in colorectal and bile duct cancer.
The evidence behind the stage I de-escalation statement on the triple-negative page: an ordinary haematoxylin and eosin slide identifies a fifth of patients whose outcome without chemotherapy matches treated cohorts. A prospective trial of chemotherapy omission is the missing step.
Biliary tumours are often diagnosed on tiny biopsies or brushings, so a blood-based panel that detects HER2 amplification and other targets in half of patients is a practical route to testing, with tissue confirmation where the blood is uninformative.
Family history misses most carriers, so the NCCN and ASCO guidelines moved to testing every patient; each carrier found is a family that can be offered surveillance and a patient who may be eligible for platinum and PARP inhibition.
A scoring tool that needs no new test and can run in primary care records; it turns the 1 percent of Chari's cohort into a 3.6 percent group in whom imaging or a blood test becomes defensible.
It defines the gene list a TNBC germline panel should report on and shows the same genes apply in African American women, the population with the highest TNBC incidence.
It stops a BRAF-mutant report being read as one uniform outlook, and it separates the class II and III mutations, which signal differently and are not covered by the encorafenib plus cetuximab label, from V600E.
This cohort underpins the guideline shift to germline BRCA1/2 testing for all TNBC patients regardless of age or family history, and it is the prevalence figure the corpus uses for germline BRCA1 in TNBC.
It is the evidence behind universal mismatch repair testing of every colorectal cancer, which is now standard in most guidelines and which, as a by-product, identifies everyone eligible for immunotherapy.
Shares Hitachi (particle therapy), Carbon-ion therapy, Gamma Knife, Stereotactic radiosurgery (Gamma Knife, CyberKnife, linac SRS).
Shares Aignostics, Atlas (Aignostics, Mayo Clinic, Charité), Stereotactic radiosurgery (Gamma Knife, CyberKnife, linac SRS), Proton therapy machines: cyclotrons, synchrotrons and single-room systems.
Shares Evanthia Galanis, Stephen J. Russell, Multiple myeloma.
Shares Hitachi (particle therapy), Carbon-ion therapy, Proton therapy machines: cyclotrons, synchrotrons and single-room systems, Proton therapy.
Shares Hitachi (particle therapy), Proton therapy machines: cyclotrons, synchrotrons and single-room systems, Proton therapy, Biliary tract cancer (cholangiocarcinoma).
Shares S. Vincent Rajkumar, Shaji K. Kumar, Multiple myeloma.
Shares Hitachi (particle therapy), Proton therapy machines: cyclotrons, synchrotrons and single-room systems, Proton therapy, Hepatocellular carcinoma.
Shares Probability of pancreatic cancer following diabetes: a population-based study, Model to Determine Risk of Pancreatic Cancer in Patients With New-Onset Diabetes, Pancreatic cancer roadmap: from Whipple's operation to gemcitabine, FOLFIRINOX, adjuvant chemotherapy, PARP inhibition, KRAS inhibition, vaccines and the surveillance question.