The NCI is the US government's cancer research agency, spending ~$7B a year and running the Cancer Centers Program, TCGA, and Rosenberg's cell therapy lab.
The National Cancer Institute, part of the US National Institutes of Health in Bethesda, is the US government's cancer research agency; it runs the Cancer Centers Program that designates seventy-four centres, The Cancer Genome Atlas and its Genomic Data Commons, the RAS Initiative, the SEER registry and the cooperative groups NRG, SWOG, Alliance and ECOG-ACRIN. Its Surgery Branch under Rosenberg developed tumour-infiltrating lymphocyte therapy and neoantigen TCR-T, and its Pediatric MATCH and myeloMATCH trials, its CPTAC and PDQ resources and the JNCI journal all sit in OnCo. It is linked to bottlenecks on data silos, hidden failures, funding that follows fashion and slow translation, and to ideas for a national non-profit CRO and perpetual platform trials. Whether it can fund infrastructure rather than projects is the standing question. Douglas R. Lowy is among the people listed. The institutions linked below are the NCI-designated cancer centres in OnCo, its intramural Center for Cancer Research and the Frederick National Laboratory; the trials are those whose sponsor field names the NCI.
From OpenAlex, oncology works in the last five years (2022 to 2026, current year in progress); counted on 2026-09-24.
Matched to National Cancer Institute, including child institutions. 2,852 works · 46,921 citations · 78% open access · 10% clinical trials · 2% reviews.
NCI oncologist who led the trial that showed atezolizumab produces lasting responses in alveolar soft part sarcoma, the first approved treatment for this rare cancer.
Invented BH3 profiling, the functional test behind venetoclax's success, before becoming NCI director.
Led the selumetinib trials that gave children with neurofibromatosis their first approved drug.
Co-developed the HPV vaccine technology that is eliminating cervical cancer in vaccinated populations.
With Emil Freireich he showed that combinations of drugs could cure childhood leukaemia, then extended the idea to Hodgkin lymphoma and to adjuvant treatment after surgery.
At the NCI in the early 1960s he and Emil Frei gave children four drugs at once, VAMP, against fierce opposition, and turned a leukaemia almost no child survived into a curable one. He also worked out platelet transfusion.
A lawyer treated for breast cancer in 1987 who built the National Breast Cancer Coalition and won the Department of Defense breast cancer programme, the first to put trained patient advocates on scientific review panels.
RAS biologist who founded Onyx Pharmaceuticals and led the NCI's national effort to drug RAS.
Runs NCI's immuno-oncology clinical programme, from prostate cancer vaccines to bifunctional checkpoint fusion proteins.
Louis Staudt defined the molecular subtypes of large B-cell lymphoma that guide targeted therapy.
NCI epidemiologist whose HPV natural history studies underpin HPV-based cervical screening and risk-based management worldwide.
She turned the American Cancer Society into a research funder in the 1940s, built the Lasker Awards, and led the lobbying that produced the 1971 National Cancer Act and the modern NCI budget.
Nirali Shah developed CD22 CAR-T for children whose leukaemia escaped CD19 therapy.
Made mesothelin a drug target, from immunotoxins to ADCs and CAR-T, and leads NCI's mesothelioma programme.
Diagnosed in 1974, she refused the standard practice of biopsy and mastectomy under one anaesthetic without the patient's say. Her campaign made the two-step procedure and informed choice the norm.
American surgeon who pioneered removing the thyroid in children with inherited RET mutations before cancer develops, led ZETA, the trial that established vandetanib for medullary thyroid cancer, and chaired the American Thyroid Association guideline for the disease.
Father of cancer immunotherapy: first to cure patients with IL-2 and with their own tumour-infiltrating lymphocytes.
Developed dose-adjusted EPOCH-R, the regimen that cures primary mediastinal B-cell lymphoma without radiotherapy.
Cancer biologist who directs the National Cancer Institute's Center for Cancer Research, the large intramural research programme in Bethesda.
The most rigorous evaluation of the Chilean programme available; read alongside Mardones and Frenz (2019) and Samaniego and colleagues (2024).
The best single starting point for a clinician or researcher new to the disease, written by the groups running the Chilean and Indian cohorts; its list of unmet needs is the skeleton of the ideas section on this page.
The external validation the 2017 paper asked for; it is why residual cancer burden is reported in UK and European pathology and used as a trial entry criterion rather than an MD Anderson curiosity.
Lifileucel proved that Steven Rosenberg's decades-old TIL concept could be industrialised into a licensed product and gave patients with checkpoint-refractory melanoma, who otherwise have few options, a chance of durable remission. It is the first cell therapy approved for any solid tumour. The treatment requires surgery to harvest tumour, hospitalisation for lymphodepletion and IL-2, and specialised centres, so its reach is limited.
Lung cancer in never-smokers is not smokers' lung cancer with the smoking removed; it is a different set of diseases with a different clock. The slow-growing piano subtype in particular is the argument that a screening test aimed at never-smokers would need to look for something other than what low-dose computed tomography was built to find.
The piece that turns a research classification into something a trial can use on one person's biopsy, with a probability attached rather than a flat label. It is the reason genetics-directed lymphoma trials became possible at all.
R-CHOP remains the standard first-line regimen for diffuse large B-cell lymphoma. The trial is also the clearest lesson in the disease about adopting a regimen on single-arm data: dose-adjusted EPOCH-R had been used widely for a decade before this comparison existed.
The genetic nosology that precision-medicine trials in diffuse large B-cell lymphoma now use to pick patients. It gives a mechanism, not just a label: two of the four subtypes point at a drug class that already exists.
Shares Publish per-patient trial cost benchmarks and target halving them, A public registry of unanswered clinical questions linked to funding calls, Disclose R&D and manufacturing costs of publicly funded cancer drugs to get coverage, Grant progress reports must list what did not work.
Shares Sylvester Comprehensive Cancer Center, University of Miami, University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Mayo Clinic Comprehensive Cancer Center in Arizona, The University of Kansas Cancer Center.
Shares Case Comprehensive Cancer Center, O'Neal Comprehensive Cancer Center at UAB, MUSC Hollings Cancer Center, Sylvester Comprehensive Cancer Center, University of Miami.
Shares Every payer covers routine care costs for trial participants, in every country, Lay trial navigators funded per centre, evaluated in a randomised trial, Stop excluding people with a prior cancer, controlled HIV, or treated hepatitis, A public equity index for trial sites and sponsors, tied to funding.
Shares ComboMATCH (EAY191), One master trial for cancer prevention drugs across many precancers, Lung-MAP S1400I: nivolumab with or without ipilimumab, A perpetual platform trial in every major cancer, funded as infrastructure.
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 command-line client for downloading from the NCI Genomic Data Commons, home of TCGA, TARGET and CPTAC genomics.
The schema that defines every entity and field in the Genomic Data Commons.
The portal of the Human Tumor Atlas Network, the NCI's single-cell and spatial atlases of tumour evolution.
The NCI's Breast Cancer Risk Assessment (Gail) model as an R package.
The NCI's tool for building and validating absolute risk models, used for breast and other cancer risk prediction.
The National Cancer Institute's evidence-based summaries on treatment, screening, genetics and supportive care in patient and health professional versions; US government work in the public domain.
The NCI's reference terminology for cancer research and care, free to download and use.
The NCI's free training on cancer registration, anatomy, staging and coding, used by registrars worldwide.
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.
The analysis software for the United States cancer registry data: incidence, survival and prevalence statistics computed from SEER itself.