Johns Hopkins is the birthplace of cancer genomics (Vogelstein), MSI-high immunotherapy (Le, Diaz), and liquid biopsy and MCED science (CancerSEEK).
Johns Hopkins Hospital and its Sidney Kimmel Comprehensive Cancer Center in Baltimore are where cancer genomics began with Vogelstein and Kinzler, and the centre holds NCI comprehensive designation and tenth place in the Newsweek/Statista oncology ranking. Its record includes pembrolizumab in mismatch-repair-deficient tumours, the first tumour-agnostic approval, led by Le and Diaz, the CancerSEEK liquid biopsy that fed Exact Sciences' multi-cancer early detection programme, and the Bloomberg-Kimmel Institute for Cancer Immunotherapy under Drew M. Pardoll and Elizabeth M. Jaffee. OnCo links it to DELFI Diagnostics, to the DETECT-A, DYNAMIC and CheckMate 816 papers, and to pathways from epigenetic reprogramming to telomere maintenance. Whether blood-based early detection lowers harm as well as finding cancers is the question its own work posed. Programmes and people 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 Johns Hopkins University, including child institutions. 2,962 works · 42,161 citations · 70% open access · 8% clinical trials · 3% reviews.
Baltimore gynaecologic oncologist who led the trial showing that adding trastuzumab to chemotherapy helps women with HER2-positive uterine serous carcinoma, an aggressive form of endometrial cancer.
Bert Vogelstein is the most-cited scientist in cancer genetics: he mapped how colorectal cancer develops and founded the field of cancer genome sequencing and blood-based detection.
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.
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.
Immunologist who helped define the PD-1 pathway's role in cancer and built one of the largest immunotherapy institutes.
First author of the studies that showed mismatch-repair-deficient tumours respond to PD-1 blockade regardless of origin.
Pancreatic cancer immunologist who developed the GVAX vaccine and led national cancer policy panels.
Her cervical cancer cells, taken in 1951 without her knowledge, became HeLa, the first immortal human cell line. Her story changed how consent and family rights in research are handled.
Led CheckMate 017, the first trial to show immunotherapy beats chemotherapy in lung cancer.
Developed the MANAFEST assay to track the tumour-specific T cells that immunotherapy awakens.
Co-discovered APC, the gatekeeper gene of colorectal cancer, and co-led the first cancer genome sequences.
In 2016 his $50 million, matched by Sidney Kimmel and others to $125 million, launched a Johns Hopkins institute that put more than a hundred scientists and clinicians to work on cancer immunotherapy.
Co-developed CancerSEEK, the blood test that showed multi-cancer early detection is possible, and ran the first prospective screening study of it.
Led CheckMate 816, which established neoadjuvant chemo-immunotherapy for resectable lung cancer.
The Jones Apparel founder has given $157 million to Johns Hopkins since 2001, which named its cancer centre for him, and put $50 million into the Bloomberg~Kimmel Institute for Cancer Immunotherapy in 2016.
Founder of cancer epigenetics, showing that abnormal DNA methylation silences tumour-suppressor genes and can be reversed by drugs.
Suzanne Topalian led the first nivolumab trials showing PD-1 blockade works across several cancers.
William Nelson is the long-time director of the Johns Hopkins cancer centre and a prostate cancer epigenetics researcher.
Patients with operable stage II-III lung cancer without EGFR or ALK alterations should have chemo-immunotherapy discussed before surgery rather than only afterwards. Three pre-operative cycles do not compromise the operation and improve cure rates. Whether to continue immunotherapy after surgery, as the perioperative trials do, and whether patients with pCR need any further treatment, remain open questions.
For stage II colon cancer, where most patients are cured by surgery alone, a blood test can identify the minority who benefit from chemotherapy and spare everyone else its side effects. It does not yet prove that treating ctDNA-positive patients improves survival compared with not treating them.
The stage shift the pancreatic cancer page quotes (about three in four surveillance-detected cancers at stage I) and the strongest argument for offering surveillance to every germline carrier found by universal testing, which the NHS does not yet do outside research.
The first randomised evidence that the order in which prostate cancer treatments are given changes how long they work, independently of which treatments they are. It is also a rare trial in which quality of life pointed one way and the primary endpoint pointed nowhere.
A blood test can find early, treatable cancers in people who feel well, including cancers for which no screening exists. It is not a replacement for mammography or colonoscopy but a possible addition. Larger randomised trials are needed to show benefit outweighs harm.
It gives surveillance a target and a timetable: catch high-grade dysplasia and there are about three years before invasion, and TGF-beta pathway loss is the event to detect.
The rulebook behind the CAPS cohorts and the UK EUROPAC programme; it is also the reason surveillance for carriers is not yet a routine NHS service, because the consortium itself asked for it to stay within research until benefit was shown.
The reference for why pancreatic microenvironment trials read as a list of failures and what the field now means by remodelling rather than removing the stroma.
Shares Pancreatic intraepithelial neoplasia: a new nomenclature and classification system for pancreatic duct lesions, A revised classification system and recommendations from the Baltimore consensus meeting for neoplastic precursor lesions in the pancreas, Precancerous neoplastic cells can move through the pancreatic ductal system, AI that spots pancreatic cancer on scans taken a year before diagnosis.
Shares Precancerous neoplastic cells can move through the pancreatic ductal system, Distant metastasis occurs late during the genetic evolution of pancreatic cancer, Whole genome sequencing defines the genetic heterogeneity of familial pancreatic cancer, Genomic characterization of malignant progression in neoplastic pancreatic cysts.
Shares Clinical implications of genomic alterations in the tumour and circulation of pancreatic cancer patients, Combined circulating tumor DNA and protein biomarker-based liquid biopsy for the earlier detection of pancreatic cancers, Detection and localization of surgically resectable cancers with a multi-analyte blood test, DETECT-A: a blood test plus PET-CT to screen 10,006 women with no symptoms.
Shares IPMNs with co-occurring invasive cancers: neighbours but not always relatives, DPC4 gene status of the primary carcinoma correlates with patterns of failure in patients with pancreatic cancer, Genomic characterization of malignant progression in neoplastic pancreatic cysts, A combination of molecular markers and clinical features improve the classification of pancreatic cysts.
Shares 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, Distant metastasis occurs late during the genetic evolution of pancreatic cancer, IPMNs with co-occurring invasive cancers: neighbours but not always relatives.
Shares A revised classification system and recommendations from the Baltimore consensus meeting for neoplastic precursor lesions in the pancreas, IPMNs with co-occurring invasive cancers: neighbours but not always relatives, Presence of somatic mutations in most early-stage pancreatic intraepithelial neoplasia, Recurrent GNAS mutations define an unexpected pathway for pancreatic cyst development.
Shares Recurrent GNAS mutations define an unexpected pathway for pancreatic cyst development, A combination of molecular markers and clinical features improve the classification of pancreatic cysts, The molecular evolution of acquired resistance to targeted EGFR blockade in colorectal cancers, Le 2017: mismatch-repair deficiency predicts response to PD-1 blockade across twelve tumour types, leading to the first tissue-agnostic drug approval.
Shares Genetic instability in colorectal cancers, Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability, Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma, Le 2017: mismatch-repair deficiency predicts response to PD-1 blockade across twelve tumour types, leading to the first tissue-agnostic drug approval.
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.
A modular variant annotation platform with a store of annotators, including cancer-specific ones, and a browser-based results viewer.
Code behind the DELFI cell-free DNA fragmentation approach to cancer detection, from the Velculescu lab at Johns Hopkins.
Classifies genes as oncogenes or tumour suppressors from their mutation patterns.
Predicts driver missense mutations, cancer type by cancer type, from the Karchin lab.