Where chemotherapy began (Farber, 1948) and where much of modern breast, lung, and myeloma oncology was defined.
Dana-Farber Brigham Cancer Center in Boston is where chemotherapy began, with Farber's aminopterin remissions in 1948, and through Dana-Farber/Harvard Cancer Center it is the largest NCI-designated centre by grant funding and fifteenth in the Newsweek/Statista oncology list. Its firsts include the discovery of EGFR mutations in lung cancer by Jänne and Johnson, KEYNOTE-522 leadership by Tolaney with Schmid in triple-negative breast cancer, Anderson's myeloma drug development and the Profile genomic testing programme. OnCo links it to BWEL and RASolute 302, to pathology foundation models from the Mahmood and Yu labs, to the Cancer Dependency Map and clonal haematopoiesis papers, and to people including Paul G. Richardson, Benjamin L. Ebert and Ann H. Partridge. Data silos are the bottleneck OnCo records against it. Its breast, lung, myeloma and paediatric 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 Dana-Farber Cancer Institute, including child institutions. 4,333 works · 74,896 citations · 65% open access · 16% clinical trials · 2% reviews.
Mapped the Fanconi anaemia/BRCA DNA repair pathway and how tumours become resistant to PARP inhibitors.
Boston sarcoma doctor who first showed that mTOR inhibitors shrink perivascular epithelioid cell tumours and then led AMPECT, the trial that made nab-sirolimus the first approved treatment for these rare cancers.
Ann Partridge led the POSITIVE trial showing women can safely pause hormone therapy to have a baby.
Created the low, intermediate and high-risk classification that every prostate cancer decision starts from.
Discovered how lenalidomide works, launching the field of molecular-glue degraders, and defined clonal haematopoiesis before leading Dana-Farber.
After his mother died of melanoma he organised a bike ride across Massachusetts in 1980 with 36 riders; the Pan-Mass Challenge has since raised $1.125 billion for Dana-Farber and passes on every rider-raised dollar.
Boston lymphoma doctor who led ZUMA-5, the trial that brought the CAR-T therapy axicabtagene ciloleucel to relapsed follicular lymphoma.
Led the first personalised neoantigen peptide vaccine trial in melanoma and mapped how CLL evolves under treatment.
A 12-year-old lymphoma patient of Sidney Farber whose 1948 radio broadcast launched the Jimmy Fund, which has funded Dana-Farber for more than 75 years.
Computational oncologist who built open tools for interpreting tumour genomes and predicting response.
Surgeon-scientist who led IMpassion031 and studies of surgery de-escalation after neoadjuvant immunotherapy.
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.
Breast cancer specialist who leads Yale Cancer Center and Smilow Cancer Hospital, and who previously ran breast oncology at Dana-Farber for more than two decades.
First author of the 2010 ipilimumab trial that proved immunotherapy could extend survival in melanoma.
Led the imatinib trial in GIST that proved a targeted drug could melt away a solid tumour, and every GIST kinase inhibitor since.
Showed that PD-L1 is the ligand for PD-1 and that the pair switches T cells off, the foundation of checkpoint immunotherapy.
Boston oncologist who led CABINET, the trial that showed cabozantinib delays progression of advanced neuroendocrine tumours after other treatments have failed.
Led ALPINE, the first head-to-head trial in which a next-generation BTK inhibitor (zanubrutinib) beat ibrutinib.
Led KEYNOTE-045, the first trial to show immunotherapy beats chemotherapy in advanced bladder cancer.
A leading authority on inherited cancer risk and how BRCA carriers should be treated and screened.
Translated bortezomib and lenalidomide from bench to bedside, helping turn myeloma from a two-year to a decade-plus disease.
Nancy Lin is the leading authority on brain metastases from breast cancer, including the HER2CLIMB tucatinib data in patients with active brain disease.
Led KarMMa, which brought idecabtagene vicleucel, the first CAR-T for myeloma, to approval.
Co-discovered EGFR mutations in lung cancer and has led the drug development that followed, from osimertinib to KRAS G12C inhibitors.
Neuro-oncologist who created the RANO response criteria used in every brain tumour trial and leads glioblastoma drug development.
Led the DETERMINATION trial and many of the myeloma drug approvals of the past two decades.
Boston lymphoma doctor who led KEYNOTE-170, the trial that showed pembrolizumab can control relapsed primary mediastinal B-cell lymphoma, and who helped bring PD-1 blockade to Hodgkin lymphoma.
Surgeon-scientist who led the first neoadjuvant pembrolizumab trial in head and neck cancer and the KEYNOTE-689 study that made it standard.
Led RATIFY, the trial that made midostaurin the first targeted therapy added to induction chemotherapy for AML.
A two-year-old with acute leukaemia treated by Sidney Farber with the folate antagonist aminopterin from December 1947. His temporary remission, reported in 1948, was the first evidence that a drug could turn back leukaemia.
Leads Dana-Farber's breast oncology division and many of the trials that moved ADCs and de-escalated therapy into breast cancer care.
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.
In 1947-48 he showed that the folate antagonist aminopterin could send childhood leukaemia into remission, the first drug ever to do so. He then built Dana-Farber and, with Mary Lasker, won the 1971 National Cancer Act.
Discovered the MYD88 mutation that defines Waldenström macroglobulinaemia and led the trial that made ibrutinib its first approved drug.
From the 1940s until his last clinic visit in 1999 the greatest hitter in baseball raised money for Dana-Farber's Jimmy Fund and visited children on the wards on condition that no one wrote about it.
Leads kidney cancer research worldwide, including the adjuvant pembrolizumab and belzutifan trials.
Ursula Matulonis led the MIRASOL trial that gave ovarian cancer its first ADC with a survival benefit.
William Kaelin is the Nobel laureate whose work on VHL and HIF-2α led directly to belzutifan.
A multi-cancer blood test can be run in ordinary clinics, and most positive results can be resolved with imaging. But six in ten positives are false alarms that take months to resolve, and the test misses most cancers. Whether it reduces late-stage cancer or deaths is unknown; that requires randomised trials.
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.
It corrected a widely repeated simplification. An STK11 or KEAP1 mutation is not by itself a reason to expect immunotherapy to fail; it is a reason to expect it in a KRAS-mutant tumour, which is how the result should be read on a report.
Patients whose kidney cancer has been removed but who are at high risk of recurrence (large or high-grade tumours, node involvement, or resected metastases) can now be offered a year of pembrolizumab, which increases the chance of being alive and cancer-free several years later. Roughly nine patients need treatment to prevent one recurrence at two years, and some will have permanent side effects, so shared decision-making matters. Why pembrolizumab succeeded where similar drugs failed is not fully understood.
TIMER2.0 is one of the most used tools in cancer immunogenomics and its multi-algorithm design is a reminder that computational immune cell estimates are model-dependent and should be cross-checked.
TMB-high is uncommon but not negligible in TNBC, rises at relapse, and the tumour-agnostic pembrolizumab indication makes it worth measuring on a metastatic biopsy.
PTEN loss, the most common PI3K-pathway lesion in TNBC, may mark primary immunotherapy resistance, and TMB may add to PD-L1 in choosing who gets checkpoint blockade.
A germline result is not the whole story: without loss of the second allele the tumour may not be repair-deficient, which is why tumour sequencing and, in trials, HRD signatures are read alongside.
Shares Break up the liquid droplets where oncogenic transcription happens, Catherine J. Wu, Let patients themselves donate their records and samples for ultra-rare cancers, Genomic correlates of immune-cell infiltrates in colorectal carcinoma.
Shares Break Through Cancer, Damon Runyon Cancer Research Foundation, National Comprehensive Cancer Network (NCCN), Sean Parker.
Shares Break Through Cancer, The V Foundation for Cancer Research, Emil "Tom" Frei III, National Comprehensive Cancer Network (NCCN).
Shares Pan-Mass Challenge, Billy Starr, Einar "Jimmy" Gustafson, Ted Williams.
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.
Dana-Farber's toolkit for computational pathology: preprocessing whole-slide and multiplex images and training models.
Reconstructs T-cell and B-cell receptor repertoires from bulk or single-cell RNA-seq of tumours.
The Van Allen lab's clinical interpretation algorithm and knowledge base for cancer genomics, matching variants to therapies and trials.