UCSF is the birthplace of oncogene biology (Bishop, Varmus) and KRAS G12C drugging (Shokat), and a leader in I-SPY adaptive breast trials.
The UCSF Helen Diller Family Comprehensive Cancer Center in San Francisco is the birthplace of oncogene biology, where Bishop and Varmus made their Nobel-winning discovery, and of KRAS G12C drugging through Shokat's switch-II pocket; it holds NCI comprehensive designation and ranks thirty-third in the Newsweek/Statista oncology list. It leads the I-SPY 2 adaptive platform trial in breast cancer under Laura J. Esserman, runs the UCSF500 panel, and pioneered PSMA PET with Thomas A. Hope, alongside neuro-oncology and prostate programmes. OnCo links it to KRAS and PSMA, to gallium-68 PSMA-11, to the Ostrem and Shokat paper, and to the MYC and telomere pathways. Whether MYC can be drugged directly, and tolerated, is the open question it is linked to. Alan Ashworth, Eric J. Small and Alan P. Venook are among the people listed.
From OpenAlex, oncology works in the last five years (2022 to 2026, current year in progress); counted on 2026-09-24.
Matched to University of California, San Francisco, including child institutions. 2,818 works · 47,444 citations · 71% open access · 11% clinical trials · 2% reviews.
Led the pivotal talquetamab trial, establishing GPRC5D as the second bispecific target in myeloma.
Co-discovered that BRCA-deficient cancers die when PARP is blocked, the idea behind an entire drug class.
GI oncologist who led CALGB/SWOG 80405 and helped show that tumour side matters in colorectal cancer.
Neuroendocrine tumour specialist who helps design the trials that set treatment for these rare cancers.
Prostate cancer trialist who helped bring abiraterone and sipuleucel-T to patients, and led ASCO in 2025-26.
RAS biologist who founded Onyx Pharmaceuticals and led the NCI's national effort to drug RAS.
The cancer centre at UCSF carries her name, and in 2017 the Helen Diller Foundation gave UCSF $500 million, the largest gift in its history, bringing the family's total there to $650 million.
The immunologist who ran the Parker Institute from its launch in 2016, building a shared research network across leading US cancer centres; he came from UCSF and now leads a regulatory T cell company.
Paediatric oncologist whose trials established transplant and 13-cis-retinoic acid for high-risk neuroblastoma.
The chemist whose lab found the hidden pocket in KRAS G12C that made the 'undruggable' target druggable.
Breast surgeon who built the I-SPY platform, the adaptive trial that tests new drugs before surgery.
Neurosurgeon who proved that removing more of a glioma extends survival and pioneered awake mapping to do it safely.
She and Mark Zuckerberg founded the Chan Zuckerberg Biohub with the stated mission to cure or prevent all disease; its programmes include engineering the immune system to detect cancer and other diseases early.
Prostate oncologist studying how tumours transform to escape hormone therapy and how to target them with radioligands.
San Francisco oncologist who was lead author of KEYNOTE-966, which showed that adding pembrolizumab to gemcitabine and cisplatin helps people with advanced bile duct cancer live longer.
In May 2025 the Weill Family Foundation's $100 million challenge launched a $200 million, ten-year cancer research partnership between UCSF and Stanford, the two big Bay Area cancer centres that usually compete.
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.
Nuclear medicine physician who led the trials that got PSMA PET approved in the United States.
ctDNA clearance may refine pCR as a surrogate: a patient with residual disease but no ctDNA may not need escalation, the hypothesis behind ctDNA-guided post-neoadjuvant trials.
This academic programme is what the FDA approved 68Ga-PSMA-11 on in December 2020, and the Illuccix and Locametz kits rest on it for the staging indication. Its message for a man being staged before surgery is that a positive PSMA PET node is very likely real, but a negative scan does not rule out small nodal deposits, so the lymph node dissection still matters.
This framework is behind the everyday language of hot and cold tumours and the design of combination trials that pair checkpoint inhibitors with treatments meant to draw T cells into the tumour.
It gives a genetic account of both immunotherapy failures: why some mismatch repair deficient tumours resist, and why the microsatellite-stable majority has no T cells in it to begin with.
The most frequently mutated oncogene in cancer stopped being undruggable, and patients with KRAS G12C lung and bowel cancers now have targeted pills. The approach, exploiting a mutation-created chemical handle and an inactive-state pocket, has become a template for other hard targets.
MYC amplification, present in a fifth to a third of TNBC, is undruggable directly; this is the synthetic-lethal logic behind CDK (especially CDK9 and CDK1/2) inhibitor trials in the disease.
It opened the subtype programme that Moffitt, Bailey and COMPASS refined; the classical versus mesenchymal or basal split has survived every re-analysis.
Shares Emerson Collective, Priscilla Chan, Sanford I. Weill, Damon Runyon Cancer Research Foundation.
Shares Diagnostic accuracy of 68Ga-PSMA-11 PET for pelvic nodal metastasis detection prior to radical prostatectomy and pelvic lymph node dissection: a multicenter prospective phase 3 imaging trial, Gallium-68 gozetotide (PSMA-11), PSMA-PreRP, PSMA.
Shares Diagnostic accuracy of 68Ga-PSMA-11 PET for pelvic nodal metastasis detection prior to radical prostatectomy and pelvic lymph node dissection: a multicenter prospective phase 3 imaging trial, Gallium-68 gozetotide (PSMA-11), PSMA-PreRP, Parker Institute for Cancer Immunotherapy.
Shares I-SPY 1 (CALGB 150007/150012, ACRIN 6657), Laura J. Esserman, I-SPY 2.2, I-SPY 2.
Shares Helen Diller, Emerson Collective, Priscilla Chan, Sanford I. Weill.
Shares Frank McCormick, Ostrem and Shokat: the hidden pocket that made KRAS G12C druggable, KRAS.