Princess Margaret is Canada's leading cancer centre and a pioneer in immunotherapy and cancer stem cell research.
Princess Margaret Cancer Centre in Toronto is Canada's leading cancer centre and ranks ninth in the Newsweek/Statista oncology list. It is where John E. Dick's group identified cancer stem cells, and it runs a major phase 1 unit under Lillian L. Siu alongside tumour-infiltrating lymphocyte and radiation medicine research, with Tak W. Mak, Pamela S. Ohashi and Aaron D. Schimmer among its scientists. OnCo links it to the CHALLENGE colon cancer exercise trial, to cBioPortal, to the cancer stem cell and phenotypic plasticity pathway, and to Ontario Health, the Ontario Institute for Cancer Research and the Canadian Cancer Society. Whether stem cell biology can yet be turned into treatments patients feel is still open. Its people page shows who to read.
From OpenAlex, oncology works in the last five years (2022 to 2026, current year in progress); counted on 2026-09-24.
Matched to Princess Margaret Cancer Centre, including child institutions. 1,477 works · 21,748 citations · 66% open access · 15% clinical trials · 3% reviews.
Keith Stewart is a myeloma researcher who leads Canada's largest cancer centre.
Leukaemia researcher who found that AML stem cells depend on mitochondrial proteases and metabolism.
Amit Oza is a gynaecologic oncologist who led early olaparib and niraparib studies in ovarian cancer.
Led TAX 327, which made docetaxel the first life-extending chemotherapy for prostate cancer, and has spent decades pressing for higher trial standards.
Discovered cancer stem cells, showing leukaemia is driven by a rare population of self-renewing cells.
Runs one of the world's largest phase 1 programmes and led trials that shaped head and neck cancer immunotherapy.
Lung cancer oncologist who showed plasma genotyping matches tissue and leads Canadian lung trials.
Immunologist who built Canada's TIL therapy programme and defined T-cell tolerance mechanisms.
Cloned the T-cell receptor and co-discovered CTLA-4's brake function, foundations of modern immunotherapy.
Genomicist who applies cell-free DNA and single-cell sequencing to track cancer and immunotherapy response.
It explains why one biopsy can mislead and why chemotherapy selects for the protective neighbourhood, an argument for spatial rather than bulk profiling.
It is the number behind 'basal-like is chemoresistant' and the validation of the GATA6 stain that lets a pathology laboratory call the subtype without RNA sequencing.
It explains why single-sample classifiers disagree on about one tumour in eight and why KRAS allelic imbalance and GATA6 copy number are being read alongside expression.
COMPASS is the prospective evidence that transcriptional subtype predicts chemotherapy response, and it produced the practical GATA6 test that trials now use to stratify.
Signatures find repair-deficient tumours that gene panels miss, and they mark the minority in which checkpoint drugs have a rationale.
The textbook PanIN-to-cancer ladder is only part of the story, and a screening programme cannot assume years of orderly progression in every patient.
The retrospective platinum signal that made platinum-based first-line chemotherapy the standard for BRCA carriers and set POLO's design of olaparib after platinum.
Shares Genomics-driven precision medicine for advanced pancreatic cancer: early results from the COMPASS trial, GATA6 expression distinguishes classical and basal-like subtypes in advanced pancreatic cancer, Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution.
Shares Genomics-driven precision medicine for advanced pancreatic cancer: early results from the COMPASS trial, GATA6 expression distinguishes classical and basal-like subtypes in advanced pancreatic cancer, Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution.
Shares Canadian Cancer Society, Health Canada, Sunnybrook Odette Cancer Centre, CHALLENGE (CCTG CO.21).
Shares A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns, Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution.
Shares The Hospital for Sick Children (SickKids), Cancer stem cells & phenotypic plasticity.
Shares A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns, Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution.
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 Bioconductor package for analysing large pharmacogenomic datasets such as GDSC and CCLE, from the Haibe-Kains lab.
Turns messy DICOM folders into analysis-ready arrays with RTSTRUCT and dose handling, from the Haibe-Kains lab.
A Bioconductor package implementing the published breast cancer molecular subtype and prognostic gene signatures, including PAM50.
A Python client for The Cancer Imaging Archive's NBIA API from the Haibe-Kains lab.