Benjamin Haibe‐Kains

ORCID: 0000-0002-7684-0079
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About
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Research Areas
  • Gene expression and cancer classification
  • Bioinformatics and Genomic Networks
  • Cancer Genomics and Diagnostics
  • Radiomics and Machine Learning in Medical Imaging
  • Computational Drug Discovery Methods
  • AI in cancer detection
  • Breast Cancer Treatment Studies
  • Cancer Immunotherapy and Biomarkers
  • Cancer Cells and Metastasis
  • Advanced Breast Cancer Therapies
  • Molecular Biology Techniques and Applications
  • Sarcoma Diagnosis and Treatment
  • RNA modifications and cancer
  • Artificial Intelligence in Healthcare and Education
  • CAR-T cell therapy research
  • HER2/EGFR in Cancer Research
  • Genetics, Bioinformatics, and Biomedical Research
  • Pharmacogenetics and Drug Metabolism
  • Single-cell and spatial transcriptomics
  • Cancer-related molecular mechanisms research
  • Medical Imaging Techniques and Applications
  • PARP inhibition in cancer therapy
  • Head and Neck Cancer Studies
  • Genetic factors in colorectal cancer
  • Epigenetics and DNA Methylation

University of Toronto
2016-2025

Princess Margaret Cancer Centre
2016-2025

University Health Network
2016-2025

Ontario Institute for Cancer Research
2016-2025

Vector Institute
2016-2025

Public Health Ontario
2021-2025

Artificial Intelligence in Medicine (Canada)
2019-2025

Kingston Health Sciences Centre
2023-2025

Queens University
2023-2025

Queen's University
2023-2025

Human cancers exhibit strong phenotypic differences that can be visualized noninvasively by medical imaging. Radiomics refers to the comprehensive quantification of tumour phenotypes applying a large number quantitative image features. Here we present radiomic analysis 440 features quantifying intensity, shape and texture, which are extracted from computed tomography data 1,019 patients with lung or head-and-neck cancer. We find have prognostic power in independent sets cancer patients, many...

10.1038/ncomms5006 article EN cc-by-nc-nd Nature Communications 2014-06-03

Background: Histologic grade in breast cancer provides clinically important prognostic information. However, 30%–60% of tumors are classified as histologic 2. This is associated with an intermediate risk recurrence and thus not informative for clinical decision making. We examined whether was gene expression profiles cancers such could be used to improve grading. Methods: analyzed microarray data from 189 invasive carcinomas three published datasets carcinomas. identified differentially...

10.1093/jnci/djj052 article EN JNCI Journal of the National Cancer Institute 2006-02-14

Abstract Purpose: Recently, a 76-gene prognostic signature able to predict distant metastases in lymph node–negative (N−) breast cancer patients was reported. The aims of this study conducted by TRANSBIG were independently validate these results and compare the outcome with clinical risk assessment. Experimental Design: Gene expression profiling frozen samples from 198 N− systemically untreated done at Bordet Institute, blinded data independent Veridex. Genomic defined Veridex, data....

10.1158/1078-0432.ccr-06-2765 article EN Clinical Cancer Research 2007-06-01

CD4⁺ T cells are critical regulators of immune responses, but their functional role in human breast cancer is relatively unknown. The goal this study was to produce an image infiltrating tumors using limited ex vivo manipulation better understand the differences associated with patient prognosis. We performed comprehensive molecular profiling isolated from untreated invasive primary and found that cell subpopulations included follicular helper (Tfh) cells, which have not previously been...

10.1172/jci67428 article EN Journal of Clinical Investigation 2013-06-16

A number of microarray studies have reported distinct molecular profiles breast cancers (BC), such as basal-like, ErbB2-like, and two to three luminal-like subtypes. These were associated with different clinical outcomes. However, although the basal ErbB2 subtypes are repeatedly recognized, identification estrogen receptor (ER) -positive has been inconsistent. Therefore, refinement their definition is needed.We previously a gene expression grade index (GGI), which defines histologic based on...

10.1200/jco.2006.07.1522 article EN Journal of Clinical Oncology 2007-03-30

Due to advances in the acquisition and analysis of medical imaging, it is currently possible quantify tumor phenotype. The emerging field Radiomics addresses this issue by converting images into minable data extracting a large number quantitative imaging features. One main challenges segmentation. Where manual delineation time consuming prone inter-observer variability, has been shown that semi-automated approaches are fast reduce variability. In study, semiautomatic region growing...

10.1371/journal.pone.0102107 article EN cc-by PLoS ONE 2014-07-15

Using gene-expression data from over 6,000 breast cancer patients, we report herein that high CD73 expression is associated with a poor prognosis in triple-negative cancers (TNBC). Because anthracycline-based chemotherapy regimens are standard treatment for TNBC, investigated the relationship between and anthracycline efficacy. In TNBC patients treated anthracycline-only preoperative chemotherapy, gene was significantly lower rate of pathological complete response or disappearance invasive...

10.1073/pnas.1222251110 article EN Proceedings of the National Academy of Sciences 2013-06-17

Abstract Summary: The survcomp package provides functions to assess and statistically compare the performance of survival/risk prediction models. It implements state-of-the-art statistics (i) measure risk models; (ii) combine these statistical estimates from multiple datasets using a meta-analytical framework; (iii) competitive Availability: R/Bioconductor is provided open source under Artistic-2.0 License with user manual containing installation, operating instructions use case scenarios on...

10.1093/bioinformatics/btr511 article EN Bioinformatics 2011-09-07

Abstract Radiomics provides a comprehensive quantification of tumor phenotypes by extracting and mining large number quantitative image features. To reduce the redundancy compare prognostic characteristics radiomic features across cancer types, we investigated cancer-specific feature clusters in four independent Lung Head & Neck (H&N) cohorts (in total 878 patients). Radiomic were extracted from pre-treatment computed tomography (CT) images. Consensus clustering resulted eleven...

10.1038/srep11044 article EN cc-by Scientific Reports 2015-06-05

Abstract Background Estrogen receptor positive (ER+) breast cancers (BC) are heterogeneous with regard to their clinical behavior and response therapies. The ER is currently the best predictor of anti-estrogen agent tamoxifen, yet up 30–40% ER+BC will relapse despite tamoxifen treatment. New prognostic biomarkers further biological understanding resistance required. We used gene expression profiling develop an outcome-based using a training set 255 ER+ BC samples from women treated adjuvant...

10.1186/1471-2164-9-239 article EN cc-by BMC Genomics 2008-05-22
Liwei Cao Chen Huang Daniel Cui Zhou Yingwei Hu T. Mamie Lih and 95 more Sara R. Savage Karsten Krug David Clark Michael Schnaubelt Lijun Chen Felipe da Veiga Leprevost Rodrigo Vargas Eguez Weiming Yang Jianbo Pan Bo Wen Yongchao Dou Wen Jiang Yuxing Liao Zhiao Shi Nadezhda V. Terekhanova Song Cao Rita Jui-Hsien Lu Yize Li Ruiyang Liu Houxiang Zhu Peter Ronning Yige Wu Matthew A. Wyczalkowski Hariharan Easwaran Ludmila Danilova Arvind Singh Mer Seungyeul Yoo Joshua M. Wang Wenke Liu Benjamin Haibe‐Kains Mathangi Thiagarajan Scott D. Jewell Galen Hostetter Chelsea J. Newton Qing Kay Li Michael H. A. Roehrl David Fenyö Pei Wang Alexey I. Nesvizhskii D.R. Mani Gilbert S. Omenn Emily S. Boja Mehdi Mesri Ana I. Robles Henry Rodriguez Oliver F. Bathe Daniel W. Chan Ralph H. Hruban Li Ding Bing Zhang Hui Zhang Mitual Amin Eunkyung An Christina Ayad Thomas Bauer Chet Birger Michael J. Birrer Simina M. Boca William Bocik Melissa Borucki Shuang Cai Steven A. Carr Sandra Cerda Huan Chen Steven Chen David Chesla Arul M. Chinnaiyan Antonio Colaprico Sandra Cottingham Magdalena Derejska Saravana M. Dhanasekaran Marcin J. Domagalski Brian J. Druker Elizabeth R. Duffy Maureen A. Dyer Nathan Edwards Matthew J. Ellis Jennifer Eschbacher Alicia Francis Jesse Francis Stacey Gabriel N Gabrovski Johanna Gardner Gad Getz Michael A. Gillette Charles A. Goldthwaite Pamela Grady Shuai Guo Pushpa Hariharan Tara Hiltke Barbara Hindenach Katherine A. Hoadley Jasmine Huang Corbin D. Jones Karen A. Ketchum

Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive cancer with poor patient survival. Toward understanding the underlying molecular alterations that drive PDAC oncogenesis, we conducted comprehensive proteogenomic analysis of 140 pancreatic cancers, 67 normal adjacent tissues, and 9 tissues. Proteomic, phosphoproteomic, glycoproteomic analyses were used to characterize proteins their modifications. In addition, whole-genome sequencing, whole-exome methylation, RNA sequencing...

10.1016/j.cell.2021.08.023 article EN cc-by Cell 2021-09-01

Breast cancer in young women is associated with poor prognosis. We aimed to define the role of gene expression signatures predicting prognosis and understand biological differences according age.Patients were assigned molecular subtypes [estrogen receptor (ER)(+)/HER2(-); HER2(+), ER(-)/HER2(-))] using a three-gene classifier. evaluated whether previously published proliferation, stroma, immune-related added prognostic information Adjuvant! online tested their interaction age Cox model for...

10.1158/1078-0432.ccr-11-2599 article EN Clinical Cancer Research 2012-01-20

Understanding the tumor immune microenvironment (TIME) promises to be key for optimal cancer therapy, especially in triple-negative breast (TNBC). Integrating spatial resolution of cells with laser capture microdissection gene expression profiles, we defined distinct TIME stratification TNBC, implications current therapies including checkpoint blockade. TNBCs an immunoreactive exhibited tumoral infiltration granzyme B+CD8+ T (GzmB+CD8+ cells), a type 1 IFN signature, and elevated multiple...

10.1172/jci96313 article EN Journal of Clinical Investigation 2019-02-12

PIK3CA mutations are reported to be present in approximately 25% of breast cancer (BC), particularly the estrogen receptor–positive (ER+) and HER2-overexpressing (HER2+) subtypes, making them one most common genetic aberrations BC. In experimental models, these have been shown activate AKT induce oncogenic transformation, hence lesions hypothesized render tumors highly sensitive therapeutic PI3K/mTOR inhibition. By analyzing gene expression protein data from nearly 1,800 human BCs, we report...

10.1073/pnas.0907011107 article EN Proceedings of the National Academy of Sciences 2010-05-17

Abstract Summary: Breast cancer is one of the most frequent cancers among women. Extensive studies into molecular heterogeneity breast have produced a plethora subtype classification and prognosis prediction algorithms, as well numerous gene expression signatures. However, reimplementation these algorithms tedious but important task to enable comparison existing signatures models between each other with new models. Here, we present genefu R/Bioconductor package, multi-tiered compendium...

10.1093/bioinformatics/btv693 article EN Bioinformatics 2015-11-24

Single sample predictors (SSPs) and Subtype classification models (SCMs) are gene expression–based classifiers used to identify the four primary molecular subtypes of breast cancer (basal-like, HER2-enriched, luminal A, B). SSPs use hierarchical clustering, followed by nearest centroid classification, based on large sets tumor-intrinsic genes. SCMs a mixture Gaussian distributions genes with expression specifically correlated three key (estrogen receptor [ER], HER2, aurora kinase A [AURKA])....

10.1093/jnci/djr545 article EN cc-by-nc JNCI Journal of the National Cancer Institute 2012-01-18
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