Robert R. McWilliams, MD, MSc, MSHA

Robert R. McWilliams, MD, MSc, MSHA

Robert McWilliams, MD, is an internationally recognized clinician, trialist, and leader in gastrointestinal oncology and skin cancers. He serves as the Deputy Director of the OSF Cancer Institute, where he continues clinical trial and outcomes research in addition to transforming the cancer clinical practice.

Dr. McWilliams completed his medical training at Georgetown University School of Medicine, graduating summa cum laude and pursued residency in Internal Medicine at Johns Hopkins. He completed Hematology/Oncology fellowship at Mayo Clinic in Rochester, MN, where he also completed a genetic epidemiology research fellowship and a Masters Degree in Clinical Research. He was on faculty at Mayo Clinic for 20 years, rising to the rank of Professor,  serving in numerous leadership roles including Clinical Practice Chair of Medical Oncology, Vice Chair of Oncology, Deputy Director of Cancer Practice, Chair of the Biospecimens Subcommittee, and Chair of the Therapeutic Strategy Subcommittee. He led redesign of the medical oncology care model at Mayo Clinic, optimizing the utilization of each team member to the top of their scope. He grew the Patient Navigator program in the Cancer Center, led the adoption of Epic EHR system for hematology and oncology, pioneered the use of patient reported systems to address financial barriers, and led the first precision oncology clinic.

He has authored more than 180 publications, including in high impact journals such as The New England Journal of Medicine, JAMA, JAMA Oncology, Lancet Oncology, the Journal of Clinical Oncology, Nature Genetics, Gut, and Clinical Cancer Research. He has served numerous roles nationally and internationally, including serving on the Pancreas Cancer Task Force and the GI Cancers Steering Committee of the National Cancer Institute, and the U.S. Lead for Small Bowel Adenocarcinoma in the International Rare Cancers Initiative. He served in several roles in the National Comprehensive Cancer Network, including on the Board of Directors, the Finance Committee, the Electronic Health Records subcommittee, and on the Best Practices Committee (alternate).  He has also served on the Epic Adult Oncology Advisory Board.

His career has focused on using genetic information to advance care for patients, tapping into increasingly available technological systems to enhance care on a population scale. He believes technology can be harnessed to enhance the prevention, detection, and treatment of cancer, while enhancing the humanistic experience for providers and patients.

 

Areas of Interest

GI and Skin Cancers

Medical Oncology

Advancing patient care with genetic information on a populations scale for prevention, detection and treatment of cancer

 

Education & Training

MD in Clinical Medicine from Georgetown University School of Medicine

Internal Medicine Residency at Johns Hopkins University School of Medicine

Hematology/oncology and a research fellowship in genetic epidemiology of cancer, at the Mayo School of Graduate Medical Education, Mayo Clinic College of Medicine

Hematology/oncology residency at Mayo School of Graduate Medical Education, Mayo Clinic College of Medicine

Master’s in healthcare administration from the University of Wisconsin – LaCrosse.

 

Select Publications

Preoperative Treatment of Locally Advanced Rectal Cancer. N Engl J Med. 2023 

BRAF V600 Mutation Detection in Plasma Cell-Free DNA: NCCTG N0879 (Alliance). Mayo Clin Proc Innov Qual Outcomes. 2021

ZEBRA: A Multicenter Phase II Study of Pembrolizumab in Patients with Advanced Small-Bowel Adenocarcinoma. Clin Cancer Res. 2021 

Effect of Germline Mutations in Homologous Recombination Repair Genes on Overall Survival of Patients with Pancreatic Adenocarcinoma. Clin Cancer Res. 2020

Association of tumour mutational burden with outcomes in patients with advanced solid tumours treated with pembrolizumab: prospective biomarker analysis of the multicohort, open-label, phase 2 KEYNOTE-158 study. Lancet Oncol. 2020

Pertuzumab plus trastuzumab for HER2-amplified metastatic colorectal cancer (MyPathway): an updated report from a multicentre, open-label, phase 2a, multiple basket study. Lancet Oncol. 2019

Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer. JAMA. 2018

A randomized phase 2 cooperative group trial of carboplatin, paclitaxel, and bevacizumab +/- everolimus for metastatic melanoma. Cancer. 2018

Rucaparib Monotherapy in Patients With Pancreatic Cancer and a Known Deleterious BRCA Mutation. JCO Precis Oncol. 2018

North Central Cancer Treatment Group N0543 (Alliance): A phase 2 trial of pharmacogenetic-based dosing of irinotecan, oxaliplatin, and capecitabine as first-line therapy for patients with advanced small bowel adenocarcinoma. Cancer. 2017

Phase II trial of gemcitabine and tanespimycin (17AAG) in metastatic pancreatic cancer: a Mayo Clinic Phase II Consortium study. Invest New Drugs. 2015

Alliance for Clinical Trials in Oncology. Patient and tumor characteristics and BRAF and KRAS mutations in colon cancer, NCCTG/Alliance N0147. J Natl Cancer Inst. 2014

Integrated genomic characterization reveals novel, therapeutically relevant drug targets in FGFR and EGFR pathways in sporadic intrahepatic cholangiocarcinoma. PLoS Genet. 2014

Current status and future directions of personalized medicine. Genome Med. 2013

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. Nat Genet. 2010

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations and risk for pancreatic adenocarcinoma. Cancer. 2010

Improved survival in metastatic colorectal cancer is associated with adoption of hepatic resection and improved chemotherapy. J Clin Oncol. 2009

Polymorphic variants in hereditary pancreatic cancer genes are not associated with pancreatic cancer risk. Cancer Epidemiol Biomarkers Prev. 2009

Polymorphisms in DNA repair genes, smoking, and pancreatic adenocarcinoma risk. Cancer Res. 2008

Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome. J Biol Chem. 2004