Cancer
Our team of cancer researchers is involved in research to improve cancer screening, prevention, treatment, survival and costs for Kaiser Permanente members and for the nation. We evaluate a variety of patient reported results and other factors to improve cancer-related care and improve quality of life for cancer survivors. We conduct research to evaluate how health system policies and processes affect care for cancer patients. Additionally, the IHR partners with local and national organizations, including the National Cancer Institute, to develop cohorts of study participants who are interested in taking part in research aimed at preventing cancer or improving cancer-related results.
Cancer Researchers
Featured Projects
Investigators: Heather Spencer Feigelson, PhD, MPH and Andrea Burnett-Hartman, PhD, MPH
This project is a collaboration of 4 Kaiser Permanente (KP) regions (Georgia, Hawaii, Northwest and Colorado) participating in the assembly of a prospective multi-center cohort study that will include up to 200,000 cancer-free adults aged 40-65 years. This cohort will serve an invaluable function in the conduct of research into cancer etiology and prevention. Kaiser Permanente represents the ideal environment to conduct this research as a pioneer in electronic medical record (EMR) technology and our decades of experience conducting research in these defined populations. We will capitalize upon these resources and experience to recruit KP members as part of this complex, intensive, prospective cohort study.
Funder: National Institutes of Health/National Cancer Institute
Study End Date: 11/03/2028
This project is a collaboration of 4 Kaiser Permanente (KP) regions (Georgia, Hawaii, Northwest and Colorado) participating in the assembly of a prospective multi-center cohort study that will include up to 200,000 cancer-free adults aged 40-65 years. This cohort will serve an invaluable function in the conduct of research into cancer etiology and prevention. Kaiser Permanente represents the ideal environment to conduct this research as a pioneer in electronic medical record (EMR) technology and our decades of experience conducting research in these defined populations. We will capitalize upon these resources and experience to recruit KP members as part of this complex, intensive, prospective cohort study.
Funder: National Institutes of Health/National Cancer Institute
Study End Date: 11/03/2028
Investigator: Andrea Burnett-Hartman, PhD, MPH
The major goals of this competitive renewal are to leverage the infrastructure and successful work of IMPULSS-1 by expanding the economic model to include treatment guidance and assess the use of the web-based interactive IMPULSS Toolkit in real-time across multiple diverse health systems.
Funder: National Cancer Institute
Study End Date: 12/31/2027
The major goals of this competitive renewal are to leverage the infrastructure and successful work of IMPULSS-1 by expanding the economic model to include treatment guidance and assess the use of the web-based interactive IMPULSS Toolkit in real-time across multiple diverse health systems.
Funder: National Cancer Institute
Study End Date: 12/31/2027
Investigator: Debra P. Ritzwoller, PhD
Funder: National Cancer Institute
Study End Date: 07/31/2026
Funder: National Cancer Institute
Study End Date: 07/31/2026
Investigator: Andrea Burnett-Hartman, PhD, MPH
The major goal of this project is to evaluate how policies that impact genomic medicine affect the implementation of precision medicine approaches in health care systems.
Funder: National Cancer Institute
Study End Date: 06/30/2025
The major goal of this project is to evaluate how policies that impact genomic medicine affect the implementation of precision medicine approaches in health care systems.
Funder: National Cancer Institute
Study End Date: 06/30/2025
Investigator: Heather Spencer Feigelson, PhD, MPH
Despite recommendations that all ovarian cancer cases should receive genetic counseling and testing, rates remain low. This study aims to increase the identification of women and their families who have a higher cancer risk by applying a traceback testing approach to retrospectively identify women who have a prior diagnosis of ovarian cancer. This study will leverage tumor registries to identify prior cases of ovarian cancer diagnosed within the past 10 years at two managed care healthcare systems (Kaiser Permanente Northwest and Kaiser Permanente Colorado). The use of archived pathology samples for germline genetic testing will allow family members of both living and deceased women to receive familial genetic cancer risk information. We will assess: 1) the feasibility of and barriers associated with using tumor registries and archived pathology samples for a traceback testing approach; 2) explore the ethical, privacy, and policy implications associated with genetic testing in deceased patients to inform familial risk; 3) characterize barriers to receiving genetic counseling at the time of diagnosis, including barriers to referral, care access, and patient follow-up.
Funder: National Institutes of Health/National Cancer Institute
Study End Date: 02/28/2024
Despite recommendations that all ovarian cancer cases should receive genetic counseling and testing, rates remain low. This study aims to increase the identification of women and their families who have a higher cancer risk by applying a traceback testing approach to retrospectively identify women who have a prior diagnosis of ovarian cancer. This study will leverage tumor registries to identify prior cases of ovarian cancer diagnosed within the past 10 years at two managed care healthcare systems (Kaiser Permanente Northwest and Kaiser Permanente Colorado). The use of archived pathology samples for germline genetic testing will allow family members of both living and deceased women to receive familial genetic cancer risk information. We will assess: 1) the feasibility of and barriers associated with using tumor registries and archived pathology samples for a traceback testing approach; 2) explore the ethical, privacy, and policy implications associated with genetic testing in deceased patients to inform familial risk; 3) characterize barriers to receiving genetic counseling at the time of diagnosis, including barriers to referral, care access, and patient follow-up.
Funder: National Institutes of Health/National Cancer Institute
Study End Date: 02/28/2024
Investigator: Heather Spencer Feigelson, PhD, MPH
The goal of this study is to evaluate the ability of a blood test (Guardant Health’s LUNAR technology) to detect early stage lung cancer among symptom-free individuals who are at high risk of lung cancer and who are undergoing low-dose CT lung screening, or who have incidentally detected lung nodules that are being clinically evaluated in pulmonology.
Funder: Guardant Health, Inc.
Study End Date: 09/30/2024
The goal of this study is to evaluate the ability of a blood test (Guardant Health’s LUNAR technology) to detect early stage lung cancer among symptom-free individuals who are at high risk of lung cancer and who are undergoing low-dose CT lung screening, or who have incidentally detected lung nodules that are being clinically evaluated in pulmonology.
Funder: Guardant Health, Inc.
Study End Date: 09/30/2024
Investigator: Debra P. Ritzwoller, PhD
Funder: National Cancer Institute
Study End Date: 08/31/2024
Funder: National Cancer Institute
Study End Date: 08/31/2024
Investigator: Andrea Burnett-Hartman, PhD, MPH
The major goal of this study is to evaluate the impact of the Nodify XL2 test on management of indeterminate lung nodules in KPCO pulmonology patients.
Funder: Biodesix, Inc.
Study End Date: 05/31/2023
The major goal of this study is to evaluate the impact of the Nodify XL2 test on management of indeterminate lung nodules in KPCO pulmonology patients.
Funder: Biodesix, Inc.
Study End Date: 05/31/2023
Investigator: Heather Spencer Feigelson, PhD, MPH
The goal of this project is to investigate the implementation of exome sequencing in practice settings that primarily serve racially, ethnically, and socioeconomically diverse patients while examining the needs of both patients and clinicians. We will evaluate the clinical utility of exome sequencing in healthy adults of reproductive age at risk for hereditary cancer syndromes (Lynch Syndrome and Hereditary Breast and Ovarian Cancer). We will evaluate and tailor for diverse populations the critical interactions in the program, including the consent process, choices for reporting additional findings, and the response to results disclosure.
Funder: National Human Genome Research Institute
Study End Date: 05/31/2023
The goal of this project is to investigate the implementation of exome sequencing in practice settings that primarily serve racially, ethnically, and socioeconomically diverse patients while examining the needs of both patients and clinicians. We will evaluate the clinical utility of exome sequencing in healthy adults of reproductive age at risk for hereditary cancer syndromes (Lynch Syndrome and Hereditary Breast and Ovarian Cancer). We will evaluate and tailor for diverse populations the critical interactions in the program, including the consent process, choices for reporting additional findings, and the response to results disclosure.
Funder: National Human Genome Research Institute
Study End Date: 05/31/2023
Investigators: Debra P. Ritzwoller, PhD and Andrea Burnett-Hartman, PhD, MPH
The long-term goal of this multi-site center grant is to identify critical gaps in the lung cancer screening process and to design innovative, multilevel interventions to reduce lung cancer mortality, particularly among underserved populations.
Funder: National Cancer Institute
Study End Date: 03/31/2024
The long-term goal of this multi-site center grant is to identify critical gaps in the lung cancer screening process and to design innovative, multilevel interventions to reduce lung cancer mortality, particularly among underserved populations.
Funder: National Cancer Institute
Study End Date: 03/31/2024
Investigator: Andrea Burnett-Hartman, PhD, MPH
The goal of the PROSPR Coordinating Center (PCC) is to coordinate the research of PROSPR Research Centers to achieve PROSPR's mission of evaluating and improving the cancer screening process (recruitment, screening, diagnosis, and referral for treatment).
Funder: National Cancer Institute
Study End Date: 03/31/2023
The goal of the PROSPR Coordinating Center (PCC) is to coordinate the research of PROSPR Research Centers to achieve PROSPR's mission of evaluating and improving the cancer screening process (recruitment, screening, diagnosis, and referral for treatment).
Funder: National Cancer Institute
Study End Date: 03/31/2023
Investigator: Larissa White, PhD, MPH, CPH
To examine the relationship between genetic testing at the time of ovarian, fallopian, or peritoneal cancer at the time of diagnosis and social determinants of health in a retrospective sample of people who received care at one of three integrated health systems from 2008-2019.
Funder: National Institutes of Health
Study End Date: 02/29/2023
To examine the relationship between genetic testing at the time of ovarian, fallopian, or peritoneal cancer at the time of diagnosis and social determinants of health in a retrospective sample of people who received care at one of three integrated health systems from 2008-2019.
Funder: National Institutes of Health
Study End Date: 02/29/2023
Investigator: Heather Spencer Feigelson, PhD, MPH
The aim of this study is to identify miRNA expression changes associated with risk of invasive breast cancer among a cohort of women initially diagnosed with DCIS.
Funder: National Cancer Institute
Study End Date: 07/31/2023
The aim of this study is to identify miRNA expression changes associated with risk of invasive breast cancer among a cohort of women initially diagnosed with DCIS.
Funder: National Cancer Institute
Study End Date: 07/31/2023
Investigator: Debra P. Ritzwoller, PhD
Funder: Gordon & Betty Moore Foundation
Study End Date: 06/30/2022
Funder: Gordon & Betty Moore Foundation
Study End Date: 06/30/2022
Investigator: Heather Spencer Feigelson, PhD, MPH
The goal of this project was to investigate the association between breast density and risk of contralateral breast cancer.
Funder: National Cancer Institute
Study End Date: 08/31/2023
The goal of this project was to investigate the association between breast density and risk of contralateral breast cancer.
Funder: National Cancer Institute
Study End Date: 08/31/2023
Investigator: Andrea Burnett-Hartman, PhD, MPH
The objective of this project is to characterize factors relating to the genetic predisposition, clinical presentation, and prognosis of serrated colorectal cancer.
Funder: National Cancer Institute
Study End Date: 04/30/2023
The objective of this project is to characterize factors relating to the genetic predisposition, clinical presentation, and prognosis of serrated colorectal cancer.
Funder: National Cancer Institute
Study End Date: 04/30/2023
Investigator: Debra P. Ritzwoller, PhD
Funder: American Cancer Society
Study End Date: 06/30/2021
Funder: American Cancer Society
Study End Date: 06/30/2021
Investigator: Debra P. Ritzwoller, PhD
Funder: Patient-Centered Outcomes Research Institute
Study End Date: 07/31/2020
Funder: Patient-Centered Outcomes Research Institute
Study End Date: 07/31/2020
Investigator: Debra P. Ritzwoller, PhD
Funder: National Cancer Institute
Study End Date: 02/28/2019
Funder: National Cancer Institute
Study End Date: 02/28/2019
Investigator: Andrea Burnett-Hartman, PhD, MPH
Recent evidence implicates an additional group of polyps, sessile serrated polyps, as potential precursors to a subset of colorectal cancer. This project investigated the clinical significance of sessile serrated polyps, with the long-term goal of identifying new groups that are high-risk for colorectal cancer and improving the effectiveness of colorectal cancer screening.
Funder: National Cancer Institute
Study End Date: 03/31/2018
Recent evidence implicates an additional group of polyps, sessile serrated polyps, as potential precursors to a subset of colorectal cancer. This project investigated the clinical significance of sessile serrated polyps, with the long-term goal of identifying new groups that are high-risk for colorectal cancer and improving the effectiveness of colorectal cancer screening.
Funder: National Cancer Institute
Study End Date: 03/31/2018