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Brief Title: ASCO Survey on COVID-19 in Oncology (ASCO) Registry
Official Title: ASCO Survey on Coronavirus Disease 2019 (COVID-19) in Oncology (ASCO) Registry
Study ID: NCT04659135
Brief Summary: The American Society of Clinical Oncology (ASCO) Survey on Coronavirus 2019 (COVID-19) in Oncology Registry (ASCO Registry) aims to help the cancer community learn more about the patterns of symptoms and severity of COVID-19 among patients with cancer, as well as how COVID-19 is impacting the delivery of cancer care and patient outcomes. The ASCO Registry collects both baseline and follow-up data on how the virus impacts cancer care and cancer patient outcomes during the COVID-19 pandemic.
Detailed Description: Rationale: The COVID-19 Pandemic presents a unique opportunity to capture information on how a disease outbreak affects delivery of high-quality cancer care. ASCO is providing the means for the oncology community to rapidly submit data that will inform both current cancer care and provide information to help guide decision-making for future disease outbreaks. While other entities have launched COVID-19 cancer registries, ASCO's registry collects information about patients undergoing treatment for cancer and with confirmed COVID-19 infection based on a positive test. Unlike other registries, ASCO's registry collects follow-up information on both COVID-19 disease and cancer outcomes at 30-day intervals for the first 90 days and 90-day intervals thereafter up to one year after COVID-19 diagnosis. Project Objectives: Capture and describe cancer and COVID-19 status at COVID-19 diagnosis, and cancer and COVID-19 outcomes of patients with cancer and COVID-19 from participating cancer practices/institutions. Data collected includes treatment approaches, cancer status, changes to cancer treatment plans in patients with confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, status of COVID-19 infection (e.g., severity of symptoms, need for ventilator, hospitalization, etc.) and cancer (e.g., cancer progression, treatment-related changes/modifications, etc.). Research Objectives: Objective 1: Describe the distribution of symptoms and severity of COVID-19 among patients with cancer (on active treatment or on adjuvant treatment within 12 months after surgical resection) who have confirmed infection of SARS-CoV-2 •Objective 1.1: Describe distribution of symptoms and severity of COVID-19 stratified according to demographic characteristics, including age, cancer type, cancer extent, race, ethnicity, geography, type of therapy received, smoking status, comorbidities, etc. •Objective 1.2: Identify characteristics independently associated with severity of COVID-19 in cancer patients. Objective 2: Examine SARS-CoV-2 viral infection outcomes (ongoing, recovery, hospitalized, not in ICU; hospitalized in ICU; placed on ventilator; death due to COVID-19 disease complications) and cancer outcomes (stable, response to treatment, progression, delayed treatment, treatment discontinued, and death) * Objective 2.1: Stratify patients with SARS-CoV-2 viral infection according to characteristics described in Objective 1.1 to examine whether any of the characteristics are independently associated with COVID-19 and/or cancer outcomes * Objective 2.2: Examine the relationship between SARS-CoV-2 viral infection outcomes and cancer outcomes and whether SARS-CoV-2 viral infection outcomes are independently associated with cancer outcomes Objective 3: To describe effects of the COVID-19 pandemic on cancer practices in the U.S., including changes in staffing and resource availability, priorities for patient care, and modification of interactions between care providers and patients (including use of telemedicine) Eligibility Criteria: The registry collects data about patients with a cancer diagnosis who have a confirmed SARS-CoV-2 infection and are being treated at participating cancer practices/institutions within the United States. Patients in one of the four categories are eligible: 1. Patients with a new cancer diagnosis and in the process of cancer staging and/or receipt of initial cancer therapy 2. Patients with clinically evident cancer receiving anti-cancer treatment, 3. Patients who are disease free, but receiving any type of adjuvant therapy within 1 year following surgical resection (including hormonal treatments), and 4. Patients with clinically evident cancer receiving supportive care only. Statistical Considerations and Reporting: ASCO's Center for Research and Analytics (CENTRA) reports via a data dashboard (https://www.asco.org/covid-resources/asco-registry/data-dashboard) to the general cancer community key characteristics of patients in the Registry. ASCO also submits abstracts for presentation and manuscripts for publication. Reports summarize overall data and stratified by patient characteristics, such as disease sites and stage, age and comorbidities. Reports or publications will also include cancer treatment delay and discontinuation of cancer treatments including surgery, radiation and drug-based therapies, due to the patient's COVID-19 disease and to other factors, with stratification by other variables as described above. Changes in practice patterns of care, staffing, resources, and interactions with patients will also be evaluated and summarized. As there is no hypothesis testing planned, there is no required sample size and providing reports also provided to other registries, with cumulative information, will not affect validity of results. Confidence intervals will be provided where appropriate to demonstrate precision of estimates.
Minimum Age:
Eligible Ages: CHILD, ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of Alabama at Birmingham, Birmingham, Alabama, United States
Infirmary Cancer Care, Mobile, Alabama, United States
Anchorage Oncology Center, Anchorage, Alaska, United States
AIS Cancer Center, Bakersfield, California, United States
Long Beach Memorial Medical Center, Fountain Valley, California, United States
Orange Coast Medical Center, Fountain Valley, California, United States
Saddleback Memorial Medical Center, Fountain Valley, California, United States
Helen Diller Family Comprehensive Cancer Center, UCSF, San Francisco, California, United States
Gene Upshaw Memorial Tahoe Forest Cancer Center, Truckee, California, United States
PIH Health, Whittier, California, United States
Hartford HealthCare Cancer Institute, Hartford, Connecticut, United States
Day Kimball Healthcare, Putnam, Connecticut, United States
Bayhealth Medical Center, Dover, Delaware, United States
Florida Precision Oncology, A Division of 21st Centry Oncology, Fort Myers, Florida, United States
Florida Cancer Specialists - Sarah Cannon Research Institute, Sarasota, Florida, United States
University of South Florida, Tampa, Florida, United States
Emory University Winship Cancer Institute, Atlanta, Georgia, United States
Augusta University, Augusta, Georgia, United States
Cancer Center of Middle Georgia, LLC, Dublin, Georgia, United States
Hawaii Cancer Care, Honolulu, Hawaii, United States
University of Chicago, Chicago, Illinois, United States
NorthShore University HealthSystem, Evanston, Illinois, United States
OSF Little Company of Mary Hospital, Evergreen Park, Illinois, United States
Joliet Oncology-Hematology Associates, Joliet, Illinois, United States
Edward-Elmhurst Healthcare, Naperville, Illinois, United States
Illinois Cancer Care, Peoria, Illinois, United States
Quincy Medical Group Cancer Institute, Quincy, Illinois, United States
Goshen Center for Cancer Care, Goshen, Indiana, United States
Michiana Hematology Oncology, Mishawaka, Indiana, United States
Midwest Oncology Associates - Sarah Cannon Research Institute, Overland Park, Kansas, United States
University of Kansas Medical Center, Westwood, Kansas, United States
Baptist Health Madisonville, Madisonville, Kentucky, United States
Greater Baltimore Medical Center, Baltimore, Maryland, United States
Saint Agnes Hospital Cancer Institute, Baltimore, Maryland, United States
Tufts Medical Center, Boston, Massachusetts, United States
Great Lakes Cancer Management Specialists, Grosse Pointe Woods, Michigan, United States
Mayo Clinic, Rochester, Minnesota, United States
Boone Hospital Center, Columbia, Missouri, United States
Mosaic Cancer Care, Saint Joseph, Missouri, United States
Nebraska Hematology Oncology, Lincoln, Nebraska, United States
Callahan Cancer Center, North Platte, Nebraska, United States
Nebraska Cancer Specialists, Omaha, Nebraska, United States
University of Nebraska Medical Center, Omaha, Nebraska, United States
Bayonne Medical Center, Bayonne, New Jersey, United States
CarePoint Health - Christ Hospital, Jersey City, New Jersey, United States
Penn Medicine, Princeton Health, Plainsboro, New Jersey, United States
Hematology Oncology Associates of Central New York, East Syracuse, New York, United States
Northwell Health Cancer Institute, Lake Success, New York, United States
Memorial Sloan Kettering Cancer Center, New York, New York, United States
University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States
Levine Cancer Institute Atrium Health, Charlotte, North Carolina, United States
East Carolina University, Greenville, North Carolina, United States
Carteret Health Care, Morehead City, North Carolina, United States
CarolinaEast Medical Center, New Bern, North Carolina, United States
Regional Medical Oncology Center, Wilson, North Carolina, United States
Aultman Hospital, Canton, Ohio, United States
Cincinnati Children's Hospital, Cincinnati, Ohio, United States
Oncology Hematology Care, Cincinnati, Ohio, United States
University Hospitals Seidman Cancer Center, Cleveland, Ohio, United States
TriCounty Hematology and Oncology, Massillon, Ohio, United States
Columbia Memorial Hospital, Astoria, Oregon, United States
Samaritan Health Services Corvallis, Corvallis, Oregon, United States
Penn Medicine, Lancaster General Health, Lancaster, Pennsylvania, United States
University of Pennsylvania, Philadelphia, Pennsylvania, United States
Thomas Jefferson University, Philadelphia, Pennsylvania, United States
Lexington Oncology, West Columbia, South Carolina, United States
Monument Health, Rapid City, South Dakota, United States
Kirkland Cancer Center, Jackson, Tennessee, United States
Baptist Clinical Research Institute, Memphis, Tennessee, United States
Tennessee Oncology, Nashville, Tennessee, United States
The START Center for Cancer Care, San Antonio, Texas, United States
University of Texas, Health Science Center, San Antonio, Texas, United States
Virginia Cancer Specialists, Fairfax, Virginia, United States
Augusta Health, Fishersville, Virginia, United States
Hematology Oncology Associates of Fredericksburg, Fredericksburg, Virginia, United States
Virginia Cancer Institute, Richmond, Virginia, United States
PeaceHealth, Vancouver, Washington, United States
Name: Julie R Gralow, MD
Affiliation: American Society of Clinical Oncology
Role: PRINCIPAL_INVESTIGATOR
Name: Suanna S Bruinooge, MPH
Affiliation: American Society of Clinical Oncology
Role: STUDY_DIRECTOR
Name: Elizabeth Garrett-Mayer, PhD
Affiliation: American Society of Clinical Oncology
Role: STUDY_DIRECTOR