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Spots Global Cancer Trial Database for ASCO Survey on COVID-19 in Oncology (ASCO) Registry

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Trial Identification

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

Interventions

Study Description

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.

Keywords

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

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

Useful links and downloads for this trial

Clinicaltrials.gov

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