Spots Global Cancer Trial Database for An Observational Pilot Study Evaluating the Feasibility of Conducting Genome-Wide Association Studies Utilizing Subject Provided Information in Subjects With Locally Recurrent or MBC, MCRC, MNSCLC, RGBM or MRCC Treated With Avastin (Bevacizumab) (InVite)
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Trial Identification
Brief Title: An Observational Pilot Study Evaluating the Feasibility of Conducting Genome-Wide Association Studies Utilizing Subject Provided Information in Subjects With Locally Recurrent or MBC, MCRC, MNSCLC, RGBM or MRCC Treated With Avastin (Bevacizumab) (InVite)
Official Title: An Observational Pilot Study Evaluating the Feasibility of Conducting Genome-Wide Association Studies Utilizing Subject Provided Information in Subjects With Locally Recurrent or Metastatic Breast Cancer, Metastatic Colorectal Cancer, Metastatic Non-Squamous Non-Small Cell Lung Cancer, Recurrent Glioblastoma, or Metastatic Renal Cell Cancer Treated With Avastin
Study ID: NCT01598597
Interventions
Study Description
Brief Summary: This pilot, non-interventional, observational, Web-based, prospective cohort study is designed to collect self-reported safety and effectiveness and genetic data from subjects with locally recurrent breast cancer (BC) or metastatic breast cancer (MBC), metastatic colorectal cancer (MCRC), metastatic non-squamous non-small cell lung cancer (MNSCLC), recurrent glioblastoma (RGBM), or metastatic renal cell cancer (MRCC) in the United States who have been previously treated with Avastin (bevacizumab). The cohort will be composed of male and female subjects who have been diagnosed with locally recurrent BC or MBC, MCRC, MNSCLC, RGBM, or MRCC who have received treatment with bevacizumab in combination with chemotherapy, which started prior to or up to 31 December 2012. Participants will be self-referred to this study. They will be recruited online via a number of sources, including through the involvement of patient advocacy groups, social media tools, traditional media, physicians, and events to raise awareness of this study. After appropriate informed consent and authorization are obtained, data will be collected directly from subjects in an online survey. Participants will be contacted electronically to complete quarterly follow-up surveys. The follow-up period will be 1 year from responding to the baseline survey. DNA collection will be performed as part of this study. DNA will be extracted from saliva, which will be provided by the subject utilizing a collection kit sent to the participants for at-home use.
Detailed Description:
Keywords
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
, Many locations, Alabama, United States
, Many locations, Alaska, United States
, Many locations, Arizona, United States
, Many locations, Arkansas, United States
, Many locations, California, United States
, Many locations, Colorado, United States
, Many locations, Connecticut, United States
, Many locations, Delaware, United States
, Many locations, Florida, United States
, Many locations, Georgia, United States
, Many locations, Hawaii, United States
, Many locations, Idaho, United States
, Many locations, Illinois, United States
, Many locations, Indiana, United States
, Many locations, Iowa, United States
, Many locations, Kansas, United States
, Many locations, Kentucky, United States
, Many locations, Louisiana, United States
, Many locations, Maine, United States
, Many locations, Maryland, United States
, Many locations, Massachusetts, United States
, Many locations, Michigan, United States
, Many locations, Minnesota, United States
, Many locations, Mississippi, United States
, Many locations, Missouri, United States
, Many locations, Montana, United States
, Many locations, Nebraska, United States
, Many locations, Nevada, United States
, Many locations, New Hampshire, United States
, Many locations, New Jersey, United States
, Many locations, New Mexico, United States
, Many locations, New York, United States
, Many locations, North Carolina, United States
, Many locations, North Dakota, United States
, Many locations, Ohio, United States
, Many locations, Oklahoma, United States
, Many locations, Oregon, United States
, Many locations, Pennsylvania, United States
, Many locations, Rhode Island, United States
, Many locations, South Carolina, United States
, Many locations, South Dakota, United States
, Many locations, Tennessee, United States
, Many locations, Texas, United States
, Many locations, Utah, United States
, Many locations, Vermont, United States
, Many locations, Virginia, United States
, Many locations, Washington, United States
, Many locations, West Virginia, United States
, Many locations, Wisconsin, United States
, Many locations, Wyoming, United States
Contact Details
Name: Clinical Trials
Affiliation: Genentech, Inc.
Role: STUDY_DIRECTOR
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