About this trial
Background:
People who join a study in the Developmental Therapeutics Clinic (DTC) have tests. These include blood draws and biopsies. Researchers collect data from these samples. Some people take part in more than one study at the DTC. At this time, data are connected only with one single study. Researchers want to access people s medical records. This will allow them to link the research data from all their studies they have or will take part in. Researchers also want to collect medical data about their diagnosis and treatment history. This will allow them to see how their cancer reacted to different drugs over time.
Objective:
To enter people into a master protocol to connect research sample and treatment data across DTC studies.
Eligibility:
People ages 18 and older who are being evaluated or treated for cancer in the DTC
Design:
Participants will allow researchers to look at all the data from their research samples. This includes those from their current, past, and any future NIH studies.
Participants will allow researchers to access some of their medical data. This includes age, diagnosis, treatment history, and response to treatment.
Participants will provide no new samples.
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Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients who are being evaluated and/or treated for cancer or benign tuumors in the Developmental Therapeutics Clinic at the NIH Clinical Center
Ability to understand and willingness to sign a written informed consent document indicating their willingness to have data from their tissue or biologic fluid research specimens and limited medial information used for research as outlined in this protocol and to allow protocol staff access to the CRIS database and their Medical Records Number (MRN).
Age greater than or equal to 18 years
Disqualifiers
None
Trial population
Patients on research protocols at the Developmental Therapeutics Clinic
Trial design
Cohort
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Obtaining informed consent
Collation of research sample and treatment data from individual patients across their participation in consecutive DTC clinical trials
Sponsors and contacts
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