University of California, Davis
Sacramento, California, 95817, United States
Location status: Recruiting
Location contact
Office of Clinical Research
CONTACT
Xiao Zhao, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT06103682
This is a phase 2 pragmatic study that evaluates the clinical benefit of continuing systemic therapy with the addition of locally ablative therapies for oligo-progressive solid tumors as the primary objective. The primary outcome measure is the time to treatment failure (defined as time to change in systemic failure or permanent discontinuation of therapy) following locally ablative therapy.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Sacramento, California, 95817, United States
Location status: Recruiting
Office of Clinical Research
CONTACT
Xiao Zhao, MD
PRINCIPAL_INVESTIGATOR
This is a phase 2 pragmatic study at a single site that evaluates the clinical benefit of continuing systemic therapy with the addition of locally ablative therapies for oligo-progressive solid tumors as the primary objective. The primary endpoint is disease control at 3 months, defined as continuation in systemic cancer therapy without any changes or permanent discontinuation for 3 months following first day of ablative local therapy. Participants will receive ablative local therapy per standard practices in addition to their systemic therapy and will be followed for up to 5 years following ablative local therapy. Participants will be assigned stereotactic ablative radiotherapy (SABR) or interventional radiology (IR) ablation therapy per the discretion of treating radiation oncologist and/or interventional radiologist.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Stereotactic ablative radiotherapy (SABR) or interventional radiology (IR) ablation therapy
Time frame: 3 months from the first day of ablative local therapy
Number of participants with controlled disease at 3 months, defined as continuation in systemic cancer therapy without any changes or permanent discontinuation for 3 months following first day of ablative local therapy
Time frame: Up to 2 years from the first day of ablative local therapy
Number of participants experiencing grade ≥ 3 adverse events (except for hematologic and electrolyte abnormalities) attributable to ablative local therapy occurring up to 2 years from the first day of ablative local therapy
Time frame: Up to 1 year from the first day of ablative local therapy
Median overall survival stratified by primary tumor type
Time frame: Up to 1 year from the first day of ablative local therapy
Time to treatment failure, defined as time to change in systemic therapy or permanent discontinuation of cancer therapy
Contact information is provided by the study sponsor or research team.
University of California, Davis
Other
Acronym: OBLITERATE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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