- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02710253
Salvage Radiation Therapy in Treating Patients With Metastatic Cancer That Has Progressed After Systemic Immunotherapy
Phase II Trial of Salvage Radiation Therapy to Induce Systemic Disease Regression After Progression on Systemic Immunotherapy
Study Overview
Status
Detailed Description
PRIMARY OBJECTIVES:
I. To identify immunotherapy-based treatments where salvage radiation produces systemic disease control after initial progressive disease.
II. To identify immunotherapy-based treatments where salvage radiation produces a high rate of treatment-related toxicities.
SECONDARY OBJECTIVES:
I. To determine the frequency of systemic disease control (objective response or stable disease) after salvage radiation following progression on immunotherapy among all patients and within each treatment group.
II. Determine the frequency of dose limiting toxicities (DLTs) with salvage radiation after progression on treatment with an immunotherapy agent among all patients and within each treatment group.
III. To determine the rate of systemic objective response among all patients and within each treatment group among all patients and within each treatment group.
IV. To determine the duration of response in patients who achieve disease control among all patients and within each treatment group.
V. To determine the overall survival after salvage radiation among all patients and within each treatment group.
VI. To determine the systemic progression free survival after salvage radiation among all patients and within each treatment group.
OUTLINE:
Patients undergo either 4, 5, or 10 fractions of stereotactic body radiation therapy (SBRT), or 5-15 fractions of external beam radiation therapy (EBRT) to any site of metastatic disease daily for any time between 4 days and 3 weeks as determined by the treating radiation oncologist. Patients with at least stable disease (SD) after the second imaging evaluation may undergo additional SBRT in 4 fractions or EBRT in 3 fractions.
After completion of study treatment, patients are followed up at 30 days, then every 12 weeks for up to 1 year.
Study Type
Enrollment (Estimated)
Phase
- Phase 2
Contacts and Locations
Study Contact
- Name: James Welsh, MD
- Phone Number: 713-563-2300
- Email: jwelsh@mdanderson.org
Study Locations
-
-
Texas
-
Conroe, Texas, United States, 77384
- Active, not recruiting
- MD Anderson in The Woodlands
-
Houston, Texas, United States, 77030
- Recruiting
- M D Anderson Cancer Center
-
Contact:
- James Welsh
- Phone Number: 713-563-2300
-
Principal Investigator:
- James Welsh
-
Houston, Texas, United States, 77079
- Active, not recruiting
- MD Anderson West Houston
-
League City, Texas, United States, 77573
- Active, not recruiting
- MD Anderson League City
-
Sugar Land, Texas, United States, 77478
- Active, not recruiting
- MD Anderson in Sugar Land
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Pathologically confirmed diagnosis of cancer
- Progressive disease via Immune-Related Response Criteria (irRC) on prior study or standard of care therapy utilizing an immunotherapy agent OR a clinical status that requires salvage radiation treatment (e.g.: palliative radiation therapy [RT]) at the discretion of treating physician and/or principal investigator (PI)
Previous progression of disease while on treatment of an immunotherapy agent or cell-based therapy
- Patients may continue with maintenance immunotherapy as part of standard of care therapy while receiving radiation
- Have at least one site of metastatic disease amenable to radiation; all lesions amenable to radiation may be irradiated at the discretion of treating radiation oncologist, depending on the location, size and number of lesions
- Be willing and able to provide written informed consent/assent for the trial
- Have a performance status of 0-2 on the Eastern Cooperative Oncology Group (ECOG) performance scale
Female subject of childbearing potential should have a negative urine or serum pregnancy within 28 days prior to study registration up to the first fraction of radiation;
- Note: if the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
- We will allow prior radiation to other sites, with no washout period, prior to study entry as long as the high dose regions of the prior and proposed radiation fields do not overlap or it can overlap, as long as the area being treated is getting low dose radiation; this can be done alone or in combination with high dose to a previously un-irradiated area
Exclusion Criteria:
- Has a diagnosis of active scleroderma, lupus, or other rheumatologic disease which in the opinion of the treating radiation oncologist precludes safe radiation therapy
- Has had prior radiation therapy within the past 3 months where the high dose area of the prior radiation would overlap with the high dose area of the intended radiation based on the judgment of the treating radiation oncologist
Has not recovered (i.e., =< grade 1 or at baseline) from adverse events due to a previous treatment
- Note: subjects with permanent =< grade 2 toxicities (e.g. neuropathy) or toxicities corrected through routine medical management (e.g. thyroid replacement for hypothyroidism) are an exception to this criterion and may qualify for the study
- Note: if subject received major surgery, they must have recovered adequately from the toxicity and/or complications from the intervention prior to starting therapy
- Note: subjects with asymptomatic =< grade 2 laboratory or dermatologic abnormalities are an exception to this criterion and may qualify for the study pending the judgment of the treating radiation oncologist
- Has an active infection requiring intravenous systemic therapy or hospital admission
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
- Is pregnant or expecting to conceive or within the projected duration of the trial, starting with the screening visit through 60 days after the last fraction of radiation
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Treatment (SBRT or EBRT)
Patients undergo either 4, 5, or 10 fractions of SBRT, or 5-15 fractions of EBRT to any site of metastatic disease daily for any time between 4 days and 3 weeks as determined by the treating radiation oncologist.
Patients with at least SD after the second imaging evaluation may undergo additional SBRT in 4 fractions or EBRT in 3 fractions.
|
Correlative studies
Undergo EBRT
Other Names:
Undergo SBRT
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of patients with stable disease
Time Frame: At 4 months
|
To be evaluable for efficacy patients must receive at least one set of systemic imaging >= 4 weeks after completion of radiation.
For all control cohorts, efficacy will be evaluated based off of retrospective review of control patients.
Corollary investigation will be conducted utilizing immune-related response criteria (ir-RC).
Significance testing will assess differences in the frequency of disease control rate via Fisher Exact (if n =< 20) or Chi-squared (if n > 20) test.
|
At 4 months
|
Objective response (partial response or complete response)
Time Frame: Up to 1 year
|
To be evaluable for efficacy patients must receive at least one set of systemic imaging >= 4 weeks after completion of radiation.
For all control cohorts, efficacy will be evaluated based off of retrospective review of control patients.
Corollary investigation will be conducted utilizing ir-RC.
Significance testing will assess differences in the frequency of objective response via Fisher exact (if n =< 20) or Chi-squared (if n > 20) test.
|
Up to 1 year
|
Incidence of adverse events
Time Frame: Up to 1 year
|
Assessed with Common Terminology Criteria for Adverse Events version 4.0. To be evaluable for toxicity, patients must be on the trial for at least 8 weeks. For a toxicity to be considered a dose limiting toxicity, the toxicity must be grade 3+ non-dermatologic and non-laboratory, grade 4+ laboratory, or grade 4+ dermatologic. In addition the toxicity must meet the following criteria:
|
Up to 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Overall survival
Time Frame: Up to 1 year
|
Will be calculated utilizing the method of Kaplan and Meier.
Exploratory analyses will compare specific treatment groups with the corresponding control group when available.
Differences in overall survival will be compared utilizing Log-Rank test and Cox proportional hazards regression adjusting for factors including treatment group, disease histology, previous response with the most recent immunotherapy based treatment.
|
Up to 1 year
|
Progression free survival
Time Frame: Up to 1 year
|
Will be calculated via RECIST 1.1 utilizing the method of Kaplan and Meier.
Exploratory analyses will compare specific treatment groups with the corresponding control group when available.
Differences in progression free survival will be compared utilizing Log-Rank test and Cox proportional hazards regression adjusting for factors including treatment group, disease histology, previous response with the most recent immunotherapy based treatment.
|
Up to 1 year
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: James Welsh, M.D. Anderson Cancer Center
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2015-0936 (Other Identifier: M D Anderson Cancer Center)
- NCI-2016-00682 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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