Post-Surgical Stereotactic Radiotherapy (SRT) Versus GammaTile-ROADS (Radiation One and Done Study)
Purpose
This trial will be a randomized controlled study comparing the efficacy and safety of intraoperative radiation therapy using GammaTilesTM (GT) versus SRT 3-4 weeks following metastatic tumor resection which is the current standard of care.
Condition
- Brain Metastases
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Patients aged 18 years old and above. Eligibility is restricted to this age group given that the battery of neurocognitive tests utilized in this protocol are not developed or validated for use in a younger population. 2. One to six newly diagnosed brain metastases, identified on the screening MRI, from an extracranial primary tumor. 3. Only one lesion, designated the index lesion, is planned for surgical resection. The index lesion must be between 2.0 and 7.0 cm in maximal extent on the screening MRI, and gross total resection is expected by the neurosurgeon. 4. Non-index lesions must measure ≤ 4.0 cm in maximal extent on the screening MRI brain scan. The unresected lesions will be treated with SRT as outlined in the treatment section of the concept. 5. All metastases must be located ≥ 5 mm from the optic chiasm and outside the brainstem. Dural based metastasis are eligible. 6. Previous and/or concurrent treatment with investigational or FDA approved systemic therapies (e.g., chemotherapy, targeted therapeutics, immunotherapy) are permitted and must follow protocol guidelines as follows: Systemic therapy is allowed a minimum of one week from last systemic therapy cycle to surgical resection, and one week after surgical resection to allow a minimum of one week before starting/resuming systemic therapy, depending on the specific systemic agent(s), as recommended by medical/neuro-oncology. Systemic therapy is not allowed 1 day before SRT, the same day as the SRT, or 1 day after the completion of the SRT or longer, depending on the specific systemic agent(s), as recommended by medical/neuro-oncology. Agents that are delivered by implant or depot injections (such as hormonal therapies) are excluded from these restrictions. 7. Karnofsky Performance Scale (KPS) score of ≥ 70. Patients with KPS < 70 can be enrolled if their baseline KPS within 14 days of screening was estimated ≥ 70 and surgical management is expected to improve KPS to ≥ 70. 8. Stable systemic disease or reasonable systemic treatment options predicting a life expectancy of ≥6 months. 9. Ability to complete an MRI of the head with contrast 10. Adequate renal and hepatic function to undergo surgery, in investigators opinion. 11. For women of childbearing potential only, a negative urine or serum pregnancy test done <7 days prior to randomization is required. Women must be willing to notify investigator immediately if they become pregnant at any time during the trial period. 12. Men and women of childbearing potential must be willing to employ adequate contraception throughout the study and for men for up to 3 months after completing treatment. 13. Subjects must be fluent in English, Spanish, or another language the study site is prepared to obtain informed consent for in this trial. English speaking subjects will complete Neurocognitive assessments. Non-English-speaking subjects are trial-eligible but will not complete the Neurocognitive assessments as the psychometric properties for translated tests are either not known or not as robust. 14. Willingness and ability to provide written informed consent and HIPAA authorization prior to performance of any study-related procedures. A legally authorized representative may provide consent if the potential subject lacks the capacity to provide consent themselves.
Exclusion Criteria
- Age <18 years. 2. Karnofsky Performance Scale (KPS) score of <70. Patients with KPS < 70 can be enrolled if their baseline KPS within 14 days of screening was estimated ≥ 70 and surgical management is expected to improve KPS to ≥ 70. 3. Sensitivity to bovine (cow) derived materials including collagen products. 4. Past radiation or surgical therapy to the index lesion or the newly diagnosed non-index lesion(s) is exclusionary. However, up to a total of 2 prior courses of SRT treatment to previously diagnosed lesions are allowed as long as any treated lesions are were ≥15mm from the index lesion. 5. Patients with >6 newly diagnosed metastases on screening MRI 6. Pregnant patients. 7. Primary germ cell tumor, small cell carcinoma, or lymphoma. 8. Leptomeningeal metastasis (LMD). Note: For the purposes of exclusion, LMD is a clinical diagnosis, defined as radiologic or clinical evidence of leptomeningeal involvement with or without positive cerebrospinal fluid (CSF) cytology. 9. Prior WBRT for brain metastases. 10. Concomitant therapy that, in the investigator's opinion, would interfere with the evaluation of the safety or efficacy of the study device. 11. Comorbid psychiatric or neurologic disease or injury impacting cognition, in the opinion of the treating physician, that might impair patient's ability to understand or comply with the requirements of the study or to provide consent 12. Subjects who, in the investigator's opinion, are unable to understand the protocol or to give informed consent, have a history of poor cooperation, noncompliance with medical treatment, or difficulty in returning for follow up care. A legally authorized representative may provide consent if the potential subject lacks the capacity to provide consent themselves.
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Surgical Resection and GammaTile Therapy |
Surgical Resection and GammaTile Therapy |
|
|
Active Comparator Surgical Resection and Stereotactic Radiation Therapy |
Surgical Resection and Stereotactic Radiation Therapy |
|
Recruiting Locations
Phoenix, Arizona 85027
John Wanebo, MD
Little Rock, Arkansas 72205
Analiz Rodriguez, MD, PhD
501-296-1138
Jacksonville, Florida 32204
Jacksonville, Florida 32207
Orange Park, Florida 32073
Michael Horowitz, MD
904-272-9981
Orlando, Florida 32804
Jack Ramsberger
407-303-2090
Orlando, Florida 32806
Hermes Garcia, MD
Tampa, Florida 33606
JENNIFER BURGESS, MS
813-844-1053
Atlanta, Georgia 30322
Kimberly Bojanowski
404-778-7215
Chicago, Illinois 60607
Ken Tatebe, MD, PhD
312-942-9619
Indianapolis, Indiana 46202
Mitesh Shah, MD
Kansas City, Kansas 66016
Paul Camarata
913-588-5575
Louisville, Kentucky 40202
Akshitkumar Mistry, MD
502-562-4370
Detroit, Michigan 48202
Raid Faddah, MBBS, CCRP
313-916-2723
Minneapolis, Minnesota 55407
Minneapolis, Minnesota 55414
Lindsey Sloan, MD, PhD
Columbia, Missouri 65212
Saint Louis, Missouri 63110
John Dombrowski, MD
Lebanon, New Hampshire 03766
Ashley E Gaughan-Maher
Neptune, New Jersey 07753
Albany, New York 12208
New York, New York 10065
Brandon Imber, MD
631-636-0677
Westchester, New York 10595
Simon Hanft, MD
914-493-2363
Chapel Hill, North Carolina 27599
Greenville, North Carolina 27834
Stuart Lee, MD
252-847-1550
Cincinnati, Ohio 45209
Vincent DiNapoli, MD
513-569-5369
Pittsburgh, Pennsylvania 15212
Providence, Rhode Island 02906
Clark Chen, MD, PhD
401-793-9166
Nashville, Tennessee 37232
Dallas, Texas 75235
Toral Patel, MD
Houston, Texas 77030
Houston, Texas 77030
Houston, Texas 77030
San Antonio, Texas 78249
John Floyd, MD
210-450-1000
The Woodlands, Texas 77380
Seattle, Washington 98101
Jamie Leitzinger
206-287-6278
More Details
- NCT ID
- NCT04365374
- Status
- Recruiting
- Sponsor
- GT Medical Technologies, Inc.
Detailed Description
GammaTile therapy results in improved clinical outcomes; however, the data is a single site experience with a limited number of subjects, including only 12 of which were patients with metastatic brain tumors. The primary objective of this randomized, controlled trial is to compare the efficacy and safety of intraoperative radiation therapy using GammaTile® (GT) versus SRT 3-4 weeks following metastatic tumor resection which is the current standard of care. The data collected in this trial design will allow for a direct comparison of a variety of outcomes including local control, overall survival, functional status, quality of life, neurocognitive status, and safety in the target population. In order to support direct comparisons, subjects will be randomized to the two equally sized arms (1:1) based on the following stratification factors: age (<60 vs ≥60), duration of extracranial disease control (≤3 months vs >3 months), number of metastases (one, 2-4 total, 5-6 total ), histology (breast cancer, lung cancer, melanoma, other), the maximal diameter of the index lesion (≤3 cm, >3 cm to ≤5cm, >5cm to ≤7cm) and use of prior or current immunotherapy (yes vs no). An index lesion meeting the criteria of ≥ 2.0-7.0 cm in maximum diameter and appropriate for gross total resection (GTR), will be identified and up to five (5) other unresected, previously untreated lesions in a patient will be allowed. After resection of the index lesion, the surgical bed will be treated with adjunct radiation (either GT or SRT) thereby following the standard of care guidelines (NCCN Guidelines, 2019). Additionally, all unresected, previously untreated metastatic lesions will be treated with stereotactic radiosurgery alone, which also adheres to standard of care guidelines (NCCN Guidelines, 2019). GammaTile is an FDA-cleared means of rapid dose delivery of radiation therapy directly to the tumor bed with predictable dosimetry at the immediate time of resection, and an intense but localized radiation treatment may confer a reduced risk for radiation necrosis compared to other therapies. It is typically easily placed with minimal additional operative time and limited staff radiation exposure. Given these benefits, the rationale for conducting this randomized controlled comparison study is to generate additional data, to further support the use of this new FDA-cleared method of delivering radiation therapy in the setting of newly diagnosed brain metastases.