Long Term Use of SAVI SCOUT: Pilot Study
Study Details
Study Description
Brief Summary
The purpose of this study is to evaluate the performance of FDA-cleared SAVI SCOUT Breast Localization and Surgical Guidance System (SCOUT) over a longer duration prior to surgery. The device is a non-wire system, which uses nonradioactive light-activated radar, to provide breast surgeons with real-time guidance to locate and remove the target lesion in the breast and/or axillary tissue. The SCOUT device standard of care use is placement up to 30 days prior to surgery to assist surgeons in the localization and retrieval of breast/axillary lesions. Routine image-guided methods (Mammography, Ultrasound, and CT) are used. In this study, investigators will assess the longer term placement of the SCOUT device over an extended time (31 - 365 days) in order to address the needs of patients who require neoadjuvant treatment prior to definitive surgery.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
The SAVI SCOUT (Cianna Medical, Inc.) surgical guidance system received 510(k) U.S. Food and Drug Administration (FDA) approval in August 2014. This system is used as a standard of care since 2015 in the Memorial Healthcare System (MHS) operating rooms by experienced breast surgeons (over 150 MHS breast cancer patients and over 5,000 U.S. breast cancer patients as of September 2016). In MHS standard of care practice, the device is placed at the target lesion(s) under image-guidance by the radiologist up to 30 days prior to surgery.
Patients with certain types of breast cancer undergo neoadjuvant treatment with biologic (hormonal) and/or chemotherapy with the goal of decreasing the tumor volume prior to definitive surgery. If the original cancer lesion(s) resolve completely, this is called complete pathologic response (pCR). pCR and even a partial response, while good for the patient, can result in disappearance or poor visualization of the target and often render pre-operative image-guided localization by the radiologist more difficult and less reliable. This can result in unintended larger, more disfiguring breast cancer surgery. Therefore, if the SCOUT device can be placed prior to treatment response, when the lesion is clearly visualized on imaging, accurate image-guided targeting is optimal and thus placement and subsequent surgery should be more accurate. If this pilot study demonstrates successful performance of the device without device-related complications, it will bring improved value to future patients who will require fewer and/or less extensive pre-operative and surgical procedures. Some value may also be provided to subjects as the targeting before tumor shrinkage is expected to be more accurate.
Thus, this pilot study will assess the performance of FDA-cleared SCOUT system over a longer duration prior to breast and/or axillary lymph node surgery.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: SCOUT device The study population consists of 25 - 35 adult surgical patient volunteers who plan to have definitive breast cancer surgery at Memorial Healthcare System (MHS) Hospitals after neoadjuvant treatment. The investigator will identify subjects who meet inclusion/exclusion criteria, obtain patient's consent and schedule the subject for the SAVI SCOUT Surgical Guidance System procedure. All study participants will receive the same treatment assignment, i.e. lesion localization with the SCOUT device 31 - 365 days prior to surgery. Neoadjuvant treatment decisions will be determined by patient's medical oncologist. |
Device: SAVI SCOUT Surgical Guidance System
SAVI SCOUT Surgical Guidance System is a non-wire system, which uses nonradioactive light-activated radar, to provide breast surgeons with real-time guidance to locate and remove the target lesion in the breast and/or axillary tissue.
|
Outcome Measures
Primary Outcome Measures
- Number of Participants Considered to Have a Successful Surgery [31 - 365 days prior to surgery]
The primary endpoint of this study is successful surgery. Successful surgery (defined as one where the device stays in place and can be removed successfully during surgery) when this device is placed 31 - 365 days prior to surgery. Unsuccessful surgery is defined as one where the device does not stay in place and/or cannot be removed successfully during surgery) when this device is placed 31 - 365 days prior to surgery.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Patient is willing and able to provide informed consent. Patient SCOUT device(s) is placed as part of routine care or study but before neoadjuvant treatment begins.
-
Patient is female.
-
Patient is between the ages of 18 and 90 years.
-
Patient has breast cancer and will undergo neoadjuvant therapy and excision at Memorial Healthcare System.
-
Patient is willing and able to comply with all study procedures and be available to follow-up for the duration of the study (1 - 13 months).
-
Patient reads or understands English or Spanish.
Exclusion Criteria:
-
Patient is pregnant.
-
Patient has pacemaker or implantable defibrillators (These have not been bench tested as of September 2016).
-
Patient has known or suspected nickel allergy.
-
Patient is scheduled or receiving investigational drugs for neoadjuvant regimen. (This could confound UADE of this device.)
-
Patient has any condition that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study.
-
Patient has other malignancy except for adequately treated and cured basal or squamous cancer, curatively treated in situ disease or any other cancer for which the patient has been disease free for greater than or equal to 5 years.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Envision Physician Scientific Research, Inc. formerly Sheridan Healthcare, Inc. | Plantation | Florida | United States | 33322 |
Sponsors and Collaborators
- Envision Healthcare Scientific Intelligence, Inc.
- Cianna Medical, Inc.
Investigators
- Principal Investigator: Mary Hayes-Macaluso, MD, Envision Healthcare Scientific Intelligence, Inc.
Study Documents (Full-Text)
More Information
Publications
- Caudle AS, Yang WT, Mittendorf EA, Black DM, Hwang R, Hobbs B, Hunt KK, Krishnamurthy S, Kuerer HM. Selective surgical localization of axillary lymph nodes containing metastases in patients with breast cancer: a prospective feasibility trial. JAMA Surg. 2015 Feb;150(2):137-43. doi: 10.1001/jamasurg.2014.1086.
- Cox CE, Garcia-Henriquez N, Glancy MJ, Whitworth P, Cox JM, Themar-Geck M, Prati R, Jung M, Russell S, Appleton K, King J, Shivers SC. Pilot Study of a New Nonradioactive Surgical Guidance Technology for Locating Nonpalpable Breast Lesions. Ann Surg Oncol. 2016 Jun;23(6):1824-30. doi: 10.1245/s10434-015-5079-x. Epub 2016 Feb 3.
- Hylton NM, Gatsonis CA, Rosen MA, Lehman CD, Newitt DC, Partridge SC, Bernreuter WK, Pisano ED, Morris EA, Weatherall PT, Polin SM, Newstead GM, Marques HS, Esserman LJ, Schnall MD; ACRIN 6657 Trial Team and I-SPY 1 TRIAL Investigators. Neoadjuvant Chemotherapy for Breast Cancer: Functional Tumor Volume by MR Imaging Predicts Recurrence-free Survival-Results from the ACRIN 6657/CALGB 150007 I-SPY 1 TRIAL. Radiology. 2016 Apr;279(1):44-55. doi: 10.1148/radiol.2015150013. Epub 2015 Dec 1.
- Mango V, Ha R, Gomberawalla A, Wynn R, Feldman S. Evaluation of the SAVI SCOUT Surgical Guidance System for Localization and Excision of Nonpalpable Breast Lesions: A Feasibility Study. AJR Am J Roentgenol. 2016 Oct;207(4):W69-W72. Epub 2016 Jun 15.
- CMI-SCOUT-001
Study Results
Participant Flow
| Recruitment Details | |
|---|---|
| Pre-assignment Detail |
| Arm/Group Title | SCOUT Device |
|---|---|
| Arm/Group Description | All study participants received the same treatment assignment, i.e. lesion localization with the SCOUT device 31 - 365 days prior to surgery. Each participant underwent the SAVI SCOUT Surgical Guidance System procedure. |
| Period Title: Overall Study | |
| STARTED | 34 |
| COMPLETED | 34 |
| NOT COMPLETED | 0 |
Baseline Characteristics
| Arm/Group Title | SCOUT Device |
|---|---|
| Arm/Group Description | All study participants received the same treatment assignment, i.e. lesion localization with the SCOUT device 31 - 365 days prior to surgery. Each participant underwent the SAVI SCOUT Surgical Guidance System procedure. |
| Overall Participants | 34 |
| Age (years) [Mean (Full Range) ] | |
| Mean (Full Range) [years] |
50
|
| Sex: Female, Male (Count of Participants) | |
| Female |
34
100%
|
| Male |
0
0%
|
| Race/Ethnicity, Customized (Count of Participants) | |
| Caucasian |
10
29.4%
|
| African American |
12
35.3%
|
| Hispanic |
11
32.4%
|
| Other |
1
2.9%
|
| Node Positive (Count of Participants) | |
| Count of Participants [Participants] |
23
67.6%
|
Outcome Measures
| Title | Number of Participants Considered to Have a Successful Surgery |
|---|---|
| Description | The primary endpoint of this study is successful surgery. Successful surgery (defined as one where the device stays in place and can be removed successfully during surgery) when this device is placed 31 - 365 days prior to surgery. Unsuccessful surgery is defined as one where the device does not stay in place and/or cannot be removed successfully during surgery) when this device is placed 31 - 365 days prior to surgery. |
| Time Frame | 31 - 365 days prior to surgery |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title | SCOUT Device |
|---|---|
| Arm/Group Description | All study participants received the same treatment assignment, i.e. lesion localization with the SCOUT device 31 - 365 days prior to surgery. Each participant underwent the SAVI SCOUT Surgical Guidance System procedure. |
| Measure Participants | 34 |
| Count of Participants [Participants] |
34
100%
|
Adverse Events
| Time Frame | 0 months - 14 months. Reportable adverse events were collected from the time after informed consent is obtained until 30 days (for non-serious AEs) or 7 days (for SAEs) after the last day of study participation | |
|---|---|---|
| Adverse Event Reporting Description | Adverse events from underlying diseases and related to neoadjuvant treatments were not intended to be collected. The written Protocol was amended to clarify this point. All reported SAEs were unrelated to the investigational device and collected prior to the Protocol amendment. The collected events were all previously known as anticipated side effects of chemotherapy and fertility preservation. | |
| Arm/Group Title | SCOUT Device | |
| Arm/Group Description | All study participants received the same treatment assignment, i.e. lesion localization with the SCOUT device 31 - 365 days prior to surgery. Each participant underwent the SAVI SCOUT Surgical Guidance System procedure. | |
All Cause Mortality |
||
| SCOUT Device | ||
| Affected / at Risk (%) | # Events | |
| Total | 0/34 (0%) | |
Serious Adverse Events |
||
| SCOUT Device | ||
| Affected / at Risk (%) | # Events | |
| Total | 0/34 (0%) | |
Other (Not Including Serious) Adverse Events |
||
| SCOUT Device | ||
| Affected / at Risk (%) | # Events | |
| Total | 0/34 (0%) | |
Limitations/Caveats
More Information
Certain Agreements
All Principal Investigators ARE employed by the organization sponsoring the study.
There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
Results Point of Contact
| Name/Title | Women's Imaging Director |
|---|---|
| Organization | Envision Healthcare Scientific Intelligence, Inc. |
| Phone | 9549397729 |
| clinicaltrials@shcr.com |
- CMI-SCOUT-001