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19F Hot Spot MRI of Human Adipose-derived Stem Cells for Breast Reconstruction

This is a First-in-man, Phase I Study Utilizing 19F Magnetic Resonance Imaging (MRI) to Track Autologous, Adipose Derived Stem Cells.

Status
Withdrawn
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02035085
Acronym
CS-1000
Enrollment
0
Registered
2014-01-14
Start date
2014-06-30
Completion date
2022-06-30
Last updated
2022-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

19F MRI

Brief summary

Six female patients (\>18 years of age, pre-menopausal) who have had loco-regional (lumpectomy and radiation) therapy for breast carcinoma and have been at least one-year disease free will undergo liposuction, the autologous SVF cell fraction will be isolated and labeled with CS-1000 in the operating room without entering cell culture, which will then be returned to the patient at the site of breast grafting. Patients will receive a pre-screening MRI . Patients will have an MRI scans over a period of 1 month at Johns Hopkins. Follow-up MRIs at 6,12, and 18 months will also be performed. Only at Johns Hopkins with fluorine being done as part of this investigational study. By performing fluorine MRI and quantification of 19F signal, we hypothesize that the engraftment of transplanted cells can be tracked in ways not possible before, using the total fluorine signal as surrogate marker for cell persistence and survival. We expect that a clinically successful outcome (maintenance of breast contour and volume) will be positively correlated with cell survival. The outcome of this study may pave the way for using 19F MRI cell tracking as a new tool for stem cell therapy in a variety of clinical applications.

Interventions

DRUGCS-1000 labeled SVF cells

Patients will undergo autologous transplantation of CS-1000 labelled SVF cells in a sterile environment.

Sponsors

Cosmeticsurg.net
CollaboratorOTHER
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patient capable and willing to sign the Informed Consent (see attached document) 2. Patient must be willing to complete all visits in this study 3. Female, \>18 years of age 4. Lumpectomy and radiation therapy for breast carcinoma 5. 18 month disease free survival 6. No evidence of metastatic disease 7. Patient is fit for surgery as determined by preoperative medical clearance workup performed by an independent primary care physician. 8. Negative pregnancy test.

Exclusion criteria

1. Evidence of metastatic disease 2. Less than 18 months disease-free interval 3. Unable to undergo MRI: 3a) Metallic implant 3b) Claustrophobic 4) High risk for surgical intervention because of comorbidities 5) Received treatment with an investigational drug within 30 days of screening.

Design outcomes

Primary

MeasureTime frameDescription
19F MRI signal over timewithin 18 monthsThe engraftment of transplanted cells will be tracked in ways not possible before, using the total fluorine signal as surrogate marker for cell persistence and survival.

Secondary

MeasureTime frameDescription
Maintenance of breast contour and volumewithin 18 monthsCTCAE/CTEP scale examination criteria (retraction, atrophy, breast and arm edema, ulceration, telangiectasia, and induration/fibrosis will be used for assessments.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026