
Patrick Swift
Clinical Professor, Radiation Oncology - Radiation Therapy
Clinical Focus
- Cancer > Radiation Oncology
- Radiation Oncology
Professional Education
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Residency: UCSF Radiation Oncology Residency (1989) CA
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Internship: St Mary's Medical Center Internal Medicine Residency (1985) CA
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Medical Education: University of Pennsylvania (1984) PA
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Board Certification: American Board of Radiology, Radiation Oncology (1989)
2022-23 Courses
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Independent Studies (6)
- Directed Reading in Radiation Oncology
RADO 299 (Win, Spr) - Early Clinical Experience in Radiation Oncology
RADO 280 (Win, Spr) - Graduate Research
RADO 399 (Win, Spr) - Medical Scholars Research
RADO 370 (Win, Spr) - Readings in Radiation Biology
RADO 101 (Win, Spr) - Undergraduate Research
RADO 199 (Win, Spr)
- Directed Reading in Radiation Oncology
All Publications
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PSMA- and GRPR-targeted PET: Results from 50 Patients with Biochemically Recurrent Prostate Cancer.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine
2021
Abstract
Rationale: Novel radiopharmaceuticals for positron emission tomography (PET) are evaluated for the diagnosis of biochemically recurrent prostate cancer (BCR PC). Here, we compare the gastrin releasing peptide receptors (GRPR) - targeting 68Ga-RM2 with the prostate specific membrane antigen (PSMA) - targeting 68Ga-PSMA11 and 18F-DCFPyL. Methods: Fifty patients had both 68Ga-RM2 PET/MRI and 68Ga-PSMA11 PET/CT (n = 23) or 18F-DCFPyL PET/CT (n = 27) at an interval ranging from 1 to 60 days (mean±SD: 15.8±17.7). Maximum standardized uptake values (SUVmax) were collected for all lesions. Results: RM2 PET was positive in 35 and negative in 15 of the 50 patients. PSMA PET was positive in 37 and negative in 13 of the 50 patients. Both scans detected 70 lesions in 32 patients. Forty-three lesions in 18 patients were identified only on one scan: 68Ga-RM2 detected 7 more lesions in 4 patients, while PSMA detected 36 more lesions in 13 patients. Conclusion: 68Ga-RM2 remains a valuable radiopharmaceutical even when compared with the more widely used 68Ga-PSMA11/18F-DCFPyL in the evaluation of BCR PC. Larger studies are needed to verify that identifying patients for whom these two classes of radiopharmaceuticals are complementary may ultimately allow for personalized medicine.
View details for DOI 10.2967/jnumed.120.259630
View details for PubMedID 33674398