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Research ArticleClinical Investigation

Predicting Outcomes of Indeterminate Bone Lesions on 18F-DCFPyL PSMA PET/CT Scans in the Setting of High-Risk Primary or Recurrent Prostate Cancer

Tim E. Phelps, Stephanie A. Harmon, Esther Mena, Liza Lindenberg, Joanna H. Shih, Deborah E. Citrin, Peter A. Pinto, Bradford J. Wood, William L. Dahut, James L. Gulley, Ravi A. Madan, Peter L. Choyke and Baris Turkbey
Journal of Nuclear Medicine March 2023, 64 (3) 395-401; DOI: https://doi.org/10.2967/jnumed.122.264334
Tim E. Phelps
1Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
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Stephanie A. Harmon
1Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
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Esther Mena
1Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
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Liza Lindenberg
1Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
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Joanna H. Shih
2Biometric Research Program, National Cancer Institute, National Institutes of Health, Rockville, Maryland;
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Deborah E. Citrin
3Radiation Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
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Peter A. Pinto
4Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
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Bradford J. Wood
5Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, Maryland;
6Center for Interventional Oncology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and
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William L. Dahut
7Genitourinary Malignancies Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland
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James L. Gulley
7Genitourinary Malignancies Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland
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Ravi A. Madan
7Genitourinary Malignancies Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland
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Peter L. Choyke
1Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
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Baris Turkbey
1Molecular Imaging Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
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Abstract

Indeterminate bone lesions (IBLs) on prostate-specific membrane antigen (PSMA) PET/CT are common. This study aimed to define variables that predict whether such lesions are likely malignant or benign using features on PSMA PET/CT. Methods: 18F-DCFPyL PET/CT imaging was performed on 243 consecutive patients with high-risk primary or biochemically recurrent prostate cancer. IBLs identified on PSMA PET/CT could not definitively be interpreted as benign or malignant. Medical records of patients with IBLs were reviewed to determine the ultimate status of each lesion. IBLs were deemed malignant or benign on the basis of evidence of progression or stability at follow-up, respectively, or by biopsy results; IBLs were deemed equivocal when insufficient or unclear evidence existed. Post hoc patient, lesion, and scan variables accounting for clustered data were evaluated using Wilcoxon rank-sum and χ2 tests to determine features that favored benign or malignant interpretation. Results: Overall, 98 IBLs within 267 bone lesions (36.7%) were identified in 48 of 243 patients (19.8%). Thirty-seven of 98 IBLs were deemed benign, and 42 were deemed malignant, of which 8 had histologic verification; 19 remained equivocal. Location and SUVmax categorical variables were predictive of IBL interpretation (P = 0.0201 and P = 0.0230, respectively). For IBLs with new interpretations, 34 of 37 (91.9%) considered benign showed an SUVmax of less than 5 or exhibited focal uptake without coexisting bone metastases; 37 of 42 (88.1%) deemed malignant demonstrated an SUVmax of at least 5 or were present with coexisting bone metastases. Logistic regression predicted IBLs with a high SUVmax (univariable: odds ratio [OR], 9.29 [P = 0.0016]; multivariable: OR, 13.87 [P = 0.0089]) or present with other bone metastases (univariable: OR, 9.87 [P = 0.0112]; multivariable: OR, 11.35 [P = 0.003]) to be malignant. Conclusion: IBLs on PSMA PET/CT are concerning; however, characterizing their location, SUV, and additional scan findings can aid interpretation. IBLs displaying an SUVmax of at least 5 or present with other bone metastases favor malignancy. IBLs without accompanying bone metastases that exhibit an SUVmax of less than 5 and are observed only in atypical locations favor benign processes. These guidelines may assist in the interpretation of IBLs on PSMA PET/CT.

  • prostate cancer
  • PET/CT
  • PSMA
  • bone metastases
  • indeterminate bone lesions

Footnotes

  • Published online Oct. 20, 2022.

  • © 2023 by the Society of Nuclear Medicine and Molecular Imaging.
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Journal of Nuclear Medicine: 64 (3)
Journal of Nuclear Medicine
Vol. 64, Issue 3
March 1, 2023
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Predicting Outcomes of Indeterminate Bone Lesions on 18F-DCFPyL PSMA PET/CT Scans in the Setting of High-Risk Primary or Recurrent Prostate Cancer
Tim E. Phelps, Stephanie A. Harmon, Esther Mena, Liza Lindenberg, Joanna H. Shih, Deborah E. Citrin, Peter A. Pinto, Bradford J. Wood, William L. Dahut, James L. Gulley, Ravi A. Madan, Peter L. Choyke, Baris Turkbey
Journal of Nuclear Medicine Mar 2023, 64 (3) 395-401; DOI: 10.2967/jnumed.122.264334

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Predicting Outcomes of Indeterminate Bone Lesions on 18F-DCFPyL PSMA PET/CT Scans in the Setting of High-Risk Primary or Recurrent Prostate Cancer
Tim E. Phelps, Stephanie A. Harmon, Esther Mena, Liza Lindenberg, Joanna H. Shih, Deborah E. Citrin, Peter A. Pinto, Bradford J. Wood, William L. Dahut, James L. Gulley, Ravi A. Madan, Peter L. Choyke, Baris Turkbey
Journal of Nuclear Medicine Mar 2023, 64 (3) 395-401; DOI: 10.2967/jnumed.122.264334
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Keywords

  • prostate cancer
  • PET/CT
  • PSMA
  • bone metastases
  • indeterminate bone lesions
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