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Prospective Pilot Study of 18F-Fluoroestradiol PET/CT in Patients With Invasive Lobular Carcinomas.
Covington, Matthew F; Hoffman, John M; Morton, Kathryn A; Buckway, Brandon; Boucher, Kenneth M; Rosenthal, Regina E; Porretta, Jane M; Brownson, Kirstyn E; Matsen, Cindy B; Vaklavas, Christos; Ward, John H; Wei, Mei; Buys, Saundra S; Chittoria, Namita; Yakish, Ellen D; Archibald, Zane G; Burrell, Lance D; Butterfield, Regan I; Yap, Jeffrey T.
Afiliação
  • Covington MF; Center for Quantitative Cancer Imaging, Huntsman Cancer Institute, 2000 Circle of Hope Dr, Salt Lake City, UT 84112.
  • Hoffman JM; Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, UT.
  • Morton KA; Center for Quantitative Cancer Imaging, Huntsman Cancer Institute, 2000 Circle of Hope Dr, Salt Lake City, UT 84112.
  • Buckway B; Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, UT.
  • Boucher KM; Center for Quantitative Cancer Imaging, Huntsman Cancer Institute, 2000 Circle of Hope Dr, Salt Lake City, UT 84112.
  • Rosenthal RE; Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, UT.
  • Porretta JM; Present affiliation: Summit Physician Specialists, Murray, UT.
  • Brownson KE; Center for Quantitative Cancer Imaging, Huntsman Cancer Institute, 2000 Circle of Hope Dr, Salt Lake City, UT 84112.
  • Matsen CB; Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT.
  • Vaklavas C; Biostatistics, Huntsman Cancer Institute, Salt Lake City, UT.
  • Ward JH; Department of Surgery, University of Utah, Salt Lake City, UT.
  • Wei M; Department of Surgery, University of Utah, Salt Lake City, UT.
  • Buys SS; Department of Surgery, University of Utah, Salt Lake City, UT.
  • Chittoria N; Department of Surgery, University of Utah, Salt Lake City, UT.
  • Yakish ED; Department of Internal Medicine, Oncology Division, University of Utah, Salt Lake City, UT.
  • Archibald ZG; Department of Internal Medicine, Oncology Division, University of Utah, Salt Lake City, UT.
  • Burrell LD; Department of Internal Medicine, Oncology Division, University of Utah, Salt Lake City, UT.
  • Butterfield RI; Department of Internal Medicine, Oncology Division, University of Utah, Salt Lake City, UT.
  • Yap JT; Department of Internal Medicine, Oncology Division, University of Utah, Salt Lake City, UT.
AJR Am J Roentgenol ; 221(2): 228-239, 2023 08.
Article em En | MEDLINE | ID: mdl-36919879
ABSTRACT
BACKGROUND. PET/CT with 18F-fluoroestradiol (FES) (FDA-approved in 2020) depicts tissues expressing estrogen receptor (ER). Invasive lobular carcinoma (ILC) is commonly ER positive. OBJECTIVE. The primary aim of this study was to assess the frequency with which sites of histologically proven ILC have abnormal uptake on FES PET/CT. METHODS. This prospective single-center pilot study, conducted from December 2020 to August 2021, enrolled patients with histologically confirmed ILC to undergo FES PET/CT; patients optionally underwent FDG PET/CT. Two nuclear radiologists assessed FES PET/CT and FDG PET/CT studies for abnormal uptake corresponding to known ILC sites at enrollment and for additional sites of abnormal uptake, resolving differences by consensus. The primary endpoint was percentage of known ILC sites showing abnormal FES uptake. The alternative to the null hypothesis was that more than 60% of sites would have abnormal FES uptake, exceeding the percentage of ILC with abnormal FDG uptake described in prior literature. A sample size of 24 biopsied lesions was preselected to provide 81% power for the alternative hypothesis (one-sided α = .10). Findings on FES PET/CT and FDG PET/CT were summarized for additional secondary endpoints. RESULTS. The final analysis included 17 patients (mean age, 59.1 ± 13.2 years) with 25 sites of histologically confirmed ILC at enrollment (22 breast lesions, two axillary lymph nodes, one distant metastasis). FES PET/CT showed abnormal uptake in 22 of 25 (88%) lesions, sufficient to reject the null hypothesis (p = .002). Thirteen patients underwent FDG PET/CT. Four of 23 (17%) sites of histologically confirmed ILC, including additional sites detected and confirmed after enrollment, were identified with FES PET/CT only, and 1 of 23 (4%) was identified only with FDG PET/CT (p = .18). FES PET/CT depicted additional lesions not detected with standard-of-care evaluation in 4 of 17 (24%) patients (two contralateral breast cancers and two metastatic axillary lymph nodes, all with subsequent histologic confirmation). Use of FES PET/CT resulted in changes in clinical stage with respect to standard-of-care evaluation in 3 of 17 (18%) patients. CONCLUSION. The primary endpoint of the trial was met. The frequency of abnormal FES uptake among sites of histologically known ILC was found to be to be significantly greater than 60%. CLINICAL IMPACT. This pilot study shows a potential role of FES PET/CT in evaluation of patients with ILC. TRIAL REGISTRATION. ClinicalTrials.gov NCT04252859.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Carcinoma Lobular Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Middle aged Idioma: En Revista: AJR Am J Roentgenol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Carcinoma Lobular Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Middle aged Idioma: En Revista: AJR Am J Roentgenol Ano de publicação: 2023 Tipo de documento: Article