18F-fluorodeoxyglucose (FDG) PET or 18F-fluorothymidine (FLT) PET to assess early response to aromatase inhibitors (AI) in women with ER+ operable breast cancer in a window-of-opportunity study

Abstract Purpose This study evaluated the ability of 18F-Fluorodeoxyglucose (FDG) and 18F-Fluorothymidine (FLT) imaging with positron emission tomography (PET) to measure early response to endocrine therapy from baseline to just prior to surgical resection in estrogen receptor positive (ER+) breast...

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Main Authors: Perrin E. Romine, Lanell M. Peterson, Brenda F. Kurland, Darrin W. Byrd, Alena Novakova-Jiresova, Mark Muzi, Jennifer M. Specht, Robert K. Doot, Jeanne M. Link, Kenneth A. Krohn, Paul E. Kinahan, David A. Mankoff, Hannah M. Linden
Format: Article
Language:English
Published: BMC 2021-08-01
Series:Breast Cancer Research
Subjects:
Online Access:https://doi.org/10.1186/s13058-021-01464-1
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spelling doaj-793a48469d8446bfa6e4e77f2e989f662021-08-29T11:14:21ZengBMCBreast Cancer Research1465-542X2021-08-0123111110.1186/s13058-021-01464-118F-fluorodeoxyglucose (FDG) PET or 18F-fluorothymidine (FLT) PET to assess early response to aromatase inhibitors (AI) in women with ER+ operable breast cancer in a window-of-opportunity studyPerrin E. Romine0Lanell M. Peterson1Brenda F. Kurland2Darrin W. Byrd3Alena Novakova-Jiresova4Mark Muzi5Jennifer M. Specht6Robert K. Doot7Jeanne M. Link8Kenneth A. Krohn9Paul E. Kinahan10David A. Mankoff11Hannah M. Linden12Division of Medical Oncology, University of Washington/Seattle Cancer Care AllianceDivision of Medical Oncology, University of Washington/Seattle Cancer Care AllianceUniversity of PittsburghDepartment of Radiology, University of WashingtonDepartment of Oncology, First Faculty of Medicine, Charles University and Thomayer HospitalDepartment of Radiology, University of WashingtonDivision of Medical Oncology, University of Washington/Seattle Cancer Care AllianceDepartment of Radiology, University of PennsylvaniaDepartment of Diagnostic Radiology, Oregon Health and Science UniversityDepartment of Diagnostic Radiology, Oregon Health and Science UniversityDepartment of Radiology, University of WashingtonDepartment of Radiology, University of PennsylvaniaDivision of Medical Oncology, University of Washington/Seattle Cancer Care AllianceAbstract Purpose This study evaluated the ability of 18F-Fluorodeoxyglucose (FDG) and 18F-Fluorothymidine (FLT) imaging with positron emission tomography (PET) to measure early response to endocrine therapy from baseline to just prior to surgical resection in estrogen receptor positive (ER+) breast tumors. Methods In two separate studies, women with early stage ER+ breast cancer underwent either paired FDG-PET (n = 22) or FLT-PET (n = 27) scans prior to endocrine therapy and again in the pre-operative setting. Tissue samples for Ki-67 were taken for all patients both prior to treatment and at the time of surgery. Results FDG maximum standardized uptake value (SUVmax) declined in 19 of 22 lesions (mean 17% (range −45 to 28%)). FLT SUVmax declined in 24 of 27 lesions (mean 26% (range −77 to 7%)). The Ki-67 index declined in both studies, from pre-therapy (mean 23% (range 1 to 73%)) to surgery [mean 8% (range < 1 to 41%)]. Pre- and post-therapy PET measures showed strong rank-order agreement with Ki-67 percentages for both tracers; however, the percent change in FDG or FLT SUVmax did not demonstrate a strong correlation with Ki-67 index change or Ki-67 at time of surgery. Conclusions A window-of-opportunity approach using PET imaging to assess early response of breast cancer therapy is feasible. FDG and FLT-PET imaging following a short course of neoadjuvant endocrine therapy demonstrated measurable changes in SUVmax in early stage ER+ positive breast cancers. The percentage change in FDG and FLT-PET uptake did not correlate with changes in Ki-67; post-therapy SUVmax for both tracers was significantly associated with post-therapy Ki-67, an established predictor of endocrine therapy response.https://doi.org/10.1186/s13058-021-01464-1FDG-PETFLT-PETKi-67ER+ breast cancerAromatase inhibitors
collection DOAJ
language English
format Article
sources DOAJ
author Perrin E. Romine
Lanell M. Peterson
Brenda F. Kurland
Darrin W. Byrd
Alena Novakova-Jiresova
Mark Muzi
Jennifer M. Specht
Robert K. Doot
Jeanne M. Link
Kenneth A. Krohn
Paul E. Kinahan
David A. Mankoff
Hannah M. Linden
spellingShingle Perrin E. Romine
Lanell M. Peterson
Brenda F. Kurland
Darrin W. Byrd
Alena Novakova-Jiresova
Mark Muzi
Jennifer M. Specht
Robert K. Doot
Jeanne M. Link
Kenneth A. Krohn
Paul E. Kinahan
David A. Mankoff
Hannah M. Linden
18F-fluorodeoxyglucose (FDG) PET or 18F-fluorothymidine (FLT) PET to assess early response to aromatase inhibitors (AI) in women with ER+ operable breast cancer in a window-of-opportunity study
Breast Cancer Research
FDG-PET
FLT-PET
Ki-67
ER+ breast cancer
Aromatase inhibitors
author_facet Perrin E. Romine
Lanell M. Peterson
Brenda F. Kurland
Darrin W. Byrd
Alena Novakova-Jiresova
Mark Muzi
Jennifer M. Specht
Robert K. Doot
Jeanne M. Link
Kenneth A. Krohn
Paul E. Kinahan
David A. Mankoff
Hannah M. Linden
author_sort Perrin E. Romine
title 18F-fluorodeoxyglucose (FDG) PET or 18F-fluorothymidine (FLT) PET to assess early response to aromatase inhibitors (AI) in women with ER+ operable breast cancer in a window-of-opportunity study
title_short 18F-fluorodeoxyglucose (FDG) PET or 18F-fluorothymidine (FLT) PET to assess early response to aromatase inhibitors (AI) in women with ER+ operable breast cancer in a window-of-opportunity study
title_full 18F-fluorodeoxyglucose (FDG) PET or 18F-fluorothymidine (FLT) PET to assess early response to aromatase inhibitors (AI) in women with ER+ operable breast cancer in a window-of-opportunity study
title_fullStr 18F-fluorodeoxyglucose (FDG) PET or 18F-fluorothymidine (FLT) PET to assess early response to aromatase inhibitors (AI) in women with ER+ operable breast cancer in a window-of-opportunity study
title_full_unstemmed 18F-fluorodeoxyglucose (FDG) PET or 18F-fluorothymidine (FLT) PET to assess early response to aromatase inhibitors (AI) in women with ER+ operable breast cancer in a window-of-opportunity study
title_sort 18f-fluorodeoxyglucose (fdg) pet or 18f-fluorothymidine (flt) pet to assess early response to aromatase inhibitors (ai) in women with er+ operable breast cancer in a window-of-opportunity study
publisher BMC
series Breast Cancer Research
issn 1465-542X
publishDate 2021-08-01
description Abstract Purpose This study evaluated the ability of 18F-Fluorodeoxyglucose (FDG) and 18F-Fluorothymidine (FLT) imaging with positron emission tomography (PET) to measure early response to endocrine therapy from baseline to just prior to surgical resection in estrogen receptor positive (ER+) breast tumors. Methods In two separate studies, women with early stage ER+ breast cancer underwent either paired FDG-PET (n = 22) or FLT-PET (n = 27) scans prior to endocrine therapy and again in the pre-operative setting. Tissue samples for Ki-67 were taken for all patients both prior to treatment and at the time of surgery. Results FDG maximum standardized uptake value (SUVmax) declined in 19 of 22 lesions (mean 17% (range −45 to 28%)). FLT SUVmax declined in 24 of 27 lesions (mean 26% (range −77 to 7%)). The Ki-67 index declined in both studies, from pre-therapy (mean 23% (range 1 to 73%)) to surgery [mean 8% (range < 1 to 41%)]. Pre- and post-therapy PET measures showed strong rank-order agreement with Ki-67 percentages for both tracers; however, the percent change in FDG or FLT SUVmax did not demonstrate a strong correlation with Ki-67 index change or Ki-67 at time of surgery. Conclusions A window-of-opportunity approach using PET imaging to assess early response of breast cancer therapy is feasible. FDG and FLT-PET imaging following a short course of neoadjuvant endocrine therapy demonstrated measurable changes in SUVmax in early stage ER+ positive breast cancers. The percentage change in FDG and FLT-PET uptake did not correlate with changes in Ki-67; post-therapy SUVmax for both tracers was significantly associated with post-therapy Ki-67, an established predictor of endocrine therapy response.
topic FDG-PET
FLT-PET
Ki-67
ER+ breast cancer
Aromatase inhibitors
url https://doi.org/10.1186/s13058-021-01464-1
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