Chemokine receptor–targeted PET/CT provides superior diagnostic performance in newly diagnosed marginal zone lymphoma patients: a head-to-head comparison with [18F]FDG
Background In patients with marginal zone lymphoma (MZL), [ 18 F]FDG PET/CT provided inconsistent diagnostic accuracy. C-X-C motif chemokine receptor 4 (CXCR4) is overexpressed in MZL and thus, may emerge as novel theranostic target. We aimed to evaluate the diagnostic performance of CXCR4-targeting...
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Published in | European journal of nuclear medicine and molecular imaging Vol. 51; no. 3; pp. 749 - 755 |
---|---|
Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.02.2024
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 1619-7070 1619-7089 |
DOI | 10.1007/s00259-023-06489-6 |
Cover
Abstract | Background
In patients with marginal zone lymphoma (MZL), [
18
F]FDG PET/CT provided inconsistent diagnostic accuracy. C-X-C motif chemokine receptor 4 (CXCR4) is overexpressed in MZL and thus, may emerge as novel theranostic target. We aimed to evaluate the diagnostic performance of CXCR4-targeting [
68
Ga]Ga-PentixaFor when compared to [
18
F]FDG PET/CT in MZL.
Methods
Thirty-two untreated MZL patients (nodal,
n
= 17; extranodal,
n
= 13; splenic,
n
= 2) received [
68
Ga]Ga-PentixaFor and [
18
F]FDG PET/CT within median 2 days. We performed a visual and quantitative analysis of the total lymphoma volume by measuring maximum/peak standardized uptake values (SUV
max/peak
), and calculating target-to-background ratios (TBR, defined as lesion-based SUV
peak
divided by SUV
mean
from blood pool). Visual comparisons for both radiotracers were carried out for all target lesions (TL), and quantitative analysis of concordant TL evident on both scans. Last, MZL subtype analyses were also conducted.
Results
On a patient-based level, [
68
Ga]Ga-PentixaFor identified MZL manifestations in 32 (100%) subjects (vs. [
18
F]FDG, 25/32 [78.1%]). Of the 256 identified TL, 127/256 (49.6%) manifestations were evident only on CXCR4-directed imaging, while only 7/256 (2.7%) were identified on [
18
F]FDG but missed by [
68
Ga]Ga-PentixaFor. In the remaining 122/256 (47.7%) concordant TL, [
68
Ga]Ga-PentixaFor consistently provided increased metrics when compared to [
18
F]FDG: SUV
max
,
10.3 (range, 2.53–37.2) vs. 5.72 (2.32–37.0); SUV
peak
, 6.23 (1.58–25.7) vs. 3.87 (1.54–27.7);
P
< 0.01, respectively. Concordant TL TBR on [
68
Ga]Ga-PentixaFor (median, 3.85; range, 1.05–16.0) was also approximately 1.8-fold higher relative to [
18
F]FDG (median, 2.08; range, 0.81–28.8;
P
< 0.01). Those findings on image contrast, however, were driven by nodal MZL (
P
< 0.01), and just missed significance for extranodal MZL (
P
= 0.06).
Conclusions
In newly diagnosed MZL patients, [
68
Ga]Ga-PentixaFor identified more sites of disease when compared to [
18
F]FDG, irrespective of MZL subtype. Quantitative PET parameters including TBR were also higher on [
68
Ga]Ga-PentixaFor PET/CT, suggesting improved diagnostic read-out using chemokine receptor-targeted imaging. |
---|---|
AbstractList | Background
In patients with marginal zone lymphoma (MZL), [
18
F]FDG PET/CT provided inconsistent diagnostic accuracy. C-X-C motif chemokine receptor 4 (CXCR4) is overexpressed in MZL and thus, may emerge as novel theranostic target. We aimed to evaluate the diagnostic performance of CXCR4-targeting [
68
Ga]Ga-PentixaFor when compared to [
18
F]FDG PET/CT in MZL.
Methods
Thirty-two untreated MZL patients (nodal,
n
= 17; extranodal,
n
= 13; splenic,
n
= 2) received [
68
Ga]Ga-PentixaFor and [
18
F]FDG PET/CT within median 2 days. We performed a visual and quantitative analysis of the total lymphoma volume by measuring maximum/peak standardized uptake values (SUV
max/peak
), and calculating target-to-background ratios (TBR, defined as lesion-based SUV
peak
divided by SUV
mean
from blood pool). Visual comparisons for both radiotracers were carried out for all target lesions (TL), and quantitative analysis of concordant TL evident on both scans. Last, MZL subtype analyses were also conducted.
Results
On a patient-based level, [
68
Ga]Ga-PentixaFor identified MZL manifestations in 32 (100%) subjects (vs. [
18
F]FDG, 25/32 [78.1%]). Of the 256 identified TL, 127/256 (49.6%) manifestations were evident only on CXCR4-directed imaging, while only 7/256 (2.7%) were identified on [
18
F]FDG but missed by [
68
Ga]Ga-PentixaFor. In the remaining 122/256 (47.7%) concordant TL, [
68
Ga]Ga-PentixaFor consistently provided increased metrics when compared to [
18
F]FDG: SUV
max
,
10.3 (range, 2.53–37.2) vs. 5.72 (2.32–37.0); SUV
peak
, 6.23 (1.58–25.7) vs. 3.87 (1.54–27.7);
P
< 0.01, respectively. Concordant TL TBR on [
68
Ga]Ga-PentixaFor (median, 3.85; range, 1.05–16.0) was also approximately 1.8-fold higher relative to [
18
F]FDG (median, 2.08; range, 0.81–28.8;
P
< 0.01). Those findings on image contrast, however, were driven by nodal MZL (
P
< 0.01), and just missed significance for extranodal MZL (
P
= 0.06).
Conclusions
In newly diagnosed MZL patients, [
68
Ga]Ga-PentixaFor identified more sites of disease when compared to [
18
F]FDG, irrespective of MZL subtype. Quantitative PET parameters including TBR were also higher on [
68
Ga]Ga-PentixaFor PET/CT, suggesting improved diagnostic read-out using chemokine receptor-targeted imaging. BackgroundIn patients with marginal zone lymphoma (MZL), [18F]FDG PET/CT provided inconsistent diagnostic accuracy. C-X-C motif chemokine receptor 4 (CXCR4) is overexpressed in MZL and thus, may emerge as novel theranostic target. We aimed to evaluate the diagnostic performance of CXCR4-targeting [68Ga]Ga-PentixaFor when compared to [18F]FDG PET/CT in MZL.MethodsThirty-two untreated MZL patients (nodal, n = 17; extranodal, n = 13; splenic, n = 2) received [68Ga]Ga-PentixaFor and [18F]FDG PET/CT within median 2 days. We performed a visual and quantitative analysis of the total lymphoma volume by measuring maximum/peak standardized uptake values (SUVmax/peak), and calculating target-to-background ratios (TBR, defined as lesion-based SUVpeak divided by SUVmean from blood pool). Visual comparisons for both radiotracers were carried out for all target lesions (TL), and quantitative analysis of concordant TL evident on both scans. Last, MZL subtype analyses were also conducted.ResultsOn a patient-based level, [68Ga]Ga-PentixaFor identified MZL manifestations in 32 (100%) subjects (vs. [18F]FDG, 25/32 [78.1%]). Of the 256 identified TL, 127/256 (49.6%) manifestations were evident only on CXCR4-directed imaging, while only 7/256 (2.7%) were identified on [18F]FDG but missed by [68Ga]Ga-PentixaFor. In the remaining 122/256 (47.7%) concordant TL, [68Ga]Ga-PentixaFor consistently provided increased metrics when compared to [18F]FDG: SUVmax, 10.3 (range, 2.53–37.2) vs. 5.72 (2.32–37.0); SUVpeak, 6.23 (1.58–25.7) vs. 3.87 (1.54–27.7); P < 0.01, respectively. Concordant TL TBR on [68Ga]Ga-PentixaFor (median, 3.85; range, 1.05–16.0) was also approximately 1.8-fold higher relative to [18F]FDG (median, 2.08; range, 0.81–28.8; P < 0.01). Those findings on image contrast, however, were driven by nodal MZL (P < 0.01), and just missed significance for extranodal MZL (P = 0.06).ConclusionsIn newly diagnosed MZL patients, [68Ga]Ga-PentixaFor identified more sites of disease when compared to [18F]FDG, irrespective of MZL subtype. Quantitative PET parameters including TBR were also higher on [68Ga]Ga-PentixaFor PET/CT, suggesting improved diagnostic read-out using chemokine receptor-targeted imaging. In patients with marginal zone lymphoma (MZL), [ F]FDG PET/CT provided inconsistent diagnostic accuracy. C-X-C motif chemokine receptor 4 (CXCR4) is overexpressed in MZL and thus, may emerge as novel theranostic target. We aimed to evaluate the diagnostic performance of CXCR4-targeting [ Ga]Ga-PentixaFor when compared to [ F]FDG PET/CT in MZL. Thirty-two untreated MZL patients (nodal, n = 17; extranodal, n = 13; splenic, n = 2) received [ Ga]Ga-PentixaFor and [ F]FDG PET/CT within median 2 days. We performed a visual and quantitative analysis of the total lymphoma volume by measuring maximum/peak standardized uptake values (SUV ), and calculating target-to-background ratios (TBR, defined as lesion-based SUV divided by SUV from blood pool). Visual comparisons for both radiotracers were carried out for all target lesions (TL), and quantitative analysis of concordant TL evident on both scans. Last, MZL subtype analyses were also conducted. On a patient-based level, [ Ga]Ga-PentixaFor identified MZL manifestations in 32 (100%) subjects (vs. [ F]FDG, 25/32 [78.1%]). Of the 256 identified TL, 127/256 (49.6%) manifestations were evident only on CXCR4-directed imaging, while only 7/256 (2.7%) were identified on [ F]FDG but missed by [ Ga]Ga-PentixaFor. In the remaining 122/256 (47.7%) concordant TL, [ Ga]Ga-PentixaFor consistently provided increased metrics when compared to [ F]FDG: SUV , 10.3 (range, 2.53-37.2) vs. 5.72 (2.32-37.0); SUV , 6.23 (1.58-25.7) vs. 3.87 (1.54-27.7); P < 0.01, respectively. Concordant TL TBR on [ Ga]Ga-PentixaFor (median, 3.85; range, 1.05-16.0) was also approximately 1.8-fold higher relative to [ F]FDG (median, 2.08; range, 0.81-28.8; P < 0.01). Those findings on image contrast, however, were driven by nodal MZL (P < 0.01), and just missed significance for extranodal MZL (P = 0.06). In newly diagnosed MZL patients, [ Ga]Ga-PentixaFor identified more sites of disease when compared to [ F]FDG, irrespective of MZL subtype. Quantitative PET parameters including TBR were also higher on [ Ga]Ga-PentixaFor PET/CT, suggesting improved diagnostic read-out using chemokine receptor-targeted imaging. |
Author | Weich, Alexander Kosmala, Aleksander Hartrampf, Philipp E. Raderer, Markus Higuchi, Takahiro Schneid, Simone Duell, Johannes Schlötelburg, Wiebke Lapa, Constantin Buck, Andreas K. Topp, Max S. Serfling, Sebastian E. Werner, Rudolf A. Einsele, Hermann |
Author_xml | – sequence: 1 givenname: Aleksander surname: Kosmala fullname: Kosmala, Aleksander email: Kosmala_A@ukw.de organization: Department of Nuclear Medicine, University Hospital Würzburg – sequence: 2 givenname: Johannes surname: Duell fullname: Duell, Johannes organization: Department of Internal Medicine II, University Hospital Würzburg – sequence: 3 givenname: Simone surname: Schneid fullname: Schneid, Simone organization: Department of Nuclear Medicine, University Hospital Würzburg – sequence: 4 givenname: Sebastian E. surname: Serfling fullname: Serfling, Sebastian E. organization: Department of Nuclear Medicine, University Hospital Würzburg – sequence: 5 givenname: Takahiro surname: Higuchi fullname: Higuchi, Takahiro organization: Department of Nuclear Medicine, University Hospital Würzburg, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University – sequence: 6 givenname: Alexander surname: Weich fullname: Weich, Alexander organization: Department of Internal Medicine II, University Hospital Würzburg – sequence: 7 givenname: Constantin surname: Lapa fullname: Lapa, Constantin organization: Nuclear Medicine, Faculty of Medicine, University of Augsburg – sequence: 8 givenname: Philipp E. surname: Hartrampf fullname: Hartrampf, Philipp E. organization: Department of Nuclear Medicine, University Hospital Würzburg – sequence: 9 givenname: Markus surname: Raderer fullname: Raderer, Markus organization: Department of Internal Medicine I, Medical University Vienna – sequence: 10 givenname: Hermann surname: Einsele fullname: Einsele, Hermann organization: Department of Internal Medicine II, University Hospital Würzburg – sequence: 11 givenname: Andreas K. surname: Buck fullname: Buck, Andreas K. organization: Department of Nuclear Medicine, University Hospital Würzburg – sequence: 12 givenname: Max S. surname: Topp fullname: Topp, Max S. organization: Department of Internal Medicine II, University Hospital Würzburg – sequence: 13 givenname: Wiebke surname: Schlötelburg fullname: Schlötelburg, Wiebke organization: Department of Nuclear Medicine, University Hospital Würzburg – sequence: 14 givenname: Rudolf A. orcidid: 0000-0003-3372-6046 surname: Werner fullname: Werner, Rudolf A. organization: Department of Nuclear Medicine, University Hospital Würzburg, Department of Radiology and Radiological Sciences, Johns Hopkins School of Medicine |
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CitedBy_id | crossref_primary_10_1007_s12254_024_00998_2 crossref_primary_10_1016_j_cpet_2024_05_002 crossref_primary_10_1097_MNM_0000000000001889 |
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Keywords | Ga]Ga-PentixaFor C-X-C motif chemokine receptor F]FDG Marginal zone lymphoma CXCR4 [ PET [68Ga]Ga-PentixaFor [18F]FDG |
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In patients with marginal zone lymphoma (MZL), [
18
F]FDG PET/CT provided inconsistent diagnostic accuracy. C-X-C motif chemokine receptor 4 (CXCR4)... In patients with marginal zone lymphoma (MZL), [ F]FDG PET/CT provided inconsistent diagnostic accuracy. C-X-C motif chemokine receptor 4 (CXCR4) is... BackgroundIn patients with marginal zone lymphoma (MZL), [18F]FDG PET/CT provided inconsistent diagnostic accuracy. C-X-C motif chemokine receptor 4 (CXCR4) is... |
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SubjectTerms | Cardiology Chemokine receptors Chemokines Computed tomography Coordination Complexes CXCR4 protein Diagnostic systems Fluorine isotopes Fluorodeoxyglucose F18 Gallium Radioisotopes Humans Image contrast Imaging Lesions Lymphoma Medical diagnosis Medical imaging Medicine Medicine & Public Health Nuclear Medicine Oncology Original Article Orthopedics Peptides, Cyclic Performance evaluation Positron emission Positron emission tomography Positron Emission Tomography Computed Tomography - methods Quantitative analysis Radioactive tracers Radiology Radionuclide Imaging Spleen |
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Title | Chemokine receptor–targeted PET/CT provides superior diagnostic performance in newly diagnosed marginal zone lymphoma patients: a head-to-head comparison with [18F]FDG |
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