Macrophage-Targeted [ <sup>11</sup> C]DPA-713 PET/CT Imaging for Early Therapeutic Evaluation of Anti–Tumor Necrosis Factor Treatment in Rheumatoid Arthritis

Anti-tumor necrosis factor (aTNF) treatment of rheumatoid arthritis (RA) requires 3-6 mo to establish efficacy, with 50%-70% response. Quantitative macrophage-targeting PET/CT previously proved to accurately represent RA activity and treatment response. This study investigated early aTNF treatment efficacy assessment using the [<sup>11</sup>C]<i>N,N</i>-diethyl-2-(4-methoxyphenyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-acetamide ([<sup>11</sup>C]DPA-713) macrophage-targeting PET/CT tracer. <b>Methods:</b> Two whole-body [<sup>11</sup>C]DPA-713 PET/CT scans, at baseline and 4 wk, were performed in 20 patients without exposure to biologic agents before starting aTNF treatment. Tracer uptake in joints was quantified by determination of SUVs in 44 joints at baseline and 4 wk of aTNF treatment. Mean SUVs of all joints and specific joint clusters were related to clinical evaluation of the 44 included joints for tenderness (tender joint count of 44 joints [TJC44]) and swelling (swollen joint count of 44 joints [SJC44]) at 26 wk using linear regression analyses. In addition, multivariable analysis, including both PET/CT and concurrent clinical outcome of independent measures versus dependent TJC44 or SJC44 at 26 wk, was performed. <b>Results:</b> Univariate regression analyses showed significant associations between mean SUV<sub>peak</sub> of all joints at baseline (TJC44, <i>r</i> <sup>2</sup> = 0.61; SJC44, <i>r</i> <sup>2</sup> = 0.50; <i>P</i> < 0.001) and 4 wk (TJC44, <i>r</i> <sup>2</sup> = 0.52; SJC44, <i>r</i> <sup>2</sup> = 0.48; <i>P</i> < 0.001) and TJC44 or SJC44 at 26 wk. For specific joint clusters, high correlations were found between SUV<sub>peak</sub> of metacarpophalangeal joints at 4 wk and SUV<sub>peak</sub> of SJC44 at 26 wk (<i>r</i> <sup>2</sup> = 0.67; <i>P</i> < 0.001). Multivariable analyses showed slightly increased correlations (<i>r</i> <sup>2</sup> ≤ 0.75) by combining PET/CT and TJC44, SJC44, and C-reactive protein measurements. <b>Conclusion:</b> Early quantitative [<sup>11</sup>C]DPA-713 PET/CT measurements at baseline and 4 wk of aTNF treatment are associated with clinical disease activity at 26 wk. Therefore, quantitative macrophage [<sup>11</sup>C]DPA-713 PET/CT may have potential clinical value for early prediction of aTNF treatment response in patients with RA.

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Journal
Journal of Nuclear Medicine
Published
2025-12-30
DOI
https://doi.org/10.2967/jnumed.125.270289
Primary Topic
Rheumatoid Arthritis Research and Therapies
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article
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article

Macrophage-Targeted [ 11 C]DPA-713 PET/CT Imaging for Early Therapeutic Evaluation of Anti–Tumor Necrosis Factor Treatment in Rheumatoid Arthritis

Jerney de Jongh, Stéphanie van der Pas, Gerben J.C. Zwezerijnen, W. Van Binsbergen et al.
Journal of Nuclear Medicine
Rheumatoid Arthritis Research and Therapies
article

Macrophage-Targeted [ 11 C]DPA-713 PET/CT Imaging for Early Therapeutic Evaluation of Anti–Tumor Necrosis Factor Treatment in Rheumatoid Arthritis

Jerney de Jongh, Stéphanie van der Pas, Gerben J.C. Zwezerijnen, W. Van Binsbergen, Maqsood Yaqub, Conny J. van der Laken, Dirkjan van Schaardenburg, Alexandre E. Voskuyl
article en

Abstract

Anti-tumor necrosis factor (aTNF) treatment of rheumatoid arthritis (RA) requires 3-6 mo to establish efficacy, with 50%-70% response. Quantitative macrophage-targeting PET/CT previously proved to accurately represent RA activity and treatment response. This study investigated early aTNF treatment efficacy assessment using the [<sup>11</sup>C]<i>N,N</i>-diethyl-2-(4-methoxyphenyl)-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-acetamide ([<sup>11</sup>C]DPA-713) macrophage-targeting PET/CT tracer. <b>Methods:</b> Two whole-body [<sup>11</sup>C]DPA-713 PET/CT scans, at baseline and 4 wk, were performed in 20 patients without exposure to biologic agents before starting aTNF treatment. Tracer uptake in joints was quantified by determination of SUVs in 44 joints at baseline and 4 wk of aTNF treatment. Mean SUVs of all joints and specific joint clusters were related to clinical evaluation of the 44 included joints for tenderness (tender joint count of 44 joints [TJC44]) and swelling (swollen joint count of 44 joints [SJC44]) at 26 wk using linear regression analyses. In addition, multivariable analysis, including both PET/CT and concurrent clinical outcome of independent measures versus dependent TJC44 or SJC44 at 26 wk, was performed. <b>Results:</b> Univariate regression analyses showed significant associations between mean SUV<sub>peak</sub> of all joints at baseline (TJC44, <i>r</i> <sup>2</sup> = 0.61; SJC44, <i>r</i> <sup>2</sup> = 0.50; <i>P</i> < 0.001) and 4 wk (TJC44, <i>r</i> <sup>2</sup> = 0.52; SJC44, <i>r</i> <sup>2</sup> = 0.48; <i>P</i> < 0.001) and TJC44 or SJC44 at 26 wk. For specific joint clusters, high correlations were found between SUV<sub>peak</sub> of metacarpophalangeal joints at 4 wk and SUV<sub>peak</sub> of SJC44 at 26 wk (<i>r</i> <sup>2</sup> = 0.67; <i>P</i> < 0.001). Multivariable analyses showed slightly increased correlations (<i>r</i> <sup>2</sup> ≤ 0.75) by combining PET/CT and TJC44, SJC44, and C-reactive protein measurements. <b>Conclusion:</b> Early quantitative [<sup>11</sup>C]DPA-713 PET/CT measurements at baseline and 4 wk of aTNF treatment are associated with clinical disease activity at 26 wk. Therefore, quantitative macrophage [<sup>11</sup>C]DPA-713 PET/CT may have potential clinical value for early prediction of aTNF treatment response in patients with RA.

Journal of Nuclear MedicineVol. 67(3)
Reade (NL), Amsterdam Neuroscience (NL), Public Health Service of Amsterdam (NL), Amsterdam University Medical Centers (NL)
Good health and well-being
Openalex Percentile: Top 27%
Rheumatoid Arthritis Research and Therapies
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