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[(89)Zr]Zr-DFO-girentuximab and [(18)F]FDG PET/CT to Predict Watchful Waiting Duration in Patients with Metastatic Clear-cell Renal Cell Carcinoma

PURPOSE: Watchful waiting (WW) can be considered for patients with metastatic clear-cell renal cell carcinoma (mccRCC) with good or intermediate prognosis, especially those with <2 International Metastatic RCC Database Consortium criteria and ≤2 metastatic sites [referred to as watch and wait (“W...

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Detalles Bibliográficos
Autores principales: Verhoeff, Sarah R., Oosting, Sjoukje F., Elias, Sjoerd G., van Es, Suzanne C., Gerritse, Sophie L., Angus, Lindsay, Heskamp, Sandra, Desar, Ingrid M.E., Menke-van der Houven van Oordt, C. Willemien, van der Veldt, Astrid A.M., Arens, Anne I.J., Brouwers, Adrienne H., Eisses, Bertha, Mulders, Peter F.A., Hoekstra, Otto S., Zwezerijnen, Gerben J.C., van der Graaf, Winette T.A., Aarntzen, Erik H.J.G., Oyen, Wim J.G., van Herpen, Carla M.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for Cancer Research 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890134/
https://www.ncbi.nlm.nih.gov/pubmed/36394882
http://dx.doi.org/10.1158/1078-0432.CCR-22-0921
Descripción
Sumario:PURPOSE: Watchful waiting (WW) can be considered for patients with metastatic clear-cell renal cell carcinoma (mccRCC) with good or intermediate prognosis, especially those with <2 International Metastatic RCC Database Consortium criteria and ≤2 metastatic sites [referred to as watch and wait (“W&W”) criteria]. The IMaging PAtients for Cancer drug SelecTion-Renal Cell Carcinoma study objective was to assess the predictive value of [(18)F]FDG PET/CT and [(89)Zr]Zr-DFO-girentuximab PET/CT for WW duration in patients with mccRCC. EXPERIMENTAL DESIGN: Between February 2015 and March 2018, 48 patients were enrolled, including 40 evaluable patients with good (n = 14) and intermediate (n = 26) prognosis. Baseline contrast-enhanced CT, [(18)F]FDG and [(89)Zr]Zr-DFO-girentuximab PET/CT were performed. Primary endpoint was the time to disease progression warranting systemic treatment. Maximum standardized uptake values (SUV(max)) were measured using lesions on CT images coregistered to PET/CT. High and low uptake groups were defined on the basis of median geometric mean SUV(max) of RECIST-measurable lesions across patients. RESULTS: The median WW time was 16.1 months [95% confidence interval (CI): 9.0–31.7]. The median WW period was shorter in patients with high [(18)F]FDG tumor uptake than those with low uptake (9.0 vs. 36.2 months; HR, 5.6; 95% CI: 2.4–14.7; P < 0.001). Patients with high [(89)Zr]Zr-DFO-girentuximab tumor uptake had a median WW period of 9.3 versus 21.3 months with low uptake (HR, 1.7; 95% CI: 0.9–3.3; P = 0.13). Patients with “W&W criteria” had a longer median WW period of 21.3 compared with patients without: 9.3 months (HR, 1.9; 95% CI: 0.9–3.9; P(one-sided) = 0.034). Adding [(18)F]FDG uptake to the “W&W criteria” improved the prediction of WW duration (P < 0.001); whereas [(89)Zr]Zr-DFO-girentuximab did not (P = 0.53). CONCLUSIONS: In patients with good- or intermediate-risk mccRCC, low [(18)F]FDG uptake is associated with prolonged WW. This study shows the predictive value of the “W&W criteria” for WW duration and shows the potential of [(18)F]FDG-PET/CT to further improve this.