| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Thunold, Solfrid |
| dc.contributor.author | Hernes, Eivor |
| dc.contributor.author | Farooqi, Saima |
| dc.contributor.author | Francis, Roslyn |
| dc.contributor.author | Simo Perdigo, Marc |
| dc.contributor.author | Öjlert, Åsa Kristina |
| dc.contributor.author | Nowak, Anna |
| dc.contributor.author | cedres, susana |
| dc.date.accessioned | 2025-03-04T08:51:19Z |
| dc.date.available | 2025-03-04T08:51:19Z |
| dc.date.copyright | 2024 |
| dc.date.issued | 2025-01 |
| dc.identifier.citation | Thunold S, Hernes E, Farooqi S, Öjlert ÅK, Francis RJ, Nowak AK, et al. Outcome prediction based on [18F]FDG PET/CT in patients with pleural mesothelioma treated with ipilimumab and nivolumab +/- UV1 telomerase vaccine. Eur J Nucl Med Mol Imaging. 2025 Jan;52:693–707. |
| dc.identifier.issn | 1619-7089 |
| dc.identifier.uri | https://hdl.handle.net/11351/12682 |
| dc.description | Immunotherapy; Pleural mesothelioma; Telomerase vaccine |
| dc.description.abstract | Purpose
The introduction of immunotherapy in pleural mesothelioma (PM) has highlighted the need for effective outcome predictors. This study explores the role of [18F]FDG PET/CT in predicting outcomes in PM treated with immunotherapy.
Methods
Patients from the NIPU trial, receiving ipilimumab and nivolumab +/- telomerase vaccine in second-line, were included. [18F]FDG PET/CT was obtained at baseline (n = 100) and at week-5 (n = 76). Metabolic tumour volume (MTV) and peak standardised uptake value (SUVpeak) were evaluated in relation to survival outcomes. Wilcoxon rank-sum test was used to assess differences in MTV, total lesion glycolysis (TLG), maximum standardised uptake value (SUVmax) and SUVpeak between patients exhibiting an objective response, defined as either partial response or complete response according to the modified Response Criteria in Solid Tumours (mRECIST) and immune RECIST (iRECIST), and non-responders, defined as either stable disease or progressive disease as their best overall response.
Results
Univariate Cox regression revealed significant associations of MTV with OS (HR 1.36, CI: 1.14, 1.62, p < 0.001) and PFS (HR 1.18, CI: 1.03, 1.34, p = 0.02), while multivariate analysis showed a significant association with OS only (HR 1.35, CI: 1.09, 1.68, p = 0.007). While SUVpeak was not significantly associated with OS or PFS in univariate analyses, it was significantly associated with OS in multivariate analysis (HR 0.43, CI: 0.23, 0.80, p = 0.008). Objective responders had significant reductions in TLG, SUVmax and SUVpeak at week-5.
Conclusion
MTV provides prognostic value in PM treated with immunotherapy. High SUVpeak was not associated with inferior outcomes, which could be attributed to the distinct mechanisms of immunotherapy. Early reductions in PET metrics correlated with treatment response.
Study registration
The NIPU trial (NCT04300244) is registered at clinicaltrials.gov. https://classic.clinicaltrials.gov/ct2/show/NCT04300244?cond=Pleural+Mesothelioma&cntry=NO&draw=2&rank=4 |
| dc.language.iso | eng |
| dc.publisher | Springer |
| dc.relation.ispartofseries | European Journal of Nuclear Medicine and Molecular Imaging;52 |
| dc.rights | Attribution 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
| dc.source | Scientia |
| dc.subject | Avaluació de resultats (Assistència sanitària) |
| dc.subject | Mesotelioma - Immunoteràpia |
| dc.subject | Pleura - Càncer - Immunoteràpia |
| dc.subject | Tomografia per emissió de positrons |
| dc.subject.mesh | Treatment Outcome |
| dc.subject.mesh | Pleural Neoplasms |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Mesothelioma |
| dc.subject.mesh | Combined Modality Therapy |
| dc.subject.mesh | Positron Emission Tomography Computed Tomography |
| dc.title | Outcome prediction based on [18F]FDG PET/CT in patients with pleural mesothelioma treated with ipilimumab and nivolumab +/- UV1 telomerase vaccine |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1007/s00259-024-06853-0 |
| dc.subject.decs | resultado del tratamiento |
| dc.subject.decs | neoplasias pleurales |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | mesotelioma |
| dc.subject.decs | tratamiento combinado |
| dc.subject.decs | tomografía por emisión de positrones-tomografía computarizada |
| dc.relation.publishversion | https://doi.org/10.1007/s00259-024-06853-0 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Thunold S, Farooqi S, Öjlert ÅK] Dept of Oncology, Oslo University Hospital, Oslo, Norway. Dept of Cancer Genetics, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway. [Hernes E] Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway. [Francis RJ] Dept of Nuclear Medicine, Sir Charles Gairdner Hospital, Perth, Australia. Medical School of The University of Western Australia, Perth, Australia. [Nowak AK] Medical School of The University of Western Australia, Perth, Australia. National Centre for Asbestos-Related Diseases, University of Western Australia, Perth, Australia. Medical Oncology, Sir Charles Gairdner Hospital, Perth, Australia. [Cedres S] Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Simo Perdigo M] Servei de Medicina Nuclear, Vall d’Hebron Hospital Universitari, Barcelona, Spain |
| dc.identifier.pmid | 39133306 |
| dc.identifier.wos | 001289939500002 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |