Prognostic value of baseline [18F]-fluorodeoxyglucose positron emission tomography parameters MTV, TLG and asphericity in an international multicenter cohort of nasopharyngeal carcinoma patients.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 07 05 2020
accepted: 14 07 2020
entrez: 31 7 2020
pubmed: 31 7 2020
medline: 25 9 2020
Statut: epublish

Résumé

[18F]-fluorodeoxyglucose (FDG) positron emission tomography (PET) parameters have shown prognostic value in nasopharyngeal carcinomas (NPC), mostly in monocenter studies. The aim of this study was to assess the prognostic impact of standard and novel PET parameters in a multicenter cohort of patients. The established PET parameters metabolic tumor volume (MTV), total lesion glycolysis (TLG) and maximal standardized uptake value (SUVmax) as well as the novel parameter tumor asphericity (ASP) were evaluated in a retrospective multicenter cohort of 114 NPC patients with FDG-PET staging, treated with (chemo)radiation at 8 international institutions. Uni- and multivariable Cox regression and Kaplan-Meier analysis with respect to overall survival (OS), event-free survival (EFS), distant metastases-free survival (FFDM), and locoregional control (LRC) was performed for clinical and PET parameters. When analyzing metric PET parameters, ASP showed a significant association with EFS (p = 0.035) and a trend for OS (p = 0.058). MTV was significantly associated with EFS (p = 0.026), OS (p = 0.008) and LRC (p = 0.012) and TLG with LRC (p = 0.019). TLG and MTV showed a very high correlation (Spearman's rho = 0.95), therefore TLG was subesequently not further analysed. Optimal cutoff values for defining high and low risk groups were determined by maximization of the p-value in univariate Cox regression considering all possible cutoff values. Generation of stable cutoff values was feasible for MTV (p<0.001), ASP (p = 0.023) and combination of both (MTV+ASP = occurrence of one or both risk factors, p<0.001) for OS and for MTV regarding the endpoints OS (p<0.001) and LRC (p<0.001). In multivariable Cox (age >55 years + one binarized PET parameter), MTV >11.1ml (hazard ratio (HR): 3.57, p<0.001) and ASP > 14.4% (HR: 3.2, p = 0.031) remained prognostic for OS. MTV additionally remained prognostic for LRC (HR: 4.86 p<0.001) and EFS (HR: 2.51 p = 0.004). Bootstrapping analyses showed that a combination of high MTV and ASP improved prognostic value for OS compared to each single variable significantly (p = 0.005 and p = 0.04, respectively). When using the cohort from China (n = 57 patients) for establishment of prognostic parameters and all other patients for validation (n = 57 patients), MTV could be successfully validated as prognostic parameter regarding OS, EFS and LRC (all p-values <0.05 for both cohorts). In this analysis, PET parameters were associated with outcome of NPC patients. MTV showed a robust association with OS, EFS and LRC. Our data suggest that combination of MTV and ASP may potentially further improve the risk stratification of NPC patients.

Identifiants

pubmed: 32730364
doi: 10.1371/journal.pone.0236841
pii: PONE-D-20-13504
pmc: PMC7392321
doi:

Substances chimiques

Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0236841

Déclaration de conflit d'intérêts

Dr. Amthauer reports personal fees from SIRTEX Medical Europe, grants from GE Healthcare, grants and personal fees from Novartis, outside the submitted work; All other authors have declared that no competing interests exist. We ensure that Dr Amthauer´s fees and grants do not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Sebastian Zschaeck (S)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.
Berlin Institute of Health (BIH), Berlin, Germany.

Yimin Li (Y)

Department of Radiation Oncology, Xiamen Cancer Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.

Qin Lin (Q)

Department of Radiation Oncology, Xiamen Cancer Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.

Marcus Beck (M)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.

Holger Amthauer (H)

Department of Nuclear Medicine, Charité-Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany.

Laura Bauersachs (L)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.

Marina Hajiyianni (M)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.

Julian Rogasch (J)

Department of Nuclear Medicine, Charité-Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany.

Vincent H Ehrhardt (VH)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.

Goda Kalinauskaite (G)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.

Julian Weingärtner (J)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.

Vivian Hartmann (V)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.

Jörg van den Hoff (J)

Department of Positron Emission Tomography, Institute of Radiopharmaceutical Cancer Research, Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany.

Volker Budach (V)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.

Carmen Stromberger (C)

Charité -Universitätsmedizin Berlin, Berlin, Germany.
Freie Universität Berlin, Berlin, Germany.
Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Radiation Oncology, Berlin Institute of Health, Berlin, Germany.

Frank Hofheinz (F)

Department of Positron Emission Tomography, Institute of Radiopharmaceutical Cancer Research, Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany.

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