Article (Scientific journals)
Non-metastatic para-aortic lymph node remodeling as a predictor of outcome in locally advanced cervical cancer.
Baudin, Louis; Zanella, Léa; Lebeau, Alizée et al.
2026In Clinical Cancer Research
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Abstract :
[en] [en] PURPOSE: Treatment of Locally Advanced Cervical Cancer (LACC) is guided notably by the European Society of Gynaecological Oncology (ESGO) guidelines; unfortunately, relapse remains frequent despite standard chemoradiotherapy and brachytherapy. We evaluated whether histological assessment of non-metastatic para-aortic lymph node (PAoLN) provides prognostic value in LACC. EXPERIMENTAL DESIGN: Primary tumor and PAoLNs from 137 non-metastatic LACC patients were stratified by pre-therapeutic 18F-FDG PET/CT into pelvic PET-positive (pPET+, N= 72) and negative (pPET-, N= 65) groups. Immunohistochemistry on whole sections assessed germinal centers, CD4+, CD8+, FOXP3+ cells, neutrophils (CD66b+, neutrophil extracellular traps: NETs) and high-endothelial venules (HEVs). Associations with progression-free survival (PFS) were examined via univariate and multivariate analyses after a median follow-up of 55.4 months. RESULTS: Primary tumor profile was not associated with outcome, whereas PAoLN features were strongly predictive. In pPET- patients, higher NETs were associated with shorter PFS (p=0.015; HR=2.768), while elevated CD4/CD8 ratio improved outcomes (p=0.047, HR=0.497). In pPET+ patients, shorter PFS was linked to FOXP3+ (p=0.04, HR=1.918) and proliferating FOXP3+ cells (p=0.018, HR=1.668) density. Across the full cohort, abundant germinal centers (p=0.0355, HR=0.273) and elevated CD4/CD8 ratio (p=0.001, HR=0.490) independently correlated with lower recurrence risk. Internal validation was conducted through a bootstrap resampling method. Combinatorial analyses revealed distinct predictive signatures according to pPET status: higher NETs, fewer germinal centers and FIGO-IIA1-IIIB status predicted relapse in pPET- patients. CONCLUSIONS: Integrating pPET status with PAoLN histological analyses improves recurrence risk stratification in LACC. PAoLN evaluation may serve as a complementary tool to guide treatment intensification and surveillance strategies.
Disciplines :
Oncology
Author, co-author :
Baudin, Louis   ;  Université de Liège - ULiège > GIGA
Zanella, Léa   ;  Université de Liège - ULiège > GIGA
Lebeau, Alizée  ;  Centre Hospitalier Universitaire de Liège - CHU > > Service d'oncologie médicale
Pleyers, Clémence ;  CHU Dinant Godinne UCL Namur Namur, Namur Belgium
Gubbels, Noémie  ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie cellulaire et moléculaire
Blacher, Silvia  ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie cellulaire et moléculaire
Seidel, Laurence  ;  Université de Liège - ULiège > Département des sciences de la santé publique
Kakkos, Athanasios  ;  Université de Liège - ULiège > Département des sciences cliniques
Goffin, Frédéric  ;  Université de Liège - ULiège > Département des sciences cliniques > Gynécologie-obstétrique, partim Gynécologie
Lovinfosse, Pierre  ;  Université de Liège - ULiège > GIGA > GIGA Platforms - In Vivo Imaging - Nuclear Medicine Division
Gennigens, Christine  ;  Université de Liège - ULiège > Département des sciences cliniques > Oncologie
Pirson, Sébastien  ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie cellulaire et moléculaire
Kridelka, Frédéric   ;  Université de Liège - ULiège > Département des sciences cliniques > Gynécologie-Obstétrique
Noël, Agnès   ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie cellulaire et moléculaire
More authors (4 more) Less
 These authors have contributed equally to this work.
Language :
English
Title :
Non-metastatic para-aortic lymph node remodeling as a predictor of outcome in locally advanced cervical cancer.
Publication date :
04 March 2026
Journal title :
Clinical Cancer Research
ISSN :
1078-0432
eISSN :
1557-3265
Publisher :
American Association for Cancer Research (AACR), United States
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 14 April 2026

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