Cellular dissociation grading on biopsies of pulmonary squamous cell carcinoma provides prognostic information across all stages and is congruent with resection specimen grading.

Jesinghaus, Moritz; Boxberg, Melanie; Schmitt, Maxime; Kriegsmann, Mark; Harms, Alexander; Lang, Corinna; Muley, Thomas; Winter, Hauke; Kriegsmann, Katharina; Warth, Arne; Stenzinger, Albrecht; Denkert, Carsten; Hoffmann, Hans; Safi, Seyer; Weichert, Wilko

doi:10.1002/cjp2.295

2022

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Title:: Cellular dissociation grading on biopsies of pulmonary squamous cell carcinoma provides prognostic information across all stages and is congruent with resection specimen grading.
Document type:: Journal Article
Author(s):: Jesinghaus, Moritz; Boxberg, Melanie; Schmitt, Maxime; Kriegsmann, Mark; Harms, Alexander; Lang, Corinna; Muley, Thomas; Winter, Hauke; Kriegsmann, Katharina; Warth, Arne; Stenzinger, Albrecht; Denkert, Carsten; Hoffmann, Hans; Safi, Seyer; Weichert, Wilko
Abstract:: Grading of squamous cell carcinomas (SCCs) based on tumour budding and cell nest size has been termed cellular dissociation grading (CDG) and was suggested as a robust outcome predictor when assessed in biopsies and resections of various extrapulmonary SCCs. In pulmonary SCC (pSCC), this has so far been shown only for resected cancers. As most lung cancers are inoperable, it is of utmost importance to clarify whether the prognostic impact of CDG is retained in the biopsy setting. Two independent pSCC biopsy cohorts from Munich (n = 134, non-resected) and Heidelberg (n = 135, resected) were assessed. Tumour budding and cell nest size measures were assembled into the three-tiered CDG system (G1-G3). Data were correlated with clinicopathological parameters and overall- (OS), disease-specific- (DSS), and disease-free survival (DFS). Interobserver variability and concordance between biopsy and resection specimen were also investigated. CDG was highly congruent between biopsy and resection specimens (κ = 0.77, p < 0.001). In both pSCC cohorts, biopsy-derived CDG strongly impacted on OS, DSS, and DFS (e.g. DFS: p < 0.001). In multivariate survival analyses, CDG remained a stage independent predictor of survival in both cohorts (DFS: p < 0.001 respectively; hazard ratio Munich cohort: CDG-G2: 4.31, CDG-G3; 5.14; Heidelberg cohort: CDG-G2: 5.87, CDG-G3: 9.07). Interobserver agreement for CDG was almost perfect (κ = 0.84, p < 0.001). We conclude that assessment of CDG based on tumour budding and cell nest size is feasible on pSCC biopsies and harbours stage independent prognostic information in resectable as well as non-resectable pSCC. Integration of this grading approach into clinicopathological routine should be considered.
Journal title abbreviation:: J Pathol Clin Res
Year:: 2022
Journal volume:: 8
Journal issue:: 6
Pages contribution:: 567-578
Fulltext / DOI:: doi:10.1002/cjp2.295
Pubmed ID:: http://view.ncbi.nlm.nih.gov/pubmed/36111649
TUM Institution:: Institut für Allgemeine Pathologie und Pathologische Anatomie (Dr. Mogler komm.); Klinik und Poliklinik für Chirurgie (Prof. Friess); Lehrstuhl für Translationale Tumorforschung (DKTK) (Prof. Saur)
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