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Morphologic intratumoral heterogeneity from routine whole-slide histopathology is prognostic for survival in primary central nervous system lymphoma: development in the LOC Network and international external validation

Lucas Rincón de la RosaiD, Noemie Barillot, Isaias Hernández-VerdíniD, Roser VelascoiD, Bertrand MathoniD, Sandrine Eimer, Jean Rodolphe Vignes, Audrey RousseauiD, Jérôme PaillassaiD, Guido AhleiD, Felix Lerintiu, Emmanuelle Uro‐CosteiD, Lucie ObériciD, Émeline TabouretiD, Romain AppayiD, Guillaume GauchotteiD, Luc TaillandieriD, Jean‐Pierre Marolleau, Clovis AdamiD, Rénata UrsuiD, Stefania CuzzubboiD, Anna SchmittiD, Lucia NichelliiD, Albert Pons‐EscodaiD, Frédéric CharlotteiD, , Agustí AlentorniD

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Abstract

Background: Clinical scores incompletely capture outcomes in primary central nervous system lymphoma (PCNSL). We quantified morphologic heterogeneity in pretreatment hematoxylin and eosin (H\&E) whole slides. Patients and methods: Three independent cohorts of immunocompetent, HIV- and EBV-negative patients treated recently were analyzed: LOC 2023 (122 slides), phase III BLOCAGE-01 (245 slides; NCT02313389), and external Barcelona (BCN; 41 slides). UNI embeddings, prototype learning, spatial metrics, and elastic-net Cox regression defined ITH-C. Results: Models achieved bootstrap-corrected concordance of 0.797--0.834. Age-, sex-, and KPS-adjusted ITH-C HRs were 1.29 (95\% CI 1.01--1.64), 1.27 (1.07--1.51), and 2.13 (1.35--3.37), respectively. Adding ITH-C increased MSKCC C-index from 0.671 to 0.717, 0.560 to 0.593, and 0.588 to 0.706. Spatial transcriptomics linked ITH-C to immune programs. Conclusions: Routine H\&E encodes prognostic spatial heterogeneity in PCNSL. ITH-C complements clinical scores, supporting prospective risk stratification.

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