<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>128(2)</volume><submitter>Xu L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>In this real-world study, we aimed to elucidate the predictive value of tumour-associated stroma for clinical prognostic and therapeutic response in upper tract urothelial carcinoma (UTUC) by reviewing the clinicopathologic characteristics of 1015 UTUC patients through a nationwide multicenter analysis.&lt;h4>Methods&lt;/h4>The tumour-stroma ratio (TSR) was assessed based on tissue sections stained for hematoxylin and eosin (H&amp;E), and patients were further stratified into stroma-high (>50% stroma) and stroma-low group (≤50% stroma). Kaplan-Meier curve and Cox regression hazard analysis were conducted to assess the survival outcomes of UTUC patients. Bioinformatics analysis and immunostaining analysis were applied to portray the tumour microenvironment (TME).&lt;h4>Results&lt;/h4>Stroma-high UTUC was significantly associated with poorer survival outcomes and inferior chemotherapeutic responsiveness. Our established nomogram achieved a high prognostic accuracy in predicting overall survival and cancer-specific survival in both of the discovery cohort (area under the curve [AUC] 0.663 and 0.712) and the validation cohort (AUC 0.741 and 0.747). Moreover, stroma-high UTUC was correlated with immunoevasive TME accompanied by increased cancer-associated fibroblasts, tumour-associated macrophages and, conspicuously a cluster of highly exhausted CD8&lt;sup>+&lt;/sup> T cells.&lt;h4>Conclusion&lt;/h4>Our results showed stroma-high UTUC was associated with an inferior prognosis and an immunoevasive TME with exhausted CD8&lt;sup>+&lt;/sup> T cells in UTUC patients. Our TSR-based nomogram could be used to refine prognosis and inform treatment decisions of patients with UTUC.</pubmed_abstract><journal>British journal of cancer</journal><pagination>310-320</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9902452</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The tumour-associated stroma correlates with poor clinical outcomes and immunoevasive contexture in patients with upper tract urothelial carcinoma: results from a multicenter real-world study (TSU-01 Study).</pubmed_title><pmcid>PMC9902452</pmcid><pubmed_authors>Xu L</pubmed_authors><pubmed_authors>Zhou L</pubmed_authors><pubmed_authors>Lin R</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Ma L</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Lin T</pubmed_authors><pubmed_authors>Yang M</pubmed_authors><pubmed_authors>Zhong W</pubmed_authors><pubmed_authors>Cheng S</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Xia K</pubmed_authors><pubmed_authors>Hong P</pubmed_authors></additional><is_claimable>false</is_claimable><name>The tumour-associated stroma correlates with poor clinical outcomes and immunoevasive contexture in patients with upper tract urothelial carcinoma: results from a multicenter real-world study (TSU-01 Study).</name><description>&lt;h4>Background&lt;/h4>In this real-world study, we aimed to elucidate the predictive value of tumour-associated stroma for clinical prognostic and therapeutic response in upper tract urothelial carcinoma (UTUC) by reviewing the clinicopathologic characteristics of 1015 UTUC patients through a nationwide multicenter analysis.&lt;h4>Methods&lt;/h4>The tumour-stroma ratio (TSR) was assessed based on tissue sections stained for hematoxylin and eosin (H&amp;E), and patients were further stratified into stroma-high (>50% stroma) and stroma-low group (≤50% stroma). Kaplan-Meier curve and Cox regression hazard analysis were conducted to assess the survival outcomes of UTUC patients. Bioinformatics analysis and immunostaining analysis were applied to portray the tumour microenvironment (TME).&lt;h4>Results&lt;/h4>Stroma-high UTUC was significantly associated with poorer survival outcomes and inferior chemotherapeutic responsiveness. Our established nomogram achieved a high prognostic accuracy in predicting overall survival and cancer-specific survival in both of the discovery cohort (area under the curve [AUC] 0.663 and 0.712) and the validation cohort (AUC 0.741 and 0.747). Moreover, stroma-high UTUC was correlated with immunoevasive TME accompanied by increased cancer-associated fibroblasts, tumour-associated macrophages and, conspicuously a cluster of highly exhausted CD8&lt;sup>+&lt;/sup> T cells.&lt;h4>Conclusion&lt;/h4>Our results showed stroma-high UTUC was associated with an inferior prognosis and an immunoevasive TME with exhausted CD8&lt;sup>+&lt;/sup> T cells in UTUC patients. Our TSR-based nomogram could be used to refine prognosis and inform treatment decisions of patients with UTUC.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-22T19:03:25.949Z</modification><creation>2025-04-06T02:38:34.321Z</creation></dates><accession>S-EPMC9902452</accession><cross_references><pubmed>36396819</pubmed><doi>10.1038/s41416-022-02049-1</doi></cross_references></HashMap>