<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ng C</submitter><funding>Shanghai Municipal Health Commission</funding><funding>Science and Technology Commission of Shanghai Municipality</funding><funding>Wu Jieping Medical Foundation</funding><funding>Beijing Xisike Clinical Oncology Research Foundation</funding><funding>National Natural Science Foundation of China</funding><pagination>304</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12433416</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>74(10)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Disitamab vedotin (DV, RC48-ADC) has shown promising efficacy and manageable safety as monotherapy or combined with immune checkpoint inhibitors (ICIs) in metastatic urothelial carcinoma (mUC) patients progressing after systemic chemotherapy. This study evaluates the efficacy and safety of RC48-ADC plus ICIs in metastatic upper tract urothelial carcinoma (mUTUC) in a real-world setting.&lt;h4>Methods&lt;/h4>This retrospective, multicenter study included 198 mUTUC patients treated with RC48-ADC plus ICI at 23 clinical centers between June 2021 and December 2023. Data were analyzed from July to September 2024.&lt;h4>Primary endpoint&lt;/h4>objective response rate (ORR). Secondary endpoints: progression-free survival (PFS), overall survival (OS), duration of response (DoR), time to obj</pubmed_abstract><journal>Cancer immunology, immunotherapy : CII</journal><pubmed_title>The efficacy and safety of disitamab vedotin combined with immune checkpoint inhibitors in metastatic upper tract urothelial carcinoma: a multicenter real-world study.</pubmed_title><pmcid>PMC12433416</pmcid><funding_grant_id>82102748</funding_grant_id><funding_grant_id>Y-Gilead2024-PT-0054</funding_grant_id><funding_grant_id>24ZR1492000</funding_grant_id><funding_grant_id>2023ZZ02014</funding_grant_id><funding_grant_id>320.6750.2022-19-92</funding_grant_id><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Ding G</pubmed_authors><pubmed_authors>Yu S</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>Wei X</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Jing T</pubmed_authors><pubmed_authors>Shen H</pubmed_authors><pubmed_authors>Xiong W</pubmed_authors><pubmed_authors>Bi H</pubmed_authors><pubmed_authors>Xue W</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Yan Z</pubmed_authors><pubmed_authors>Tang Q</pubmed_authors><pubmed_authors>Ng C</pubmed_authors><pubmed_authors>Xia D</pubmed_authors><pubmed_authors>Jia Z</pubmed_authors><pubmed_authors>Yuan Y</pubmed_authors><pubmed_authors>Chen M</pubmed_authors><pubmed_authors>Bao Y</pubmed_authors><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Huang Z</pubmed_authors><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Xiao J</pubmed_authors><pubmed_authors>Hu H</pubmed_authors><pubmed_authors>Yang Q</pubmed_authors><pubmed_authors>Ye J</pubmed_authors></additional><is_claimable>false</is_claimable><name>The efficacy and safety of disitamab vedotin combined with immune checkpoint inhibitors in metastatic upper tract urothelial carcinoma: a multicenter real-world study.</name><description>&lt;h4>Background&lt;/h4>Disitamab vedotin (DV, RC48-ADC) has shown promising efficacy and manageable safety as monotherapy or combined with immune checkpoint inhibitors (ICIs) in metastatic urothelial carcinoma (mUC) patients progressing after systemic chemotherapy. This study evaluates the efficacy and safety of RC48-ADC plus ICIs in metastatic upper tract urothelial carcinoma (mUTUC) in a real-world setting.&lt;h4>Methods&lt;/h4>This retrospective, multicenter study included 198 mUTUC patients treated with RC48-ADC plus ICI at 23 clinical centers between June 2021 and December 2023. Data were analyzed from July to September 2024.&lt;h4>Primary endpoint&lt;/h4>objective response rate (ORR). Secondary endpoints: progression-free survival (PFS), overall survival (OS), duration of response (DoR), time to obj</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-01T06:34:54.388Z</modification><creation>2026-04-08T10:05:12.527Z</creation></dates><accession>S-EPMC12433416</accession><cross_references><pubmed>40944727</pubmed><doi>10.1007/s00262-025-04154-5</doi></cross_references></HashMap>