<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>111(7)</volume><submitter>Osawa T</submitter><pubmed_abstract>The present study aimed to evaluate the efficacy of the real-world use of axitinib and to develop a prognostic model for stratifying patients who could derive long-term benefit from axitinib. This was a retrospective, descriptive study evaluating the efficacy of axitinib in patients with metastatic renal cell carcinoma that had been treated with 1 or 2 systemic antiangiogenic therapy regimens at 1 of 36 hospitals belonging to the Japan Urologic Oncology Group between January 2012 and February 2019. The primary outcome was overall survival (OS). Using a split-sample method, candidate variables that exhibited significant relationships with OS were chosen to create a model. The new model was validated using the rest of the cohort. In total, 485 patients were enrolled. The median OS was 34 mon</pubmed_abstract><journal>Cancer science</journal><pagination>2460-2471</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7385391</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Oncological outcomes of a multicenter cohort treated with axitinib for metastatic renal cell carcinoma.</pubmed_title><pmcid>PMC7385391</pmcid><pubmed_authors>Osawa T</pubmed_authors><pubmed_authors>Suzuki T</pubmed_authors><pubmed_authors>Morita K</pubmed_authors><pubmed_authors>Nishiyama H</pubmed_authors><pubmed_authors>Japanese Urological Oncology Group</pubmed_authors><pubmed_authors>Tamura K</pubmed_authors><pubmed_authors>Uemura M</pubmed_authors><pubmed_authors>Mitsuzuka K</pubmed_authors><pubmed_authors>Tomida R</pubmed_authors><pubmed_authors>Goto T</pubmed_authors><pubmed_authors>Shinohara N</pubmed_authors><pubmed_authors>Anai S</pubmed_authors><pubmed_authors>Minami K</pubmed_authors><pubmed_authors>Takeuchi A</pubmed_authors><pubmed_authors>Ueda K</pubmed_authors><pubmed_authors>Miyauchi Y</pubmed_authors><pubmed_authors>Hara T</pubmed_authors><pubmed_authors>Ohba K</pubmed_authors><pubmed_authors>Kusakabe N</pubmed_authors><pubmed_authors>Murakami M</pubmed_authors><pubmed_authors>Ito YM</pubmed_authors><pubmed_authors>Kashiwagi A</pubmed_authors><pubmed_authors>Sugimoto M</pubmed_authors><pubmed_authors>Murai S</pubmed_authors><pubmed_authors>Inoue T</pubmed_authors><pubmed_authors>Kojima T</pubmed_authors><pubmed_authors>Sazuka T</pubmed_authors><pubmed_authors>Nakai Y</pubmed_authors><pubmed_authors>Ozawa M</pubmed_authors><pubmed_authors>Ikeshiro S</pubmed_authors><pubmed_authors>Yasumoto H</pubmed_authors><pubmed_authors>Iwamoto H</pubmed_authors><pubmed_authors>Yamada S</pubmed_authors><pubmed_authors>Shimazui T</pubmed_authors><pubmed_authors>Shindo T</pubmed_authors><pubmed_authors>Yokomizo A</pubmed_authors><pubmed_authors>Kitamura H</pubmed_authors><pubmed_authors>Komiyama M</pubmed_authors><pubmed_authors>Nakagomi H</pubmed_authors><pubmed_authors>Eto M</pubmed_authors><pubmed_authors>Kohei N</pubmed_authors><pubmed_authors>Yamamoto Y</pubmed_authors><pubmed_authors>Morooka D</pubmed_authors><pubmed_authors>Mochizuki T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Oncological outcomes of a multicenter cohort treated with axitinib for metastatic renal cell carcinoma.</name><description>The present study aimed to evaluate the efficacy of the real-world use of axitinib and to develop a prognostic model for stratifying patients who could derive long-term benefit from axitinib. This was a retrospective, descriptive study evaluating the efficacy of axitinib in patients with metastatic renal cell carcinoma that had been treated with 1 or 2 systemic antiangiogenic therapy regimens at 1 of 36 hospitals belonging to the Japan Urologic Oncology Group between January 2012 and February 2019. The primary outcome was overall survival (OS). Using a split-sample method, candidate variables that exhibited significant relationships with OS were chosen to create a model. The new model was validated using the rest of the cohort. In total, 485 patients were enrolled. The median OS was 34 mon</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-04T07:40:45.788Z</modification><creation>2025-04-04T07:40:45.788Z</creation></dates><accession>S-EPMC7385391</accession><cross_references><pubmed>32402135</pubmed><doi>10.1111/cas.14449</doi></cross_references></HashMap>