<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Puliani G</submitter><funding>Ministero della Salute</funding><pagination>e240386</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12023733</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(2)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Little is known about sex differences in lenvatinib treatment safety and efficacy.&lt;h4>Methods&lt;/h4>Real-word retrospective Italian multicenter study enrolling patients with radioiodine-refractory differentiated thyroid cancer treated with lenvatinib.&lt;h4>Results&lt;/h4>A total of 138 patients (64 females) were included, with a median follow-up of 26 months (2-72). More men performed physical activities (34% vs 17%, P = 0.024). The frequency of smoking and alcohol consumption was higher in men (58% vs 33%, P = 0.003; 45% vs 17%, P = 0.001). We did not find sex differences in lenvatinib dose reduction due to adverse events (AEs) (78% females vs 85% males). Ninety-nine percent of patients developed at least one adverse event (AE), with no sex difference in their number and the time to first AE. Severe AEs occurred in 74% of males and 66% of females (P = 0.398), with a mean dose of 18.2 mg (±5.7), and a median time to the first serious AE of 9 weeks (1-154). Stomatitis/mucositis and hematological disorders were more frequent in females (48% vs 30%, P = 0.016; 17% vs 4%, P = 0.011). Gastrointestinal disorders were higher in males (15% vs 2%, P = 0.010). Eighty-seven patients interrupted lenvatinib due to AEs (median time: 3 months (0-48), mean dose: 17 mg ±5.5). Discontinuation occurred in 21 patients, five for severe AEs. No sex differences were found in progression-free survival, overall survival or disease control rate. Liver metastases were associated with disease progression (HR: 3.73, 95% CI: 1.06-13.12, P = 0.040) or death (HR: 4.82, 95% CI: 1.75-13.25, P = 0.002) only in females.&lt;h4>Conclusion&lt;/h4>Lenvatinib is effective in both sexes and exhibits a good safety profile, with a sex difference in the frequencies of some adverse events.</pubmed_abstract><journal>European thyroid journal</journal><pubmed_title>Gender impact on safety and efficacy in lenvatinib treated patients with radioiodine-refractory differentiated thyroid cancer (GISEL study).</pubmed_title><pmcid>PMC12023733</pmcid><funding_grant_id>Ricerca Corrente</funding_grant_id><pubmed_authors>Valerio L</pubmed_authors><pubmed_authors>Sapuppo G</pubmed_authors><pubmed_authors>Puliani G</pubmed_authors><pubmed_authors>Durante C</pubmed_authors><pubmed_authors>Elisei R</pubmed_authors><pubmed_authors>Nervo A</pubmed_authors><pubmed_authors>Zovato S</pubmed_authors><pubmed_authors>Giani C</pubmed_authors><pubmed_authors>Fugazzola L</pubmed_authors><pubmed_authors>Castagna MG</pubmed_authors><pubmed_authors>Terrenato I</pubmed_authors><pubmed_authors>Mormando M</pubmed_authors><pubmed_authors>De Leo S</pubmed_authors><pubmed_authors>Grani G</pubmed_authors><pubmed_authors>Arvat E</pubmed_authors><pubmed_authors>Bianchini M</pubmed_authors><pubmed_authors>Appetecchia M</pubmed_authors><pubmed_authors>Lauretta R</pubmed_authors><pubmed_authors>Pellegriti G</pubmed_authors><pubmed_authors>Dalmiglio C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gender impact on safety and efficacy in lenvatinib treated patients with radioiodine-refractory differentiated thyroid cancer (GISEL study).</name><description>&lt;h4>Introduction&lt;/h4>Little is known about sex differences in lenvatinib treatment safety and efficacy.&lt;h4>Methods&lt;/h4>Real-word retrospective Italian multicenter study enrolling patients with radioiodine-refractory differentiated thyroid cancer treated with lenvatinib.&lt;h4>Results&lt;/h4>A total of 138 patients (64 females) were included, with a median follow-up of 26 months (2-72). More men performed physical activities (34% vs 17%, P = 0.024). The frequency of smoking and alcohol consumption was higher in men (58% vs 33%, P = 0.003; 45% vs 17%, P = 0.001). We did not find sex differences in lenvatinib dose reduction due to adverse events (AEs) (78% females vs 85% males). Ninety-nine percent of patients developed at least one adverse event (AE), with no sex difference in their number and the time to first AE. Severe AEs occurred in 74% of males and 66% of females (P = 0.398), with a mean dose of 18.2 mg (±5.7), and a median time to the first serious AE of 9 weeks (1-154). Stomatitis/mucositis and hematological disorders were more frequent in females (48% vs 30%, P = 0.016; 17% vs 4%, P = 0.011). Gastrointestinal disorders were higher in males (15% vs 2%, P = 0.010). Eighty-seven patients interrupted lenvatinib due to AEs (median time: 3 months (0-48), mean dose: 17 mg ±5.5). Discontinuation occurred in 21 patients, five for severe AEs. No sex differences were found in progression-free survival, overall survival or disease control rate. Liver metastases were associated with disease progression (HR: 3.73, 95% CI: 1.06-13.12, P = 0.040) or death (HR: 4.82, 95% CI: 1.75-13.25, P = 0.002) only in females.&lt;h4>Conclusion&lt;/h4>Lenvatinib is effective in both sexes and exhibits a good safety profile, with a sex difference in the frequencies of some adverse events.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-06-01T13:02:22.517Z</modification><creation>2025-07-01T03:05:43.601Z</creation></dates><accession>S-EPMC12023733</accession><cross_references><pubmed>40198664</pubmed><doi>10.1530/ETJ-24-0386</doi></cross_references></HashMap>