<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>36(10)</volume><submitter>Kubasch AS</submitter><funding>Amgen</funding><pubmed_abstract>The EUROPE phase 2 trial investigated the predictive value of biomarkers on the clinical efficacy of single agent romiplostim (ROM) treatment in patients with lower-risk myelodysplastic neoplasms (LR-MDS) and thrombocytopenia within the 'European Myelodysplastic Neoplasms Cooperative Group' (EMSCO) network. A total of 77 patients with LR-MDS and a median platelet count of 25/nl were included, all patients received ROM at a starting dose of 750 μg by SC injection weekly. Thirty-two patients (42%) achieved a hematologic improvement of platelets (HI-P) with a median duration of 340 days. Neutrophil (HI-N) and erythroid (HI-E) responses were observed in three (4%) and seven (9%) patients, respectively. We could not confirm previous reports that HI-P correlated with baseline endogenous thrombop</pubmed_abstract><journal>Leukemia</journal><pagination>2519-2527</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9522582</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prospective validation of a biomarker-driven response prediction model to romiplostim in lower-risk myelodysplastic neoplasms - results of the EUROPE trial by EMSCO.</pubmed_title><pmcid>PMC9522582</pmcid><pubmed_authors>Thiede C</pubmed_authors><pubmed_authors>Huetter-Kroenke ML</pubmed_authors><pubmed_authors>Slama B</pubmed_authors><pubmed_authors>Ades L</pubmed_authors><pubmed_authors>Giagounidis A</pubmed_authors><pubmed_authors>Gotze KS</pubmed_authors><pubmed_authors>Fenaux P</pubmed_authors><pubmed_authors>De Renzis B</pubmed_authors><pubmed_authors>Cony-Makhoul P</pubmed_authors><pubmed_authors>Metzeler KH</pubmed_authors><pubmed_authors>Mies A</pubmed_authors><pubmed_authors>Sapena R</pubmed_authors><pubmed_authors>Kubasch AS</pubmed_authors><pubmed_authors>Schlenk RF</pubmed_authors><pubmed_authors>Jersemann K</pubmed_authors><pubmed_authors>Gloaguen S</pubmed_authors><pubmed_authors>Gourin MP</pubmed_authors><pubmed_authors>Metzgeroth G</pubmed_authors><pubmed_authors>Platzbecker U</pubmed_authors><pubmed_authors>Diaz JMT</pubmed_authors><pubmed_authors>Dimicoli-Salazar S</pubmed_authors><pubmed_authors>Schipp D</pubmed_authors><pubmed_authors>Herbst R</pubmed_authors><pubmed_authors>Laribi K</pubmed_authors><pubmed_authors>Park S</pubmed_authors><pubmed_authors>Sockel K</pubmed_authors><pubmed_authors>Jonasova A</pubmed_authors><pubmed_authors>Tiebel O</pubmed_authors><pubmed_authors>Chermat F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prospective validation of a biomarker-driven response prediction model to romiplostim in lower-risk myelodysplastic neoplasms - results of the EUROPE trial by EMSCO.</name><description>The EUROPE phase 2 trial investigated the predictive value of biomarkers on the clinical efficacy of single agent romiplostim (ROM) treatment in patients with lower-risk myelodysplastic neoplasms (LR-MDS) and thrombocytopenia within the 'European Myelodysplastic Neoplasms Cooperative Group' (EMSCO) network. A total of 77 patients with LR-MDS and a median platelet count of 25/nl were included, all patients received ROM at a starting dose of 750 μg by SC injection weekly. Thirty-two patients (42%) achieved a hematologic improvement of platelets (HI-P) with a median duration of 340 days. Neutrophil (HI-N) and erythroid (HI-E) responses were observed in three (4%) and seven (9%) patients, respectively. We could not confirm previous reports that HI-P correlated with baseline endogenous thrombop</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-05-31T15:57:12.162Z</modification><creation>2024-12-04T01:58:26.498Z</creation></dates><accession>S-EPMC9522582</accession><cross_references><pubmed>36071100</pubmed><doi>10.1038/s41375-022-01669-z</doi></cross_references></HashMap>