<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Madaci L</submitter><funding>ADEREM, Marseille, France</funding><pubmed_abstract>After decades during which the treatment of acute myeloblastic leukemia was limited to variations around a skeleton of cytarabine/anthracycline, targeted therapies appeared. These therapies, first based on monoclonal antibodies, also rely on specific inhibitors of various molecular abnormalities. A significant but modest prognosis improvement has been observed thanks to these new treatments that are limited by a high rate of relapse, due to the intrinsic chemo and immune-resistance of leukemia stem cell, together with the acquisition of these resistances by clonal evolution. Relapses are also influenced by the equilibrium between the pro or anti-tumor signals from the bone marrow stromal microenvironment and immune effectors. What should be the place of the targeted therapeutic options in </pubmed_abstract><journal>Biomarker research</journal><pagination>50</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8237443</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The contribution of single-cell analysis of acute leukemia in the therapeutic strategy.</pubmed_title><pmcid>PMC8237443</pmcid><pubmed_authors>Loriod B</pubmed_authors><pubmed_authors>Madaci L</pubmed_authors><pubmed_authors>Costello R</pubmed_authors><pubmed_authors>Colle J</pubmed_authors><pubmed_authors>Venton G</pubmed_authors><pubmed_authors>Farnault L</pubmed_authors></additional><is_claimable>false</is_claimable><name>The contribution of single-cell analysis of acute leukemia in the therapeutic strategy.</name><description>After decades during which the treatment of acute myeloblastic leukemia was limited to variations around a skeleton of cytarabine/anthracycline, targeted therapies appeared. These therapies, first based on monoclonal antibodies, also rely on specific inhibitors of various molecular abnormalities. A significant but modest prognosis improvement has been observed thanks to these new treatments that are limited by a high rate of relapse, due to the intrinsic chemo and immune-resistance of leukemia stem cell, together with the acquisition of these resistances by clonal evolution. Relapses are also influenced by the equilibrium between the pro or anti-tumor signals from the bone marrow stromal microenvironment and immune effectors. What should be the place of the targeted therapeutic options in </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jun</publication><modification>2025-04-04T09:10:42.293Z</modification><creation>2022-02-10T17:44:05.918Z</creation></dates><accession>S-EPMC8237443</accession><cross_references><pubmed>34176517</pubmed><doi>10.1186/s40364-021-00300-0</doi></cross_references></HashMap>