<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>84(2)</volume><submitter>Hack CC</submitter><funding>Novartis Germany GmbH</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Adjuvant treatment of patients with early-stage breast cancer (BC) should include an aromatase inhibitor (AI). Especially patients with a high recurrence risk might benefit from an upfront therapy with an AI for a minimum of five years. Nevertheless, not much is known about the patient selection for this population in clinical practice. Therefore, this study analyzed the prognosis and patient characteristics of postmenopausal patients selected for a five-year upfront letrozole therapy.&lt;h4>Patients and methods&lt;/h4>From 2009 to 2011, 3529 patients were enrolled into the adjuvant phase IV PreFace clinical trial (NCT01908556). Postmenopausal hormone receptor-positive BC patients, for whom an upfront five-year therapy with letrozole (2.5 mg/day) was indicated, were eligible</pubmed_abstract><journal>Geburtshilfe und Frauenheilkunde</journal><pagination>185-195</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10853028</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Long-term Follow-up and Safety of Patients after an Upfront Therapy with Letrozole for Early Breast Cancer in Routine Clinical Care - The PreFace Study.</pubmed_title><pmcid>PMC10853028</pmcid><pubmed_authors>Sutterlin MW</pubmed_authors><pubmed_authors>Marme F</pubmed_authors><pubmed_authors>Bohm S</pubmed_authors><pubmed_authors>Muller V</pubmed_authors><pubmed_authors>Bayer CM</pubmed_authors><pubmed_authors>Thomssen C</pubmed_authors><pubmed_authors>Huebner H</pubmed_authors><pubmed_authors>Fehm TN</pubmed_authors><pubmed_authors>Wolf C</pubmed_authors><pubmed_authors>Uhrig S</pubmed_authors><pubmed_authors>Hofmann NM</pubmed_authors><pubmed_authors>Luck HJ</pubmed_authors><pubmed_authors>Jackisch C</pubmed_authors><pubmed_authors>Theuser AK</pubmed_authors><pubmed_authors>Kellner S</pubmed_authors><pubmed_authors>Brucker SY</pubmed_authors><pubmed_authors>Kolberg HC</pubmed_authors><pubmed_authors>Brucker C</pubmed_authors><pubmed_authors>Almstedt K</pubmed_authors><pubmed_authors>Dall P</pubmed_authors><pubmed_authors>Schneeweiss A</pubmed_authors><pubmed_authors>Hanf V</pubmed_authors><pubmed_authors>Aktas B</pubmed_authors><pubmed_authors>Kummel S</pubmed_authors><pubmed_authors>Wallwiener D</pubmed_authors><pubmed_authors>Uleer C</pubmed_authors><pubmed_authors>Maass N</pubmed_authors><pubmed_authors>Ruebner M</pubmed_authors><pubmed_authors>Rack B</pubmed_authors><pubmed_authors>Rody A</pubmed_authors><pubmed_authors>Fasching PA</pubmed_authors><pubmed_authors>Hack CC</pubmed_authors><pubmed_authors>Kalder M</pubmed_authors><pubmed_authors>Juhasz-Boss I</pubmed_authors><pubmed_authors>Belleville E</pubmed_authors><pubmed_authors>Janni W</pubmed_authors><pubmed_authors>Haberle L</pubmed_authors><pubmed_authors>Gass P</pubmed_authors><pubmed_authors>Schmatloch S</pubmed_authors><pubmed_authors>Rauh C</pubmed_authors><pubmed_authors>Hein A</pubmed_authors><pubmed_authors>Goossens C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long-term Follow-up and Safety of Patients after an Upfront Therapy with Letrozole for Early Breast Cancer in Routine Clinical Care - The PreFace Study.</name><description>&lt;h4>Introduction&lt;/h4>Adjuvant treatment of patients with early-stage breast cancer (BC) should include an aromatase inhibitor (AI). Especially patients with a high recurrence risk might benefit from an upfront therapy with an AI for a minimum of five years. Nevertheless, not much is known about the patient selection for this population in clinical practice. Therefore, this study analyzed the prognosis and patient characteristics of postmenopausal patients selected for a five-year upfront letrozole therapy.&lt;h4>Patients and methods&lt;/h4>From 2009 to 2011, 3529 patients were enrolled into the adjuvant phase IV PreFace clinical trial (NCT01908556). Postmenopausal hormone receptor-positive BC patients, for whom an upfront five-year therapy with letrozole (2.5 mg/day) was indicated, were eligible</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2026-06-02T19:21:30.131Z</modification><creation>2024-11-06T02:20:11.904Z</creation></dates><accession>S-EPMC10853028</accession><cross_references><pubmed>38344045</pubmed><doi>10.1055/a-2238-3153</doi></cross_references></HashMap>