<?xml version="1.0"?><rdf:RDF xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:edm="http://www.europeana.eu/schemas/edm/" xmlns:wgs84_pos="http://www.w3.org/2003/01/geo/wgs84_pos" xmlns:foaf="http://xmlns.com/foaf/0.1/" xmlns:rdaGr2="http://rdvocab.info/ElementsGr2" xmlns:oai="http://www.openarchives.org/OAI/2.0/" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:ore="http://www.openarchives.org/ore/terms/" xmlns:skos="http://www.w3.org/2004/02/skos/core#" xmlns:dcterms="http://purl.org/dc/terms/"><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-6HA9OQOJ/701fb1a7-9d8b-4945-81dd-4e4d5d47afe6/HTML"><dcterms:extent>55 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-6HA9OQOJ/cac3792a-3210-4514-9beb-892bb06e9e2f/PDF"><dcterms:extent>121 KB</dcterms:extent></edm:WebResource><edm:WebResource rdf:about="http://www.dlib.si/stream/URN:NBN:SI:DOC-6HA9OQOJ/737c9572-222c-4539-adbb-2534c890ac86/TEXT"><dcterms:extent>29 KB</dcterms:extent></edm:WebResource><edm:TimeSpan rdf:about="1929-2026"><edm:begin xml:lang="en">1929</edm:begin><edm:end xml:lang="en">2026</edm:end></edm:TimeSpan><edm:ProvidedCHO rdf:about="URN:NBN:SI:DOC-6HA9OQOJ"><dcterms:isPartOf rdf:resource="https://www.dlib.si/details/urn:nbn:si:spr-a30mfzkp" /><dcterms:issued>2008</dcterms:issued><dc:creator>Černelč, Peter</dc:creator><dc:creator>Kodre, Veronika</dc:creator><dc:format xml:lang="sl">številka:1</dc:format><dc:format xml:lang="sl">6 strani</dc:format><dc:format xml:lang="sl">letnik:77</dc:format><dc:format xml:lang="sl">str. I-87-I-92</dc:format><dc:identifier>ISSN:1318-0347</dc:identifier><dc:identifier>COBISSID:24129753</dc:identifier><dc:identifier>URN:URN:NBN:SI:doc-6HA9OQOJ</dc:identifier><dc:language>sl</dc:language><dc:publisher xml:lang="sl">Slovensko zdravniško društvo</dc:publisher><dcterms:isPartOf xml:lang="sl">Zdravniški vestnik</dcterms:isPartOf><dc:subject xml:lang="en">Bence Jones Protein</dc:subject><dc:subject xml:lang="sl">Bence Jonesova beljakovina</dc:subject><dc:subject xml:lang="en">Beta 2-Microglobulin</dc:subject><dc:subject xml:lang="sl">Beta 2-mikroglobulini</dc:subject><dc:subject xml:lang="en">Drug Therapy</dc:subject><dc:subject xml:lang="sl">hematologija</dc:subject><dc:subject xml:lang="en">Immunoglobulins</dc:subject><dc:subject xml:lang="sl">Imunoglobulini</dc:subject><dc:subject xml:lang="en">Multiple Myeloma</dc:subject><dc:subject xml:lang="sl">Multipli mielom</dc:subject><dc:subject xml:lang="sl">plazmocitom</dc:subject><dc:subject xml:lang="en">therapy</dc:subject><dc:subject xml:lang="en">Treatment Outcome</dc:subject><dc:subject xml:lang="sl">zdravljenje</dc:subject><dc:subject xml:lang="sl">Zdravljenje, izid</dc:subject><dcterms:temporal rdf:resource="1929-2026" /><dc:title xml:lang="sl">Zdravljenje diseminiranega plazmocitoma z zdravilom bortezomib| Treatment of multiple myeloma with bortezomib|</dc:title><dc:description xml:lang="sl">Background In this retrospective study we evaluated effectiveness and safety of bortezomib, comparing our results with already published clinical studies. Methods Patients received bortezomib as part of everyday clinical practice andin the range of approved indications. We evaluated bortezomib effectivenessin 66 patients according to modified SWOG criteria and treatment responsiveness (CR, VGPR, PR, MR) or unresponsiveness (SD, PD). Treatment responsiveness was compared according to high risk (beta-2 microglobulin &gt;= 5,5 mg/L) or standard risk (beta-2 mikroglobulin &lt; 5.5 mg/L), patient's age (&gt;65 ali &lt; 65 let), number of previous treatments (1 ali &gt; 1) and previous treatment with thalidomid. Side effects and reasons for early treatment discontinuation were also evaluated. Results Patients received 1-7 previous treatments (median 1.5). Treatment responsiveness was observed in 80.3% patients (1.5% CR, 45.5 % VGPR, 21.2% PR and 12.1% MR). No statistical significant influence was observed according to: high risk (p = 0.178), age above 65 years (p = 0.756), &gt; 1 previous treatment (p = 0.419) or previous treatment with thalidomid (p = 0.475). Side effects of bortezomib treatment were: anemia (40.9%), peripheral neuropathy grade 3 or more (28.7%), infections (21.2%), herpes zooster (12.1%), neutropenia (10.6%), trombocitopenia (9%) and gastro-intestinal problems (7.5%). Early discontinuation was observed due to: peripheral neuropathy (28.7%), other serious side effects (6%), bortezomib uneffectiveness (19.7%) or planned autologous transplant (15.1%). Conclusions Bortezomib (Velcade) is effective and safe treatment also for patients with multiple myeloma that developed resistance to previous treatments or belong to high risk patient group</dc:description><edm:type>TEXT</edm:type><dc:type xml:lang="sl">znanstveno časopisje</dc:type><dc:type xml:lang="en">journals</dc:type><dc:type rdf:resource="http://www.wikidata.org/entity/Q361785" /></edm:ProvidedCHO><ore:Aggregation rdf:about="http://www.dlib.si/?URN=URN:NBN:SI:DOC-6HA9OQOJ"><edm:aggregatedCHO rdf:resource="URN:NBN:SI:DOC-6HA9OQOJ" /><edm:isShownBy rdf:resource="http://www.dlib.si/stream/URN:NBN:SI:DOC-6HA9OQOJ/cac3792a-3210-4514-9beb-892bb06e9e2f/PDF" /><edm:rights rdf:resource="http://creativecommons.org/licenses/by-nc/4.0/" /><edm:provider>Slovenian National E-content Aggregator</edm:provider><edm:intermediateProvider xml:lang="en">National and University Library of Slovenia</edm:intermediateProvider><edm:dataProvider xml:lang="sl">Slovensko zdravniško društvo</edm:dataProvider><edm:object rdf:resource="http://www.dlib.si/streamdb/URN:NBN:SI:DOC-6HA9OQOJ/maxi/edm" /><edm:isShownAt rdf:resource="http://www.dlib.si/details/URN:NBN:SI:DOC-6HA9OQOJ" /></ore:Aggregation></rdf:RDF>