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dc.contributor.authorTangen, Jon-Magnus
dc.contributor.authorTjønnfjord, Geir Erland
dc.contributor.authorGulbrandsen, Nina
dc.contributor.authorGedde-Dahl, Thobias
dc.contributor.authorStormorken, Espen
dc.contributor.authorAnderson, Kristina
dc.contributor.authorVo, Camilla Dao
dc.contributor.authorSchjesvold, Fredrik Hellem
dc.contributor.authorMyeloma Center, Oslo
dc.date.accessioned2020-08-28T09:15:22Z
dc.date.available2020-08-28T09:15:22Z
dc.date.created2018-11-20T12:24:58Z
dc.date.issued2018
dc.identifier.citationBMC Cancer. 2018, 18:801 1-9.en_US
dc.identifier.issn1471-2407
dc.identifier.urihttps://hdl.handle.net/11250/2675496
dc.description.abstractBackground: With the advent of novel drugs improved overall survival in patients with multiple myeloma, including patients who received up-front autologous stem cell transplantation (ASCT), has been reported from several centers. Here we report on overall survival in a population-based cohort of patients receiving ASCT as first line treatment and in whom novel agents were an option for second and later lines of treatment. Methods: Patients with multiple myeloma ≤ 65 years of age who were considered for ASCT from 01.01.2001-31.06.2005 (period 1) and from 01.07.2005 until 31.12.2009 (period 2) at Oslo University Hospital (OUH) were identified. Relevant data were collected from the patients' medical records. Results: Altogether, 293/355 patients received ASCT. In all, median OS was 82.9 months in patients ≤ 60 years of age and 59.0 months in patients 61-65 years. For patients ≤ 60 years of age median OS increased from 70.6 months to 87.7 months (p = 0. 22) and median survival after start of second line therapy increased from 34.5 months to 46.5 months (p = 0.015) between the two periods. For patients 61-65 years of age median OS increased from 57.3 months to 61.2 months (p = 0. 87) and median survival after start of second line therapy was practically unchanged (32.6 months vs. 33.1 months (p = 0.97) between the periods. In patients ≤ 60 years of age salvage ASCT was used in 34% of the patients while in patients 61-65 years of age salvage ASCT was used in 7.3% of the patients. The use of salvage ASCT and novel drugs, as well as the number of treatment lines, were higher in patients ≤ 60 years of age and increased during the study period. Conclusion: In patients ≤ 60 years of age an increased median OS of 17 months between the two periods were noted, but the difference failed to reach statistical significance. However, a statistically significant difference in median survival of 12 months after start of second line therapy was found in this age group, which may be explained by a more active second line treatment. In patients 61-65 years only a slight increase of survival, not statistically significant, was noted between the periods.en_US
dc.language.isoengen_US
dc.relation.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083560/pdf/12885_2018_Article_4722.pdf
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectAutologous stem cell transplantation;en_US
dc.subjectMultiple myeloma;en_US
dc.subjectNovel drugs;en_US
dc.subjectOverall survival;en_US
dc.titleImproved outcome in patients following autologous stem cell transplantation for multiple myeloma in south eastern Norway 2001-2010: A retrospective, population based analysisen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_US
dc.source.pagenumber1-9en_US
dc.source.volume18:801en_US
dc.source.journalBMC Canceren_US
dc.source.issue1en_US
dc.identifier.doi10.1186/s12885-018-4722-x
dc.identifier.cristin1632592
cristin.unitcode1991,3,0,0
cristin.unitnameDiv Gjøvik
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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