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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00006348naa a2200685 4500
001oai:DiVA.org:umu-97219
003SwePub
008141212s2014 | |||||||||||000 ||eng|
009oai:lup.lub.lu.se:f69f4c56-faa0-4731-bfae-d084e78b6a5d
009oai:DiVA.org:uu-239383
009oai:DiVA.org:liu-112815
009oai:prod.swepub.kib.ki.se:130075034
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-972192 URI
024a https://doi.org/10.1093/annonc/mdu3752 DOI
024a https://lup.lub.lu.se/record/46149262 URI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-2393832 URI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-1128152 URI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1300750342 URI
040 a (SwePub)umud (SwePub)lud (SwePub)uud (SwePub)liud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Tandstad, T.u St Olavs University Hospital, Norway4 aut
2451 0a One course of adjuvant BEP in clinical stage I nonseminoma mature and expanded results from the SWENOTECA group
264 1b Elsevier BV,c 2014
338 a print2 rdacarrier
500 a Funding Agencies|National Cancer Fund of Sweden
520 a The SWENOTECA group treated 517 clinical stage I nonseminoma patients with one course of adjuvant BEP in a prospective study. The median follow-up is 7.9 years. One course of adjuvant BEP reduced the risk of relapse by over 90%. The relapse rates were 1.6% in low-risk disease and 3.2% in high-risk disease. One course of adjuvant BEP should be considered a standard adjuvant treatment option.SWENOTECA has since 1998 offered patients with clinical stage I (CS I) nonseminoma, adjuvant chemotherapy with one course of bleomycin, etoposide and cisplatin (BEP). The aim has been to reduce the risk of relapse, sparing patients the need of toxic salvage treatment. Initial results on 312 patients treated with one course of adjuvant BEP, with a median follow-up of 4.5 years, have been previously published. We now report mature and expanded results. In a prospective, binational, population-based risk-adapted treatment protocol, 517 Norwegian and Swedish patients with CS I nonseminoma received one course of adjuvant BEP. Patients with lymphovascular invasion (LVI) in the primary testicular tumor were recommended one course of adjuvant BEP. Patients without LVI could choose between surveillance and one course of adjuvant BEP. Data for patients receiving one course of BEP are presented in this study. At a median follow-up of 7.9 years, 12 relapses have occurred, all with IGCCC good prognosis. The latest relapse occurred 3.3 years after adjuvant treatment. The relapse rate at 5 years was 3.2% for patients with LVI and 1.6% for patients without LVI. Five-year cause-specific survival was 100%. The updated and expanded results confirm a low relapse rate following one course of adjuvant BEP in CS I nonseminoma. One course of adjuvant BEP should be considered a standard treatment in CS I nonseminoma with LVI. For patients with CS I nonseminoma without LVI, one course of adjuvant BEP is also a treatment option.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Cancer och onkologi0 (SwePub)302032 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cancer and Oncology0 (SwePub)302032 hsv//eng
653 a testicular cancer
653 a adjuvant chemotherapy
653 a nonseminoma
700a Ståhl, Olofu Lund University,Lunds universitet,Reproduktionsmedicin, Malmö,Forskargrupper vid Lunds universitet,Reproductive medicine, Malmö,Lund University Research Groups,Skåne University Hospital, Sweden4 aut0 (Swepub:lu)kir-ost
700a Håkansson, Ulfu Lund University,Lunds universitet,Institutionen för kliniska vetenskaper, Malmö,Medicinska fakulteten,Department of Clinical Sciences, Malmö,Faculty of Medicine,Skåne University Hospital, Sweden4 aut0 (Swepub:lu)kir-uha
700a Dahl, O.u University of Bergen, Norway; Haukeland Hospital, Norway4 aut
700a Haugnes, H. S.u University of Tromso, Norway; University Hospital North Norway, Norway4 aut
700a Klepp, O. H.u Alesund Hospital, Norway4 aut
700a Langberg, C. W.u Oslo University Hospital, Norway4 aut
700a Laurell, Annau Uppsala universitet,Enheten för onkologi,University of Uppsala Hospital, Sweden4 aut0 (Swepub:uu)annajohn
700a Oldenburg, J.u Oslo University Hospital, Norway4 aut
700a Solberg, A.u St Olavs University Hospital, Norway4 aut
700a Söderström, Karinu The Cancer Clinic, Norrland University Hospital, Umeå,Norrland University Hospital, Sweden4 aut0 (Swepub:umu)kansom97
700a Cavallin-Ståhl, Evau Lund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,Skåne University Hospital, Sweden4 aut0 (Swepub:lu)onk-ecs
700a Stierner, U.u Sahlgrens University Hospital, Sweden4 aut
700a Wahlquist, R.u Oslo University Hospital, Norway4 aut
700a Wall, Najmeu Östergötlands Läns Landsting,Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet,Onkologiska kliniken US4 aut0 (Swepub:liu)najwa86
700a Cohn-Cedermark, G.u Karolinska Institutet4 aut
710a St Olavs University Hospital, Norwayb Reproduktionsmedicin, Malmö4 org
773t Annals of Oncologyd : Elsevier BVg 25:11, s. 2167-2172q 25:11<2167-2172x 0923-7534x 1569-8041
856u https://doi.org/10.1093/annonc/mdu375
856u http://www.ncbi.nlm.nih.gov/pubmed/25114021?dopt=Abstracty FULLTEXT
856u http://dx.doi.org/10.1093/annonc/mdu375y FULLTEXT
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-97219
8564 8u https://doi.org/10.1093/annonc/mdu375
8564 8u https://lup.lub.lu.se/record/4614926
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-239383
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-112815
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:130075034

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