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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004175naa a2200505 4500
001oai:DiVA.org:liu-36136
003SwePub
008091010s2006 | |||||||||||000 ||eng|
009oai:DiVA.org:uu-25381
009oai:prod.swepub.kib.ki.se:1932412
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-361362 URI
024a https://doi.org/10.1093/annonc/mdj0602 DOI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-253812 URI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:19324122 URI
040 a (SwePub)liud (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Pfeiffer, P4 aut
2451 0a Short-time infusion of oxaliplatin in combination with capecitabine (XELOX30) as second-line therapy in patients with advanced colorectal cancer after failure to irinotecan and 5-fluorouracil
264 1b Elsevier BV,c 2006
338 a print2 rdacarrier
520 a Background: The efficacy of oxaliplatin combined with capecitabine (XELOX) as second-line therapy in patients with advanced colorectal cancer (ACRC) resistant to irinotecan is not well established. Oxaliplatin induces acute, cold-induced neuropathy in most patients. The incidence is claimed to be infusion rate-dependent and therefore a 2-h infusion is recommended. Patients and methods: For practical and economic reasons, but also for patient's convenience, we performed a phase II study to examine XELOX30 (capecitabine 1000 mg/m2 orally twice daily on days 1-14 and oxaliplatin 130 mg/m2 as a 30 min infusion on day 1) in patients with ACRC resistant to irinotecan. In addition the pharmacokinetics of oxaliplatin was studied. Results: From November 2002 to September 2003, 70 patients with ACRC were treated with XELOX30. Median age was 62 (range 33-74 years) years and median performance status was 1 (range 0-2). The median number of courses was four (range 1-12) and median cumulative dose of oxaliplatin was 530 (range 125-1560) mg/m2. The response rate was 17% (95% CI 10-23), median time to progression (TTP) was 5.4 months (95% CI 4.6-6.4) and median survival 9.5 months (95% CI 8.5-11.2). White blood cell count (WBC) and performance status were significantly correlated to TTP. Neurotoxicity was moderate: grade 1 56%, grade 2 17% and grade 3 6%. Other grade 3 toxicities were nausea/ vomiting 9%, diarrhoea 14% and PPE 8%. The maximum blood concentration and total body clearance of oxaliplatin was higher than previously reported in studies examining 2-h infusions, but the volume of distribution and terminal half-life was in close agreement with previous results. Conclusion: XELOX30 is a very convenient second-line regimen in ACRC with an activity and safety profile similar to other oxaliplatin schedules. © 2005 European Society for Medical Oncology.
653 a MEDICINE
653 a MEDICIN
700a Sörbye, H4 aut
700a Ehrsson, H4 aut
700a Fokstuen, T4 aut
700a Mortensen, JP4 aut
700a Baltesgard, L4 aut
700a Tveit, KM4 aut
700a Ögreid, D4 aut
700a Starkhammar, Hans,d 1948-u Östergötlands Läns Landsting,Linköpings universitet,Hälsouniversitetet,Onkologi,Onkologiska kliniken US4 aut0 (Swepub:liu)hanst87
700a Wallin, I4 aut
700a Qvortrup, C4 aut
700a Glimelius, Bu Karolinska Institutet,Uppsala universitet,Institutionen för onkologi, radiologi och klinisk immunologi4 aut
710a Linköpings universitetb Hälsouniversitetet4 org
773t Annals of Oncologyd : Elsevier BVg 17:2, s. 252-258q 17:2<252-258x 0923-7534x 1569-8041
856u https://doi.org/10.1093/annonc/mdj060
856u http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=16291583&dopt=Citation
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-36136
8564 8u https://doi.org/10.1093/annonc/mdj060
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-25381
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:1932412

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