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dc.contributor.authorEto, Masatoshien
dc.contributor.authorKawano, Yoshiakien
dc.contributor.authorHirao, Yoshihikoen
dc.contributor.authorMita, Kojien
dc.contributor.authorArai, Yoichien
dc.contributor.authorTsukamoto, Taijien
dc.contributor.authorHashine, Katsuyoshien
dc.contributor.authorMatsubara, Akioen
dc.contributor.authorFujioka, Tomoakien
dc.contributor.authorKimura, Goen
dc.contributor.authorShinohara, Nobuoen
dc.contributor.authorTatsugami, Katsunorien
dc.contributor.authorHinotsu, Shiroen
dc.contributor.authorNaito, Seijien
dc.contributor.alternative樋之津, 史郎ja
dc.date.accessioned2016-05-25T01:59:33Z-
dc.date.available2016-05-25T01:59:33Z-
dc.date.issued2015-10-09-
dc.identifier.issn1471-2407-
dc.identifier.urihttp://hdl.handle.net/2433/212504-
dc.description.abstractBackground: To improve antitumor effects against metastatic renal cell carcinoma (mRCC), use of molecular target-based drugs in sequential or combination therapy has been advocated. In combination therapy, interferon (IFN)-aα amplified the effect of sorafenib in our murine model (J Urol 184:2549, 2010), and cytokine-treated mRCC patients in Japan had good prognoses (Eur Urol 57:317, 2010). We thus conducted a phase II clinical trial of sorafenib plus IFN-aα for untreated mRCC patients in Japan. Methods: In this multicenter, prospective study, provisionally registered patients with histologically confirmed metastatic clear cell RCC received natural IFN-aα (3 dosages of 3 million U per week) for 2 weeks. Only IFN-aα-tolerant patients were registered to this trial, and treated additionally with oral sorafenib (400 mg, bid). The primary end point of the study was rate of response (CR + PR) to sorafenib plus IFN-aα treatment assessed using RECIST v1.0. The secondary end points were disease control rate (CR + PR + SD), progression free survival (PFS), overall survival (OS), and safety of the combined treatment. PFS and OS curves were plotted using the Kaplan-Meier method. Results: From July 2009 to July 2012, a total of 53 untreated patients were provisionally registered, and 51 patients were finally registered. Rate of Response to the combined therapy of sorafenib plus IFN-aα was 26.2 % (11/42) (CR 1, PR 10). The median PFS was 10.1 months (95 % CI, 6.4 to 18.5 months), and the median OS has not been reached yet. The combined therapy increased neither the incidence of adverse effects (AE) nor the incidence of unexpected AE. A limitation was that a relatively high number of patients (9 patients) were excluded for eligibility criteria violations. Conclusion: Our data have demonstrated that sorafenib plus IFN-aα treatment is safe and effective for untreated mRCC patients. Trial registration:UMIN000002466 , 9th September, 2009en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherBioMed Central Ltd.en
dc.rights© 2015 Eto et al. 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.en
dc.subjectSorafeniben
dc.subjectInterferon-alphaen
dc.subjectRenal cell carcinomaen
dc.titlePhase II clinical trial of sorafenib plus interferon-alpha treatment for patients with metastatic renal cell carcinoma in Japanen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleBMC Canceren
dc.identifier.volume15-
dc.relation.doi10.1186/s12885-015-1675-1-
dc.textversionpublisher-
dc.identifier.artnum667-
dc.identifier.pmid26452347-
dcterms.accessRightsopen access-
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