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dc.contributor.author | Rudick, RA | |
dc.contributor.author | Stuart, WH | |
dc.contributor.author | Calabresi, PA | |
dc.contributor.author | Confavreux, C | |
dc.contributor.author | Galetta, SL | |
dc.contributor.author | Radue, EW | |
dc.contributor.author | Lublin, FD | |
dc.contributor.author | Weinstock-Guttman, B | |
dc.contributor.author | Wynn, DR | |
dc.contributor.author | Lynn, F | |
dc.contributor.author | ERAKSOY, Mefküre | |
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dc.contributor.author | Sarove-Pinhas, I | |
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dc.contributor.author | Millefiorini, E | |
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dc.contributor.author | Perini, P | |
dc.contributor.author | Laroni, A | |
dc.contributor.author | Marrosu, M | |
dc.contributor.author | Marchi, ECP | |
dc.contributor.author | Spinicci, G | |
dc.contributor.author | Massole, S | |
dc.contributor.author | Mascia, M | |
dc.contributor.author | Floris, G | |
dc.contributor.author | Trojano, M | |
dc.contributor.author | Bellacosa, A | |
dc.contributor.author | Paolicelli, D | |
dc.contributor.author | Zimatore, GB | |
dc.contributor.author | Simone, IL | |
dc.contributor.author | Giorelli, M | |
dc.contributor.author | Di Monte, E | |
dc.contributor.author | Mancardi, G | |
dc.contributor.author | Pizzorno, M | |
dc.contributor.author | Murialdo, A | |
dc.contributor.author | Narciso, E | |
dc.contributor.author | Capello, A | |
dc.contributor.author | Comi, G | |
dc.contributor.author | Martinelli, V | |
dc.contributor.author | Rodegher, M | |
dc.contributor.author | Esposito, F | |
dc.contributor.author | Colombo, B | |
dc.contributor.author | Rossi, P | |
dc.contributor.author | Polman, CH | |
dc.contributor.author | Jasperse, MMS | |
dc.contributor.author | Zwemmer, JNP | |
dc.contributor.author | Nielsen, J | |
dc.contributor.author | Kragt, JJ | |
dc.contributor.author | Jongen, PJH | |
dc.contributor.author | De Smet, E | |
dc.contributor.author | Tacken, H | |
dc.contributor.author | Frequin, STFM | |
dc.contributor.author | Siegers, HP | |
dc.contributor.author | Mauser, HW | |
dc.contributor.author | Fernandez-Fernandez, O | |
dc.contributor.author | Leon, A | |
dc.date.accessioned | 2021-03-04T11:31:38Z | |
dc.date.available | 2021-03-04T11:31:38Z | |
dc.date.issued | 2006 | |
dc.identifier.citation | Rudick R., Stuart W., Calabresi P., Confavreux C., Galetta S., Radue E., Lublin F., Weinstock-Guttman B., Wynn D., Lynn F., et al., "Natalizumab plus interferon beta-1a for relapsing multiple sclerosis", NEW ENGLAND JOURNAL OF MEDICINE, cilt.354, sa.9, ss.911-923, 2006 | |
dc.identifier.issn | 0028-4793 | |
dc.identifier.other | av_72be90f9-5a54-4e58-916b-991bcb56b39a | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/78977 | |
dc.identifier.uri | https://avesis.istanbul.edu.tr/api/publication/72be90f9-5a54-4e58-916b-991bcb56b39a/file | |
dc.identifier.uri | https://doi.org/10.1056/nejmoa044396 | |
dc.description.abstract | .AbstractBackgroundInterferon beta is used to modify the course of relapsing multiple sclerosis. Despiteinterferon beta therapy, many patients have relapses. Natalizumab, an α4 integrinantagonist, appeared to be safe and effective alone and when added to interferonbeta-1a in preliminary studies.MethodsWe randomly assigned 1171 patients who, despite interferon beta-1a therapy, hadhad at least one relapse during the 12-month period before randomization to receivecontinued interferon beta-1a in combination with 300 mg of natalizumab (589patients) or placebo (582 patients) intravenously every 4 weeks for up to 116 weeks.The primary end points were the rate of clinical relapse at 1 year and the cumulativeprobability of disability progression sustained for 12 weeks, as measured by theExpanded Disability Status Scale, at 2 years.ResultsCombination therapy resulted in a 24 percent reduction in the relative risk of sustaineddisability progression (hazard ratio, 0.76; 95 percent confidence interval, 0.61to 0.96; P = 0.02). Kaplan–Meier estimates of the cumulative probability of progressionat two years were 23 percent with combination therapy and 29 percent withinterferon beta-1a alone. Combination therapy was associated with a lower annualizedrate of relapse over a two-year period than was interferon beta-1a alone (0.34vs. 0.75, P<0.001) and with fewer new or enlarging lesions on T2-weighted magneticresonance imaging (0.9 vs. 5.4, P<0.001). Adverse events associated with combinationtherapy were anxiety, pharyngitis, sinus congestion, and peripheral edema.Two cases of progressive multifocal leukoencephalopathy, one of which was fatal,were diagnosed in natalizumab-treated patients.ConclusionsNatalizumab added to interferon beta-1a was significantly more effective than interferonbeta-1a alone in patients with relapsing multiple sclerosis. Additional researchis needed to elucidate the benefits and risks of this combination treatment.(ClinicalTrials.gov number, NCT00030966.) | |
dc.language.iso | eng | |
dc.subject | Klinik Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Temel Tıp Bilimleri | |
dc.subject | Family Practice | |
dc.subject | Fundamentals and Skills | |
dc.subject | General Health Professions | |
dc.subject | Pathophysiology | |
dc.subject | Internal Medicine | |
dc.subject | Assessment and Diagnosis | |
dc.subject | Medicine (miscellaneous) | |
dc.subject | General Medicine | |
dc.subject | Health Sciences | |
dc.subject | TIP, GENEL & İÇECEK | |
dc.title | Natalizumab plus interferon beta-1a for relapsing multiple sclerosis | |
dc.type | Makale | |
dc.relation.journal | NEW ENGLAND JOURNAL OF MEDICINE | |
dc.contributor.department | , , | |
dc.identifier.volume | 354 | |
dc.identifier.issue | 9 | |
dc.identifier.startpage | 911 | |
dc.identifier.endpage | 923 | |
dc.contributor.firstauthorID | 2522240 | |