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001-es BibID:	BIBFORM083110
Első szerző:	Sands, Bruce E.
Cím:	Ustekinumab as Induction and Maintenance Therapy for Ulcerative Colitis / Sands Bruce E., Sandborn William J., Panaccione Remo, O'Brien Christopher D., Zhang Hongyan, Johanns Jewel, Adedokun Omoniyi J., Li Katherine, Peyrin-Biroulet Laurent, Van Assche Gert, Danese Silvio, Targan Stephan, Abreu Maria T., Hisamatsu Tadakazu, Szapary Philippe, Marano Colleen, UNIFI Study Group
Dátum:	2019
ISSN:	0028-4793
Megjegyzések:	BACKGROUND The efficacy of ustekinumab, an antagonist of the p40 subunit of interleukin-12 and interleukin-23, as induction and maintenance therapy in patients with ulcerative colitis is unknown. METHODS We evaluated ustekinumab as 8-week induction therapy and 44-week maintenance therapy in patients with moderate-to-severe ulcerative colitis. A total of 961 patients were randomly assigned to receive an intravenous induction dose of ustekinumab (either 130 mg [320 patients] or a weight-range?based dose that approximated 6 mg per kilogram of body weight [322]) or placebo (319). Patients who had a response to induction therapy 8 weeks after administration of intravenous ustekinumab were randomly assigned again to receive subcutaneous maintenance injections of 90 mg of ustekinumab (either every 12 weeks [172 patients] or every 8 weeks [176]) or placebo (175). The primary end point in the induction trial (week 8) and the maintenance trial (week 44) was clinical remission (defined as a total score of ?2 on the Mayo scale [range, 0 to 12, with higher scores indicating more severe disease] and no subscore >1 [range, 0 to 3] on any of the four Mayo scale components). RESULTS The percentage of patients who had clinical remission at week 8 among patients who received intravenous ustekinumab at a dose of 130 mg (15.6%) or 6 mg per kilogram (15.5%) was significantly higher than that among patients who received placebo (5.3%) (P<0.001 for both comparisons). Among patients who had a response to induction therapy with ustekinumab and underwent a second randomization, the percentage of patients who had clinical remission at week 44 was significantly higher among patients assigned to 90 mg of subcutaneous ustekinumab every 12 weeks (38.4%) or every 8 weeks (43.8%) than among those assigned to placebo (24.0%) (P = 0.002 and P<0.001, respectively). The incidence of serious adverse events with ustekinumab was similar to that with placebo. Through 52 weeks of exposure, there were two deaths (one each from acute respiratory distress syndrome and hemorrhage from esophageal varices) and seven cases of cancer (one each of prostate, colon, renal papillary, and rectal cancer and three nonmelanoma skin cancers) among 825 patients who received ustekinumab and no deaths and one case of cancer (testicular cancer) among 319 patients who received placebo. CONCLUSIONS Ustekinumab was more effective than placebo for inducing and maintaining remission in patients with moderate-to-severe ulcerative colitis. (Funded by Janssen Research and Development; UNIFI ClinicalTrials.gov number, NCT02407236.)
Tárgyszavak:	Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban colitis ulcerative colitis ustekinumab
Megjelenés:	New England Journal Of Medicine. - 381 : 13 (2019), p. 1201-1214. -
További szerzők:	Sandborn, William J. Panaccione, Remo O'Brien, Christopher D. Zhang, Hongyan Johanns, Jewel Adedokun, Omoniyi J. Li, Katherine Peyrin-Biroulet, Laurent Van Assche, Gert Danese, Silvio Targan, Stephan Abreu, Maria T. Hisamatsu, Tadakazu Szapary, Philippe Marano, Colleen Altorjay István (1954-) (belgyógyász, gasztroenterológus, onkológus) UNIFI Study Group
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