Phase III Study of Adjuvant Ipilimumab (3 or 10 mg/kg) Versus High-Dose Interferon Alfa-2b for Resected High-Risk Melanoma: North American Intergroup E1609

被引:107
|
作者
Tarhini, Ahmad A. [1 ]
Lee, Sandra J. [2 ,3 ]
Hodi, F. Stephen [3 ]
Rao, Uma N. M. [4 ]
Cohen, Gary I. [5 ]
Hamid, Omid [6 ]
Hutchins, Laura F. [7 ]
Sosman, Jeffrey A. [8 ]
Kluger, Harriett M. [9 ]
Eroglu, Zeynep [1 ]
Koon, Henry B. [10 ]
Lawrence, Donald P. [11 ]
Kendra, Kari L. [12 ]
Minor, David R. [13 ]
Lee, Carrie B. [14 ]
Albertini, Mark R. [15 ]
Flaherty, Lawrence E. [16 ]
Petrella, Teresa M. [17 ]
Streicher, Howard [18 ]
Sondak, Vernon K. [1 ]
Kirkwood, John M. [4 ]
机构
[1] H Lee Moffitt Comprehens Canc Ctr, Tampa, FL USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[5] Greater Baltimore Med Ctr, Baltimore, MD USA
[6] Angeles Clin & Res Inst, Santa Monica, CA USA
[7] Univ Arkansas, Little Rock, AR 72204 USA
[8] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[9] Yale Univ, New Haven, CT USA
[10] Case Western Reserve Univ, Cleveland, OH 44106 USA
[11] Massachusetts Gen Hosp, Boston, MA 02114 USA
[12] Ohio State Univ, Columbus, OH 43210 USA
[13] Sutter Calif Pacific Med Ctr, San Francisco, CA USA
[14] Univ N Carolina, Chapel Hill, NC 27515 USA
[15] Univ Wisconsin, Madison, WI USA
[16] Wayne State Univ, Karmanos Canc Inst, Detroit, MI USA
[17] Odette Canc Ctr, Toronto, ON, Canada
[18] NCI, Rockville, MD USA
基金
美国国家卫生研究院;
关键词
STAGE-III; DOUBLE-BLIND; TRIAL; SURVIVAL; THERAPY; DISEASE; PLACEBO; RELAPSE;
D O I
10.1200/JCO.19.01381
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Phase III adjuvant trials have reported significant benefits in both relapse-free survival (RFS) and overall survival (OS) for high-dose interferon alfa (HDI) and ipilimumab at 10 mg/kg (ipi10). E1609 evaluated the safety and efficacy of ipilimumab at 3 mg/kg (ipi3) and ipi10 versus HDI. PATIENTS AND METHODS E1609 was a phase III trial in patients with resected cutaneous melanoma (American Joint Committee on Cancer 7th edition stage IIIB, IIIC, M1a, or M1b). It had 2 coprimary end points: OS and RFS. A 2-step hierarchic approach first evaluated ipi3 versus HDI followed by ipi10 versus HDI. RESULTS Between May 2011 and August 2014, 1,670 adult patients were centrally randomly assigned (1:1:1) to ipi3 (n = 523), HDI (n = 636), or ipi10 (n = 511). Treatment-related adverse events grade ? 3 occurred in 37% of patients receiving ipi3, 79% receiving HDI, and 58% receiving ipi10, with adverse events leading to treatment discontinuation in 35%, 20%, and 54%, respectively. Comparison of ipi3 versus HDI used an intent-to-treat analysis of concurrently randomly assigned patient cases (n = 1,051) and showed significant OS difference in favor of ipi3 (hazard ratio [HR], 0.78; 95.6% repeated CI, 0.61 to 0.99; P = .044; RFS: HR, 0.85; 99.4% CI, 0.66 to 1.09; P = .065). In the second step, for ipi10 versus HDI (n = 989), trends in favor of ipi10 did not achieve statistical significance. Salvage patterns after melanoma relapse showed significantly higher rates of ipilimumab and ipilimumab/anti?programmed death 1 use in the HDI arm versus ipi3 and ipi10 (P ? .001). CONCLUSION Adjuvant therapy with ipi3 benefits survival versus HDI; for the first time to our knowledge in melanoma adjuvant therapy, E1609 has demonstrated a significant improvement in OS against an active control regimen. The currently approved adjuvant ipilimumab dose (ipi10) was more toxic and not superior in efficacy to HDI.
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页码:567 / +
页数:10
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