Adjuvant Pembrolizumab versus IFNα2b or Ipilimumab in Resected High-Risk Melanoma

被引:43
|
作者
Grossmann, Kenneth F. [1 ]
Othus, Megan [2 ]
Patel, Sapna P. [3 ]
Tarhini, Ahmad A. [4 ]
Sondak, Vernon K. [4 ]
Knopp, Michael, V [5 ]
Petrella, Teresa M. [6 ]
Truong, Thach-Giao [7 ]
Khushalani, Nikhil, I [4 ]
Cohen, Justine, V [8 ]
Buchbinder, Elizabeth, I [9 ]
Kendra, Kari [5 ]
Funchain, Pauline [10 ]
Lewis, Karl D. [11 ]
Conry, Robert M. [12 ]
Chmielowski, Bartosz [13 ]
Kudchadkar, Ragini R. [14 ]
Johnson, Douglas B. [15 ]
Li, Hongli [2 ]
Moon, James [2 ]
Eroglu, Zeynep [4 ]
Gastman, Brian [10 ]
Kovacsovics-Bankowski, Magdalena [1 ]
Gunturu, Krishna S. [16 ]
Ebbinghaus, Scot W. [17 ]
Ahsan, Sama [17 ]
Ibrahim, Nageatte [17 ]
Sharon, Elad [18 ]
Korde, Larissa A. [18 ]
Kirkwood, John M. [19 ]
Ribas, Antoni [13 ]
机构
[1] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT USA
[2] SWOG Stat & Data Management Ctr, Seattle, WA USA
[3] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[4] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[5] Ohio State Univ, Columbus, OH 43210 USA
[6] Sunnybrook Hlth Sci Ctr, Odette Canc Ctr, Toronto, ON, Canada
[7] Kaiser Permanente NCAL, Vallejo, CA USA
[8] Massachusetts Gen Hosp, Boston, MA 02114 USA
[9] Dana Farber Canc Inst, Boston, MA 02115 USA
[10] Cleveland Clin, Cleveland, OH 44106 USA
[11] Univ Colorado, Canc Ctr, Aurora, CO USA
[12] Univ Alabama Birmingham, Canc Ctr, Birmingham, AL USA
[13] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90024 USA
[14] Emory Univ, Winship Canc Inst, Atlanta, GA USA
[15] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[16] Lahey Hosp & Med Ctr, Burlington, NJ USA
[17] Merck & Co Inc, Kenilworth, Warwick, England
[18] NCI, Canc Therapy Evaluat Program, Bethesda, MD USA
[19] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
关键词
DOUBLE-BLIND; STAGE-III; NIVOLUMAB; SURVIVAL; PLACEBO; BRAF;
D O I
10.1158/2159-8290.CD-21-1141
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We conducted a randomized phase III trial to evaluate whether adjuvant pembrolizumab for one year (647 patients) improved recurrence-free survival (RFS) or overall survival (OS) in comparison with high-dose IFN alpha -2b for one year or ipilimumab for up to three years (654 patients), the approved standard-of-care adjuvant immunotherapies at the time of enrollment for patients with high-risk resected melanoma. At a median follow-up of 47.5 months, pembrolizumab was associated with significantly longer RFS than prior standard-of-care adjuvant immunotherapies [HR, 0.77; 99.62% confidence interval (CI), 0.59-0.99; P= 0.002]. There was no statistically significant association with OS among all patients (HR, 0.82; 96.3% CI, 0.61-1.09; P = 0.15). Proportions of treatmentrelated adverse events of grades 3 to 5 were 19.5% with pembrolizumab, 71.2% with IFN alpha-2b, and 49.2% with ipilimumab. Therefore, adjuvant pembrolizumab significantly improved RFS but not OS compared with the prior standard-of-care immunotherapies for patients with high-risk resected melanoma. SIGNIFICANCE: Adjuvant PD-1 blockade therapy decreases the rates of recurrence, but not survival, in patients with surgically resectable melanoma, substituting the prior standard-of-care immunotherapies for this cancer.
引用
收藏
页码:644 / 653
页数:10
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