Phase II Study of Pembrolizumab Plus GVD As Second-Line Therapy for Relapsed or Refractory Classical Hodgkin Lymphoma

被引:0
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作者
Moskowitz, Alison J. [1 ]
Shah, Gunjan [2 ]
Schoder, Heiko [1 ]
Ganesan, Nivetha [1 ]
Hancock, Helen [1 ]
Davey, Theresa [1 ]
Sohail, Samia [1 ]
Santarosa, Alayna [1 ]
Pomerantz, Lauren [1 ]
Jarjies, Christine [1 ]
Galasso, Natasha [1 ]
Neuman, Rachel [1 ]
Kumar, Anita [1 ]
Lahoud, Oscar B. [3 ]
Batlevi, Connie Lee [1 ]
Hamlin, Paul A. [1 ]
Straus, David J. [1 ]
Rodriguez-Rivera, Ildefonso [1 ]
Owens, Colette [1 ]
Caron, Philip [1 ]
Intlekofer, Andrew M. [1 ]
Hamilton, Audrey [1 ]
Horwitz, Steven M. [1 ]
Falchi, Lorenzo [1 ]
Joffe, Erel [1 ]
Palomba, Maria Lia [1 ]
Noy, Ariela [4 ]
Matasar, Matthew J. [1 ]
Pongas, Georgios [5 ]
Vardhana, Santosha [1 ]
von Keudell, Gottfried R. [1 ]
Yahalom, Joachim [1 ]
Zelenetz, Andrew D. [1 ]
Moskowitz, Craig H. [5 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Lymphoma Serv, 1275 York Ave, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, Adult Bone Marrow Transplant Serv, 1275 York Ave, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Med, Adult Bone Marrow Transplant Serv, Brooklyn, NY USA
[4] Mem Sloan Kettering Canc Ctr, Dept Med, Lymphoma Serv, 1275 York Ave, New York, NY 10021 USA
[5] Univ Miami Hlth Syst, Sylvester Comprehens Canc Ctr, Miami, FL USA
关键词
STEM-CELL TRANSPLANTATION; PET;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The international phase 2 CAPTIVATE (PCYC-1142) study evaluated ibrutinib (420 mg daily) plus venetoclax (ramped up to 400 mg daily) as first-line therapy in patients with CLL (Abstract 123). After 12 cycles of treatment, patients with confirmed undetectable MRD were randomly assigned in a double-blind manner to receive ibrutinib or placebo, and those with detectable MRD or unconfirmed undetectable MRD were randomly assigned to receive open-label ibrutinib monotherapy or ibrutinib plus venetoclax. The median age of the 164 patients was 58 years (range, 28-69), and the majority had at least 1 high-risk genetic feature. Among the patients with confirmed undetectable MRD before randomization, the rate of disease-free survival at 1 year after randomization was 100.0% in the ibrutinib group vs 95.3% in the placebo group (P=.1475). Across all 4 randomized cohorts, the 30-month PFS was between 95% and 100%. No new safety signals arose.
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页码:14 / 15
页数:2
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