Polatuzumab Vedotin in Relapsed or Refractory Diffuse Large B-Cell Lymphoma

被引:552
|
作者
Sehn, Laurie H. [1 ,2 ]
Herrera, Alex F. [3 ]
Flowers, Christopher R. [4 ]
Kamdar, Manali K. [5 ]
McMillan, Andrew [6 ]
Hertzberg, Mark [7 ,8 ]
Assouline, Sarit [9 ]
Kim, Tae Min [10 ]
Kim, Won Seog [11 ]
Ozcan, Muhit [12 ]
Hirata, Jamie [13 ]
Penuel, Elicia [13 ]
Paulson, Joseph N. [13 ]
Cheng, Ji [14 ]
Ku, Grace [13 ]
Matasar, Matthew J. [15 ]
机构
[1] BC Canc Ctr Lymphoid Canc, 600 West 10th Ave, Vancouver, BC V5Z 4E6, Canada
[2] Univ British Columbia, Vancouver, BC, Canada
[3] City Hope Natl Med Ctr, Duarte, CA USA
[4] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[5] Univ Colorado, Aurora, CO USA
[6] Nottingham Univ Hosp, Nottingham, England
[7] Prince Wales Hosp, Sydney, NSW, Australia
[8] Univ NSW, Sydney, NSW, Australia
[9] Jewish Gen Hosp, Montreal, PQ, Canada
[10] Seoul Natl Univ Hosp, Seoul, South Korea
[11] Samsung Med Ctr, Seoul, South Korea
[12] Ankara Univ, Ankara, Turkey
[13] Genentech Inc, San Francisco, CA 94080 USA
[14] F Hoffmann La Roche & Cie AG, Mississauga, ON, Canada
[15] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
关键词
ANTIBODY-DRUG CONJUGATE; NON-HODGKIN-LYMPHOMA; PLUS RITUXIMAB; EXPRESSION; LEUKEMIA; BINDING;
D O I
10.1200/JCO.19.00172
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Patients with transplantation-ineligible relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) fare poorly, with limited treatment options. The antibody-drug conjugate polatuzumab vedotin targets CD79b, a B-cell receptor component. METHODS Safety and efficacy of polatuzumab vedotin with bendamustine and obinutuzumab (pola-BG) was evaluated in a single-arm cohort. Polatuzumab vedotin combined with bendamustine and rituximab (pola-BR) was compared with bendamustine and rituximab (BR) in a randomly assigned cohort of patients with transplantation-ineligible R/R DLBCL (primary end point: independent review committee [IRC] assessed complete response [CR] rate at the end of treatment). Duration of response, progression-free survival (PFS), and overall survival (OS) were analyzed using Kaplan-Meier and Cox regression methods. RESULTS Pola-BG and pola-BR had a tolerable safety profile. The phase Ib/II pola-BG cohort (n = 27) had a CR rate of 29.6% and a median OS of 10.8 months (median follow-up, 27.0 months). In the randomly assigned cohort (n = 80; 40 per arm), pola-BR patients had a significantly higher IRC-assessed CR rate (40.0% v 17.5%; P = .026) and longer IRC-assessed PFS (median, 9.5 v 3.7 months; hazard ratio [HR], 0.36, 95% CI, 0.21 to 0.63; P < .001) and OS (median, 12.4 v 4.7 months; HR, 0.42; 95% CI, 0.24 to 0.75; P = .002; median follow-up, 22.3 months). Pola-BR patients had higher rates of grade 3-4 neutropenia (46.2% v 33.3%), anemia (28.2% v 17.9%), and thrombocytopenia (41% v 23.1%), but similar grade 3-4 infections (23.1% v 20.5%), versus the BR group. Peripheral neuropathy associated with polatuzumab vedotin (43.6% of patients) was grade 1-2 and resolved in most patients. CONCLUSION Polatuzumab vedotin combined with BR resulted in a significantly higher CR rate and reduced the risk of death by 58% compared with BR in patients with transplantation-ineligible R/R DLBCL. (C) 2019 by American Society of Clinical Oncology
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页码:155 / +
页数:22
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