Polatuzumab Vedotin in Previously Untreated Diffuse Large B-Cell Lymphoma

被引:407
|
作者
Tilly, Herve [1 ,2 ,3 ]
Morschhauser, Franck [4 ]
Sehn, Laurie H. [8 ,9 ]
Friedberg, Jonathan W. [12 ]
Trneny, M. [14 ,15 ]
Sharman, Jeff P. [16 ]
Herbaux, Charles [5 ]
Burke, John M. [17 ]
Matasar, Matthew [13 ,18 ]
Rai, Shinya [19 ]
Izutsu, Koji [20 ]
Mehta-Shah, Neha [21 ]
Oberic, Lucie [6 ]
Chauchet, Adrien [7 ]
Jurczak, Wojciech [22 ]
Song, Yuqin [23 ]
Greil, Richard [24 ,25 ]
Mykhalska, Larysa [26 ]
Bergua-Burgues, Juan M. [27 ]
Cheung, Matthew C. [10 ]
Pinto, Antonio [29 ]
Shin, Ho-Jin [30 ]
Hapgood, Greg [31 ]
Munhoz, Eduardo [32 ]
Abrisqueta, Pau [28 ]
Gau, Jyh-Pyng [33 ]
Hirata, Jamie [34 ]
Jiang, Yanwen [34 ]
Yan, Mark [11 ]
Lee, Calvin [34 ]
Flowers, Christopher R. [35 ]
Salles, Gilles [13 ]
机构
[1] Ctr Henri Becquerel, Dept Hematol, Rouen, France
[2] Ctr Henri Becquerel, INSERM Unit 1245, Rouen, France
[3] Univ Rouen, Rouen, France
[4] Univ Lille, Ctr Hosp Univ CHU Lille, ULR 7365 GRITA Grp Rech Sur Formes Injectables &, Lille, France
[5] CHU Montpellier, Montpellier, France
[6] Inst Univ Canc, Dept Hematol, Toulouse Oncopole, Toulouse, France
[7] Ctr Hosp Reg Univ Besancon, Dept Hematol, Besancon, France
[8] BC Canc, Ctr Lymphoid Canc, Vancouver, BC, Canada
[9] Univ British Columbia, Vancouver, BC, Canada
[10] Univ Toronto, Odette Canc Ctr, Sunnybrook Hlth Sci Ctr, Toronto, ON, Canada
[11] F Hoffmann La Roche, Mississauga, ON, Canada
[12] Univ Rochester, Wilmot Canc Inst, Rochester, NY USA
[13] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[14] Charles Univ Prague, Fac Med 1, Prague, Czech Republic
[15] Gen Univ Hosp, Prague, Czech Republic
[16] US Oncol Network, Willamette Valley Canc Inst & Res Ctr, Eugene, OR USA
[17] Rocky Mt Canc Ctr, Aurora, CO USA
[18] Mem Sloan Kettering Canc Ctr, Montvale, NJ USA
[19] Kindai Univ, Fac Med, Dept Hematol & Rheumatol, Osaka, Japan
[20] Natl Canc Ctr, Tokyo, Japan
[21] Washington Univ, St Louis, MO 63110 USA
[22] Maria Sklodowska Curie Natl Res Inst Oncol, Krakow, Poland
[23] Peking Univ Canc Hosp, Beijing, Peoples R China
[24] Paracelsus Med Univ, Salzburg Canc Res Inst, Med Dept 3, Ctr Clin Canc & Immunol Trials, Salzburg, Austria
[25] Canc Cluster Salzburg, Salzburg, Austria
[26] Feofaniya Clin Hosp, Kiev, Ukraine
[27] Hosp San Pedro de Alcantara, Caceres, Spain
[28] Vall dHebron Univ Hosp, Vall dHebron Inst Oncol, Dept Hematol, Barcelona, Spain
[29] IRCCS, Hematol Oncol & Stem Cell Transplantat Unit, Ist Nazl Tumori, Fdn G Pascale, Naples, Italy
[30] Pusan Natl Univ, Pusan Natl Univ Hosp, Res Inst Med Sci, Dept Internal Med,Div Hematol Oncol,Sch Med, Busan, South Korea
[31] Princess Alexandra Hosp, Brisbane, Qld, Australia
[32] Hosp Erasto Gaertner, Curitiba, Parana, Brazil
[33] Taipei Vet Gen Hosp, Taipei, Taiwan
[34] Genentech Inc, San Francisco, CA 94080 USA
[35] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2022年 / 386卷 / 04期
关键词
RITUXIMAB PLUS CYCLOPHOSPHAMIDE; NON-HODGKIN-LYMPHOMA; ANTIBODY-DRUG CONJUGATE; ELDERLY-PATIENTS; PHASE-III; R-CHOP; VINCRISTINE; DOXORUBICIN; TRIAL; CHEMOTHERAPY;
D O I
10.1056/NEJMoa2115304
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Diffuse large B-cell lymphoma (DLBCL) is typically treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). However, only 60% of patients are cured with R-CHOP. Polatuzumab vedotin is an antibody-drug conjugate targeting CD79b, which is ubiquitously expressed on the surface of malignant B cells. METHODS We conducted a double-blind, placebo-controlled, international phase 3 trial to evaluate a modified regimen of R-CHOP (pola-R-CHP), in which vincristine was replaced with polatuzumab vedotin, as compared with standard R-CHOP, in patients with previously untreated intermediate-risk or high-risk DLBCL. Patients 18 to 80 years of age were randomly assigned in a 1:1 ratio to receive six cycles of either pola-R-CHP or R-CHOP, plus two cycles of rituximab alone. The primary end point was investigator-assessed progression-free survival. Secondary end points included overall survival and safety. RESULTS Overall, 879 patients underwent randomization: 440 were assigned to the pola-R-CHP group and 439 to the R-CHOP group. After a median follow-up of 28.2 months, the percentage of patients surviving without progression was significantly higher in the pola-R-CHP group than in the R-CHOP group (76.7% [95% confidence interval (CI), 72.7 to 80.8] vs. 70.2% [95% CI, 65.8 to 74.6] at 2 years; stratified hazard ratio for progression, relapse, or death, 0.73 by Cox regression; 95% CI, 0.57 to 0.95; P=0.02). Overall survival at 2 years did not differ significantly between the groups (88.7% [95% CI, 85.7 to 91.6] in the pola-R-CHP group and 88.6% [95% CI, 85.6 to 91.6] in the R-CHOP group; hazard ratio for death, 0.94; 95% CI, 0.65 to 1.37; P=0.75). The safety profile was similar in the two groups. CONCLUSIONS Among patients with previously untreated intermediate-risk or high-risk DLBCL, the risk of disease progression, relapse, or death was lower among those who received pola-R-CHP than among those who received R-CHOP.
引用
收藏
页码:351 / 363
页数:13
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