A Three-Arm Randomized Phase II Study of Bendamustine/Rituximab with Bortezomib Induction or Lenalidomide Continuation in Untreated Follicular Lymphoma: ECOG-ACRIN E2408

被引:17
作者
Evens, Andrew M. [1 ]
Hong, Fangxin [2 ]
Habermann, Thomas M. [3 ]
Advani, Ranjana H. [4 ]
Gascoyne, Randy D. [5 ]
Witzig, Thomas E. [3 ]
Quon, Andrew [6 ]
Ranheim, Erik A. [7 ]
Ansell, Stephen M. [3 ]
Cheema, Puneet Singh [8 ]
Dy, Philip A. [9 ]
O'Brien, Timothy E. [10 ]
Winter, Jane N. [11 ]
Cescon, Terrence P. [12 ]
Chang, Julie E. [7 ]
Kahl, Brad S. [13 ]
机构
[1] Rutgers Canc Inst New Jersey, New Brunswick, NJ 08901 USA
[2] Dana Farber Canc Inst, ECOG ACRIN Biostat Ctr, Boston, MA 02115 USA
[3] Mayo Clin, Rochester, MN USA
[4] Stanford Canc Inst, Stanford, CA USA
[5] British Columbia Canc Agcy, Vancouver, BC, Canada
[6] Univ Calif Los Angeles, Los Angeles, CA 90024 USA
[7] Univ Wisconsin, Madison, WI USA
[8] St Johns Hosp Hlth East Care Syst, Maplewood, MN USA
[9] Decatur Mem Hosp, Effingham, IL USA
[10] Case Western Reserve Univ, Cleveland, OH 44106 USA
[11] Northwestern Univ, Chicago, IL 60611 USA
[12] Reading Hosp, W Reading, PA USA
[13] Washington Univ, St Louis, MO 63110 USA
关键词
PROTEASOME INHIBITOR BORTEZOMIB; MANTLE-CELL LYMPHOMAS; NON-HODGKINS-LYMPHOMA; TERM-FOLLOW-UP; 1ST-LINE TREATMENT; PLUS RITUXIMAB; COMPLETE RESPONSE; INDOLENT; SURVIVAL; THERAPY;
D O I
10.1158/1078-0432.CCR-20-1345
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We sought to improve upon frontline bendamustine/rituximab (BR) induction therapy followed by rituximab maintenance in untreated high-risk follicular lymphoma (FL). Patients and Methods: Patients were randomized to BR induction followed by 2-year rituximab maintenance (BR-R), BR with bortezomib and rituximab maintenance (BVR-R), or BR followed by lenalidomide (1 year) with rituximab maintenance (BR-LR). Dual primary objectives were complete remission (CR) rate and 1-year disease-free survival (DFS); 289 patients enrolled (NCT01216683). Results: For induction, 92%, 87%, and 86% of patients randomized to BR-R, BVR-R, or BR-LR received six cycles, respectively. CR rate with BR versus BVR induction was 62% versus 75%, respectively (P = 0.04). One-year DFS rates with BR-R versus BR-LR were 85% versus 67%, respectively (P = 0.0009). This was due to an imbalance in CR rates post-BR induction and discontinuation due to adverse events (AEs). The most common grade 3-4 AEs for BVR versus BR were neutropenia and sensory neuropathy (12% vs <1%); 83% of the latter occurred with intravenous bortezomib. The most common grade 3-4 AEs related to LR versus rituximab maintenance were neutropenia 66% versus 21%, respectively (P < 0.0001), and febrile neutropenia 10% versus 2%, respectively (P = 0.05). The overall treatment-related mortality was 1.4%. With 5-year median follow-up, 3-year PFS rates for BR-R, BVR-R, and BR-LR were 77%, 82%, and 76%, respectively (P = 0.36) with OS rates of 87%, 90%, and 84%, respectively (P = 0.79). For prognostication, CR rate and POD-24 were associated with survival. Conclusions: Altogether, neither bortezomib added to BR induction nor lenalidomide added to rituximab maintenance immediately post-BR induction is recommended in untreated FL.
引用
收藏
页码:4468 / 4477
页数:10
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