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A Three-Arm Randomized Phase II Study of Bendamustine/Rituximab with Bortezomib Induction or Lenalidomide Continuation in Untreated Follicular Lymphoma: ECOG-ACRIN E2408.
Evens, Andrew M; Hong, Fangxin; Habermann, Thomas M; Advani, Ranjana H; Gascoyne, Randy D; Witzig, Thomas E; Quon, Andrew; Ranheim, Erik A; Ansell, Stephen M; Cheema, Puneet Singh; Dy, Philip A; O'Brien, Timothy E; Winter, Jane N; Cescon, Terrence P; Chang, Julie E; Kahl, Brad S.
Affiliation
  • Evens AM; Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey. ae378@cinj.rutgers.edu.
  • Hong F; Dana Farber Cancer Institute, ECOG-ACRIN Biostatistics Center, Boston, Massachusetts.
  • Habermann TM; Mayo Clinic, Rochester, Minnesota.
  • Advani RH; Stanford Cancer Institute, Stanford, California.
  • Gascoyne RD; British Columbia Cancer Agency, Vancouver, Canada.
  • Witzig TE; Mayo Clinic, Rochester, Minnesota.
  • Quon A; University of California at Los Angeles, California.
  • Ranheim EA; University of Wisconsin, Madison, Wisconsin.
  • Ansell SM; Mayo Clinic, Rochester, Minnesota.
  • Cheema PS; Saint John's Hospital Health East Care System, Maplewood, Minnesota.
  • Dy PA; Decatur Memorial Hospital, Effingham, Illinois.
  • O'Brien TE; Case Western Reserve University, Cleveland, Ohio.
  • Winter JN; Northwestern University, Chicago, Illinois.
  • Cescon TP; Reading Hospital, West Reading, Pennsylvania.
  • Chang JE; University of Wisconsin, Madison, Wisconsin.
  • Kahl BS; Washington University, St. Louis, Missouri.
Clin Cancer Res ; 26(17): 4468-4477, 2020 09 01.
Article in En | MEDLINE | ID: mdl-32532790
ABSTRACT

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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Lymphoma, Follicular / Neoplasm Recurrence, Local Type of study: Clinical_trials Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Lymphoma, Follicular / Neoplasm Recurrence, Local Type of study: Clinical_trials Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2020 Document type: Article