Outcomes of patients with limited-stage aggressive large B-cell lymphoma with high-risk cytogenetics

Author:

Torka Pallawi1ORCID,Kothari Shalin K.2,Sundaram Suchitra1,Li Shaoying3ORCID,Medeiros L. Jeffrey3ORCID,Ayers Emily C.4ORCID,Landsburg Daniel J.4,Bond David A.5ORCID,Maddocks Kami J.5,Giri Anshu6,Hess Brian6,Pham Luu Q.7,Advani Ranjana7,Liu Yang8,Barta Stefan Klaus8,Vose Julie M.9ORCID,Churnetski Michael C.10,Cohen Jonathon B.10ORCID,Burkart Madelyn11ORCID,Karmali Reem11,Zurko Joanna12,Mehta Amitkumar12ORCID,Olszewski Adam J.13,Lee Sarah14ORCID,Hill Brian T.14,Burns Timothy F.15,Lansigan Frederick15ORCID,Rabinovich Emma16,Peace David16,Groman Adrienne1,Attwood Kristopher1,Hernandez-Ilizaliturri Francisco J.1

Affiliation:

1. Roswell Park Comprehensive Cancer Center, Buffalo, NY;

2. Department of Medicine, Yale University, New Haven, CT;

3. The University of Texas MD Anderson Cancer Center, Houston, TX;

4. Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA;

5. The Ohio State University Cancer Center, Columbus, OH;

6. Division of Hematology and Oncology, Medical University of South Carolina, Charleston, SC;

7. Lymphoma Division, Stanford University, Stanford, CA;

8. Fox Chase Cancer Center, Philadelphia, PA;

9. University of Nebraska Medical Center, Omaha, NE;

10. Winship Cancer Institute, Emory University, Atlanta, GA;

11. Feinberg School of Medicine, Northwestern University, Chicago, IL;

12. Division of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL;

13. Department of Medicine, Alpert Medical School, Brown University, Providence, RI;

14. Taussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, OH;

15. Dartmouth-Hitchcock Medical Center, Lebanon, NH; and

16. Division of Hematology & Oncology, University of Illinois at Chicago, Chicago, IL

Abstract

Abstract There is a paucity of data regarding outcomes and response to standard therapy in patients with limited-stage (LS) agressive B-cell lymphoma (LS-ABCL) who harbor MYC rearrangement (MYC-R) with or without BCL2 and/or BCL6 rearrangements. We conducted a multicenter retrospective study of MYC-R LS-ABCL patients who received either rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP), or more intensive immunochemotherapy (IIC) plus or minus consolidative involved-field radiation therapy (IFRT). One hundred four patients from 15 academic centers were included. Forty four patients (42%) received R-CHOP, of whom 52% had IFRT. Sixty patients (58%) received IIC, of whom 40% had IFRT. Overall response rate was 91% (84% complete response [CR]; 7% partial response). Patients with double-hit lymphoma (DHL; n = 40) had a lower CR rate compared with patients with MYC-R only (75% vs 98%; P = .003). CR rate was higher in the IFRT vs no-IFRT group (98% vs 72%; P < .001). Median follow-up was 3.2 years; 2-year progression-free survival (PFS) and overal survival (OS) were 78% and 86% for the entire cohort, and 74% and 81% for the DHL patients, respectively. PFS and OS were similar across treatment groups (IFRT vs no IFRT, R-CHOP vs IIC) in the entire cohort and in DHL patients. Our data provide a historical benchmark for MYC-R LS-ABCL and LS-DHL patients and show that outcomes for this population may be better than previously recognized. There was no benefit of using IIC over R-CHOP in patients with MYC-R LS-ABCL and LS-DHL.

Publisher

American Society of Hematology

Subject

Hematology

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