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Author Notes:

Correspondence: Pallawi Torka, Roswell Park Comprehensive Cancer Center, Elm and Carlton Streets, Buffalo, NY 14263; pallawi.torka@roswellpark.org

Contribution: All authors provided study materials or patients, contributed to data collection and assembly, reviewed the data analysis, edited and revised the manuscript, and approved the final version of the manuscript;

in addition, P.T. and S.K.K. participated in study design, analyzed and interpreted the data, and wrote and revised the manuscript;

and A. Groman and K.A. performed data analysis and interpretation.

Conflict-of-interest disclosure: K.J.M. has received research support from Bristol-Myers Squibb, Merck, Pharmacyclics, and Novartis, and has been an advisory board member for Pharmacyclics, Celgene, Teva, Seattle Genetics, AstraZeneca, and Bayer.

R.K. has received research support from Kite/Gilead, Celgene/Juno, Takeda, and Bristol-Myers Squibb; has been an advisory board member for Kite/Gilead and Celgene/Juno; and has been on speakers’ bureaus for Kite/Gilead and AstraZeneca.

A.J.O. has received research support from Genentech/Roche, Spectrum Pharmaceuticals, and TG Pharmaceuticals.

B.H. has received research support and consulting remuneration from Genentech.

D.P. has equity holdings in Bristol-Myers Squibb and Merck, and has received associate research funding from Celgene and ER Squibb and Sons.

The remaining authors declare no competing financial interests.

Subject:

Research Funding:

This work was supported by a biostatistics shared resource supported by a Roswell Park Comprehensive Cancer Center support grant from the National Institutes of Health, National Cancer Institute (P30CA016056).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Hematology
  • DOUBLE-HIT LYMPHOMA
  • SOUTHWEST-ONCOLOGY-GROUP
  • PLUS RADIOTHERAPY
  • ELDERLY-PATIENTS
  • POOR-PROGNOSIS
  • INVOLVED-FIELD
  • R-CHOP
  • RITUXIMAB
  • MYC
  • CHEMOTHERAPY

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

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Journal Title:

Blood Advances

Volume:

Volume 4, Number 2

Publisher:

, Pages 253-262

Type of Work:

Article | Final Publisher PDF

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.

Copyright information:

© 2020 by The American Society of Hematology.

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