4.4 Article

Outcomes of Burkitt lymphoma with central nervous system involvement: evidence from a large multicenter cohort study

Journal

HAEMATOLOGICA
Volume 106, Issue 7, Pages 1932-1942

Publisher

FERRATA STORTI FOUNDATION
DOI: 10.3324/haematol.2020.270876

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Funding

  1. Takeda
  2. Merck
  3. Aptose Biosciences
  4. Gilead Sciences
  5. Takeda Oncology
  6. Bristol-Myers Squibb
  7. AstraZeneca
  8. Genentech
  9. Bayer Oncology
  10. Verastem Oncology
  11. Incyte Corporation
  12. Seattle Genetics
  13. Portola Pharmaceuticals
  14. Pharmacyclics
  15. Acerta Pharma BV
  16. Denovo Biopharma
  17. Merck Sharp Dohme Corp
  18. Astra Zeneca
  19. Ignyta
  20. Ayala
  21. BMS
  22. Kite Pharma
  23. Bristol Myers
  24. Denovo
  25. Incyte
  26. LAM Therapeutics
  27. MEI
  28. Millenium/Takeda
  29. Trillium
  30. Kite
  31. Gilead
  32. Celgene
  33. Juno
  34. MiRagen
  35. Curis
  36. TG Therapeutics
  37. Juno Therapeutics
  38. Janssen Scientific Affairs, LLC
  39. Xencor
  40. Roche/Genentech
  41. Infinity
  42. AbbVie
  43. Acerta/AstraZeneca
  44. BeiGene
  45. NIH
  46. Adaptive Biotechnologies
  47. Spectrum Pharmaceuticals

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CNS involvement in Burkitt lymphoma is common and associated with poorer prognosis regardless of treatment regimen. Treatment regimens with good CNS penetration may reduce the risk of CNS recurrence.
Central nervous system (CNS) involvement in Burkitt lymphoma poses a major therapeutic challenge, and the relative ability of contemporary regimens to treat CNS involvement remains uncertain. We describe the prognostic significance of CNS involvement and the incidence of CNS recurrence/progression after contemporary immunochemotherapy using real-world clinicopathological data from adults with Burkitt lymphoma diagnosed between 2009 and 2018 in 30 institutions in the USA. We examined associations between baseline CNS involvement, patients' characteristics, complete response rates, and survival. We also examined risk factors for CNS recurrence. Of 641 patients (aged 18 to 88 years), 120 (19%) had CNS involvement. CNS involvement was independently associated with human immunodeficiency virus infection, poor performance status, involvement of >= 2 extranodal sites, and bone marrow involvement. Selection of the first-line treatment regimen was unaffected by CNS involvement (P=0.93). Patients with CNS disease had significantly lower rates of complete response (59% vs. 77% for patients with and without CNS involvement, respectively; P<0.001), worse 3-year progression-free survival (adjusted hazard ratio [aHR]=1.53, 95% confidence interval [95% CI]: 1.14-2.06; P=0.004) and overall survival (aHR=1.62, 95% CI: 1.18-2.22; P=0.003). The 3-year cumulative incidence of CNS recurrence was 6% (95% CI: 4-8%) and was significantly lower among patients receiving other regimens (CODOX-M/IVAC, 4%, or hyperCVAD/MA, 3%) compared with DA-EPOCH-R (13%; adjusted sub-distribution HR=4.38, 95% CI:, 2.16-8.87; P<0.001). Baseline CNS involvement in Burkitt lymphoma is relatively common and portends inferior prognosis independently of the first-line treatment regimen selected. In real-world practice, regimens including intravenous systemic agents with pronounced CNS penetrance were associated with a lower risk of CNS recurrence. This finding may be influenced by observed suboptimal adherence to the strict CNS staging and intrathecal therapy procedures incorporated in the DA-EPOCH-R regimen.

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