Single-route CNS prophylaxis for aggressive non-Hodgkin lymphomas: real-world outcomes from 21 US academic institutions

Victor M. Orellana‐Noia(Emory University), Daniel Reed(Wake Forest University), Ashley McCook(Emory University), Jeremy Sen(University of Virginia), Christian Barlow(University of Virginia), Mary‐Kate Malecek(Washington University in St. Louis), Marcus P. Watkins(Washington University in St. Louis), Brad S. Kahl(Washington University in St. Louis), Michael A. Spinner(Stanford Medicine), Ranjana H. Advani(Stanford Medicine), Timothy Voorhees(University of North Carolina at Chapel Hill), Anson Snow(University of North Carolina at Chapel Hill), Natalie S. Grover(University of North Carolina at Chapel Hill), Amy Ayers(Emory University), Jason T. Romancik(Emory University), Yuxin Liu(Yale University), Scott F. Huntington(Yale University), Julio C. Chávez(Moffitt Cancer Center), Hayder Saeed(Moffitt Cancer Center), Aleksandr Lazaryan(Moffitt Cancer Center), Vikram Raghunathan(Oregon Health & Science University), Stephen E. Spurgeon(Oregon Health & Science University), Thomas Ollila(Brown University), Christopher Del Prete(Brown University), Adam J. Olszewski(Brown University), Emily C. Ayers(UPMC Hillman Cancer Center), Daniel J. Landsburg(UPMC Hillman Cancer Center), Benjamin Echalier(University of Colorado Denver), Jun Lee(University of Colorado Denver), Manali Kamdar(University of Colorado Denver), Paolo F. Caimi(Cleveland Clinic), Timothy Fu(Rutgers, The State University of New Jersey), Jieqi Liu(Rutgers, The State University of New Jersey), Kevin A. David(Rutgers, The State University of New Jersey), Hanan Alharthy(University of Maryland, Baltimore), Jennie Y. Law(University of Maryland, Baltimore), Reem Karmali(Northwestern University), Harsh Shah(University of Utah), Deborah M. Stephens(University of Utah), Ajay Major(University of Chicago), Alexandra E. Rojek(University of Chicago), Sonali M. Smith(University of Chicago), Amulya Yellala(University of Nebraska Medical Center), Avyakta Kallam(University of Nebraska Medical Center), Shazi Nakhoda(Fox Chase Cancer Center), Nadia Khan(Fox Chase Cancer Center), Mohammad Sohail(Cleveland Clinic), Brian T. Hill(Cleveland Clinic), Odeth Barrett-Campbell(Dartmouth College), Frederick Lansigan(Dartmouth College), Jeffrey M. Switchenko(Emory University), Jonathon B. Cohen(Emory University), Craig A. Portell(University of Virginia)
Blood
September 27, 2021
Cited by 94Open Access
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Abstract

Prophylaxis is commonly used to prevent central nervous sy stem (CNS) relapse in diffuse large B-cell lymphoma (DLBCL), with no clear standard of care. We retrospectively evaluated 1162 adult patients across 21 US academic centers with DLBCL or similar histologies who received single-route CNS prophylaxis as part of frontline therapy between 2013 and 2019. Prophylaxis was administered intrathecally(IT) in 894 (77%) and using systemic high-dose methotrexate (HD-MTX) in 236 (20%); 32 patients (3%) switched route due to toxicity and were assessed separately. By CNS-International Prognostic Index (IPI), 18% were considered low-risk, 51% moderate, and 30% high. Double-hit lymphoma (DHL) was confirmed in 243 of 866 evaluable patients (21%). Sixty-four patients (5.7%) had CNS relapse after median 7.1 months from diagnosis, including 15 of 64 (23%) within the first 6 months. There was no significant difference in CNS relapse between IT and HD-MTX recipients (5.4% vs 6.8%, P = .4), including after propensity score matching to account for differences between respective recipient groups. Weighting by CNS-IPI, expected vs observed CNS relapse rates were nearly identical (5.8% vs 5.7%). Testicular involvement was associated with high risk of CNS relapse (11.3%) despite most having lower CNS-IPI scores. DHL did not significantly predict for CNS relapse after single-route prophylaxis, including with adjustment for treatment regimen and other factors. This large study of CNS prophylaxis recipients with DLBCL found no significant difference in CNS relapse rates between routes of administration. Relapse rates among high-risk subgroups remain elevated, and reconsideration of prophylaxis strategies in DLBCL is of critical need.


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