TY - JOUR
T1 - High-grade B-cell lymphoma, not otherwise specified
T2 - CNS involvement and outcomes in a multi-institutional series
AU - Epperla, Narendranath
AU - Zayac, Adam S.
AU - Landsburg, Daniel J.
AU - Bock, Allison M.
AU - Nowakowski, Grzegorz S.
AU - Ayers, Emily C.
AU - Girton, Mark
AU - Hu, Marie
AU - Beckman, Amy
AU - Li, Shaoying
AU - Medeiros, L. Jeffrey
AU - Chang, Julie E.
AU - Kurt, Habibe
AU - Sandoval-Sus, Jose
AU - Ansari-Lari, Mohammad Ali
AU - Kothari, Shalin K.
AU - Kress, Anna
AU - Xu, Mina L.
AU - Torka, Pallawi
AU - Sundaram, Suchitra
AU - Smith, Stephen D.
AU - Naresh, Kikkeri N.
AU - Karimi, Yasmin
AU - Bond, David A.
AU - Evens, Andrew M.
AU - Naik, Seema G.
AU - Kamdar, Manali
AU - Haverkos, Bradley M.
AU - Karmali, Reem
AU - Farooq, Umar
AU - Vose, Julie M.
AU - Rubinstein, Paul
AU - Chaudhry, Amina
AU - Olszewski, Adam J.
N1 - Publisher Copyright:
© 2024 by The American Society of Hematology. Licensed under.
PY - 2024/10/22
Y1 - 2024/10/22
N2 - Little is known about the central nervous system (CNS) risk in high-grade B-cell lymphoma, not otherwise specified (HGBL NOS). Hence, we sought to describe the rates of baseline CNS involvement, risk of CNS recurrence after primary therapy, and management strategies in HGBL NOS. In this multicenter retrospective study, we included 160 adults with newly diagnosed HGBL NOS treated between 2016 and 2021 at 20 US institutions. Eleven patients (7%) had baseline CNS involvement at diagnosis (leptomeningeal = 6, parenchymal = 4, and both = 1). Baseline CNS involvement was significantly associated only with MYC rearrangement (OR = 3.5) and testicular (in men) or female pelvic (in women) involvement (OR = 8.1). There was no significant difference in survival outcomes between patients with HGBL NOS with (median PFS = 4 years) or without (median PFS = 2.4 years) baseline CNS involvement (P = 0.45). The cumulative incidence of CNS recurrence at 3 years was 11%. Patients with baseline CNS involvement were at the highest risk (48.5% vs 8% for those without baseline CNS involvement) and were excluded from the risk factors analysis for CNS recurrence. The risk for CNS recurrence was significantly associated with blood or bone marrow involvement, CD5 expression, non–germinal center B-cell subtype, and “dual-expresser lymphoma” phenotype, however, high CNS IPI was not.
AB - Little is known about the central nervous system (CNS) risk in high-grade B-cell lymphoma, not otherwise specified (HGBL NOS). Hence, we sought to describe the rates of baseline CNS involvement, risk of CNS recurrence after primary therapy, and management strategies in HGBL NOS. In this multicenter retrospective study, we included 160 adults with newly diagnosed HGBL NOS treated between 2016 and 2021 at 20 US institutions. Eleven patients (7%) had baseline CNS involvement at diagnosis (leptomeningeal = 6, parenchymal = 4, and both = 1). Baseline CNS involvement was significantly associated only with MYC rearrangement (OR = 3.5) and testicular (in men) or female pelvic (in women) involvement (OR = 8.1). There was no significant difference in survival outcomes between patients with HGBL NOS with (median PFS = 4 years) or without (median PFS = 2.4 years) baseline CNS involvement (P = 0.45). The cumulative incidence of CNS recurrence at 3 years was 11%. Patients with baseline CNS involvement were at the highest risk (48.5% vs 8% for those without baseline CNS involvement) and were excluded from the risk factors analysis for CNS recurrence. The risk for CNS recurrence was significantly associated with blood or bone marrow involvement, CD5 expression, non–germinal center B-cell subtype, and “dual-expresser lymphoma” phenotype, however, high CNS IPI was not.
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U2 - 10.1182/bloodadvances.2024013791
DO - 10.1182/bloodadvances.2024013791
M3 - Article
C2 - 39189932
AN - SCOPUS:85208252682
SN - 2473-9529
VL - 8
SP - 5355
EP - 5364
JO - Blood Advances
JF - Blood Advances
IS - 20
ER -