TY - JOUR
T1 - Impact of contemporary regimens on the outcomes and toxicity of primary CNS lymphoma
T2 - a single-center retrospective analysis of 73 patients
AU - Sarid, Nadav
AU - Bokstein, Felix
AU - Blumenthal, Deborah T.
AU - Weiss-Meilik, Ahuva
AU - Gibstein, Lili
AU - Avivi, Irit
AU - Perry, Chava
AU - Ram, Ron
N1 - Publisher Copyright:
© 2020, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2021/1
Y1 - 2021/1
N2 - Introduction: Primary central nervous system lymphoma (PCNSL) is a rare disease with a dismal prognosis compared to its systemic large B-cell lymphoma counterpart. Real world data are limited, when considering a uniform backbone treatment. Methods: A retrospective study of all adult patients treated sequentially with a high-dose methotrexate (HD MTX)-based regimen in a single tertiary medical center between 2003 and 2019. Results: The 2015–2019 period differed from its predecessor in that most patients were treated with an HD MTX-based polychemotherapy regimen as opposed to HD MTX monotherapy (81% vs. 13%, P <.001), rituximab was given as standard of care (100% vs. 56%, P <.01), and most induction-responsive patients received consolidation treatment (70% vs. 18%, P =.01). The median progression-free and overall survival (OS) for the entire cohort (n = 73, mean age 64 years) was 9.9 and 29.8 months, respectively. Patients diagnosed between 2015 and 2019 had superior OS (P =.03) compared to those treated earlier. An interim partial response (PR) state, documented after two cycles of chemotherapy, was associated with increased incidence of progression, with only 33% of those patients achieving end-of-induction complete response. Twenty-three percent of patients developed thrombotic events and 44% developed grade 3–4 infections. HD MTX-based polychemotherapy induction was associated with both increase in thrombotic and infection incidence. Conclusions: Contemporary HD MTX-based combination therapies suggestively improved the outcomes for PCNSL, but at a cost of increased incidence of toxicity. Patients who achieve an interim PR status are at a high risk for treatment failure.
AB - Introduction: Primary central nervous system lymphoma (PCNSL) is a rare disease with a dismal prognosis compared to its systemic large B-cell lymphoma counterpart. Real world data are limited, when considering a uniform backbone treatment. Methods: A retrospective study of all adult patients treated sequentially with a high-dose methotrexate (HD MTX)-based regimen in a single tertiary medical center between 2003 and 2019. Results: The 2015–2019 period differed from its predecessor in that most patients were treated with an HD MTX-based polychemotherapy regimen as opposed to HD MTX monotherapy (81% vs. 13%, P <.001), rituximab was given as standard of care (100% vs. 56%, P <.01), and most induction-responsive patients received consolidation treatment (70% vs. 18%, P =.01). The median progression-free and overall survival (OS) for the entire cohort (n = 73, mean age 64 years) was 9.9 and 29.8 months, respectively. Patients diagnosed between 2015 and 2019 had superior OS (P =.03) compared to those treated earlier. An interim partial response (PR) state, documented after two cycles of chemotherapy, was associated with increased incidence of progression, with only 33% of those patients achieving end-of-induction complete response. Twenty-three percent of patients developed thrombotic events and 44% developed grade 3–4 infections. HD MTX-based polychemotherapy induction was associated with both increase in thrombotic and infection incidence. Conclusions: Contemporary HD MTX-based combination therapies suggestively improved the outcomes for PCNSL, but at a cost of increased incidence of toxicity. Patients who achieve an interim PR status are at a high risk for treatment failure.
KW - High-dose methotrexate
KW - Primary central nervous system lymphoma
KW - Prognosis
KW - Toxicity
UR - http://www.scopus.com/inward/record.url?scp=85093517950&partnerID=8YFLogxK
U2 - 10.1007/s11060-020-03654-x
DO - 10.1007/s11060-020-03654-x
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C2 - 33099747
AN - SCOPUS:85093517950
SN - 0167-594X
VL - 151
SP - 211
EP - 220
JO - Journal of Neuro-Oncology
JF - Journal of Neuro-Oncology
IS - 2
ER -