Is more better? Increased doses of high dose methotrexate and addition of rituximab is associated with improved outcomes in a large primary CNS lymphoma cohort.

Primary central nervous system lymphoma (PCNSL) methotrexate rituximab standard of care survival

Journal

Annals of lymphoma
Titre abrégé: Ann Lymphoma
Pays: China
ID NLM: 101718324

Informations de publication

Date de publication:
28 Feb 2023
Historique:
medline: 18 4 2023
entrez: 17 4 2023
pubmed: 18 4 2023
Statut: ppublish

Résumé

Primary central nervous system lymphoma (PCNSL) is a rare and aggressive primary brain tumor. While high dose methotrexate (HDMTX) regimens remain standard of care, it remains unclear if optimization of HDMTX doses and the addition of rituximab provide clinical benefit. Over the last 30 years, standard care given at Memorial Sloan Kettering Cancer Center (MSKCC) has evolved, allowing the comparison of patients receiving different numbers of HDMTX doses and those treated with and without rituximab. The purpose of this study was to describe outcomes based on treatment pattern changes. This single-center, retrospective, IRB-approved study at MSKCC included patients with immunocompetent PCNSL, age ≥18 years and diagnosed between 1/1983-12/2017. Overall survival (OS) was modeled from date of last HDMTX for analyses associating HDMTX and OS. Multivariable Cox regression models estimated hazard ratios (HR) and corresponding 95% confidence intervals (CI). There were 546 patients identified with newly diagnosed PCNSL. Median overall survival (mOS) of the entire population was 4.7 years (95% CI: 3.8-5.7 years); 3.3 years (95% CI: 2.7-3.9 years) in patients diagnosed prior to 2006 and 8.1 years (95% CI: 6.6-11.1 years) in patients diagnosed 2006 onwards. Patients receiving ≥6 doses of HDMTX had improved survival compared to those receiving <6 doses of HDMTX (mOS: 7.8 OS for PCNSL has improved significantly over the last few decades. Patients seem to benefit with ≥6 doses of HDMTX and the addition of rituximab, an effect independent of treatment era, age, and KPS.

Sections du résumé

Background UNASSIGNED
Primary central nervous system lymphoma (PCNSL) is a rare and aggressive primary brain tumor. While high dose methotrexate (HDMTX) regimens remain standard of care, it remains unclear if optimization of HDMTX doses and the addition of rituximab provide clinical benefit. Over the last 30 years, standard care given at Memorial Sloan Kettering Cancer Center (MSKCC) has evolved, allowing the comparison of patients receiving different numbers of HDMTX doses and those treated with and without rituximab. The purpose of this study was to describe outcomes based on treatment pattern changes.
Methods UNASSIGNED
This single-center, retrospective, IRB-approved study at MSKCC included patients with immunocompetent PCNSL, age ≥18 years and diagnosed between 1/1983-12/2017. Overall survival (OS) was modeled from date of last HDMTX for analyses associating HDMTX and OS. Multivariable Cox regression models estimated hazard ratios (HR) and corresponding 95% confidence intervals (CI).
Results UNASSIGNED
There were 546 patients identified with newly diagnosed PCNSL. Median overall survival (mOS) of the entire population was 4.7 years (95% CI: 3.8-5.7 years); 3.3 years (95% CI: 2.7-3.9 years) in patients diagnosed prior to 2006 and 8.1 years (95% CI: 6.6-11.1 years) in patients diagnosed 2006 onwards. Patients receiving ≥6 doses of HDMTX had improved survival compared to those receiving <6 doses of HDMTX (mOS: 7.8
Conclusions UNASSIGNED
OS for PCNSL has improved significantly over the last few decades. Patients seem to benefit with ≥6 doses of HDMTX and the addition of rituximab, an effect independent of treatment era, age, and KPS.

Identifiants

pubmed: 37067886
doi: 10.21037/aol-22-19
pmc: PMC10100595
mid: NIHMS1887687
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Références

Neuro Oncol. 2013 Aug;15(8):1068-73
pubmed: 23502429
Sci Rep. 2021 Jan 22;11(1):2125
pubmed: 33483528
Br J Haematol. 2016 Aug;174(3):417-24
pubmed: 27018254
J Clin Oncol. 2006 Dec 20;24(36):5711-5
pubmed: 17116938
Am J Hematol. 2015 Dec;90(12):1149-54
pubmed: 26414492
Neurology. 2014 Jul 15;83(3):235-9
pubmed: 24928128
Clin Transl Oncol. 2007 Jul;9(7):465-7
pubmed: 17652061
Neuro Oncol. 2018 Apr 9;20(5):687-694
pubmed: 29036697
Leukemia. 2022 Jul;36(7):1870-1878
pubmed: 35562406
Lancet Oncol. 2019 Feb;20(2):216-228
pubmed: 30630772
Neurology. 2011 Mar 8;76(10):929-30
pubmed: 21383331
Cancer. 2004 Jul 1;101(1):139-45
pubmed: 15221999
Leuk Lymphoma. 2016 Dec;57(12):2777-2783
pubmed: 27087066
Neurology. 2004 Sep 14;63(5):901-3
pubmed: 15365145

Auteurs

Prakirthi Yerram (P)

Department of Pharmacy, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Samantha N Reiss (SN)

Department of Pharmacy, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Lisa Modelevsky (L)

Department of Pharmacy, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Lauren Schaff (L)

Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Anne S Reiner (AS)

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Katherine S Panageas (KS)

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Christian Grommes (C)

Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Classifications MeSH