Real-time intracranial pressure monitoring during high-dose methotrexate treatment for primary central nervous system lymphoma.


Journal

Cancer treatment and research communications
ISSN: 2468-2942
Titre abrégé: Cancer Treat Res Commun
Pays: England
ID NLM: 101694651

Informations de publication

Date de publication:
2020
Historique:
received: 07 05 2020
revised: 27 10 2020
accepted: 30 10 2020
pubmed: 9 11 2020
medline: 18 11 2021
entrez: 8 11 2020
Statut: ppublish

Résumé

Primary central nervous system lymphoma (PCNSL) is an aggressive non-Hodgkin lymphoma with exclusive central nervous system (CNS) and/or ocular involvement. Increased intracranial pressure (ICP) from cerebral edema can commonly presents secondary to the mass effect of PCNSL. Methotrexate-based induction chemotherapy is the gold standard for treatment, however, several neurotoxic complications have been associated with high-dose methotrexate (HD-MTX) treatment. Tumor lysis and other biochemical disruptions following administration of HD-MTX are postulated to increase cerebral edema and ICP in predisposed patients, therefore, in the setting of ring-enhancing lesions with significant mass effect, monitoring of ICP to prevent cerebral herniation may be necessary. We present the case of a patient with diffuse cerebral edema secondary to PCNSL, who was treated with methotrexate-based induction chemotherapy and underwent real-time ICP monitoring to allow for early recognition, and management with aggressive medical therapy to prevent worsening cerebral edema and potential fatal herniation. Treatment of patients with high tumor burden PCNSL can prove to be challenging, particularly at the time of initiation of methotrexate based induction chemotherapy in the setting of impending cerebral herniation, as in the case presented. Close monitoring of the patient's ICP proved advantageous in rapidly recognizing, and successfully treating elevations in ICP that could have worsened mass effect and lead to fatal herniation.

Sections du résumé

BACKGROUND
Primary central nervous system lymphoma (PCNSL) is an aggressive non-Hodgkin lymphoma with exclusive central nervous system (CNS) and/or ocular involvement. Increased intracranial pressure (ICP) from cerebral edema can commonly presents secondary to the mass effect of PCNSL. Methotrexate-based induction chemotherapy is the gold standard for treatment, however, several neurotoxic complications have been associated with high-dose methotrexate (HD-MTX) treatment. Tumor lysis and other biochemical disruptions following administration of HD-MTX are postulated to increase cerebral edema and ICP in predisposed patients, therefore, in the setting of ring-enhancing lesions with significant mass effect, monitoring of ICP to prevent cerebral herniation may be necessary.
PRESENTATION OF CASE
We present the case of a patient with diffuse cerebral edema secondary to PCNSL, who was treated with methotrexate-based induction chemotherapy and underwent real-time ICP monitoring to allow for early recognition, and management with aggressive medical therapy to prevent worsening cerebral edema and potential fatal herniation.
DISCUSSION AND CONCLUSIONS
Treatment of patients with high tumor burden PCNSL can prove to be challenging, particularly at the time of initiation of methotrexate based induction chemotherapy in the setting of impending cerebral herniation, as in the case presented. Close monitoring of the patient's ICP proved advantageous in rapidly recognizing, and successfully treating elevations in ICP that could have worsened mass effect and lead to fatal herniation.

Identifiants

pubmed: 33161322
pii: S2468-2942(20)30069-1
doi: 10.1016/j.ctarc.2020.100234
pii:
doi:

Substances chimiques

Methotrexate YL5FZ2Y5U1

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

100234

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Antonio Dono (A)

Vivian L. Smith Department of Neurosurgery, the University of Texas Health Science Center at Houston - McGovern Medical School, 6431 Fannin St. Houston, TX, 77030, United States.

Nuruddin Husein (N)

Vivian L. Smith Department of Neurosurgery, the University of Texas Health Science Center at Houston - McGovern Medical School, 6431 Fannin St. Houston, TX, 77030, United States; Memorial Hermann Hospital-Texas Medical Center, 6411 Fannin St. Houston, TX, 77030, United States.

Cristian Ybarra (C)

Vivian L. Smith Department of Neurosurgery, the University of Texas Health Science Center at Houston - McGovern Medical School, 6431 Fannin St. Houston, TX, 77030, United States.

Rodrigo Hasbun (R)

Department of Internal Medicine - Division of Infectious Diseases, the University of Texas Health Science Center at Houston - McGovern Medical School, 6431 Fannin St. Houston, TX, 77030, United States.

H Alex Choi (HA)

Vivian L. Smith Department of Neurosurgery, the University of Texas Health Science Center at Houston - McGovern Medical School, 6431 Fannin St. Houston, TX, 77030, United States; Memorial Hermann Hospital-Texas Medical Center, 6411 Fannin St. Houston, TX, 77030, United States.

Leomar Y Ballester (LY)

Vivian L. Smith Department of Neurosurgery, the University of Texas Health Science Center at Houston - McGovern Medical School, 6431 Fannin St. Houston, TX, 77030, United States; Memorial Hermann Hospital-Texas Medical Center, 6411 Fannin St. Houston, TX, 77030, United States; Department of Pathology and Laboratory Medicine, the University of Texas Health Science Center at Houston - McGovern Medical School, 6431 Fannin St. Houston, TX, 77030, United States. Electronic address: Leomar.Y.Ballester@uth.tmc.edu.

Yoshua Esquenazi (Y)

Vivian L. Smith Department of Neurosurgery, the University of Texas Health Science Center at Houston - McGovern Medical School, 6431 Fannin St. Houston, TX, 77030, United States; Memorial Hermann Hospital-Texas Medical Center, 6411 Fannin St. Houston, TX, 77030, United States; Center for Precision Health, School of Biomedical Informatics, the University of Texas Health Science Center at Houston - McGovern Medical School, 6431 Fannin St. Houston, TX, 77030, United States. Electronic address: Yoshua.EsquenaziLevy@uth.tmc.edu.

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