Blood–Brain Barrier Disruption (BBBD)-Based Immunochemotherapy for Primary Central Nervous System Lymphoma (PCNSL), Early Results of a Phase II Study

Primary central nervous system lymphoma is a rare but aggressive brain malignancy. It is associated with poor prognosis even with the current standard of care. The aim of this study was to evaluate the effect and tolerability of blood–brain barrier disruption treatment combined with high-dose treatm...

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Main Authors: Hanne K. Kuitunen, Aino L. K. Rönkä, Eila M. Sonkajärvi, Juha-Matti Isokangas, Marja Pyörälä, Kari A. A. Palosaari, Anna S. Jokimäki, Anu E. Partanen, Harri J. Littow, Merja A. Vakkala, Esa J. Jantunen, Mirja E. Huttunen, Katja J. Marin, Annikki M. K. Aromaa-Häyhä, Päivi K. Auvinen, Tuomas Selander, Inka K. Puhakka, Outi M. Kuittinen
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/15/4/1341
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author Hanne K. Kuitunen
Aino L. K. Rönkä
Eila M. Sonkajärvi
Juha-Matti Isokangas
Marja Pyörälä
Kari A. A. Palosaari
Anna S. Jokimäki
Anu E. Partanen
Harri J. Littow
Merja A. Vakkala
Esa J. Jantunen
Mirja E. Huttunen
Katja J. Marin
Annikki M. K. Aromaa-Häyhä
Päivi K. Auvinen
Tuomas Selander
Inka K. Puhakka
Outi M. Kuittinen
author_facet Hanne K. Kuitunen
Aino L. K. Rönkä
Eila M. Sonkajärvi
Juha-Matti Isokangas
Marja Pyörälä
Kari A. A. Palosaari
Anna S. Jokimäki
Anu E. Partanen
Harri J. Littow
Merja A. Vakkala
Esa J. Jantunen
Mirja E. Huttunen
Katja J. Marin
Annikki M. K. Aromaa-Häyhä
Päivi K. Auvinen
Tuomas Selander
Inka K. Puhakka
Outi M. Kuittinen
author_sort Hanne K. Kuitunen
collection DOAJ
description Primary central nervous system lymphoma is a rare but aggressive brain malignancy. It is associated with poor prognosis even with the current standard of care. The aim of this study was to evaluate the effect and tolerability of blood–brain barrier disruption treatment combined with high-dose treatment with autologous stem cell transplantation as consolidation on primary central nervous system lymphoma patients. We performed a prospective phase II study for 25 patients with previously untreated primary central nervous system lymphoma. The blood–brain barrier disruption treatment was initiated 3–4 weeks after the MATRix regimen using the previously optimized therapy protocol. Briefly, each chemotherapy cycle included two subsequent intra-arterial blood–brain barrier disruption treatments on days 1 and 2 via either one of the internal carotid arteries or vertebral arteries. Patients received the therapy in 3-week intervals. The treatment was continued for two more courses after achieving a maximal radiological response to the maximum of six courses. The complete treatment response was observed in 88.0% of the patients. At the median follow-up time of 30 months, median progression-free and overall survivals were not reached. The 2-year overall and progression-free survival rates were 67.1% and 70.3%, respectively. Blood–brain barrier disruption treatment is a promising option for primary central nervous system lymphoma with an acceptable toxicity profile.
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spelling doaj.art-abc7b1b4382f4629a7de50373877556a2023-11-16T19:39:39ZengMDPI AGCancers2072-66942023-02-01154134110.3390/cancers15041341Blood–Brain Barrier Disruption (BBBD)-Based Immunochemotherapy for Primary Central Nervous System Lymphoma (PCNSL), Early Results of a Phase II StudyHanne K. Kuitunen0Aino L. K. Rönkä1Eila M. Sonkajärvi2Juha-Matti Isokangas3Marja Pyörälä4Kari A. A. Palosaari5Anna S. Jokimäki6Anu E. Partanen7Harri J. Littow8Merja A. Vakkala9Esa J. Jantunen10Mirja E. Huttunen11Katja J. Marin12Annikki M. K. Aromaa-Häyhä13Päivi K. Auvinen14Tuomas Selander15Inka K. Puhakka16Outi M. Kuittinen17Cancer Center, Oulu University Hospital, 90220 Oulu, FinlandDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, FinlandSurgery and Anaesthesia Center, Oulu University Hospital, 90220 Oulu, FinlandService for Medical Care, Oulu University Hospital Diagnostics, 90220 Oulu, FinlandDepartment of Medicine, Kuopio University Hospital, 70210 Kuopio, FinlandService for Medical Care, Oulu University Hospital Diagnostics, 90220 Oulu, FinlandCancer Center, Oulu University Hospital, 90220 Oulu, FinlandDepartment of Medicine, Kuopio University Hospital, 70210 Kuopio, FinlandService for Medical Care, Oulu University Hospital Diagnostics, 90220 Oulu, FinlandSurgery and Anaesthesia Center, Oulu University Hospital, 90220 Oulu, FinlandDepartment of Medicine, Kuopio University Hospital, 70210 Kuopio, FinlandSurgery and Anaesthesia Center, Oulu University Hospital, 90220 Oulu, FinlandDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, FinlandDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, FinlandDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, FinlandScience Service Center, Kuopio University Hospital, 70210 Kuopio, FinlandDepartment of Neurology, Kuopio University Hospital, 70210 Kuopio, FinlandDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, FinlandPrimary central nervous system lymphoma is a rare but aggressive brain malignancy. It is associated with poor prognosis even with the current standard of care. The aim of this study was to evaluate the effect and tolerability of blood–brain barrier disruption treatment combined with high-dose treatment with autologous stem cell transplantation as consolidation on primary central nervous system lymphoma patients. We performed a prospective phase II study for 25 patients with previously untreated primary central nervous system lymphoma. The blood–brain barrier disruption treatment was initiated 3–4 weeks after the MATRix regimen using the previously optimized therapy protocol. Briefly, each chemotherapy cycle included two subsequent intra-arterial blood–brain barrier disruption treatments on days 1 and 2 via either one of the internal carotid arteries or vertebral arteries. Patients received the therapy in 3-week intervals. The treatment was continued for two more courses after achieving a maximal radiological response to the maximum of six courses. The complete treatment response was observed in 88.0% of the patients. At the median follow-up time of 30 months, median progression-free and overall survivals were not reached. The 2-year overall and progression-free survival rates were 67.1% and 70.3%, respectively. Blood–brain barrier disruption treatment is a promising option for primary central nervous system lymphoma with an acceptable toxicity profile.https://www.mdpi.com/2072-6694/15/4/1341BBBDPCNSLASCT
spellingShingle Hanne K. Kuitunen
Aino L. K. Rönkä
Eila M. Sonkajärvi
Juha-Matti Isokangas
Marja Pyörälä
Kari A. A. Palosaari
Anna S. Jokimäki
Anu E. Partanen
Harri J. Littow
Merja A. Vakkala
Esa J. Jantunen
Mirja E. Huttunen
Katja J. Marin
Annikki M. K. Aromaa-Häyhä
Päivi K. Auvinen
Tuomas Selander
Inka K. Puhakka
Outi M. Kuittinen
Blood–Brain Barrier Disruption (BBBD)-Based Immunochemotherapy for Primary Central Nervous System Lymphoma (PCNSL), Early Results of a Phase II Study
Cancers
BBBD
PCNSL
ASCT
title Blood–Brain Barrier Disruption (BBBD)-Based Immunochemotherapy for Primary Central Nervous System Lymphoma (PCNSL), Early Results of a Phase II Study
title_full Blood–Brain Barrier Disruption (BBBD)-Based Immunochemotherapy for Primary Central Nervous System Lymphoma (PCNSL), Early Results of a Phase II Study
title_fullStr Blood–Brain Barrier Disruption (BBBD)-Based Immunochemotherapy for Primary Central Nervous System Lymphoma (PCNSL), Early Results of a Phase II Study
title_full_unstemmed Blood–Brain Barrier Disruption (BBBD)-Based Immunochemotherapy for Primary Central Nervous System Lymphoma (PCNSL), Early Results of a Phase II Study
title_short Blood–Brain Barrier Disruption (BBBD)-Based Immunochemotherapy for Primary Central Nervous System Lymphoma (PCNSL), Early Results of a Phase II Study
title_sort blood brain barrier disruption bbbd based immunochemotherapy for primary central nervous system lymphoma pcnsl early results of a phase ii study
topic BBBD
PCNSL
ASCT
url https://www.mdpi.com/2072-6694/15/4/1341
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