Evidence map›Paper›PMID 36831682›Full record

ArticleCancers2023

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

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 and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 1 country.

Hanne K KuitunenCancer Center, Oulu University Hospital, 90220 Oulu, Finland.
Aino L K RönkäDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, Finland.ORCID 0000-0001-6007-3648
Eila M SonkajärviSurgery and Anaesthesia Center, Oulu University Hospital, 90220 Oulu, Finland.
Juha-Matti IsokangasService for Medical Care, Oulu University Hospital Diagnostics, 90220 Oulu, Finland.
Marja PyöräläDepartment of Medicine, Kuopio University Hospital, 70210 Kuopio, Finland.
Kari A A PalosaariService for Medical Care, Oulu University Hospital Diagnostics, 90220 Oulu, Finland.
Anna S JokimäkiCancer Center, Oulu University Hospital, 90220 Oulu, Finland.
Anu E PartanenDepartment of Medicine, Kuopio University Hospital, 70210 Kuopio, Finland.ORCID 0000-0002-5634-2582
Harri J LittowService for Medical Care, Oulu University Hospital Diagnostics, 90220 Oulu, Finland.
Merja A VakkalaSurgery and Anaesthesia Center, Oulu University Hospital, 90220 Oulu, Finland.
Esa J JantunenDepartment of Medicine, Kuopio University Hospital, 70210 Kuopio, Finland.
Mirja E HuttunenSurgery and Anaesthesia Center, Oulu University Hospital, 90220 Oulu, Finland.
Katja J MarinDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, Finland.
Annikki M K Aromaa-HäyhäDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, Finland.
Päivi K AuvinenDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, Finland.
Tuomas SelanderScience Service Center, Kuopio University Hospital, 70210 Kuopio, Finland.
Inka K PuhakkaDepartment of Neurology, Kuopio University Hospital, 70210 Kuopio, Finland.
Outi M KuittinenDepartment of Oncology and Radiotherapy, Kuopio University Hospital, 70210 Kuopio, Finland.
Kuopio University Hospital · FIOulu University Hospital · FIUniversity of Eastern Finland · FI

Funding

Pohjois-Suomen terveydenhuollon tukisäätiö
6 · The paper itself

Abstract

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.

Indexed as

ASCTBBBDPCNSL

Identifiers

PMID36831682
PMCPMC9953868
OpenAlexW4321372481

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.