Evidence map›Paper›PMID 40575412›Full record

ArticleNeuro-oncology advances

Refinement of primary central nervous system lymphoma prognostication and response assessment using 3-dimensional MRI.

Jack O'Shaughnessy, Arina Martynchyk, Sze Ting Lee, Geoff Chong, Shivam Agrawal, Maciej Tatarczuch, Nariza Alysa Azryn, Gareth P Gregory, Leonid Churilov, Michael Wang and 2 more

Abstract read
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Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Observational
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

12 authors.

Jack O'ShaughnessyOlivia Newton John Cancer Research Institute at Austin Health, Australia.
Arina MartynchykOlivia Newton John Cancer Research Institute at Austin Health, Australia.ORCID https://orcid.org/0009-0009-3094-8867
Sze Ting LeeAustin Health, Molecular Imaging and therapy, Melbourne, Australia.ORCID https://orcid.org/0000-0001-8641-456X
Geoff ChongUniversity of Melbourne, Australia.ORCID https://orcid.org/0000-0003-4006-2380
Shivam AgrawalOlivia Newton John Cancer Research Institute at Austin Health, Australia.
Maciej TatarczuchSchool of Clinical Sciences at Monash Health, Faculty of Medicine, Nursing & Health Sciences, Monash University, Australia.ORCID https://orcid.org/0000-0002-5335-4481
Nariza Alysa AzrynAustin Health, Molecular Imaging and therapy, Melbourne, Australia.
Gareth P GregorySchool of Clinical Sciences at Monash Health, Faculty of Medicine, Nursing & Health Sciences, Monash University, Australia.ORCID https://orcid.org/0000-0002-4170-0682
Leonid ChurilovUniversity of Melbourne, Australia.ORCID https://orcid.org/0000-0002-9807-6606
Michael WangAustin Health, Molecular Imaging and therapy, Melbourne, Australia.
Colm KeaneFrazer Institute, University of Queensland, Australia.ORCID https://orcid.org/0000-0002-9009-9934
Eliza A HawkesSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.ORCID https://orcid.org/0000-0002-0376-2559

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Primary central nervous system lymphoma (PCNSL) is an aggressive lymphoma restricted to the CNS in which outcomes cannot be reliably predicted. The International PCNSL Collaborative Group developed standardized response assessment utilizing 2-dimensional (2D) Magnetic Resonance Imaging (MRI) tumor measurements. Considerable challenges of this approach exist due to many reasons. Recent glioblastoma and PCNSL data demonstrated that radiological assessment of baseline 3-dimensional volume (3DV) as well as 3DV reduction (3DVR) may be a sensitive prognostic parameter. Methods: Our multicentre retrospective study evaluated semiautomated 3DV in 74 PNCSL patients undergoing curative-intent chemoimmunotherapy. Results: Baseline tumor 3DV was not associated with survival. Compared to 3DVR < 58% (ROC-determined threshold based on our cohort), both interim and End-of-Treatment (EOT) 3DVR ≥ 58% in responding patients were associated with statistically significant prolonged 2-year progression-free survival (PFS) (interim: 73% (95%CI 57-83) versus 22% (95%CI 3-51), Conclusion: Although PCNSL tumor 3DV at baseline is not associated with survival outcomes, 3DVR of ≥58% in interim and EOT confers superior PFS and OS. Whereas, no difference in survival was observed using standard 2D CR versus PR response assessment at the same time-points. 3DV calculations may offer a sensitive method of response assessment for PCNSL. We are currently validating this in clinical trials.

Indexed as

3-dimensional tumor volumelymphomaMRIPCNSLprimary central nervous system lymphoma

Identifiers

PMID40575412
PMCPMC12202003

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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.