Evidence map›Paper›PMID 40717546›Full record

ArticleBritish journal of haematology2025

CLOX and neurotox: Utility of the clock drawing task in monitoring for immune effector cell-associated neurotoxicity syndrome following chimeric antigen receptor T-cell therapy.

Christina Kazzi, Ty Simpson, Miriam Wronski, Nabil Seery, Robb Wesselingh, Tracie H Tan, Katherine Y Ko, Daniel J Pearce, Cassandra Abbott, Jian Li and 13 more

Abstract read
In one paragraph

Article in British journal of haematology, 2025. 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. Article
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

23 authors.

Christina KazziDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0001-6737-5489
Ty SimpsonMalignant Haematology Transplantation and Cellular Therapy Services, Alfred Hospital, Melbourne, Victoria, Australia.
Miriam WronskiDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Nabil SeeryDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Robb WesselinghDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Tracie H TanDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Katherine Y KoDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Daniel J PearceDepartment of Neurology, Alfred Health, Melbourne, Victoria, Australia.
Cassandra AbbottMalignant Haematology Transplantation and Cellular Therapy Services, Alfred Hospital, Melbourne, Victoria, Australia.
Jian LiMalignant Haematology Transplantation and Cellular Therapy Services, Alfred Hospital, Melbourne, Victoria, Australia.
Sarah P GriffithDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Shu Min WongMalignant Haematology Transplantation and Cellular Therapy Services, Alfred Hospital, Melbourne, Victoria, Australia.
Michael WestworthDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Shafqat InamMalignant Haematology Transplantation and Cellular Therapy Services, Alfred Hospital, Melbourne, Victoria, Australia.
Constantine S TamMalignant Haematology Transplantation and Cellular Therapy Services, Alfred Hospital, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-9759-5017
Shaun FlemingMalignant Haematology Transplantation and Cellular Therapy Services, Alfred Hospital, Melbourne, Victoria, Australia.
Anneke Van Der WaltDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Terence J O'BrienDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Rubina AlpitsisDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Andrew SpencerMalignant Haematology Transplantation and Cellular Therapy Services, Alfred Hospital, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-0531-7424
Charles B MalpasDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Paul SanfilippoDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.
Mastura MonifDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.

Funding

Australian Government Department of Education Research and Training Program
6 · The paper itself

Abstract

Immune effector cell-associated neurotoxicity syndrome (ICANS)-associated cognitive impairment is common in patients who receive chimeric antigen receptor T-cell (CAR-T) therapy. This study evaluated the utility of the clock drawing task (CDT) in detecting ICANS in patients with haematological cancers following CAR-T therapy. Data were collected from CAR-T patients at The Alfred Hospital, Melbourne, Australia. Patients underwent frequent assessments using the immune effector cell-associated encephalopathy (ICE) score and the CDT, scored using a modified CLOX (CLOX-M) rating scale, during their admission. We retrospectively reviewed the medical records of consecutive patients who received CAR-T therapy between September 2022 and February 2024 to assess for ICANS and changes in ICE score and CLOX-M. A total of 1208 clock drawings were time matched within an hour of an ICE score for 54 patients (39% female, 64.36 ± 13.25 years). Fourteen (26%) patients developed ICANS. Change in CLOX-M scores from baseline and ICE scores was significantly correlated (ρ = 0.34, p < 0.001). Receiver operating characteristic (ROC) analysis demonstrated that the CLOX-M score has moderate discriminatory power (Area Under the Curve [AUC] = 0.737). A decrease in CLOX-M score of 2 or more had high specificity (0.994) but low sensitivity (0.263) for detecting ICANS. The CDT can be used to complement the ICE score to improve ICANS monitoring.

Indexed as

Hematologic NeoplasmsImmunotherapy, AdoptiveNeurotoxicity SyndromesAdultAgedFemaleHumansMaleMiddle AgedReceptors, Chimeric AntigenRetrospective Studiescell-associated neurotoxicityReceptors, Chimeric Antigenchimeric antigen receptor T‐cell (CAR‐T) therapycognitionICANSimmune effector cell‐associated neurotoxicity syndromeneurotoxicity

Identifiers

PMID40717546
PMCPMC12512059

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.