Evidence map›Paper›PMID 39951161›Full record

ReviewDiscover oncology2025

Improving access to chimeric antigen receptor T-cells for refractory or relapsing diffuse large B cell lymphoma therapy in Asia.

Ya Hwee Tan, Dok Hyun Yoon, Andrew J Davies, Christian Buske, Yang Liang Boo, Nagavalli Somasundaram, Francesca Lim, Shin Yeu Ong, Anand Jeyasekharan, Koji Izutsu and 2 more

Abstract readReview
In one paragraph

Review in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Ya Hwee TanDivision of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
Dok Hyun YoonDepartment of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Andrew J DaviesSchool of Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Christian BuskeInstitute of Experimental Cancer Research, University Hospital of Ulm, Ulm, Germany.
Yang Liang BooDepartment of Hematology, Hospital Sultanah Aminah, Johor Bahru, Malaysia.
Nagavalli SomasundaramDivision of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
Francesca LimDuke-NUS Medical School, National Cancer Centre Singapore, Singapore, Singapore.
Shin Yeu OngDepartment of Haematology, Singapore General Hospital, Singapore, Singapore.
Anand JeyasekharanDepartment of Haematology-Oncology, National University Cancer Institute, Singapore, Singapore.
Koji IzutsuDepartment of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Won Seog KimSamsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Jason Yongsheng ChanDivision of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore. jason.chan.y.s@singhealth.com.sg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T-cell (CAR-T)-mediated therapies have shown promising clinical benefit in patients with refractory or relapsing (R/R) diffuse large B-cell lymphoma (DLBCL). However, CAR-T treatment presents challenges such as lack of drug accessibility, financial barriers, variable physician preference or experience, and risk assessment based on patient-specific characteristics. This article thus aims to provide an overview of the CAR-T landscape for R/R DLBCL in Asia, with a focus on identifying barriers to access, from the perspective of Asian and international lymphoma experts. Presently, existing clinical data indicate that CAR-T therapy is a potentially curative strategy for R/R DLBCL in addition to stem cell transplantation, provided the patient's disease profile and treatment history have been thoroughly considered. However, longer-term follow-up data from large-scale studies are needed to confirm curative potential and define optimal sequencing of CAR-T in the context of novel emerging treatments, such as bi-specific antibodies, in the management of R/R DLBCL. Consequently, further research into CAR-T would benefit from collaboration between institutions. Furthermore, there is a wide disparity in CAR-T accessibility across regions due to complicated logistics and cost, which represent a significant barrier to patients in Asia. Hence, there is a need to increase representation and engagement across different stakeholders such as policymakers, payers, and the industry to arrive at a consensus on patient selection, establish clear guidelines, and develop strategies to lower CAR-T costs. Ultimately, data can support a multi-stakeholder approach when devising strategies to make CAR-T feasible and sustainable for patients.

Indexed as

CAR-TDiffuse large B-cell lymphomaImmunotherapyLymphomaNovel therapy

Identifiers

PMID39951161
PMCPMC11828776

What Socratic 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 Socratic graph.