Evidence map›Paper›PMID 42642819›Full record

ArticleJournal of Korean medical science2026

Real-World Outcomes of Tisagenlecleucel Versus Standard-of-Care Salvage Chemotherapy in Relapsed or Refractory Diffuse Large B-Cell Lymphoma: A Propensity Score-Matched Analysis From Korea.

Seonggyu Byeon, Suein Choi, Seungpil Jung, Ka Young Kim, Dae Hun Kwag, Gi-June Min, Jung Yeon Lee, Sung-Soo Park, Silvia Park, Jae-Ho Yoon and 8 more

Abstract read
In one paragraph

Article in Journal of Korean medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Seonggyu Byeon *Catholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-4989-002X
Suein Choi *Pharmacometrics Institute for Practical Education and Training (PIPET), College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0001-5438-7819
Seungpil JungPharmacometrics Institute for Practical Education and Training (PIPET), College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0003-3005-0925
Ka Young KimCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-4126-5916
Dae Hun KwagCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0003-3353-882X
Gi-June MinCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0001-7636-4693
Jung Yeon LeeCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0003-2034-9835
Sung-Soo ParkCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-8826-4136
Silvia ParkCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0003-2845-2933
Jae-Ho YoonCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-2145-9131
Sung-Eun LeeCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-9810-2050
Byung-Sik ChoCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-4524-6616
Yoo-Jin KimCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0001-6653-2956
Chang-Ki MinCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-1940-0392
Hee-Je KimCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0003-4098-3366
Seok-Goo ChoCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.ORCID https://orcid.org/0000-0002-5429-4839
Young-Woo JeonCatholic Hematology Hospital, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea. native47@catholic.ac.kr.ORCID https://orcid.org/0000-0003-3362-8200
Ki-Seong EomCatholic Hematology Hospital, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea. dreom@catholic.ac.kr.ORCID https://orcid.org/0000-0002-0578-126X

Funding

Ministry of Food and Drug Safety RS-2023-00216446
6 · The paper itself

Abstract

backgroundTisagenlecleucel, a CD19-directed chimeric antigen receptor T-cell (CAR-T) therapy, has shown durable efficacy in relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL). However, comparative real-world data against standard-of-care (SOC) therapies remain scarce in Asian populations.

methodsWe performed a retrospective, propensity score-matched cohort study at two tertiary hospitals in Korea. Adult patients with R/R DLBCL treated in the third-line (3L) or later setting received either tisagenlecleucel (CAR-T cohort) or SOC salvage chemoimmunotherapy. Propensity score matching (1:1) was conducted using age, sex, line of therapy, International Prognostic Index, Eastern Cooperative Oncology Group status, and year of diagnosis. Outcomes included response rates, progression-free survival (PFS), overall survival (OS), and safety.

resultsAmong 178 eligible patients (CAR-T, n = 67; SOC, n = 111), 100 were matched (50 per group). The CAR-T cohort achieved a significantly higher overall response rate (68% vs. 28%) and complete response rate (60% vs. 22%). Median PFS was 4.8 months for CAR-T vs. 1.6 months for SOC (hazard ratio [HR], 0.49;

conclusionIn this real-world propensity score-matched comparison from Asia, tisagenlecleucel demonstrated superior survival and response outcomes compared with SOC salvage chemotherapy in Korean patients with R/R DLBCL, supporting its role as the standard of care in the ≥ 3L setting.

Indexed as

Immunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseReceptors, Antigen, T-CellSalvage TherapyAdultAgedFemaleHumansMaleMiddle AgedProgression-Free SurvivalPropensity ScoreRepublic of KoreaRetrospective StudiesStandard of CareTreatment OutcomeReceptors, Antigen, T-CelltisagenlecleucelChimeric Antigen Receptor T-Cell TherapyDiffuse Large B-Cell LymphomaPropensity Score MatchingReal-World EvidenceTisagenlecleucel

Identifiers

PMID42642819
PMCPMC13503052

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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.