Evidence map›Paper›PMID 41968224›Full record

ArticleInternational journal of clinical oncology2026

Real-world outcomes of chimeric antigen receptor T-cell therapy with pembrolizumab as holding and/or bridging therapy in relapsed/refractory primary mediastinal large B-cell lymphoma.

Risa Nishiyama, Shinichi Makita, Anna Hiratsuka, Akiko Miyagi Maeshima, Kimiteru Ito, Yu Aruga, Chiaki Ikeda, Hirotaka Matsui, Wataru Takeda, Mai Takeuchi and 5 more

Abstract read
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Article in International journal of clinical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

15 authors.

Risa NishiyamaDepartment of Hematology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Shinichi MakitaDepartment of Hematology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan. smakita@ncc.go.jp.ORCID http://orcid.org/0000-0001-6609-8088
Anna HiratsukaDepartment of Hematology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Akiko Miyagi MaeshimaDepartment of Pathology, National Cancer Center Hospital, Tokyo, Japan.
Kimiteru ItoDepartment of Diagnostic Radiology, National Cancer Center Hospital, Tokyo, Japan.
Yu ArugaDepartment of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.
Chiaki IkedaDepartment of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.
Hirotaka MatsuiDepartment of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.
Wataru TakedaDepartment of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Mai TakeuchiDepartment of Pathology, National Cancer Center Hospital, Tokyo, Japan.
Tetsuro OchiDepartment of Hematology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Noriko IwakiDepartment of Hematology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Suguru FukuharaDepartment of Hematology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Wataru MunakataDepartment of Hematology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.
Koji IzutsuDepartment of Hematology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-Ku, Tokyo, 104-0045, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClinical data on chimeric antigen receptor (CAR) T-cell therapy in Japanese patients with relapsed/refractory primary mediastinal large B-cell lymphoma (R/R PMBCL) are limited. This study evaluated the safety and long-term outcomes of CAR T-cell therapy in R/R PMBCL, including the impact of pembrolizumab used as holding (pre-apheresis) and/or bridging (post-apheresis) therapy.

methodsWe retrospectively analyzed patients with R/R PMBCL receiving axicabtagene ciloleucel or lisocabtagene maraleucel at our institution between October 2021 and October 2025. Treatment efficacy and survival outcomes were compared with those of patients with other large B-cell lymphoma (LBCL) treated with CAR T-cell therapy. Pembrolizumab administration as holding and/or bridging therapy was also assessed.

resultsTwelve patients with PMBCL received CAR T-cell therapy, with a median follow-up of 24 months. The overall and complete response rates were both 92%. The 2-year progression-free survival (PFS) and overall survival rates were also 92%. Cytokine release syndrome was limited to grade 2, and immune effector cell-associated neurotoxicity syndrome occurred in one patient. Ten patients received pembrolizumab, which was associated with reduced metabolic tumor volume from leukapheresis to CAR T-cell infusion and manageable immune-related adverse events. Compared with other LBCL, PMBCL demonstrated favorable outcomes, with a 1-year PFS of 92% versus 65% in other LBCL (hazard ratio, 5.25; 95% confidence interval, 0.720-38.21; p = 0.067).

conclusionsCAR T-cell therapy demonstrated durable responses and a manageable safety profile in R/R PMBCL, including in patients receiving pembrolizumab as holding and/or bridging therapy, supporting its use as a promising treatment option.

Indexed as

Antibodies, Monoclonal, HumanizedImmunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseMediastinal NeoplasmsAdultAgedBiological ProductsBridge TherapyFemaleHumansMaleMiddle AgedNeoplasm Recurrence, LocalReceptors, Chimeric AntigenRetrospective StudiesTreatment OutcomeAntibodies, Monoclonal, Humanizedaxicabtagene ciloleucelBiological ProductspembrolizumabReceptors, Chimeric AntigenCAR T-cell therapyPembrolizumabPrimary mediastinal large B-cell lymphoma

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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.