Evidence map›Paper›PMID 40940718›Full record

ReviewCells2025

Impact of Novel Agents on Allogeneic Hematopoietic Cell Transplantation in Patients with T-Cell Lymphomas.

Yoshitaka Inoue, Jun-Ichirou Yasunaga

Abstract readReview
In one paragraph

Review in Cells, 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. Review
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

2 authors.

Yoshitaka InoueBlood and Marrow Transplant Program, Division of Hematology and Oncology, Penn State Cancer Institute, Hershey, PA 17033, USA.ORCID 0000-0002-3967-7356
Jun-Ichirou YasunagaDepartment of Hematology, Kumamoto University, Kumamoto 860-8556, Japan.ORCID 0000-0002-7939-2080

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell lymphomas (TCLs) are generally associated with a poorer prognosis compared to B-cell lymphomas, and allogeneic hematopoietic cell transplantation (allo-HCT) is often considered for eligible patients. One of the primary reasons for the inferior outcomes in TCLs has been the lack of effective novel agents for many years, resulting in a continued reliance on traditional cytotoxic chemotherapy regimens. However, over the past decade, several novel agents with promising efficacy against TCLs have been developed. Notably, many of these agents not only exert direct anti-tumor effects but also modulate host immune function, raising clinical questions regarding the optimal integration of these agents with allo-HCT. In this review, we aim to summarize how the use of novel agents that are approved for the treatment of TCLs-such as mogamulizumab, brentuximab vedotin, lenalidomide, histone deacetylase inhibitors, enhancer of zeste homolog inhibitors, and immune checkpoint inhibitors-before or after allo-HCT may impact transplantation outcomes in patients with TCLs.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, T-CellAnimalsAntibodies, Monoclonal, HumanizedAntineoplastic AgentsBrentuximab VedotinHistone Deacetylase InhibitorsHumansImmune Checkpoint InhibitorsLenalidomideTransplantation, HomologousAntibodies, Monoclonal, HumanizedAntineoplastic AgentsBrentuximab VedotinHistone Deacetylase InhibitorsImmune Checkpoint InhibitorsLenalidomidemogamulizumaballogeneic hematopoietic cell transplantationbrentuximab vedotinenhancer of zeste homolog 1/2 (EZH1/2) inhibitorshistone deacetylase inhibitors (HDACis)lenalidomidemogamulizumabnovel agentsT-cell lymphomas

Identifiers

PMID40940718
PMCPMC12428570

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Registered trials

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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.