Evidence map›Paper›PMID 39428323›Full record

ArticleCancer science2025

Spheroid culture to select theoretical therapeutic drugs in intravascular large B-cell lymphoma.

Mika Takai, Kazuyuki Shimada, Katsuya Furukawa, Yusuke Yamaga, Soichi Yoshiyama, Yusuke Kagaya, Takashi Suzuki, Kazuhiko Hayashi, Satoko Shimada, Kennosuke Karube and 1 more

Abstract read
In one paragraph

Article in Cancer science, 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. Review
  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

11 authors.

Mika TakaiDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Kazuyuki ShimadaDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.ORCID https://orcid.org/0000-0002-1075-9219
Katsuya FurukawaDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Yusuke YamagaDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Soichi YoshiyamaDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Yusuke KagayaDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Takashi SuzukiDepartment of Research Management, Tokushima Research Center for Drug Discovery, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Kazuhiko HayashiDepartment of Research Management, Tokushima Research Center for Drug Discovery, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Satoko ShimadaDepartment of Pathology and Clinical Laboratories, Nagoya University Hospital, Nagoya, Aichi, Japan.
Kennosuke KarubeDepartment of Pathology and Clinical Laboratories, Nagoya University Hospital, Nagoya, Aichi, Japan.
Hitoshi KiyoiDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.ORCID https://orcid.org/0000-0001-6382-9498

Funding

Japan Society for the Promotion of Science 14443918Japan Society for the Promotion of Science 17K09922Japan Society for the Promotion of Science 20K08751
6 · The paper itself

Abstract

Intravascular large B-cell lymphoma (IVLBCL) is a rare type of extranodal large B-cell lymphoma that is characterized by the proliferation of lymphoma cells in the lumina of small vessels. Recent progress uncovering the genetic characteristics associated with MYD88/CD79B mutations has stimulated interest in the use of drugs targeting B-cell receptor signaling, including Bruton's tyrosine kinase. However, difficulties in culturing ex vivo IVLBCL cells has hampered research on the development of novel therapies. In the present study, we demonstrated the establishment of an ex vivo culture system of IVLBCL cells obtained from patient-derived xenograft (PDX) models. The spheroid culture enabled us to culture IVLBCL PDX cells for more than 10 days and to explore the efficacy of drug treatments acting on these cells. We found that carfilzomib and ibrutinib were effective for treating IVLBCL in ex vivo experiments and conducted in vivo analyses to assess the efficacy of these drugs. Although the efficacy of carfilzomib was difficult to confirm due to its toxicity in our models, ibrutinib showed comparable efficacy to a standard combination of chemotherapy drugs. Together, our data provide a new culture method for IVLBCL PDX cells and a rationale for translating ibrutinib to clinical use in IVLBCL patients.

Indexed as

AdenineLymphoma, Large B-Cell, DiffusePiperidinesSpheroids, CellularXenograft Model Antitumor AssaysAgammaglobulinaemia Tyrosine KinaseAnimalsAntineoplastic AgentsCD79 AntigensHumansMiceMice, Inbred NODMyeloid Differentiation Factor 88OligopeptidesPyrazolesPyrimidinesAdenineAgammaglobulinaemia Tyrosine KinaseAntineoplastic AgentsCD79 AntigensibrutinibMyeloid Differentiation Factor 88OligopeptidesPiperidinesPyrazolesPyrimidinesBruton's tyrosine kinaseex vivo cultureintravascular large B‐cell lymphomapatient‐derived xenograft modelspheroid culture

Identifiers

PMID39428323
PMCPMC11711046

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.