Evidence map›Paper›PMID 26968188›Full record

ArticleThe Korean journal of internal medicine2017

Clinicopathologic significance of tumor microenvironment CD11c, and FOXP3 expression in diffuse large B-cell lymphoma patients receiving rituximab, cyclophosphamide, anthracycline, vincristine, and prednisone (R-CHOP) combination chemotherapy.

Seul Lee, Dong Hyun Kim, Sung Yong Oh, So Yeon Kim, Myeong Seok Koh, Ji Hyun Lee, Suee Lee, Sung-Hyun Kim, Jong-Young Kwak, Min Gyoung Pak and 3 more

Open access · goldAbstract read
In one paragraph

Article in The Korean journal of internal medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact, top 99% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Inflammatory Cells in Diffuse Large B Cell Lymphoma.Journal of clinical medicine · 2020
    Review
  9. Article
  10. 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

13 authors at 1 institution in 1 country.

Seul LeeDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Dong Hyun KimDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Sung Yong OhDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
So Yeon KimDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Myeong Seok KohDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Ji Hyun LeeDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Suee LeeDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Sung-Hyun KimDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Jong-Young KwakImmune-Network Pioneer Research Center, Dong-A University College of Medicine, Busan, Korea.
Min Gyoung PakDepartment of Pathology, Dong-A University College of Medicine, Busan, Korea.
Mi Ha JuImmune-Network Pioneer Research Center, Dong-A University College of Medicine, Busan, Korea.
Hyo-Jin KimDepartment of Internal Medicine, Dong-A University College of Medicine, Busan, Korea.
Jin Sook JeongImmune-Network Pioneer Research Center, Dong-A University College of Medicine, Busan, Korea.
Dong-A University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsCD11c is a dendritic cell marker in humans, which potentially induces a cytotoxic effect on lymphoma cells. Forkhead boxP3 (FOXP3) is a regulator of T lymphocyte in the microenvironment of the lymphoma. The principal objective of this study was to determine whether the tumors' microenvironment expressions of CD11c and FOXP3 are predictive of clinical outcomes in diffuse large B-cell lymphoma (DLBCL) patients receiving treatment with rituximab, cyclophosphamide, anthracycline, vincristine, and prednisone (R-CHOP) combination chemotherapy.

methodsThe study population consisted of 100 patients with DLBCL. The CD11c and FOXP3 expression in primary tumors' microenvironment were evaluated using an immunohistochemistry (IHC).

resultsCD11c and FOXP3 expression positivity in microenvironment were 25% and 35%, respectively. Each one counted for 1 point. In CD11c and FOXP3 stain, positive was counted as 0 and negative was 1. The points were separated into low risk (0 to 1) and high risk (2) groups. Only the extranodal DLBCL patient group analysis conveyed significant differences of progression-free survival (

conclusionsWe can achieve possible clinical significance of lymphoma tumor microenvironments through CD11c and FOXP3 IHC stains in extranodal DLBCL patients receiving R-CHOP therapy.

Indexed as

AdolescentAdultAgedAged, 80 and overAntibodies, Monoclonal, Murine-DerivedAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCD11c AntigenCyclophosphamideDoxorubicinFemaleForkhead Transcription FactorsHumansImmunohistochemistryLymphoma, Large B-Cell, DiffuseMaleAntibodies, Monoclonal, Murine-DerivedBiomarkers, TumorCD11c AntigenCyclophosphamideDoxorubicinForkhead Transcription FactorsFOXP3 protein, humanPrednisoneR-CHOP protocolRituximabVincristineCD11cFOXP3Lymphoma, large B-cell, diffuseTumor microenvironment

Identifiers

PMID26968188
PMCPMC5339461
OpenAlexW2295812943

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.