Evidence map›Paper›PMID 34466000›Full record

ArticleOncoTargets and therapy2021

Potential Role of Pleural Fluid Cytokine Profile in Myelomatous Pleural Effusions.

Junhui Xu, Liang Gao, Miao Yan, Bingjie Wang, Zhengyang Song, Huihui Liu, Kunyan Sun, Lin Nong, Mangju Wang, Xinan Cen

Open access · goldAbstract readCase Reports
In one paragraph

Article in OncoTargets and therapy, 2021. 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
0.1field-weighted citation impact, top 48% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

10 authors at 1 institution in 1 country.

Junhui Xu *Department of Hematology, Peking University First Hospital, Beijing, People's Republic of China.
Liang Gao *Department of Hematology, Peking University First Hospital, Beijing, People's Republic of China.
Miao YanDepartment of Hematology, Peking University First Hospital, Beijing, People's Republic of China.
Bingjie WangDepartment of Hematology, Peking University First Hospital, Beijing, People's Republic of China.
Zhengyang SongDepartment of Hematology, Peking University First Hospital, Beijing, People's Republic of China.ORCID 0000-0002-8014-7103
Huihui LiuDepartment of Hematology, Peking University First Hospital, Beijing, People's Republic of China.
Kunyan SunDepartment of Respiration, Peking University First Hospital, Beijing, People's Republic of China.
Lin NongDepartment of Pathology, Peking University First Hospital, Beijing, People's Republic of China.ORCID 0000-0002-1331-2420
Mangju WangDepartment of Hematology, Peking University First Hospital, Beijing, People's Republic of China.
Xinan CenDepartment of Hematology, Peking University First Hospital, Beijing, People's Republic of China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyelomatous pleural effusion (MPE), as a presentation of extramedullary infiltration of multiple myeloma (MM), is rare and currently associated with poor outcomes without effective therapy. The potential value of cytokine detection in pleural effusion to MPE has not been reported to date. CASE PRESENTATION: We herein report a case of refractory and relapsed multiple myeloma that developed bilateral MPE due to disease progression caused by intolerance to various chemotherapy regimens. Cytomorphology and flow cytometry were adopted for diagnosis confirmation. Chemotherapy containing immunomodulators combined with thoracic catheterization drainage was applied to the patient, showing a certain therapeutic effect. During the course of disease, the change of cytokine profile in pleural effusion was monitored by cytometric bead array (CBA) technology, revealing that cytokines related to tumor load such as interleukin 6 (IL-6) and interleukin 10 (IL-10) in pleural effusion decreased with the improvement of disease, while other cytokines such as interleukin 2 (IL-2), interleukin 4 (IL-4), interleukin 17A (IL-17A), tumor necrosis factor α (TNF-α), interferon γ (IFN-γ), granzyme A, granzyme B, perforin and granulysin increased with the improvement of disease.

conclusionThere is a prospect that cytokine level in pleural effusion may indicate treatment response of MPE, and in light of this case, immunomodulators may be utilized in treating patients suffering MPE. Due to limitations of our single case, we urge more groups to evaluate the potential role of cytokine profile in MPE.

Indexed as

cytokineIFN-γIL-2immunomodulatormyelomatous pleural effusions

Identifiers

PMID34466000
PMCPMC8403078
OpenAlexW3195160877

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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.