Evidence map›Paper›PMID 32020764›Full record

ArticleThoracic cancer2020

Pegylated recombinant human granulocyte colony-stimulating factor regulates the immune status of patients with small cell lung cancer.

Jing Sun, Hua Bai, Zhijie Wang, Jianchun Duan, Jin Li, Ruimin Guo, Jie Wang

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  3. Integration analysis ofBiochemistry and biophysics reports · 2024
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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

7 authors at 3 institutions in 1 country.

Jing SunDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID 0000-0002-4345-0293
Hua BaiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Zhijie WangDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Jianchun DuanDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID 0000-0003-1479-2304
Jin LiDepartment of Research and Development, Geneplus-Beijing, Beijing, China.
Ruimin GuoMedical Department, China Shijiazhuang Pharmaceutical Group Co., Ltd. (CSPC), Shijiazhuang, China.
Jie WangDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNEnvironmental Development Centre · CNShijiazhuang Yiling Pharmaceutical (China) · CN

Funding

Aiyou foundation KY201701CAMS Innovation Fund for Medical Sciences CIFMS 2016-I2M-3-008CAMS Key lab of translational research on lung cancer 2018PT31035China Shijiazhuang Pharmaceutical Group Co., LtdMinistry of Education Innovation Team development project IRT-17R10National Natural Sciences Foundation Key Program 81630071
6 · The paper itself

Abstract

backgroundSmall cell lung cancer (SCLC) is an aggressive disease involving immunodeficiency for which chemotherapy is the standard treatment. Pegylated recombinant human granulocyte colony-stimulating factor (PEG-rhG-CSF) is widely used for primary or secondary prophylaxis of febrile neutropenia (FN) in chemotherapy. However, whether PEG-rhG-CSF influences immune cells, such as lymphocytes, remains unclear.

methodsA total of 17 treatment-naïve SCLC patients were prospectively enrolled and divided into the PEG-rhG-CSF and control groups according to their FN risk. Longitudinal sampling of peripheral blood was performed before, after and 4-6 days after the first cycle of chemotherapy. Flow cytometry was used to assess lymphocyte subsets, including CD3

resultsIn the PEG-rhG-CSF group, the proportions of CD3

conclusionsPEG-rhG-CSF regulates the immune status of SCLC patients; CD4 KEY POINTS: PEG-rhG-CSF regulates SCLC immunity. PEG-rhG-CSF increased CD3

Indexed as

AgedAntineoplastic Combined Chemotherapy ProtocolsCarboplatinCase-Control StudiesCisplatinEtoposideFemaleFollow-Up StudiesGranulocyte Colony-Stimulating FactorHumansLung NeoplasmsLymphocytesMalePolyethylene GlycolsPrognosisProspective StudiesCarboplatinCisplatinEtoposideGranulocyte Colony-Stimulating Factorpegylated granulocyte colony-stimulating factor, humanPolyethylene GlycolsReceptors, Antigen, T-CellRecombinant Proteinsimmune statuslymphocyte subsetspegylated recombinant human granulocyte colony-stimulating factorsmall cell lung cancerT-cell receptor

Identifiers

PMID32020764
PMCPMC7049512
OpenAlexW3005263181

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.