Evidence map›Paper›PMID 25412106›Full record

SynthesisPloS one2014

Adoptive immunotherapy of cytokine-induced killer cell therapy in the treatment of non-small cell lung cancer.

Min Wang, Jun-Xia Cao, Jian-Hong Pan, Yi-Shan Liu, Bei-Lei Xu, Duo Li, Xiao-Yan Zhang, Jun-Li Li, Jin-Long Liu, Hai-Bo Wang and 1 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
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  10. Combination of DC/CIK adoptive T cell immunotherapy with chemotherapy in advanced non-small-cell lung cancer (NSCLC) patients: a prospective patients' preference-based study (PPPS).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
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  19. AFAP1-AS1, a long noncoding RNA upregulated in lung cancer and promotes invasion and metastasis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    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 at 1 institution in 1 country.

Min WangBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Jun-Xia CaoBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Jian-Hong PanDepartment of Biostatistics, Peking University Clinical Research Institute, Peking University Health Science Center, Beijing, China.
Yi-Shan LiuBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Bei-Lei XuBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Duo LiBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Xiao-Yan ZhangBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Jun-Li LiBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Jin-Long LiuBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Hai-Bo WangBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Zheng-Xu WangBiotherapy Center, General Hospital of Beijing Military Command, Beijing, China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe aim of this study was to systemically evaluate the therapeutic efficacy of cytokine-induced killer (CIK) cells for the treatment of non-small cell lung cancer. MATERIALS AND

methodsA computerized search of randomized controlled trials for CIK cell-based therapy was performed. The overall survival, clinical response rate, immunological assessment and side effects were evaluated.

resultsOverall, 17 randomized controlled trials of non-small cell lung cancer (NSCLC) with a total of 1172 patients were included in the present analysis. Our study showed that the CIK cell therapy significantly improved the objective response rate and overall survival compared to the non-CIK cell-treated group. After CIK combined therapy, we observed substantially increased percentages of CD3+, CD4+, CD4+CD8+, CD3+CD56+ and NK cells, whereas significant decreases were noted in the percentage of CD8+ and regulatory T cell (Treg) subgroups. A significant increase in Ag-NORs was observed in the CIK-treated patient group (p = 0.00001), whereas carcinoembryonic antigen (CEA) was more likely to be reduced to a normal level after CIK treatment (p = 0.0008). Of the possible major side effects, only the incidence of fever in the CIK group was significantly higher compared to the group that received chemotherapy alone.

conclusionThe CIK cell combined therapy demonstrated significant superiority in the overall survival, clinical response rate, and T lymphocytes responses and did not present any evidence of major adverse events in patients with NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungCell- and Tissue-Based TherapyCombined Modality TherapyCytokine-Induced Killer CellsHumansImmunotherapy, AdoptiveLung NeoplasmsRandomized Controlled Trials as TopicSurvival AnalysisTreatment Outcome

Identifiers

PMID25412106
PMCPMC4239020
OpenAlexW2078907481

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.