Evidence map›Paper›PMID 25968637›Full record

ArticleJournal of translational medicine2015

Cellular immunotherapy as maintenance therapy prolongs the survival of the patients with small cell lung cancer.

Xiao Ding, He Cao, Xiao Chen, Haofan Jin, Ziling Liu, Guanjun Wang, Lu Cai, Dan Li, Chao Niu, Huimin Tian and 4 more

Open access · goldAbstract readClinical Study
In one paragraph

Article in Journal of translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Non-histone lactylation: unveiling its functional significance.Frontiers in cell and developmental biology · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Advances and challenges in immunotherapy of small cell lung cancer.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2020
    Article
  10. Role of natural killer cells in lung cancer.Journal of cancer research and clinical oncology · 2018
    Review
  11. Review
  12. Article
  13. Cancer stem cells in small cell lung cancer.Translational lung cancer research · 2016
    Review
  14. Article
  15. [Research Progression of Maintenance Therapy in Small Cell Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2015
    Review
  16. Review
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

14 authors at 3 institutions in 2 countries.

Xiao DingCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. dingxiao70070135@sina.com.
He CaoCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. caohe2014@sina.com.
Xiao ChenCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. chenxiaojdyy2014@sina.com.
Haofan JinCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. jinhaofan2014@sina.com.
Ziling LiuCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. liuziling2014@sina.com.
Guanjun WangCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. wangguanjun2014@sina.com.
Lu CaiKosair Children's Hospital Research Institute, Department of Pediatrics, the University of Louisville, Louisville, KY, 40202, USA. cailu2014@sina.com.
Dan LiCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. lidanjdyy2014@sina.com.
Chao NiuCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. niuchao2014@sina.com.
Huimin TianCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. tianhuimin2014@sina.com.
Lei YangCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. yangleijdyy2014@sina.com.
Yuguang ZhaoCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. zhaoyuguang2014@sina.com.
Wei LiCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. drweili@yahoo.com.
Jiuwei CuiCancer Center, the First Hospital of Jilin University, No. 71. Xinmin Street, Changchun, 130021, China. cuijiuwei@yahoo.com.
Jilin University · CNFirst Hospital of Jilin University · CNUniversity of Louisville · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSmall cell lung cancer (SCLC) relapses rapidly after the initial response to chemotherapy and shows drug-resistance. This study was to investigate the efficacy and safety of cellular immunotherapy (CIT) with autologous natural killer (NK), γδT, and cytokine-induced killer (CIK) cells as maintenance therapy for SCLC patients.

methodsA pilot prospective cohort study was conducted with SCLC patients who had responded to initial chemotherapy. Patients elected to receive either CIT as maintenance therapy (study group), or to be followed-up without further treatment (control group). Progression-free survival (PFS), overall survival (OS), and adverse effects were investigated.

resultsWe recruited 58 patients (29 in each group). The patient characteristics of the 2 groups were well balanced. PFS was not significantly different between the groups, but OS was significantly longer in the study group than the control (20 vs. 11.5 months, P = 0.005; hazard ratio [HR], 0.434, 95 % confidence interval [CI], 0.236-0.797, P = 0.007). Among patients with limited-stage disease, there was no difference in PFS between the groups, but OS was longer in the study group compared to the control (26.5 vs. 11.8 months, P = 0.033; HR, 0.405, 95 % CI, 0.169-0.972, P = 0.043). Among patients with extensive-stage disease, both PFS and OS were longer in the study group than the control (5 vs. 2.7 months, P = 0.037; HR, 0.403, 95 % CI, 0.162-1.003, P = 0.051, and 14.5 vs. 9 months, P = 0.038; HR, 0.403, 95 % CI, 0.165-0.987, P = 0.047, respectively). No significant adverse reactions occurred in patients undergoing CIT.

conclusionsCIT maintenance therapy in SCLC prolonged survival with only minimal side effects. Integrating CIT into current treatment may be a novel strategy for SCLC therapy, although further multi-center randomized studies are needed.

Indexed as

AdultAgedAged, 80 and overCytokine-Induced Killer CellsCytokinesDisease-Free SurvivalDisease ProgressionFemaleHumansImmunotherapyKiller Cells, NaturalLung NeoplasmsMaleMiddle AgedNeoplasm Recurrence, LocalPhenotypeCytokines

Identifiers

PMID25968637
PMCPMC4446113
OpenAlexW1518703914

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.