Evidence map›Paper›PMID 31209436›Full record

ArticleBeijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences2019

[Efficacy and peripheral immunity analysis of allogeneic natural killer cells therapy in patients with hepatocellular carcinoma].

Y B Xie, J Y Zhang, M L DU, F P Meng, J L Fu, L M Liu, S S Wang, R Qu, F Lian, F Qiao and 5 more

Open access · greenAbstract read
In one paragraph

Article in Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 52% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. [Advances in the study of cellular immunotherapy for liver cancer].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2020
    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

15 authors at 1 institution in 1 country.

Y B XieInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
J Y ZhangInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
M L DUInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
F P MengInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
J L FuInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
L M LiuInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
S S WangInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
R QuInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
F LianInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
F QiaoInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
Y L ChenInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
Y Y GaoInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
R N XuInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
M ShiInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
F S WangInstitute of Infectious Diseases, the Fifth Medical Center of PLA General Hospital, Beijing 100039, China.
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the safety and efficacy of allogeneic natural killer (NK) cells in the treatment of primary hepatocellular carcinoma (HCC), and to elucidate the mechanism of NK cells therapy.

methodsTwenty-one patients with primary HCC treated with allogeneic NK cells at the Fifth Medical Center of the PLA General Hospital were followed up for 1 year. Peripheral blood mononuclear cells (PBMCs) were isolated from patient-related donors and cultured in vitro for 15 days and infused to the patients in two consecutive days. Clinical data and laboratory data were collected and analyzed, including survival, clinical features, imaging changes, hematology, immunology, and biochemical indicators to evaluate the safety and efficacy of allogeneic NK cell therapy. The changes of peripheral blood lymphocyte subsets after treatment were also analyzed to explore the possible anti-tumor mechanisms.

results(1) Of the 21 patients with primary HCC, 11 patients were treated once, 5 patients were treated twice, and 5 patients were treated 3 times. After allogeneic NK cells infusion, 10 patients had fever, 1 patient had slight hepatalgia and 1 patient had slight headache, no other adverse events occurred including acute and chronic graft-versus-host disease (GVHD). They resolved spontaneously within 8 hours without other treatment. (2) The total disease control rate was 76.2% during one-year follow-up. Among them, the patients with Barcelona clinic liver cancer (BCLC) stage A had a disease control rate of 100%, stable disease (SD) in 10 cases; BCLC stage B patients had a disease control rate of 60%, partial response (PR) in 1 case, and SD 2 in cases; BCLC stage C patients had a disease control rate of 50%, complete response (CR) in 1 case, and 2 cases of PR. (3) The frequencies of NK cells and CD8+ T cells in peripheral blood were significantly lower than that before at 24 hours after treatment, and the frequencies of CD4+ T cells and CD4/CD8 were significantly higher than the baseline.

conclusionAllogeneic NK cells have good safety and efficacy in the treatment of primary HCC. The anti-tumor effect of the allogeneic NK cells may play an important role in the activation of the patient's natural immune system and delay disease progression, suggesting that allogeneic NK cells combined with sorafenib may be a very effective treatment for advanced HCC, and further large-sample multicenter randomized controlled clinical trials are needed to validate this result.

Indexed as

Carcinoma, HepatocellularGraft vs Host DiseaseLiver NeoplasmsHumansKiller Cells, NaturalLeukocytes, Mononuclear

Identifiers

PMID31209436
PMCPMC7439043
OpenAlexW2988135179

What OpenQuestion holds

Textmetadata
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.