Evidence map›Paper›PMID 31261712›Full record

ArticleInternational journal of molecular sciences2019

Phase I Clinical Trial Using Autologous Ex Vivo Expanded NK Cells and Cytotoxic T Lymphocytes for Cancer Treatment in Vietnam.

Nguyen Thanh Liem, Nguyen Van Phong, Nguyen Trung Kien, Bui Viet Anh, Truong Linh Huyen, Chu Thi Thao, Nguyen Dac Tu, Doan Trung Hiep, Do Thi Hoai Thu, Hoang Thi My Nhung

Open access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Reprogramming natural killer cells for cancer therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Advances in NK cell production.Cellular & molecular immunology · 2022
    Review
  12. Review
  13. Article
  14. Article
  15. 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

10 authors at 2 institutions in 1 country.

Nguyen Thanh LiemVinmec Research Institute of Stem Cell and Gene Technology, 458 Minh Khai, Hanoi 100000, Vietnam. v.liemnt@vinmec.com.
Nguyen Van PhongVinmec Research Institute of Stem Cell and Gene Technology, 458 Minh Khai, Hanoi 100000, Vietnam.
Nguyen Trung KienVinmec Research Institute of Stem Cell and Gene Technology, 458 Minh Khai, Hanoi 100000, Vietnam.ORCID 0000-0002-6654-8015
Bui Viet AnhVinmec Research Institute of Stem Cell and Gene Technology, 458 Minh Khai, Hanoi 100000, Vietnam.
Truong Linh HuyenVinmec Research Institute of Stem Cell and Gene Technology, 458 Minh Khai, Hanoi 100000, Vietnam.
Chu Thi ThaoVinmec Research Institute of Stem Cell and Gene Technology, 458 Minh Khai, Hanoi 100000, Vietnam.
Nguyen Dac TuVinmec Research Institute of Stem Cell and Gene Technology, 458 Minh Khai, Hanoi 100000, Vietnam.
Doan Trung HiepVinmec Research Institute of Stem Cell and Gene Technology, 458 Minh Khai, Hanoi 100000, Vietnam.
Do Thi Hoai ThuFaculty of Biology, VNU University of Science, 334 Nguyen Trai, Hanoi 100000, Vietnam.
Hoang Thi My NhungVinmec Research Institute of Stem Cell and Gene Technology, 458 Minh Khai, Hanoi 100000, Vietnam. v.nhunghtm@vinmec.com.ORCID 0000-0003-1717-1570
Vinmec International Hospital · VNVNU University of Science · VN

Funding

Vingroup 001
6 · The paper itself

Abstract

(1) Background: Immune cell therapy recently attracted enormous attention among scientists as a cancer treatment, but, so far, it has been poorly studied and applied in Vietnam. The aim of this study was to assess the safety of autologous immune cell therapy for treating lung, liver, and colon cancers-three prevalent cancers in Vietnam. (2) Method: This was an open-label, single-group clinical trial that included 10 patients with confirmed diagnosis of colon, liver, or lung cancer, conducted between March 2016 and December 2017. (3) Results: After 20-21 days of culture, the average number of cytotoxic T lymphocytes (CTLs) increased 488.5-fold and the average cell viability was 96.3%. The average number of natural killer cells (NKs) increased 542.5-fold, with an average viability of 95%. Most patients exhibited improved quality of life, with the majority of patients presenting a score of 1 to 2 in the Eastern Cooperative Oncology Group (ECOG) performance status (ECOG/PS) scale, a decrease in symptoms on fatigue scales, and an increase in the mean survival time to 18.7 months at the end of the study. (4) Conclusion: This method of immune cell expansion met the requirements for clinical applications in cancer treatment and demonstrated the safety of this therapy for the cancer patients in Vietnam.

Indexed as

AdultAgedAged, 80 and overBlood Transfusion, AutologousCells, CulturedColonic NeoplasmsFemaleHumansImmunotherapyKiller Cells, NaturalLiver NeoplasmsLung NeoplasmsMaleMiddle AgedT-Lymphocytes, Cytotoxiccancercytotoxic T lymphocytesimmune cell therapynatural killer cellsperipheral blood mononuclear cells

Identifiers

PMID31261712
PMCPMC6651639
OpenAlexW2955397772

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.