Evidence map›Paper›PMID 40056167›Full record

ArticleCancer immunology, immunotherapy : CII2025

Combination therapy with expanded natural killer cells and atezolizumab exerts potent antitumor immunity in small cell lung cancer.

Manh-Cuong Vo, Van-Tan Nguyen, Van-Dinh-Huan Tran, Hyung-Joo Oh, Sung-Hoon Jung, Woo Kyun Bae, Je-Jung Lee, In-Jae Oh

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2025. 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
–field-weighted citation impact
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. 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

8 authors.

Manh-Cuong VoInstitute of Research and Development, Duy Tan University, Danang, Vietnam.
Van-Tan NguyenDepartment of Internal Medicine, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, 322 Seoyang-Ro, Hwasun-Eup, Hwasun-gun, Jeollanam-do, 58128, Republic of Korea.
Van-Dinh-Huan TranDepartment of Internal Medicine, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, 322 Seoyang-Ro, Hwasun-Eup, Hwasun-gun, Jeollanam-do, 58128, Republic of Korea.
Hyung-Joo OhDepartment of Internal Medicine, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, 322 Seoyang-Ro, Hwasun-Eup, Hwasun-gun, Jeollanam-do, 58128, Republic of Korea.
Sung-Hoon JungDepartment of Internal Medicine, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, 322 Seoyang-Ro, Hwasun-Eup, Hwasun-gun, Jeollanam-do, 58128, Republic of Korea.
Woo Kyun BaeDepartment of Internal Medicine, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, 322 Seoyang-Ro, Hwasun-Eup, Hwasun-gun, Jeollanam-do, 58128, Republic of Korea.
Je-Jung LeeDepartment of Internal Medicine, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, 322 Seoyang-Ro, Hwasun-Eup, Hwasun-gun, Jeollanam-do, 58128, Republic of Korea.
In-Jae OhDepartment of Internal Medicine, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, 322 Seoyang-Ro, Hwasun-Eup, Hwasun-gun, Jeollanam-do, 58128, Republic of Korea. droij@chonnam.ac.kr.

Funding

the Bio & Medical Technology Development Program of the National Research Foundation (NRF) funded by the Korean government (MSIT) NRF-2020M3A9G3080330
6 · The paper itself

Abstract

Despite an initial response to platinum-based chemotherapy, most patients with extensive stage of small cell lung cancer (SCLC) have a poor prognosis due to recurrence. Additionally, the benefit of immune checkpoint inhibitors is more modest than non-small cell lung cancer. Natural killer (NK) cells can directly eliminate cancer cells without prior sensitization; this is largely governed by inflammatory cytokines, which serve as killing signals to cancer cells. Here, we investigated whether the combination of NK cells plus atezolizumab, a fully humanized monoclonal antibody that specifically targets the protein programmed death-ligand 1 (PD-L1), has a synergistic effect against SCLC. NK cells were expanded and activated using irradiated K562 feeder cells in the presence of interleukin (IL)-2/IL-15/IL-21/41BB ligand for 14 days. Expanded and activated NK cells (eNK) were combined with atezolizumab and used to treat SCLC cells in both in vitro and in vivo studies. The results revealed increased PD-L1 expression in SCLC cells after the eNK challenge. eNK cells plus atezolizumab demonstrated increased cytotoxicity toward target SCLC cells, as evidenced by increased interferon-γ and tumor necrosis factor-α production, and higher levels of SCLC stem cell (CD44

Indexed as

Antibodies, Monoclonal, HumanizedKiller Cells, NaturalLung NeoplasmsSmall Cell Lung CarcinomaAnimalsB7-H1 AntigenCell Line, TumorCombined Modality TherapyFemaleHumansMiceXenograft Model Antitumor AssaysAntibodies, Monoclonal, HumanizedatezolizumabB7-H1 AntigenAnti-PD-L1AtezolizumabCombination therapyNK cellsSmall cell lung cancer

Identifiers

PMID40056167
PMCPMC11890499

What OpenQuestion holds

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Registered trials

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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.