Evidence map›Paper›PMID 32413834›Full record

ArticleTranslational oncology2020

Safety and Long-Term Outcome of Intratumoral Injection of OK432-Stimulated Dendritic Cells for Hepatocellular Carcinomas After Radiofrequency Ablation.

Masaaki Kitahara, Eishiro Mizukoshi, Takeshi Terashima, Hidetoshi Nakagawa, Rika Horii, Noriho Iida, Kuniaki Arai, Taro Yamashita, Yoshio Sakai, Tatsuya Yamashita and 3 more

Open access · goldAbstract read
In one paragraph

Article in Translational oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
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  9. New insights into mechanisms and interventions of locoregional therapies for hepatocellular carcinoma.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2024
    Article
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  12. Article
  13. Frontiers in immunology · 2023
    Review
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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

13 authors at 2 institutions in 1 country.

Masaaki KitaharaDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Eishiro MizukoshiDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan. Electronic address: eishirom@m-kanazawa.jp.
Takeshi TerashimaDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Hidetoshi NakagawaDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Rika HoriiDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Noriho IidaDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Kuniaki AraiDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Taro YamashitaDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Yoshio SakaiDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Tatsuya YamashitaDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Masao HondaDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Yasunari NakamotoSecond Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
Shuichi KanekoDepartment of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan.
Kanazawa University · JPUniversity of Fukui · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cell (DC)-based immunotherapies are believed to help eradicate residual tumor cells, including hepatocellular carcinoma (HCC). Here, we assessed the safety and clinical response to OK432-stimulated monocyte-derived DCs (MoDCs) in treating HCC after radiofrequency ablation (RFA). MoDCs were derived from 30 HCC patients in the presence of interleukin-4 and granulocyte-macrophage colony stimulating factor for 5 days and then cultured for 2 more days in the medium (basic protocol) or stimulated with OK432. On day 7, DCs were harvested and percutaneously injected into HCC tumors after RFA. We observed no grade 3 or 4 National Cancer Institute Common Toxicity Criteria adverse events. Kaplan-Meier analysis indicated that patients treated with RFA + OK432-stimulated DCs transfer had longer recurrence-free survival than those treated with RFA + basic-protocol DCs (median: 24.8 vs 13.0 months; P = .003). RFA with DC infusion can enhance various tumor-associated antigen (TAA)-specific T-cell responses. Additionally, the 5-year RFS rate for patients with significantly increased TAA-specific T-cell responses was much higher than for other patients (50.0% vs. 7.7%; P = .030). Our study provides useful information for development of HCC immunotherapies (trial registration: UMIN000001701).

Identifiers

PMID32413834
PMCPMC7226894
OpenAlexW3024568686

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.