Evidence map›Paper›PMID 31415377›Full record

ArticleMedicine2019

Immune adjuvant therapy using Bacillus Calmette-Guérin cell wall skeleton (BCG-CWS) in advanced malignancies: A phase 1 study of safety and immunogenicity assessments.

Sumiyuki Nishida, Akihiro Tsuboi, Atsushi Tanemura, Toshinori Ito, Hiroko Nakajima, Toshiaki Shirakata, Soyoko Morimoto, Fumihiro Fujiki, Naoki Hosen, Yusuke Oji and 6 more

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

Article in Medicine, 2019. 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
1.4field-weighted citation impact, top 18% 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, 38 citations in OpenAlex.

  1. Bacteria in neoplastic diseases: A brief note on Wilms tumor.World journal of experimental medicine · 2025
    Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. 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

16 authors at 3 institutions in 1 country.

Sumiyuki NishidaDepartment of Respiratory Medicine and Clinical Immunology.
Akihiro TsuboiDepartment of Cancer Immunotherapy.
Atsushi TanemuraDepartment of Dermatology.
Toshinori ItoDepartment of Gastroenterological Surgery.
Hiroko NakajimaDepartment of Cancer Immunology.
Toshiaki ShirakataDepartment of Cancer Immunotherapy.
Soyoko MorimotoDepartment of Cancer Immunotherapy.
Fumihiro FujikiDepartment of Cancer Immunology.
Naoki HosenDepartment of Cancer Stem Cell Biology.
Yusuke OjiDepartment of Functional Diagnostic Science, Osaka University Graduate School of Medicine.
Atsushi KumanogohDepartment of Respiratory Medicine and Clinical Immunology.
Ichiro KawaseDepartment of Respiratory Medicine and Clinical Immunology.
Yoshihiro OkaDepartment of Respiratory Medicine and Clinical Immunology.
Ichiro AzumaHokkaido University, Sapporo.
Satoshi MoritaDepartment of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Haruo SugiyamaDepartment of Cancer Immunology.
Osaka University · JPHokkaido University · JPKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cell wall skeleton of Bacillus Calmette-Guérin (BCG-CWS) is a bioactive component that is a strong immune adjuvant for cancer immunotherapy. BCG-CWS activates the innate immune system through various pattern recognition receptors and is expected to elicit antigen-specific cellular immune responses when co-administered with tumor antigens. To determine the recommended dose (RD) of BCG-CWS based on its safety profile, we conducted a phase I dose-escalation study of BCG-CWS in combination with WT1 peptide for patients with advanced cancer.The primary endpoint was the proportion of treatment-related adverse events (AEs) at each BCG-CWS dose. The secondary endpoints were immune responses and clinical effects. A BCG-CWS dose of 50, 100, or 200 μg/body was administered intradermally on days 0, 7, 21, and 42, followed by 2 mg of WT1 peptide on the next day. For the escalation of a dose level, 3 + 3 design was used.Study subjects were 18 patients with advanced WT1-expressing cancers refractory to standard anti-cancer therapies (7 melanoma, 5 colorectal, 4 hepatobiliary, 1 ovarian, and 1 lung). Dose-limiting toxicity occurred in the form of local skin reactions in 2 patients at a dose of 200 μg although no serious treatment-related systemic AEs were observed. Neutrophils and monocytes transiently increased in response to BCG-CWS. Some patients demonstrated the induction of the CD4 T cell subset and its differentiation from the naïve to memory phenotype, resulting in a tumor response.The RD of BCG-CWS was determined to be 100 μg/body. This dose was well tolerated and showed promising clinical effects with the induction of an appropriate immune response.

Indexed as

Mycobacterium bovisAdjuvants, ImmunologicAdultAgedBCG VaccineCD4 Lymphocyte CountCell Wall SkeletonColorectal NeoplasmsFemaleHumansLiver NeoplasmsLung NeoplasmsMaleMelanomaMiddle AgedOvarian NeoplasmsAdjuvants, ImmunologicBCG VaccineCell Wall Skeleton

Identifiers

PMID31415377
PMCPMC6831317
OpenAlexW2969036107

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.