Evidence map›Paper›PMID 36307410›Full record

ArticleNature communications2022

A phase I study of an adenoviral vector delivering a MUC1/CD40-ligand fusion protein in patients with advanced adenocarcinoma.

Tira J Tan, W X Gladys Ang, Who-Whong Wang, Hui-Shan Chong, Sze Huey Tan, Rachael Cheong, John Whay-Kuang Chia, Nicholas L Syn, Wai Ho Shuen, Rebecca Ba and 16 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02140996 (Ad-sig-hMUC-1/ecdCD40L Vector Vaccine for Immunotherapy of Epithelial Cancers), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.4field-weighted citation impact, top 7% 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.

NCT02140996 phase1unknown statusnot on this map

Ad-sig-hMUC-1/ecdCD40L Vector Vaccine for Immunotherapy of Epithelial Cancers

TypeinterventionalSponsorSingapore Clinical Research InstituteRan2014 to 2017Enrolled24ConditionsEpithelial Cancers of the Lung, Breast, Ovary, Prostate and ColonArmsAd-sig-hMUC-1/ecdCD40L vector vaccine
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 19 citations in OpenAlex.

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  10. [Research Progress of Lung Cancer Vaccines].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 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

26 authors at 7 institutions in 1 country.

Tira J Tan *Division of Medical Oncology, National Cancer Centre, Singapore, Singapore.
W X Gladys Ang *Translational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.ORCID 0000-0002-9105-0550
Who-Whong Wang *Division of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Hui-Shan ChongDivision of Clinical Trials and Epidemiological Sciences, National Cancer Centre, Singapore, Singapore.
Sze Huey TanDivision of Clinical Trials and Epidemiological Sciences, National Cancer Centre, Singapore, Singapore.ORCID 0000-0002-3089-7379
Rachael CheongDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
John Whay-Kuang ChiaCurie Oncology, Singapore, Singapore.
Nicholas L SynYong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Wai Ho ShuenDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.ORCID 0000-0001-9305-7652
Rebecca BaDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Nivashini KaliaperumalInstitute of Molecular and Cellular Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Bijin AuInstitute of Molecular and Cellular Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Richard HopkinsInstitute of Molecular and Cellular Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Xinhua LiSingapore Clinical Research Institute (SCRI), Singapore, Singapore.
Aaron C TanDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.ORCID 0000-0001-7292-1114
Amanda O L SeetDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
John E ConnollyInstitute of Molecular and Cellular Biology (IMCB), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Thaschawee ArkachaisriRheumatology and Immunology Service, KK Women's and Children's Hospital, Singapore, Singapore.ORCID 0000-0002-1387-1169
Valerie ChewTranslational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.ORCID 0000-0002-5617-0936
Ahmad Bin Mohamed LajamTranslational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Dianyan GuoTranslational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Marvin Z W ChewTranslational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Martin WasserTranslational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.ORCID 0000-0002-8753-2346
Pavanish KumarTranslational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Salvatore AlbaniTranslational Immunology Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore. salvo@duke-nus.edu.sg.ORCID 0000-0002-5602-6256
Han Chong TohDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore. toh.han.chong@singhealth.com.sg.ORCID 0000-0003-0642-3453
National Cancer Centre Singapore · SGSingHealth Duke-NUS Academic Medical Centre · SGAgency for Science, Technology and Research · SGKK Women's and Children's Hospital · SGNational University of Singapore · SGSingapore Clinical Research Institute · SGSingHealth · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer vaccines as immunotherapy for solid tumours are currently in development with promising results. We report a phase 1 study of Ad-sig-hMUC1/ecdCD40L (NCT02140996), an adenoviral-vector vaccine encoding the tumour-associated antigen MUC1 linked to CD40 ligand, in patients with advanced adenocarcinoma. The primary objective of this study is safety and tolerability. We also study the immunome in vaccinated patients as a secondary outcome. This trial, while not designed to determine clinical efficacy, reports an exploratory endpoint of overall response rate. The study meets its pre-specified primary endpoint demonstrating safety and tolerability in a cohort of 21 patients with advanced adenocarcinomas (breast, lung and ovary). The maximal dose of the vaccine is 1 ×10

Indexed as

AdenocarcinomaCancer VaccinesAdenoviridaeCD40 LigandFemaleGenetic VectorsHumansLigandsMucin-1Cancer VaccinesCD40 LigandLigandsMUC1 protein, humanMucin-1

Identifiers

PMID36307410
PMCPMC9616917
OpenAlexW4307723006

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.