Evidence map›Paper›PMID 39004526›Full record

ArticleVaccine2024

Meeting report: Considerations for trial design and endpoints in licensing therapeutic HPV16/18 vaccines to prevent cervical cancer.

Peter M Dull, Sharon L Achilles, Rafi Ahmed, Ruanne V Barnabas, Nicole G Campos, Keith Chirgwin, Jamie A Cohen, Silvia de Sanjosé, John Doorbar, Mark H Einstein and 15 more

Abstract readConference Proceedings
In one paragraph

Article in Vaccine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Cancer vaccines: advances, hurdles, and future directions.Exploration of targeted anti-tumor therapy · 2025
    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

25 authors.

Peter M DullBill & Melinda Gates Foundation, Seattle, WA, USA. Electronic address: Peter.Dull@gatesfoundation.org.
Sharon L AchillesBill & Melinda Gates Foundation, Seattle, WA, USA.
Rafi AhmedEmory Vaccine Center, Atlanta, GA, USA.
Ruanne V BarnabasDivision of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA; School of Medicine, Harvard Medical School, Boston, MA, USA; Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Nicole G CamposHarvard T.H. Chan School of Public Health, Boston, MA, USA.
Keith ChirgwinIndependent Consultant, Seattle, WA, USA.
Jamie A CohenBill & Melinda Gates Foundation, Seattle, WA, USA.
Silvia de SanjoséISGlobal, Barcelona, Spain; National Cancer Institute, Bethesda, MD, USA.
John DoorbarUniversity of Cambridge, Cambridge, UK.
Mark H EinsteinRutgers New Jersey Medical School, Newark, NJ, USA.
Claudia I EmersonMcMaster University, Hamilton, Ontario, Canada.
Sami L GottliebWorld Health Organization, Geneva, Switzerland.
Allan HildesheimIndependent Consultant, Willis, VA, USA.
Youlin QiaoChinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Paul RuffUniversity of Witwatersrand Faculty of Health Sciences, Johannesburg, South Africa.
Joshua N SampsonNational Cancer Institute, Bethesda, MD, USA.
Peter SasieniQueen Mary University of London, London, UK.
Mark SchiffmanDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.
Haina ShinBill & Melinda Gates Foundation, Seattle, WA, USA.
Margaret A StanleyUniversity of Cambridge, Cambridge, UK.
Cornelia L TrimbleJohns Hopkins University School of Medicine, Baltimore, MD, USA.
Nicholas WentzensenDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.
Angelika B RiemerGerman Cancer Research Center (DKFZ), Heidelberg, Germany; German Center for Infection Research (DZIF), Partner Site Heidelberg, Germany.
John T SchillerCenter for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Aimée R KreimerDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.

Funding

Understanding Papillomavirus Virion Proteins and VaccinesZIABC009052 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SCHILLER, JOHN T. · 2009 to 2025
$38.4M
World Health Organization 001
6 · The paper itself

Abstract

Cervical cancer is a major cause of morbidity and mortality globally with a disproportionate impact on women in low- and middle-income countries. In 2021, the World Health Organization (WHO) called for increased vaccination, screening, and treatment to eliminate cervical cancer. However, even with widespread rollout of human papillomavirus (HPV) prophylactic vaccines, millions of women who previously acquired HPV infections will remain at risk for progression to cancer for decades to come. The development and licensing of an affordable, accessible therapeutic HPV vaccine, designed to clear or control carcinogenic HPV and/or to induce regression precancer could significantly contribute to the elimination efforts, particularly benefiting those who missed out on the prophylactic vaccine. One barrier to development of such vaccines is clarity around the regulatory pathway for licensure. In Washington, D.C. on September 12-13, 2023, a meeting was convened to provide input and guidance on trial design with associated ethical and regulatory considerations. This report summarizes the discussion and conclusions from the meeting. Expert presentation topics included the current state of research, potential regulatory challenges, WHO preferred product characteristics, modeling results of impact of vaccine implementation, epidemiology and natural history of HPV infection, immune responses related to viral clearance and/or precancer regression including potential biomarkers, and ethical considerations. Panel discussions were held to explore specific trial design recommendations to support the licensure process for two vaccine indications: (1) treatment of prevalent HPV infection or (2) treatment of cervical precancers. Discussion covered inclusion/exclusion criteria, study endpoints, sample size and power, safety, study length, and additional data needed, which are reported here. Further research of HPV natural history is needed to address identified gaps in regulatory guidance, especially for therapeutic vaccines intended to treat existing HPV infections.

Indexed as

Papillomavirus InfectionsPapillomavirus VaccinesUterine Cervical NeoplasmsClinical Trials as TopicFemaleHuman papillomavirus 16Human papillomavirus 18HumansLicensureResearch DesignVaccinationPapillomavirus VaccinesCervical cancerHPVHPV therapeutic vaccineHuman papillomavirus

Identifiers

PMID39004526
PMCPMC11413486

What OpenQuestion holds

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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.