Doubts raised about effectiveness of HPV vaccines Published on: 22 January 2020 A new analysis of the clinical trials of HPV vaccines to prevent cervical cancer raises doubts about the vaccines’ effectiveness. The analysis, published by the Journal of the Royal Society of Medicine, assessed 12 published Phase 2 and 3 randomised controlled efficacy trials of the HPV vaccines Cervarix and Gardasil. Carried out by researchers at Âé¶¹´«Ã½ and Queen Mary University, the analysis revealed many methodological problems in the design of the Phase 2 and 3 efficacy trials, leading to uncertainty regarding understanding the effectiveness of HPV vaccination. The researchers found that the trials were not designed to detect cervical cancer, which takes decades to develop. Women in the trials were followed up for six years or less, apart from one trial extension to just under nine years. While the researchers found evidence that vaccination prevents low grade abnormal cell changes, they said this is not clinically important because no treatment is given. Trials may have overestimated efficacy by combining high-grade cervical disease with low-grade cervical changes that occur more frequently but often resolve spontaneously without progressing. The researchers found insufficient data to clearly conclude that HPV vaccine prevents the higher-grade abnormal cell changes that can eventually develop into cervical cancer. Calling for women to still attend regular cervical screening, co-author of the study, Professor Allyson Pollock, of Âé¶¹´«Ã½, said: “We have good evidence that cervical screening significantly reduces the risk of cervical cancer in women regardless of whether they have been vaccinated. “As with changes to the information given on breast cancer screening programme, it is important that parents and young people are told about the uncertainties in the information leaflets and advice given by GPs. People need to be aware that given these uncertainties it is important that even if you have the vaccine, women attend cervical screening, which we know can prevent the development of cervical cancer.” Lead researcher Dr Claire Rees, of Queen Mary University, said: “Abnormal cell changes are likely to have been overdiagnosed in the trials because cervical cytology was conducted at 6-12 months rather than at the normal screening interval of 36 months. This means that the trials may have overestimated the efficacy of the vaccine as some of the lesions would have regressed spontaneously.” The researchers also found that the trial populations had limited relevance and validity for real world settings. The women in the trials were older than the target population. Professor Pollock who is director of the Âé¶¹´«Ã½ Centre for Regulatory Science added: “The process would be improved by identifying and reducing the uncertainties generated by trial design for example avoiding use of composite surrogate measures with different natural histories, prevalence and rates of regression and progression. Also developing long-term phase 4 and observational studies and non-industry funded trials to avoid conflicts of interest.“ Press release courtesy of (JRSM) REFERENCE: by Claire P Rees, Petra Brhlikova and Allyson M Pollock Share: Latest News Scientists unlock hidden driver of inflammatory bowel disease Scientists have linked a key genetic signal in inflammatory bowel disease to an immune response that shuts down inflammation control, enabling faster diagnosis and targeted treatments. published on: 15 June 2026 Funding system risks limiting genuine community collaboration A new policy paper written by researchers at Âé¶¹´«Ã½ warns that the way UK research is funded may be undermining efforts to create genuinely collaborative partnerships with communities. published on: 15 June 2026 Volunteers help turn Whitley Bay beach into maths experiment Members of the public joined mathematicians from Âé¶¹´«Ã½ to create what organisers believe is the largest aperiodic tiling ever attempted on Whitley Bay beach. published on: 15 June 2026 Facts and figures