Cancer Risk From Tainted Polio Vaccine Undetermined: IOM Report

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 11 No 12
Volume 11
Issue 12

WASHINGTON-There is insufficient evidence to prove or disprove whether polio vaccine doses contaminated with simian virus-40 (SV40) between 1955 and 1963 can trigger certain cancers in humans, according to a report by the Institute of Medicine (IOM), a part of the National Academy of Sciences. Although most population studies have not found an increase in the cancers among people inoculated with the vaccine between 1955 and 1963, a possible link cannot be completely ruled out because of substantial statistical and design limitations in the 13 studies, an IOM committee concluded.

WASHINGTON—There is insufficient evidence to prove or disprove whether polio vaccine doses contaminated with simian virus-40 (SV40) between 1955 and 1963 can trigger certain cancers in humans, according to a report by the Institute of Medicine (IOM), a part of the National Academy of Sciences. Although most population studies have not found an increase in the cancers among people inoculated with the vaccine between 1955 and 1963, a possible link cannot be completely ruled out because of substantial statistical and design limitations in the 13 studies, an IOM committee concluded.

The committee recommended the development of sensitive blood tests and standardized techniques to more definitively detect SV40 in infected individuals. These techniques should then be used to determine the incidence of SV40 infection prior to 1955 and after 1963. This information would reveal how much of the SV40 infection in humans can be attributed to the contaminated vaccine.

Newsletter

Stay up to date on recent advances in the multidisciplinary approach to cancer.

Recent Videos
Treatment-related toxicities during neuro-oncology therapy appear well managed with dose modifications and treatment cycle holds.
The phase 3 NIVOSTOP trial evaluated an anti–PD-1 immunotherapy, nivolumab, in a patient population similar in the KEYNOTE-689 trial.
CAR T-cell therapies appear to be an evolving modality in the treatment of those with intracranial tumors, said Sylvia Kurz, MD, PhD.
Opportunities to further reduce relapses include pembrolizumab-based combination therapy and evaluating the agent’s contribution before and after surgery.
For patients with locally advanced head and neck cancers, the current standard of care for curative therapy has a cure rate of less than 50%.
According to Maurie Markman, MD, patient-reported outcomes pertain to more relevant questions surrounding the impact of therapy for patients.
CancerNetwork® spoke with Neha Mehta-Shah, MD, MSCI, about the clinical landscape for patients undergoing treatment for rare lymphomas.