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Self-collected HPV samples are as accurate as clinician samples and reach women who never attend screening

A meta-analysis of 56 accuracy studies and 25 randomised trials found that self-sampled swabs tested with PCR detect precancer as well as clinician-taken samples, and mailing kits to under-screened women roughly doubles participation.

Arbyn and colleagues pooled diagnostic accuracy studies comparing HPV testing on self-collected versus clinician-collected samples, and randomised trials comparing strategies to reach under-screened women.

With PCR-based assays, sensitivity for CIN2+ and CIN3+ on self samples was equivalent to clinician samples (relative sensitivity 0.99) and specificity was marginally lower (0.98). Signal-amplification assays performed worse on self samples. Mailing self-sampling kits to all under-screened women increased participation more than twofold compared with an invitation letter, as did door-to-door offers; opt-in kits produced smaller gains.

The findings underpin WHO and national guidance that self-sampling is an acceptable primary screening method.

Meta-analysisChanged practice
Authors
Arbyn M, Smith SB, Temin S, Sultana F, Castle P
Published
BMJ, 2018
What it found
  • PCR-based assays: pooled relative sensitivity of self vs clinician samples 0.99 for CIN2+, relative specificity 0.98
  • Signal-amplification assays were less sensitive on self samples (relative sensitivity 0.85 for CIN2+)
  • Mailing kits to under-screened women increased participation about 2.3-fold versus invitation letters
  • Opt-in approaches (women must request a kit) gave only modest participation gains
What it means

Women can collect their own screening sample at home with no loss of accuracy if the laboratory uses a PCR test. Sending kits directly is the most effective way to reach women who do not attend, which matters because most cervical cancers occur in under-screened women.

Be careful
  • Accuracy equivalence holds only for PCR-based assays validated for self samples
  • Triage of positive self-samples still requires a clinic visit; follow-up completion is the weak point
  • Participation trials were heterogeneous in setting and delivery
  • Self-sampling for cytology (rather than HPV) is not supported

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