SS 09-06CONSECUTIVE HPV GENOTYPING OF INVASIVE CERVICAL CANCER IN SWEDEN

11. Genotyping - Sequencing
C. Lagheden 1, C. Eklund 1, H. Lamin 2, S. Nordqvist Kleppe 1, M. Elfström 1, K. Sundström 1, P. Sparén 3, J. Dillner 1.
1Dept of Laboratory medicine, Karolinska Institutet (Sweden), 2Dept of Laboratory medicine, Karolinska University Hospital, Stockholm (Sweden), 3Dept of Medical Epidemiology and Biostatistics, Karolinska Institutet (Sweden)

Background / Objectives

The Swedish National Cervical Screening Registry evaluates and provides data to optimize cervical cancer prevention in Sweden. All cervical cancers diagnosed in Sweden during 10 years, 2002-2011, were identified. 4272 confirmed cancer cases were subjected to a national audit including HPV genotyping.


Methods

Formalin-fixed paraffin-embedded (FFPE) samples were used for HPV genotyping. In between each case-block, a blank-block was sectioned, as a control for contamination. The sections were extracted with a heating method and HPV genotyped using modified general primer (MGP)-PCR and Luminex. “HPV negative” cases are being sequenced.


Results

For a valid result the blank-block had to be negative in all tests and the case-block positive for beta-globin. 1560 cases were analysed until February 2016. The most common type was HPV 16 (47%), followed by HPV18 (15%), HPV 45 (7%), HPV 31 (3%), HPV 33 (2%), HPV 52 (1%), HPV 6 (1%), HPV 56 (1%), HPV 39 (1%), HPV 70 (1%), HPV 58 (1%), HPV 59 (1%) and HPV 35 (1%). Single infection was detected in 78% of cases.


Conclusion

Systematic HPV genotyping of all cases of invasive cervical cancer in a country is readily doable as part of monitoring the effectiveness of prevention and continued monitoring of the HPV-type specific disease burden.


References