Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Cervical dysplasia during pregnancy - Effects on oncological and psychological outcome: a case control study
1Department of Obstetrics and Gynecology, Ludwig-Maximilians-Universität, Campus Grosshadern, Munich, Germany
*Corresponding Author(s): T.M. Kolben E-mail: Theresa.Kolben@med.uni-muenchen.de
Pregnant patients with cervical intraepithelial neoplasia Grade 3 (CIN 3) are monitored in 8- to 12-weekly intervals unless invasive carcinoma is suspected. The aim of this case-control study was to evaluate differences in regression and healing rates as well as posttraumatic stress levels. Materials and Methods: Treatment and outcome were analysed retrospectively. Stress levels were measured using the standardized German version of the Impact of Event Scale-Revised (IES-R) questionnaire. Results: Spontaneous regression was seen in 26.9% of cases. Progression to invasive cancer was not detected. 88.2% of all pregnant and 88.3% of all non-pregnant women were regarded as healed. Stress level was not significantly higher in non-pregnant patients. Conclusion: Cervical dysplasia in pregnancy shows high spontaneous regression potential. Regression is associated with long-time healing of dysplasia. An observant approach in patients with CIN3 during pregnancy does not cause higher stress levels.
HSIL; CIN; Cervical dysplasia; Pregnancy; Post-traumatic stress levels.
S. Rueckert,K. Oestreich,J. Gallwas,T. Kolben,N. Ditsch,T. Starrach,C. Blume,C. Dannecker,T.M. Kolben. Cervical dysplasia during pregnancy - Effects on oncological and psychological outcome: a case control study. European Journal of Gynaecological Oncology. 2018. 39(3);399-403.
[1] Jemal A., Bray F., Center M.M., Ferlay J., Ward E., Forman D.: “Global cancer statistics’. CA Cancer J. Clin., 2011, 61, 69.
[2] Smith L.H., Danielsen B., Allen M.E., Cress R.: “Cancer associated with obstetric delivery: Results of linkage with the california cancer registry”. Am. J. Obstet. Gynecol., 2003, 189, 1128.
[3] Weiss D.: “The impact of event scale: Revised”. In:Wilson J.P. (eds). Cross-cultural assessment of psychological trauma and PTSD. New York, NY: Springer Sciene and Business Media, 2007, 219.
[4] Herbert A., Smith J.A.: “Cervical intraepithelial neoplasia grade iii (cin iii) and invasive cervical carcinoma: The yawning gap revisited and the treatment of risk”. Cytopathology, 1999, 10, 161.
[5] Massad L.S., Einstein M.H., Huh W.K., Katki H.A., Kinney W.K., Schiffman M., et al.: “2012 updated consensus guidelines for the management of abnormal cervical cancer screening tests and cancer precursors”. Obstet. Gynecol,, 2013, 121, 829.
[6] Maercker A.: “Erfassung von psychischen belastungsfolgen: Die impact of event skala-revidierte version (ies-r)”. Diagnostica, 1998, 44, 130.
[7] Arbyn M., Kyrgiou M., Simoens C., Raifu A.O., Koliopoulos G., Martin-Hirsch P., et al.: “Perinatal mortality and other severe adverse pregnancy outcomes associated with treatment of cervical intraepithelial neoplasia: Meta-analysis”. BMJ, 2008, 337, a1284.
[8] Kyrgiou M., Koliopoulos G., Martin-Hirsch P., Arbyn M., Prendiville W., Paraskevaidis E.: “Obstetric outcomes after conservative treatment for intraepithelial or early invasive cervical lesions: Systematic review and meta-analysis”. Lancet, 2006, 367, 489.
[9] Noehr B., Jensen A., Frederiksen K., Tabor A., Kjaer S.K.: “Depth of cervical cone removed by loop electrosurgical excision procedure and subsequent risk of spontaneous preterm delivery”. Obstet. Gynecol., 2009, 114, 1232.
[10] Jin G., Lanlan Z., Li C., Dan Z.: “Pregnancy outcome following loop electrosurgical excision procedure (leep) a systematic review and meta-analysis”. Arch. Gynecol. Obstet., 2014, 289, 85.
[11] Holowaty P., Miller A.B., Rohan T., To T.: “Natural history of dysplasia of the uterine cervix”. J. Natl. Cancer Inst., 1999, 91, 252.
[12] Serati M., Uccella S., Laterza R.M., Salvatore S., Beretta P., Riva C., Bolis P.F.: “Natural history of cervical intraepithelial neoplasia during pregnancy”. Acta Obstet. Gynecol. Scand., 2008, 87, 1296.
[13] Ackermann S., Gehrsitz C., Mehlhorn G., Beckmann M.W.: “Management and course of histologically verified cervical carcinoma in situ during pregnancy”. Acta Obstet. Gynecol. Scand., 2006, 85,
1134.
[14] Fader A.N., Alward E.K., Niederhauser A., Chirico C., Lesnock J.L., Zwiesler D.J., et al.: “Cervical dysplasia in pregnancy: A multi-institutional evaluation”. Am. J. Obstet. Gynecol., 2010, 203, 113 e1.
[15] Yost N.P., Santoso J.T., Mcintire D.D., Iliya F.A.: “Postpartum regression rates of antepartum cervical intraepithelial neoplasia ii and iii lesions”. Obstet. Gynecol., 1999, 93, 359.
[16] Wu Y.M., Wang T., He Y., Song F., Wang Y., Zhu L., et al.: “Clinical management of cervical intraepithelial neoplasia in pregnant andpostpartum women”. Arch. Gynecol. Obstet., 2014, 289, 1071.
[17] Arends M.J., Buckley C.H., Wells M.: “Aetiology, pathogenesis, and pathology of cervical neoplasia”. J. Clin. Pathol., 1998, 51, 96.
[18] Gallwas J., Ditsch N., Hillemanns P., Friese K., Thaler C., Dannecker C.: “The significance of hpv in the follow-up period after treatment for CIN”. Eur. J. Gynaecol. Oncol., 2010, 31, 27.
[19] Chua K.L., Hjerpe A.: “Human papillomavirus analysis as a prognostic marker following conization of the cervix uteri”. Gynecol. Oncol., 1997, 66, 108.
[20] Lin C.T., Tseng C.J., Lai C.H., Hsueh S., Huang K.G., Huang H.J., Chao A.: “Value of human papillomavirus deoxyribonucleic acid testing after conization in the prediction of residual disease in the subsequent hysterectomy specimen”. Am. J. Obstet. Gynecol., 2001, 184, 940.
[21] Jain S., Tseng C.J., Horng S.G., Soong Y.K., Pao C.C.: “Negative predictive value of human papillomavirus test following conization of the cervix uteri”. Gynecol. Oncol., 2001, 82, 177.
[22] Nagai Y., Maehama T., Asato T., Kanazawa K.: “Persistence of human papillomavirus infection after therapeutic conization for cin 3: Is it an alarm for disease recurrence?” Gynecol. Oncol., 2000, 79, 294.
[23] Bollen L.J., Tjong A.H.S.P., Van Der Velden J., Mol B.W., Lammes F.B., Ten Kate F.W., et al.: “Human papillomavirus DNA after treatment of cervical dysplasia: Low prevalence in normal cytologic smears”. Cancer, 1996, 77, 2538.
[24] Bollen L.J., Tjong A.H.S.P, Van Der Velden J., Mol B.W., Boer K., Ten Kate F.J., et al.: “Clearance of cervical human papillomavirus infection by treatment for cervical dysplasia”. Sex.
Transm. Dis., 1997, 24, 456.
[25] Distefano A.L., Picconi M.A., Alonio L.V., Dalbert D., Mural J., Bartt O., et al.: “Persistence of human papillomavirus DNA in cervical lesions after treatment with diathermic large loop excision”. Infect. Dis. Obstet. Gynecol., 1998, 6, 214.
[26] Kanamori Y., Kigawa J., Minagawa Y., Irie T., Oishi T., Itamochi H., et al.: “Residual disease and presence of human papillomavirus after conization”. Oncology, 1998, 55, 517.
[27] Strand A., Wilander E., Zehbe I., Rylander E.: “High risk hpv persists after treatment of genital papillomavirus infection but not after treatment of cervical intraepithelial neoplasia”. Acta Obstet. Gynecol. Scand., 1997, 76, 140.
[28] Vlahos G., Rodolakis A., Diakomanolis E., Stefanidis K., Haidopoulos D., Abela K., et al.: “Conservative management of cervical intraepithelial neoplasia (cin(2-3)) in pregnant women”. Gynecol. Obstet. Invest., 2002, 54, 78.
[29] Nobbenhuis M.A., Helmerhorst T.J., Van Den Brule A.J., Rozendaal L., Bezemer P.D., Voorhorst F.J., Meijer C.J.: “High-risk human papillomavirus clearance in pregnant women: trends for lower clearance during pregnancy with a catch-up postpartum”. Br. J. Cancer, 2002, 87, 75.
[30] Schneider A., Hotz M., Gissmann L.: “Increased prevalence of human papillomaviruses in the lower genital tract of pregnant women”. Int. J. Cancer, 1987, 40, 198.
[31] Sethi S., Muller M., Schneider A., Blettner M., Smith E., Turek L., et al.: “Serologic response to the e4, e6, and e7 proteins of human papillomavirus type 16 in pregnant women”. Am. J. Obstet. Gynecol., 1998, 178, 360.
[32] Siristatidis C., Vitoratos N., Michailidis E., Syciotis C., Panagiotopoulos N., Kassanos D., Salamalekis E.: “The role of the mode of delivery in the alteration of intrapartum pathological cervical cytologic findings during the postpartum period”. Eur. J. Gynaecol. Oncol., 2002, 23, 358.
[33] Chung S.M., Son G.H., Nam E.J., Kim Y.H., Kim Y.T., Park Y.W., Kwon J.Y.: “Mode of delivery influences the regression of abnormal cervical cytology”. Gynecol. Obstet. Invest., 2011, 72, 234.
[34] Kaneshiro B.E., Acoba J.D., Holzman J., Wachi K., Carney M.E.: “Effect of delivery route on natural history of cervical dysplasia”. Am. J. Obstet. Gynecol., 2005, 192, 1452.
Top