Persistence of human papillomavirus infection after therapeutic conizationfor CIN 3: Is it an alarm for disease recurrence?

Citation
Y. Nagai et al., Persistence of human papillomavirus infection after therapeutic conizationfor CIN 3: Is it an alarm for disease recurrence?, GYNECOL ONC, 79(2), 2000, pp. 294-299
Citations number
29
Categorie Soggetti
Reproductive Medicine
Journal title
GYNECOLOGIC ONCOLOGY
ISSN journal
00908258 → ACNP
Volume
79
Issue
2
Year of publication
2000
Pages
294 - 299
Database
ISI
SICI code
0090-8258(200011)79:2<294:POHPIA>2.0.ZU;2-W
Abstract
Objective. The aims of this study were (1) to examine whether HPV DNA is pe rsistently detected in the cervix after therapeutic conization for CIN 3 an d (2) to explore whether a patient with persistence of HPV infection is at risk of developing recurrent disease. Methods. Of 74 patients referred with CIN 3, 58 who were tested for HPV DNA in the pretreatment cervical lesions were enrolled in the study. After sta ndard therapeutic conization, patients were followed prospectively at the o utpatient clinic. Our follow-up protocol was to follow patients without the rapeutic intervention as long as they developed no recurrence or recurrence of CIN 1 or 2, while patients who experienced recurrence of CIN 3 were rec ommended for reconization or hysterectomy. The polymerase chain reaction fo r detecting HPV DNA was performed using fresh cell samples from the cervix. Results. In 56 of 58 patients (96.6%), HPV DNAs were detected in their prim ary cervical lesions prior to conization. With regard to the distribution o f HPV types, HPV type 16 family (types 16, 31, and 35) was identified in 28 cases (50.0%), type 18 family (types 18, 33 and 58) in 15 (26.8%), and typ e X in 18 (32.1%). Up to August 1999, all of the 58 patients have been foll owed with a mean follow-up period of 31.8 months (range: 12 to 73 months). After treatment, HPV DNA was persistently detected in 11 (19.6%) but negati ve in 45 (80.4%) of 56 HPV DNA-positive patients. HPV DNA was not detected in both HPV DNA-negative patients. Five of 11 persistently HPV DNA-positive patients (45.5%) developed CIN recurrence, while none of 45 persistently H PV DNA-negative patients did. Thus, there was a significant difference betw een the recurrence rates of these two groups (P < 0.0001). Both patients wh o were initially HPV DNA-negative developed no recurrence. Accordingly, the overall recurrence following conservative treatment for CIN 3 was 5 of 58 patients (8.6%). Conclusions. Patients with persistent HPV infection after conization for CI N 3 should be especially closely followed because they are at increased ris k of developing disease recurrence. (C) 2000, Academic Press.