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
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.