Recurrence of genitals warts in pre-HPV vaccine era after laser treatment

Data collection was divided in one main data set und two subsets.

The first subset (data set 2) consisted of data on topography of genital warts, pregnancy status and cervical smear being available for women treated from 2003 to 2009 (n = 825). Pap smears were classified according to the Second Munich Nomenclature [24]. Location of lesions was retrieved from surgical report.

Standard methods of descriptive statistics (median, minimum, maximum, range, frequencies) were used. Associations between categorical variables were tested with Pearson’s chi-square test. The Mann–Whitney U test was used to assess differences between the means of independent groups in case of non-normally distributed variables. The Kaplan–Meier method was used for univariate analysis, and the log rank test to assess the difference between recurrence curves. The Cox proportional hazards analysis was used to estimate hazard ratios and corresponding 95% confidence intervals for various prognostic variables. The multivariate analysis included patients’ age, location of genital warts (dichotomous variables for vagina, vulva, perineum/perianal region, and anus) and number of affected sites (dichotomous variable: unifocal vs multifocal) as independent variables. A p value < 0.05 was considered statistically significant. All statistical analyses were performed with SPSS, version 22.0 (IBM Corporation, Armonk, NY).

The study was approved by the Ethics Committee of Medical University Innsbruck (reference number 4198/2011).

At least one recurrence was observed in 306 (17.0%) of the 1798 study patients. Two recurrences occurred in 3.2%, three recurrences in 1.1% and nine women (0.5%) had more than three recurrences (Table 1).

Highest percentage of recurrence was observed in the age group 10–15 years and percentage of recurrence decreased with increasing age (Fig. 1).

For the women who were treated for genital warts with carbon dioxide laser at our institution from 2003 to 2009 (n = 825; Table 1) additional information concerning topography of genitals warts, pregnancy status and cervical smear was available. In these 825 women, unifocal genital warts were observed in 195 (23.6%) and multifocal lesions in various combinations in 630 (76.4%) women (Table 2). The most frequently affected site (i.e. including uni- and multifocal warts) was the vulva (n = 748; 90.7%) followed by the perineum/perianal region (n = 489; 59.3%), the vagina (n = 390; 47.3%), the anus (n = 239; 29%) and the cervix (n = 110; 13.3%). Women with unifocal lesions had significantly fewer recurrences (11.3%) in comparison to women with multifocal lesions (18.9%) (χ² = 6.08, p = 0.01). Additionally, increasing frequency of affected sites correlated with increasing percentage of recurrence. Of those women with genital warts in only one location 11.3% experienced a recurrence, whereas of those patients with four and five affected sites 21.8% and 24.0%, respectively, showed recurrences (Table 2). Anal genital warts were observed in 239 (28.9%) patients. In two (0.8%) of these 239 women additional lesions of the vagina or cervix were observed, whereas 99.2% (237 of 239) had additional lesions of the perineum, perianal region or vulva.

Of the 825 patients with genital warts who underwent laser vaporisation between 2003 and 2009, 91 (11.0%) were pregnant. No significant differences in distribution of unifocal or multifocal genital warts were observed between pregnant and non-pregnant women (χ² = 2.06, p = 0.15). Median week of gestation at the time of laser vaporisation was 21 (range 10–36) weeks. Recurrence rate in the 91 pregnant women was 18.7% (n = 17; non-pregnant patients 16.9%; p = 0.65). Of the 17 patients 15 (88.2%) experienced recurrence within the same pregnancy. Patients with a recurrence during pregnancy were treated earlier (median week of gestation: 16; range 10–33 weeks) than pregnant women without a recurrence (median week of gestation: 22; range 12–36 weeks; U = 414.0; p = 0.03).

Pap smear at time of primary treatment of genital warts was available for 712 (86.3%) of 825 women treated between 2003 and 2009. Abnormal cervical cytology was seen in 161 (22.6%) of these patients. The most frequent abnormal Pap smear was Pap IIID (64.6%) followed by Pap IIw (31.0%), Pap IV (2.5%) and Pap III (1.9%). Women with cervical genital warts significantly more frequently had abnormal Pap smears (43.7%) than did women with no involvement of the cervix (19.0%) (χ² = 30.6, p < 0.001).

For women with genital warts treated between 2006 and 2007 (n = 242) systematic follow-up data were available. Median follow-up was 3.1 years (range 4 weeks to 5.9 years). Of these 242 women at least one recurrence was observed in 68 (28.1%) patients and more than three recurrences were seen in 2.5% (Table 1). Median time from primary treatment to first recurrence was 12.7 weeks (range 2.3 weeks to 2.4 years). First recurrence was observed within three months in 51.5% of these patients, while 86.8% of these patients showed the first recurrence within 12 months. Besides laser vaporisation, recurrence of genital warts was treated with imiquimod 5% cream (14.7%), excision (11.8%), podophyllotoxin (2.9%) and electrocoagulation (2.9%).

Pregnant women did not suffer significantly more often from recurrences than non-pregnant patients (p = 0.175, Fig. 2a).

Women with multifocal genital warts significantly more frequently had recurrences than did those with unifocal lesions (p = 0.01; Fig. 2b).

Multivariate analysis confirmed multifocal lesions as an independent risk factor for recurrence with a hazard ratio of 2.9 (Table 3). Specific locations of genital warts and age did not influence the risk of recurrence (Table 3). This analysis was performed on the subset of women treated in 2006 and 2007.

Comparison of the analysed periods from 1992 to 2000 and from 2001 to 2009 showed an increase of 42% in new diagnosed cases of genital warts. Several other studies have also described an increased incidence and prevalence of genital warts within the past two decades [5, 7]. Possible reasons for this increase are changes in sexual behaviour [25], especially a greater number of sex partners, increased awareness, smoking [26], and oral contraceptive use [7]. On the other hand, implementation of the HPV vaccination has led to a decline of infection rates [22, 23, 27]. Both factors- an increase in the non- vaccinated population and a decline in the vaccinated population- underline the importance of the HPV vaccination.

Analysis of all women showed at least one recurrence in 306 of 1798 patients (17%). Interestingly, 30% of the recurrences occurred after more than six months, suggesting that a short follow-up would dramatically underestimate the recurrence rate. It cannot be determined whether the specific recurrence was due to a new infection with a new HPV genotype, a re- infection with the former HPV genotype or a reactivation of the latent HPV genotype.

We collected systematic follow-up information from the gynecologist and/or general practitioner of each woman treated between 2006 and 2007 to estimate the true recurrence rate following laser treatment. These two years were chosen, because they were representative and allow a substantial follow-up period (median 3.1 years). At least one recurrence was observed in 28.1% of these women by contrast to 17.0% in the entire cohort. It is noteworthy that in about 13% of these women first recurrence was observed more than one year after primary treatment. This observation underlines the need to follow up women with genital warts for more than 1 year.

Genital warts have been suggested as a marker for exposure to HPV and subsequently for cervical neoplasia. Munk et al. reported a 1.9-fold increased risk for self-reported abnormal Pap smear in women with a history of genital warts [26]. Additionally, Friis et al. described a 2.0- and a 2.6-fold increased risk for cervical cancer and CIN III, respectively, for women following hospitalization for condylomata acuminate [28]. In the present study abnormal Pap smear was observed in 22.6% of our patients. Abnormal Pap smears were twice as frequent in women with cervical genital warts (43.7%) than in women without cervical involvement (19.0%) and were most frequent within the first two years of the first episode [26]. Based on the high percentage of abnormal Pap smears in women with genital warts and an increased risk for cervical neoplasia, Pap smear at the time of diagnosis of genital warts and regular Pap smear after treatment are recommended.

Little research has been conducted on the determinants influencing the recurrence of genital warts after primary treatment. In our study we observed a decrease in recurrences with increasing age. A possible explanation for this observation is that the number of sexual partners per year usually decreases with increasing age and therefore HPV viral load and HPV reinfections are less frequent.

Women with multifocal genital warts had an almost three times higher risk of recurrence than women with unifocal lesions.

The most affected site was the vulva followed by the perineum/perianal region, the vagina and anus. About one-third of all investigated women had anal warts and almost all these patients additionally had warts in the perineum/perianal region or vulva. Given the fact that unknown anal warts are a frequent cause of relapse of genital warts, proctoscopic evaluation of all women with genital warts of the vulva or the perineum/perianal region is recommended to improve the management of anogenital warts. Proctoscopic examination would also allow the detection of dysplastic lesions in this area.

In pregnancy treatment options for genital warts are limited. Topical treatment with podophyllotoxin or imiquimod cream is contraindicated. The most frequently recommended treatment strategies for pregnant women are surgical therapies including carbon dioxide laser vaporisation. In our cohort 11% of the women were pregnant and recurrence rates were comparable with those in non-pregnant patients. In accordance with Ferency et al. [29] we observed significantly fewer recurrences when laser vaporisation was performed in the third trimester than in the first or second trimester. Genital warts in pregnancy are a strong risk factor for juvenile-onset recurrent respiratory papillomatosis [30]. Due to the rarity of juvenile respiratory papillomatosis, there is no proof that treatment of genital warts in pregnancy reduces the risk of vertical HPV transmission. Nevertheless, treatment of genital warts in pregnancy and reduction of viral burden is recommended.

To the best of our knowledge this is the largest study of recurrence of genital warts in a not- vaccinated population. Main strengths are the large sample size, the period of time women were followed and the same treatment modality in all patients.

Our study encounters several limitations. Due to the retrospective design we cannot exclude a selection bias, although the large number of investigated women and the long follow-up could reduce a possible bias. Another weakness of this study is the lack of data on known risk factors for incident genital warts like sexual behaviour, smoking, and history of sexually transmitted diseases. The influence of these risk factors in the development of genital wart recurrence after primary treatment remains to be elucidated. In some cases we also lack information about former treatments.