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. 2020 May 23;8(2):245. doi: 10.3390/vaccines8020245

Table 4.

Persistent/recurrent disease at the end of follow-up in vaccinated and non-vaccinated women related to the first post-conization control status. Values are absolute numbers and percentages.

Clinical Outcome at the End of Follow-Up
Status at the First Post-Conization Control (6 Months) No Disease Persistent/Recurrent LSIL/HPV Persistent/Recurrent HSIL p *
No disease (n = 153) 0.032
Non-vaccinated 55 (83.3) 7 (10.7) 4 (6.1)
Vaccinated 78 (89.7) 9 (10.3) 0 (0.0)
Persistent LSIL/HPV (n = 101) 0.173
Non-vaccinated 28 (65.1) 9 (20.9) 6 (14.0)
Vaccinated 33 (56.9) 21 (36.2) 4 (6.9)
Persistent HSIL/CIN2-3 (n = 11) 0.131
Non-vaccinated 0 (0.0) 1 (33.3) 2 (66.7)
Vaccinated 3 (37.5) 4 (50.0) 1 (12.5)

LSIL: low-grade squamous intraepithelial lesion; HPV: human papillomavirus; HSIL/CIN2-3: high-grade squamous intraepithelial lesion/cervical intraepithelial neoplasia grade 2–3. Status at first control post-conization are defined as follows: (1) persistent HSIL (histologically confirmed HSIL/CIN2-3); (2) persistent LSIL/HPV (abnormal cytology of any grade, and/or positive HPV test result, with biopsy diagnosis of LSIL/CIN1 or negative or no biopsy performed), and (3) no disease (negative HPV test, negative Pap test, and if available, negative biopsy). (1) persistent/recurrent HSIL (presence of histologically confirmed HSIL/CIN2-3, or a repeated HSIL result in at least two Pap smears separated by six months and positive HPV testing result, independently of the histological diagnosis); (2) persistent/recurrent LSIL/HPV (persistent abnormal cytological result of LSIL, ASC-US or AGUS, a single cytology result of HSIL and/or a positive HPV test result without histological diagnosis of HSIL/CIN2-3); and (3) no disease (negative HPV test, negative Pap test, and, if available, a negative biopsy). * Fisher exact test.