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Cervical Disease

Human papillomavirus Posttreatment Clearance Time in Cervical Intraepithelial Neoplasia and Invasive Cervical Cancer

Abudurexiti, Guligeina MSc; Tuerxun, Gulixian PhD; Abulizi, Guzhalinuer PhD; Mijiti, Patiman MD; Aierken, Kailibinuer PhD; Maimaiti, Anaerguli MSc; Li, Hua MSc

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Journal of Lower Genital Tract Disease: January 2020 - Volume 24 - Issue 1 - p 34-37
doi: 10.1097/LGT.0000000000000495
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Cervical cancer is the second most common malignancy worldwide and is responsible for 280,000 deaths annually.1 High-risk human papillomavirus (HPV) was found to be associated with cervical cancer (CC);2 later, the diagnosis, treatment, and follow-up study of CC have been focused on HPV infection.3 Medical treatments can treat cervical lesions caused by HPV infection and can also help the body to clear the virus. The loop electrosurgical excision procedure and the cervical cold-knife conization are the most common surgical procedures for high-grade squamous intraepithelial lesion (HSIL), whereas radical hysterectomy plus pelvic lymph node dissection is the classic surgery for early invasive CC. Radiotherapy and chemotherapy are primary treatments for middle- and late-stage invasive CC. It is shown that the risk of invasive CC for women who had received prior cervical lesion excisions was 10 times greater than that for women without any cervical lesion history.4 Although symptoms and signs of CC may disappear after treatment, the disease recurs in some patients. Treatment is difficult for recurrent CC, and the prognosis is poor. Most patients will die within 2 years after recurrence, and the 5-year survival rate is approximately 10%.5–7

It has also been reported that persistent HPV infection after treatment is the key factor for relapse of cervical intraepithelial neoplasia (CIN) and CC. Therefore, it is crucial to evaluate HPV infection status in the follow-up period.8,9 According to the Society of Gynecologic Oncology guideline, the components of posttreatment surveillance include physical examination, cytology, and HPV testing. Physical examinations are simple and inexpensive. However, microscopic lesions cannot be found only by physical examination. Cytology is widely used for posttreatment surveillance in clinic.10 However, the accuracy of the cytology is closely related to sampling site. Human papillomavirus testing has high specificity and sensitivity and is reported to be effective in monitoring for CC recurrence.11,12 The National Comprehensive Cancer Network guidelines recommend a follow-up strategy of every 3 to 6 month in the first 2 years for cervical lesions after therapy; however, which detection methods should be adopted, including HPV testing and cytology, is not specified. The rationale for HPV DNA testing in the follow-up of patients13 relies primarily on its high negative predictive value, which could enormously reduce the burden of follow-up visits.

On average, 900 cases of CC and 350 cases of CIN are treated at the Affiliated Tumor Hospital of Xinjiang Medical University every year, who should be monitored for posttreatment recurrence. Therefore, in this study, we aimed to establish a reasonable follow-up management strategy for these patients.


This was a retrospective study. Human papillomavirus–infected patients with HSIL (CIN 2–3) and early invasive CC (stages I–II (IIa) squamous cell cervical carcinoma) treated at the Affiliated Tumor Hospital of Xinjiang Medical University between 2012 and 2013 were recruited for the study. A total of 696 HSIL and 1904 early invasive CC patients were treated during that period. Finally, a total of 534 patients (97 HSIL and 437 early invasive CC) with complete available medical information were enrolled. The eligibility criteria were as follows: positive preoperative HPV DNA test results when HSIL or early invasive CC was first diagnosed; treated by electrosurgical excisional procedure; histologically confirmed diagnosis of HSIL and early invasive CC; and no recurrence of HSIL or early invasive CC during follow-up. Cytology and HPV testing are performed during follow-up after treatment. In some patients, although the cytology result is negative, HPV testing result is positive.

The HC-2 detection method was used before treatment and at every posttreatment follow-up visit. Each patient was diagnosed based on pathological results of a cervical biopsy. Clinical stages for invasive CC patients were determined by 2 chief physicians with extensive experience in gynecological oncology. Standard treatments, including cervical conization, radical hysterectomy plus pelvic lymph node dissection, chemotherapy, and radiotherapy, were performed according to patients' diagnoses, and all therapeutic methods complied with the National Comprehensive Cancer Network guidelines. Follow-up procedures were scheduled at 3, 6, 9, 12, 18, and 24 months after treatment. All patients were examined by HC-2 and Pap smears; in the case of abnormal results, colposcopy was performed. Patients' medical information, including personal information, pathological diagnosis, HPV infection status, and therapeutic strategies, was obtained through the hospital's medical record management system. The final follow-up visits of patients were completed by December 2015. Written informed consent was obtained from each study participant before the study. The ethical committee of the Affiliated Tumor Hospital of Xinjiang Medical University approved the study.

Viral clearance was defined as a viral load of less than 1, as detected by the HC-2 method, without conversion to positive status through the remaining follow-up visits. The clearance time of HPV was determined using the Kaplan-Meier method (StataCorp, 2007; StataCorp. Survival analysis and epidemiological tables. Reference manual. Release 10. College Station, TX: Stata Press; 2007). Clearance time of HPV among different age groups, different grades, and different clinical stages were compared using the log-rank test. The significance level was determined as α level of 0.05.

Role of Funding Source

This work was supported by a grant from the Italian Ministry of Health (Applied Research Projects on Screening Programmes, Protocol Number 4, February 4, 2008). The funder had no role whatsoever in the study.


The study population was composed of 97 HSIL patients and 437 early invasive CC patients. Among these HSIL patients, the numbers of CIN 2 and CIN 3 patients were 20 and 77, respectively, whereas the numbers of stage I and II (IIa) CC patients were 147 and 290, respectively.

The 3-, 6-, 9-, 12-, 18-, and 24-month HPV clearance rates of all HSIL and early invasive CC after treatment were 25.84% (138/534), 46.25% (247/534), 54.31% (290/534), 72.47% (387/534), 82.95% (443/534), and 91.95% (491/534). A total of 147, 91, and 43 patients had persistent HPV infection at 12, 18, and 24 months, respectively. All these patients were tested by cytology. Biopsy under colposcopy was performed in cases of atypical squamous cells with undetermined significance. All patients were pathologically normal. The clearance rate of HPV increased along with the length of follow-up. The median clearance time was 10.4 months (see Figure 1).

Analysis of median human papilloma virus clearance time.

The youngest patient in the study was 23 years old, whereas the oldest one was 78 years old. When different age groups of patients were analyzed, the median clearance time at ages 40 years or younger, 41 to 60, and older than 60 were 9 months (95% CI = 6.91–11.09 months), 9 months (95% CI = 7.74–10.27 months), and 12 months (95% CI = 9.21–14.79 months), respectively. No statistically significant difference was found among different age groups (p > .05) (see Figure 2).

Analysis of median human papilloma virus clearance time among different age groups of patients.

The median HPV clearance times of HSIL and early invasive CC were 9 months (95% CI = 7.89–10.11 months) and 6 months (95% CI = 4.28–7.72 months), respectively. The clearance time of HSIL was longer than that of early invasive CC (p < .05) (see Figure 3). The median clearance times of CIN 2 and CIN 3 were 12 months (95% CI = 8.50–15.50 months) and 6 months (95% CI = 4.24–7.76 months), respectively. The median clearance times of CC stages I and II (IIa) were 9 months (95% CI = 7.13–10.87 months) and 9 months (95% CI = 7.62–10.38 months), respectively. No statistical difference was found among different CIN grades (p > .05, p = .31) (see Figure 4) or different CC stages (p > .05, p = .93) (see Figure 5).

Analysis of median human papilloma virus clearance time among different disease types of patients.
Analysis of median human papilloma virus clearance time among different cervical intraepithelial neoplasia grades of patients.
Analysis of median human papilloma virus clearance time among different cervical cancer stages of patients.


There is HPV DNA in almost all CC specimens. Human papillomavirus testing is, therefore, important for screening and monitoring of patients after treatment for HSIL and early invasive CC. In addition, cytology and virology detection methods have been widely used in gynecological oncology, thus enabling cervical-lesion patients to receive timely and accurate treatment.14

Clinical research and epidemiological data have demonstrated that most HPV infections are temporary and can be cleared naturally. Different median time to viral clearance have been reported (e.g., 7 and 19 months)15 in the literature based on different study populations, different detection methods, and different follow-up methods. During follow-ups, clinical physicians often find that the virus clearance needs a certain amount of time in most HSIL and early invasive CC patients after treatment. Surgery, radiotherapy, and chemotherapy cannot clear all HPV and clearing the remnants of HPV relies on the immune function of the body. Therefore, the specific HPV clearance times for HSIL and early invasive CC are not fully clear. In this study, the 3-, 6-, 9-, 12-, 18, and 24-month HPV clearance times of HSIL and early invasive CC after treatment were 25.84%, 46.25%, 54.31%, 72.47%, 82.95%, and 91.95%, respectively, and the median time of HPV clearance was 10.4 months. Nearly half of the patients were HPV positive with negative ThinPrep cytology or cervical biopsy at first and second visits, indicating that HPV testing for follow-up after treatment could be started at 6 to 9 months. This could enormously reduce the burden of follow-up visits, and thus, the physicians' efforts could concentrate on HPV-positive patients. It is also reported that the sensitivity and specificity of HPV testing are higher than those of physical examination and cytology testing.16 Thus, standard HPV testing in follow-up of patients treated for HSIL or early invasive CC is an optional strategy for detecting HPV clearance and for early detection of recurrence of disease.

One prior report has pointed out that HPV clearance was associated with age.17 However, Gulibanu et al18 found that HPV clearance and age were unrelatedin a recent study of Chinese women. In our study, patients' ages were not related to their clearance times for both HSIL and early invasive CC, which is consistent with the findings of Gulibanu et al.18 However, the relationship between age and HPV clearance time needs to be further studied with a larger sample size.

It can take decades for cervical HPV infection to develop into HSIL and progress into early invasive CC. Therefore, early detection and early treatment for patients with cervical lesions will not only improve their quality of life but also reduce the morbidity and mortality of CC. One study in China reported19 that the median HPV clearance time of early invasive CC patients was shorter than that of HSIL patients. We found similar results in this study. This may be because the range of radical CC surgery is large enough for effective and rapid HPV clearance and can also remove the residual cancerous tissue, thereby preventing recurrence as much as possible. However, no statistically significant difference in HPV clearance time was found among different grades of HSIL and different stages of early invasive CC in the current study.


Based on our findings, the median clearance time of HPV was 10.4 months, so delaying first posttreatment follow-up time to 9 months in patients at high risk of noncompliance could potentially reduce burden of cost and repeated clinical visits without significantly compromising patient's safety. This follow-up approach could be consistently applied to all women regardless of age, severity, and extent of disease.


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cervical cancer; cervical intraepithelial neoplasia; human papilloma virus infection; clearance time; post treatment

Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the ASCCP.