JAIDS Journal of Acquired Immune Deficiency Syndromes:
Brief Report: Clinical Science
Factors Associated With Recurrence of Cervical Intraepithelial Neoplasia 2+ After Treatment Among HIV-Infected Women in Western Kenya
Huchko, Megan J. MD, MPH*; Leslie, Hannah MPH†; Maloba, May RN‡; Bukusi, Elizabeth A. MBChB, MMed, MPH, PhD‡,§; Cohen, Craig R. MD, MPH*
*Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, San Francisco, CA;
†Department of Epidemiology, University of California, Berkeley, CA;
‡Kenya Medical Research Institute, Nairobi, Kenya; and
Correspondence to: Megan J. Huchko, MD, MPH, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, 50 Beale Street, Ste 1200, San Francisco, CA 94105 (e-mail: firstname.lastname@example.org).
Salary of M.J.H. is supported by the National Center for Advancing Translational Sciences, National Institutes of Health, through UCSF-CTSI Grant KL2 TR000143. The remaining authors have no funding or conflicts of interest to disclose.
Received November 12, 2013
Accepted January 06, 2014
Abstract: HIV-infected women are at increased risk for recurrence of cervical dysplasia after treatment. Short-term recurrence rates may reflect treatment efficacy and therefore impact screening protocols and follow-up planning. We conducted a prospective study of 297 HIV-infected women undergoing loop electrosurgical excision procedure for cervical intraepithelial neoplasia 2+ (CIN2+) in an HIV clinic in Kisumu, Kenya. By 6 months after the procedure, 20 (7.1%) of women had recurrent CIN2+. Recurrence was significantly associated with CD4+ nadir but not with highly active antiretroviral therapy use. Longer-term follow-up of this cohort will illustrate the potential impact of highly active antiretroviral therapy and immune status on CIN2/3 disease recurrence.
The global burden of both cervical cancer and HIV is borne by women in low- and middle-income countries, where health care infrastructure is limited.1,2 In addition to the lack of cervical cancer prevention programs in these settings, HIV infection increases women's risk for cervical cancer through an increase in the prevalence of human papillomavirus infections and development of human papillomavirus–related precancerous and cancerous lesions.3–6 Cervical cancer risk and outcomes worsen with increasing immune dysfunction.7,8 HIV-infected women also have increased rates of recurrence after treatment for cervical intraepithelial neoplasia 2+ (CIN2+), the immediate cervical cancer precursor.9,10 Although access to highly active antiretroviral therapy (HAART) in many countries has dramatically increased over the past decade, the impact of HAART on the development of cervical precancer and recurrence after treatment remain unclear.11–15 This means that an increasing number of HIV-infected women are living longer with a potentially higher risk for cervical cancer.
Risk for cervical cancer can be greatly reduced if women have access to screening programs with effective treatment for precancerous lesions. Efforts to implement screening programs in low- and middle-income countries focus on cost and infrastructure requirements, and often aim to achieve a single lifetime screening, with treatment as needed.16 For HIV-infected women, the high risk of disease recurrence may make the single lifetime screening model inadequate. Estimates for the incidence of disease recurrence after treatment vary widely from 25% to 55% at 12 months in HIV-infected women17–19 compared with 5%–16% in HIV-negative women.20,21 There are very few studies focusing on early posttreatment outcomes (6 months) in HIV-infected women.18 Disease identified at 6 months or less may represent either treatment failure or disease recurrence, both of which necessitate additional follow-up and possibly retreatment. Identification of clinical and demographic factors that may put HIV-infected women at increased risk for early posttreatment recurrence of CIN2+ are also important, as they may potentially impact clinical care decisions and posttreatment follow-up guidelines.
Cervical cancer prevention strategies must be modified to address the increased risk of disease in HIV-infected women. To inform cervical cancer prevention programs offered to HIV-infected women, we sought to examine the early recurrence rate and factors associated with recurrence, for biopsy-confirmed CIN2+ after treatment with loop electrosurgical excision procedure (LEEP) among HIV-infected women attending a cervical cancer screening program in Kisumu, Kenya.22
We conducted a prospective cohort study among HIV-infected women undergoing primary treatment for biopsy-confirmed CIN2+ between March 2008 and December 2012 at the family AIDS care and education services program (FACES). We sought to enroll 300 women, with a 2:1 ratio of HAART users to nonusers. HAART users were defined as women who had been on HAART for at least 3 months and reported at least 90% adherence during the past 3 months. HAART use was defined as a triple antiretroviral drug regimen prescribed for clinical or immunologic indications. Nonusers were defined as women not on HAART at the time of their LEEP, who did not meet clinical or immunologic criteria to initiate HAART and had not received antiretrovirals for prevention of mother-to-child transmission within the past 6 months. Exclusion criteria included pregnancy, HAART use less than 3 months, or (for nonusers) in the past, <90% HAART adherence and plans to move out of the clinic area during the 24-month follow-up period.
LEEP was performed by trained and certified clinical officers in the clinic in 1–3 passes using the coagulation setting.23 Women who underwent LEEP for CIN2+ were given an appointment to return to the clinic at 4–6 weeks posttreatment. At that visit, they were offered enrollment in the follow-up study and signed a written informed consent. Women who enrolled in the study participated in a post-LEEP questionnaire to assess their experience with the LEEP, including any post-LEEP symptoms or adverse events.24 They were then scheduled to come back for colposcopy at 6, 12, and 24 months postprocedure. Colposcopy was performed by trained and certified providers with biopsy performed for any lesions suggestive of CIN2+ on colposcopy during those follow-up visits.25 Biopsy specimens were immediately placed in 10% buffered formalin and stored at room temperature until they were sent to the Kenya Medical Research Institute pathology laboratory in Nairobi. Final diagnoses were based on the colposcopy, and if taken, histopathology results. Results were categorized as negative (normal squamous epithelium), inflammation, CIN1, CIN2/3, or invasive cancer. For specimens with more than 1 diagnosis, the outcome was defined as the most severe diagnosis. Repeat LEEP was offered to women who had recurrence of CIN2/3.
Information from the cervical cancer screening visit was collected on a paper form and entered into an access database (Microsoft, Redmond, WA). Clinical and demographic variables from the FACES clinical encounter closest (within 6 months) to the time of the LEEP were obtained through the electronic medical record system (OpenMRS). Clinical variables that were likely to change between enrollment and 6-month follow-up visit, including CD4+ cell count, World Health Organization (WHO) stage, family planning method, and any HAART initiation or regimen change were collected from patient interviews as well as review of clinical data in OpenMRS.
Sample size calculations were based on an assumption of at least 10% recurrence defined as CIN2+. We calculated that a sample size of 270 was needed to determine a difference in recurrence of 15% between women on HAART and not on HAART. We modeled time to recurrence using Cox proportional hazards models because of individual variation in exact time of follow-up; clinical variables that changed between baseline and follow-up were included as time-varying covariates. We implemented 2 sets of models: (1) individual assessment of each predictor adjusting for age and (2) regressing HAART on time to recurrence controlling for CD4+ nadir and covariates that were significant at P < 0.10 in the first model. We selected CD4+ nadir as the best available indicator of pre-HAART immune dysfunction out of recent CD4+ nadir, most recent CD4+ count, and worst WHO stage. Sensitivity analyses were performed without HAART in the model and excluding women who initiated HAART between enrollment and the 6-month follow-up visit. We performed an additional sensitivity model including CIN1 as an outcome. All statistical analyses were performed in Stata 11 (StataCorp LP, College Station, TX).
Ethical approval was obtained from the University of California San Francisco Committee for Human Subjects Research and the Kenya Medical Research Institute Ethical Review Committee.
Two hundred ninety-seven women with CIN2+ underwent LEEP at FACES between March 2008 and December 2012 and enrolled in the follow-up study, of whom 283 (95.2%) contributed a total of 1758 months (mean: 6.2 months) of valid follow-up time. Among the 15 (5.1%) women without follow-up data, 4 were lost-to-follow-up at FACES, 1 died of other opportunistic infections, 1 sought a second opinion and had a hysterectomy, 5 were missing results, and 4 came in for follow-up within 3 months or after 12 months of LEEP and thus were not included in this analysis. At the time of LEEP, the average age of participants was 32.6 years (±6.3), average CD4+ count was 418 (±252), 52% were WHO clinical stage 1 or 2, and 194 (65.3%) were on HAART (Table 1).
Twenty [7.1%, 95% confidence interval (CI): 4.4 to 10.7] women had CIN2+ and 8 (2.8%, 95% CI: 1.2 to 5.5) had CIN1 detected at their 6-month follow-up. Among the CIN2+ cases, there were 2 invasive cancers diagnosed on biopsy. The incidence of recurrent CIN2+ over follow-up period was 13.7 per 100 person-years. Rates of recurrence did not differ significantly by HAART status. The incidence rate ratio for recurrence among women on HAART compared with HAART naive women was 2.25 (95% CI: 0.7 to 12.0). On bivariate analysis controlling for age, significant predictors of recurrence were gravidity, CD4+ count before the 6-month visit <350 cells per cubic millimeter CD4+ nadir <200 cells per cubic millimeter and WHO stage 4 (Table 2; column 1). HAART use was not significantly associated with recurrence, even when adjusting for CD4+ nadir and other covariates (Table 2; column 2) and after restricting to prestudy HAART use (data not shown). Gravidity remained associated with reduced recurrence in the adjusted model, although this association became insignificant in both sensitivity analyses (data not shown). CD4+ nadir remained associated with recurrence in all models.
This prospective cohort of HIV-infected women undergoing LEEP for CIN2+ showed a lower than expected rate of disease recurrence (7.1%) at 6 months based on earlier reports.18,26 In a final multivariable model, women with a lower CD4+ nadir had an increased risk of disease recurrence at 6 months. We did not find a difference in recurrence rates among women on HAART compared with those not on HAART, even after controlling for clinical variables reflective of disease status and restricting analysis to women on HAART before LEEP.
This study has several strengths. This is a primary data analysis from a relatively large number of HIV-infected women followed prospectively, so we were able to determine incidence and incidence ratio of disease recurrence, which can be more universally applied across populations. We studied a single treatment modality, LEEP, which can be safely performed in a low-resource setting23; others studied a combination of LEEP and cold knife cone.18,26 Another strength of this study is that we defined recurrence as biopsy-proven CIN2+, in contrast with other studies that have included CIN1 and/or abnormal cytology results as recurrence.17 We chose this outcome because it is the most clinically relevant in terms of guiding decisions about additional treatment. Finally, because this study took place within the FACES-supported HIV care clinic, we had a high rate of follow-up and were able to use laboratory and medical record data to update clinical and demographic variables throughout the study.
There were also several limitations in this study. We did not see a significant difference in recurrence rates between women on HAART and not on HAART. This could be due to a true lack of biological difference, or insufficient power to detect a true difference because of low numbers of women not on HAART, and/or a lower than expected CIN2+ recurrence rate. In addition, we were not able to look at the impact of specific HAART regimens or classifications on recurrence risk. This was due to both sample size and limited availability of different HAART regimens in our settings (less than 10% of participants were on protease inhibitor–containing regimens). Finally, although we were able to look at the size of the LEEP specimen, we were not able to comment on margins at the time of treatment because LEEP was performed using the coagulation function. Because disease margin status has been shown to be predictive of recurrence in the past,21 we considered altering the LEEP protocol. However, optimizing the procedure to reduce the risk for postprocedure bleeding in this outpatient setting was thought more important.
Although HAART was not significantly associated with recurrence outcomes, our cohort had an overall better immune status than previous studies, reflected in a higher proportion of women on HAART, greater mean CD4+ count and less advanced WHO stage.26 It is possible that our overall lower rate of recurrence is related to the better immune status, and that HAART would have a greater impact in women who have more immune dysfunction. It will be important to evaluate CIN2+ prevalence at 12 and 24 months postprocedure to see if the 6-month outcomes are predictive of lower rates of recurrence in the long term and to further explore factors associated with recurrence at later time points. These findings will help define the need for follow-up after treatment for CIN2+ in HIV-infected women, especially in settings implementing a “screen & treat” protocol. Low rates of early recurrence as seen in this study suggest that it may be safe to lengthen the first post-LEEP follow-up in selected populations and support the new WHO recommendations for a 1-year posttreatment follow-up among HIV-infected women in resource-limited settings.27
1. Ferlay J, Shin HR, Bray F, et al.. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010;127:2893–2917.
2. UNAIDS. Global Report: UNAIDS Report on the Global AIDS Epidemic 2010. 2010.
3. De Vuyst H, Gichangi P, Estambale B, et al.. Human papillomavirus types in women with invasive cervical carcinoma by HIV status in Kenya. Int J Cancer. 2008;122:244–246.
4. Chaturvedi AK, Madeleine MM, Biggar RJ, et al.. Risk of human papillomavirus-associated cancers among persons with AIDS. J Natl Cancer Inst. 2009;101:1120–1130.
5. Palefsky J. Biology of HPV in HIV infection. Adv Dent Res. 2006;19:99–105.
6. Strickler HD, Burk RD, Fazzari M, et al.. Natural history and possible reactivation of human papillomavirus in human immunodeficiency virus-positive women. J Natl Cancer Inst. 2005;97:577–586.
7. Denny L, Boa R, Williamson AL, et al.. Human papillomavirus infection and cervical disease in human immunodeficiency virus-1-infected women. Obstet Gynecol. 2008;111:1380–1387.
8. Engels EA, Biggar RJ, Hall HI, et al.. Cancer risk in people infected with human immunodeficiency virus in the United States. Int J Cancer. 2008;123:187–194.
9. Cejtin HE, Malapati R, Chaparala S. A comparison of loop electrosurgical excision procedures between human immunodeficiency virus-seropositive and -seronegative women. J Lower Genital Tract Dis. 2011;15:37–41.
10. Lodi CT, Michelin MA, Lima MI, et al.. Factors associated with recurrence of cervical intraepithelial neoplasia after conization in HIV-infected and noninfected women. Arch Gynecol Obstet. 2011;284:191–197.
11. World Health Organization. Global HIV/AIDS Response: Progress Report 2011. Key Facts on HIV Epidemic and Progress in Regions and Countries in 2010, Sub-Saharan Africa. 2011.
12. Bratcher LF, Sahasrabuddhe VV. The impact of antiretroviral therapy on HPV and cervical intraepithelial neoplasia: current evidence and directions for future research. Infect Agent cancer. 2010;5:8.
13. Franceschi S, Lise M, Clifford GM, et al.. Changing patterns of cancer incidence in the early- and late-HAART periods: the Swiss HIV Cohort Study. Br J Cancer. 2010;103:416–422.
14. Adler DH, Kakinami L, Modisenyane T, et al.. Increased regression and decreased incidence of human papillomavirus-related cervical lesions among HIV-infected women on HAART. AIDS. 2012;26:1645–1652.
15. Zeier MD, Nachega JB, Van Der Merwe FH, et al.. Impact of timing of antiretroviral therapy initiation on survival of cervical squamous intraepithelial lesions: a cohort analysis from South Africa. Int J STD AIDS. 2012;23:890–896.
16. World Health Organization. Comprehensive Cervical Cancer Prevention and Control: A Healthier Future for Girls and Women. Geneva, Switzerland: World Health Organization; 2013.
17. Malapati R, Chaparala S, Cejtin HE. Factors influencing persistence or recurrence of cervical intraepithelial neoplasia after loop electrosurgical excision procedure. J Low Genit Tract Dis. 2011;15:177–179.
18. Reimers LL, Sotardi S, Daniel D, et al.. Outcomes after an excisional procedure for cervical intraepithelial neoplasia in HIV-infected women. Gynecol Oncol. 2010;119:92–97.
19. Massad LS, Fazzari MJ, Anastos K, et al.. Outcomes after treatment of cervical intraepithelial neoplasia among women with HIV. J Low Genit Tract Dis. 2007;11:90–97.
20. Katki HA, Schiffman M, Castle PE, et al.. Five-year risk of recurrence after treatment of CIN 2, CIN 3, or AIS: performance of HPV and Pap cotesting in posttreatment management. J Low Genit Tract Dis. 2013;17:S78–S84.
21. Ryu A, Nam K, Kwak J, et al.. Early human papillomavirus testing predicts residual/recurrent disease after LEEP. J Gynecol Oncol. 2012;23:217–225.
22. Lewis Kulzer J, Penner JA, Marima R, et al.. Family model of HIV care and treatment: a retrospective study in Kenya. J Int AIDS Soc. 2012;15:8.
23. Huchko MJ, Maloba M, Bukusi EA. Safety of the loop electrosurgical excision procedure performed by clinical officers in an HIV primary care setting. Int J Gynaecol Obstet. 2010;111:89–90.
24. Woo VG, Cohen CR, Bukusi EA, et al.. Loop electrosurgical excision procedure: safety and tolerability among human immunodeficiency virus-positive Kenyan women. Obstet Gynecol. 2011;118:554–559.
25. Huchko MJ, Bukusi EA, Cohen CR. Building capacity for cervical cancer screening in outpatient HIV clinics in the Nyanza province of western Kenya. Int J Gynaecol Obstet. 2011;114:106–110.
26. Pantanowitz L. Treatment failure and recurrence of cervical intraepithelial neoplasia in HIV-infected women. Womens Health (Lond Engl). 2010;6:781–783.
27. WHO Guidelines for Screening and Treatment of Precancerous Lesions for Cervical cancer Prevention. Geneva, Switzerland: World Health Organization; 2013.
cervical cancer prevention; HIV; women's global health; Kenya; loop electrosurgical excision procedure; treatment recurrence
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