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Recurrence of cervical intraepithelial neoplasia in human immunodeficiency virus-infected women treated by means of electrosurgical excision of the transformation zone (LLETZ) in Rio de Janeiro, Brazil

Recorrência de neoplasias intraepiteliais cervicais em mulheres infectadas com o vírus da imunodeficiência humana tratadas pela exérese eletrocirúrgica da zona de transformação (EZT) no Rio de Janeiro, Brasil

Abstracts

CONTEXT AND OBJECTIVE:

Human immunodeficiency virus (HIV)-infected women have higher incidence, prevalence, persistence and recurrence of pre-invasive cervical lesions (CIN II or III). The aim here was to investigate the risk of recurrence of CIN II/III among HIV-infected women (HIV+) and uninfected women in a cohort treated by means of large-loop excision of the transformation zone (LLETZ).

DESIGN AND SETTING:

Cohort study conducted at Instituto Fernandes Figueira/Fundação Oswaldo Cruz (IFF/Fiocruz).

METHODS:

60 HIV+ and 209 HIV-negative patients were included in a cohort for follow-up after undergoing LLETZ to treat CIN II/III. A histopathological diagnosis of CIN II/III during the follow-up was taken to constitute recurrence. The following possible confounding variables were assessed: age at treatment and at end of follow-up; histological grade of intraepithelial disease treated; surgical margin involvement; adequacy of colposcopy during the follow-up; CD4+ lymphocyte count; HIV viral load; and type of antiretroviral therapy.

RESULTS:

Among the 60 HIV+ women, six showed recurrent disease during the follow-up. However, among the 209 HIV-negative women, seven showed a new precursor lesion. The relative risk of disease recurrence in the HIV+ women was 4.21 (95% CI = 1.42 to 12.43). The Kaplan-Meyer curve showed that the risk of recurrence was significantly higher among HIV+ women (log-rank test: P = 0.0111).

CONCLUSION:

The HIV+ women in our cohort presented a risk of CIN II/III recurrence at least 42% higher than among the HIV-negative women. These patients should form part of a rigorous screening and follow-up protocol for identification and appropriate treatment of cervical cancer precursor lesions.

Cervical intraepithelial neoplasia; Electrosurgery; Recurrence; Cohort studies; HIV


CONTEXTO E OBJETIVOS:

Mulheres infectadas pelo vírus da imunodeficiência humana (HIV) apresentam maior incidência, prevalência, persistência e recorrência após tratamentos de lesões pré-invasivas do colo uterino (NIC II ou III). O objetivo foi verificar o risco de recorrência de NIC II/III em mulheres infectadas pelo HIV (HIV+) e não infectadas (HIV-) em uma coorte tratada pela exérese eletrocirúrgica da zona de transformação do colo uterino (EZT).

TIPO DE ESTUDO E LOCAL:

Estudo de tipo coorte realizado no Instituto Fernandes Figueira/Fundação Oswaldo Cruz (IFF/Fiocruz).

MÉTODOS:

60 HIV+ e 209 HIV- foram incluídas em uma coorte após terem sido submetidas à EZT para tratamento de NIC II/III. Foi considerado como recorrência o diagnóstico histopatológico de NIC II/III. Foram estudadas as seguintes variáveis possivelmente confundidoras: idade no tratamento e ao final do seguimento, grau histológico da doença intra-epitelial tratada, comprometimento de margens, adequação da colposcopia no seguimento, contagem de linfócitos CD4+, carga viral de HIV e tipo de terapia antiretroviral.

RESULTADOS:

Dentre as 60 mulheres HIV+, 6 apresentaram doença recorrente durante o seguimento. De 209 HIV-, 7 apresentaram uma nova lesão precursora. O risco relativo de recorrência de doença nas HIV+ foi de 4,21 (IC 95% 1,42-12,43). Uma curva de Kaplan-Meyer mostra que o risco de recorrência é significativamente maior em mulheres HIV+ (teste de log-rank: P = 0,0111).

CONCLUSÃO:

Mulheres HIV+ em nossa coorte apresentaram risco de recorrência pelo menos 42% maior do que mulheres HIV-. Essas pacientes devem fazer parte de um protocolo de rastreio e acompanhamento rigoroso para identificação e tratamento adequado das lesões precursoras do câncer de colo uterino.

Neoplasia intra-epitelial cervical; Eletrocirurgia. Recidiva; Estudos de coortes; HIV


INTRODUCTION

The epidemic caused by the human immunodeficiency virus (HIV) infection has spread throughout the world. However, the survival of HIV-infected patients has increased significantly through improvement of its clinical management and with the advent of potent antiretroviral therapy (highly active antiretroviral therapy, HAART).11. Palella FJ Jr, Delaney KM, Moorman AC, et al. Declining morbidity and mortality among patients with advanced immunodeficiency virus infection, HIV Outpatient Study Investigators. N Engl J Med. 1998;338(13):853-60. , 22. Marins JRP, Jamal LF, Chen S, et al. Sobrevivência atual dos pacientes com aids no Brasil. Evidência dos resultados de um esforço nacional. Boletim Epidemiológico - AIDS. 2002;XV(1):49-59. Available from: http://bvsms.saude.gov.br/bvs/periodicos/bol_marco_2002.pdf. Accessed in 2013 (Mar 4).
Available from: http://bvsms.saud...
Consequently, these patients have become a target for chronic and degenerative diseases. Among these diseases, increased frequency of cervical cancer precursors, i.e. cervical intraepithelial neoplasia II and III (CIN II/III), has been observed. These precursors take on special characteristics among HIV-infected women.

HIV-infected women, especially those with low levels of CD4+ cells, present higher risk of persistent infection by HPV (human papillomavirus) and higher rates of low and high-grade squamous intraepithelial lesions and invasive carcinoma of the uterine cervix, in comparison with HIV-negative women. Because of this relationship, presence of CIN is considered to be a condition related to HIV infection, whereas invasive carcinoma of the cervix is an AIDS-defining illness.33. Pantanowitz L. Treatment failure and recurrence of cervical intraepithelial neoplasia in HIV-infected women. Womens Health (Lond Engl). 2010;6(6):781-3.

Cervical cancer is still a health problem in Brazil, since it is the third most frequent tumor in women, according to 2012 estimates from the National Cancer Institute (Instituto National de Cancer, INCA),44. Instituto Nacional do Câncer José Alencar Gomes da Silva. Coordenação Geral de Ações Estratégicas. Coordenação de Prevenção e Vigilância. Estimativa 2012: incidência de câncer no Brasil. Rio de Janeiro: INCA, 2011. Available from: http://www1.inca.gov.br/estimativa/2012/estimativa20122111.pdf. Accessed in 2013 (Mar 4).
Available from: http://www1.inca....
and it accounts for the deaths of 230,000 women per year.55. O desafio feminino do câncer. Rede Câncer. 2009;9(capa). Available from: http://www2.inca.gov.br/wps/wcm/connect/2dec21004eb69218854797f11fae00ee/20_capa.pdf?MOD=AJPERES. Accessed in 2012 (Apr 4).
Available from: http://www2.inca....

There is broad evidence that treating CIN, especially high-grade cases (CIN II and III), is an effective measure for preventing cervical cancer. Several studies have shown that HIV+ women present increased risk of persistence or recurrence of CIN after treatment,66. Russomano F, Reis A, Camargo MJ, Grinsztejn B, Tristão MA. Recurrence of cervical intraepithelial neoplasia grades 2 or 3 in HIV-infected women treated by large loop excision of the transformation zone (LLETZ). Sao Paulo Med J. 2008;126(1):17-22. which is usually related to immunodepression and low levels of CD4+ T lymphocytes,77. Lima MI, Tafuri A, Araújo AC, de Miranda Lima L, Melo VH. Cervical intraepithelial neoplasia recurrence after conization in HIV-positive and HIV-negative women. Int J Gynaecol Obstet. 2009;104(2):100-4. as well as to the extent of endocervical CIN.33. Pantanowitz L. Treatment failure and recurrence of cervical intraepithelial neoplasia in HIV-infected women. Womens Health (Lond Engl). 2010;6(6):781-3. It seems that CD3 T lymphocytes may participate in recurrence of CIN III in HIV+ women who were treated by means of cervical conization.88. Maluf PJ, Michelin MA, Etchebehere RM, Adad SJ, Murta EF. T lymphocytes (CD3) may participate in the recurrence of cervical intraepithelial neoplasia grade III. Arch Gynecol Obstet. 2008;278(6):525-30.

Large-loop excision of the transformation zone (LLETZ) is a first-line therapeutic method for treating high-grade CIN and, in some cases, low-grade CIN.77. Lima MI, Tafuri A, Araújo AC, de Miranda Lima L, Melo VH. Cervical intraepithelial neoplasia recurrence after conization in HIV-positive and HIV-negative women. Int J Gynaecol Obstet. 2009;104(2):100-4. The success rates from treating CIN with LLETZ are high, ranging from 73% to 98%. When used to treat type I or II transformation zones (completely ectocervical or partially endocervical, with the squamocolumnar junction, SCJ, seen within the first centimeter of the endocervical canal), LLETZ is comparable to cold conization and other ablative procedures.99. World Health Organization. International Agency for Research on Cancer. IARC. Monographs on the Evaluation of Carcinogenic Risks to Humans. Volume 90. Human Papillomaviruses. Lyon: World Health Organization. International Agency for Research on Cancer; 2007. Available from: http://monographs.iarc.fr/ENG/Monographs/vol90/mono90.pdf. Accessed in 2013 (Mar 4).
Available from: http://monographs...

10. Prendiville W. LLETZ: theoretical rationale, practical aspects, clinical experience, optimizing the technique. In: Prendiville W, Ritter J, Tatti SA, Twiggs LB, editors. Colposcopy: management options. London: Saunders; 2003. p. 75-89.
- 1111. Instituto Nacional de Câncer (Brasil). Coordenação Geral de Ações Estratégicas. Divisão de Apoio à Rede de Atenção Oncológica. Diretrizes brasileiras para o rastreamento do câncer do colo do útero. Rio de Janeiro: INCA; 2011. Available from: http://www1.inca.gov.br/inca/Arquivos/Diretrizes_rastreamento_cancer_colo_utero.pdf. Accessed in 2013 (Mar 4).
Available from: http://www1.inca...
It presents less morbidity due to shorter duration of surgery, use of local anesthesia and lower blood loss.1212. Boonlikit S, Junghuttakarnsatit P, Asavapiriyanont S. Treatment failure following large loop excision of the transformation zone for the treatment of cervical intraepithelial neoplasia at Rajavithi Hospital. J Med Assoc Thai. 2008;91(1):31-6.

In an initial paper on the risk of recurrence of these diseases during the first years of follow-up of this cohort, we demonstrated that the CIN II/III recurrence rate was 30.06/10,000 women per month among HIV-positive women, and of 4.88/10,000 women per month in the HIV-negative group (relative risk, RR = 6.16; 95% confidence interval, CI = 2.07-18.34).66. Russomano F, Reis A, Camargo MJ, Grinsztejn B, Tristão MA. Recurrence of cervical intraepithelial neoplasia grades 2 or 3 in HIV-infected women treated by large loop excision of the transformation zone (LLETZ). Sao Paulo Med J. 2008;126(1):17-22. The present study shows the results from a longer follow-up and with a larger number of participants in the cohort.

OBJECTIVES

To estimate the incidence and relative risk of recurrence of CIN II/III among HIV-infected women, after LLETZ, compared with women who were not infected by this virus.

METHODS

Study design

Our study was a non-concurrent (prospective and retrospective) comparative cohort study among women with and without HIV infection who underwent LLETZ to treat CIN II/III. The patients were included in the study from the time of their treatment and were monitored by means of colpocytology and colposcopy every six months.

Inclusion criteria

Study Group: HIV+ women diagnosed with CIN II/III who were treated with LLETZ in the Cervical Pathology and Colposcopy Sector, Department of Gynecology, Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira Fundação Oswaldo Cruz (IFF/Fiocruz). These women did not have any history of treatment preceding the therapy that led to their inclusion in the cohort, for the same level of disease, and they underwent at least one cytological and colposcopic evaluation six months after treatment.

Control group: HIV-negative women diagnosed with CIN II/III, with the same characteristics, who were treated and monitored at IFF/Fiocruz.

Sampling, storage, and data processing

In this study, information on the study factor and outcome, and on confounding variables associated with the study factor and/or outcome that possibly influenced this relationship, was gathered.1313. Laupacis A, Wells G, Richardson WS, Tugwell P. Users' guides to the medical literature. V. How to use an article about prognosis. Evidence-Based Medicine Working Group. JAMA. 1994;272(3):234-7. Thus, the variables measured were: presence of HIV; diagnosis of recurrent CIN II/III, which was histologically verified at any time during monitoring after LLETZ; age at treatment and at end of follow-up; histological grade of intraepithelial disease treated by LLETZ (before inclusion); surgical margin involvement in the segment excised by means of LLETZ (possible incomplete excision), as reported from the histopathological examination (before inclusion); adequacy of colposcopy during the follow-up (satisfactory or unsatisfactory); CD4+ T lymphocyte count; HIV viral load quantification; and type of antiretroviral therapy. All these variables were obtained at the time of the diagnosis/treatment and at every follow-up appointment after treatment. Pap smears were provided on these occasions, and, at the next appointment, guided by the result from this test, colposcopy was performed by one of the colposcopists in charge of the Cervical Pathology and Colposcopy Sector of IFF/Fiocruz. In the event of major colposcopic alterations, or minor ones with cytological findings suggesting CIN II or III, a biopsy was applied. When the SCJ was not completely visible and the cytology showed high grade atypia, cervical conization was indicated. Recurrence was considered to have occurred if a diagnosis of CIN II or III was observed in histological specimens obtained by colposcopically guided biopsy or other surgical method (LLETZ or conization).

Information on the HIV-related disease was obtained from documents supplied by the patients themselves or by consulting the medical records in the units where they were being monitored for their HIV infection to be treated. The measures taken into consideration were the ones closest to the follow-up visits.

The patient losses were due to moving home to other states or, mostly among HIV patients, death due to causes other than cervical neoplasia.

The data were stored in a local database at IFF/Fiocruz. At each visit, data relating to that cervical disease and HIV infection, when applicable, were collected. The data were stored in Microsoft Access and then processed using the Epi-Info version 6.4d and Stata 10.0 statistical packages.

Measurements applied and analysis

To estimate the incidence and relative risk of recurrence of pre-invasive lesions, we used a measurement of cumulative incidence in the first and second years and incidence density over the course of the study in each group. In this measurement method, each patient contributed proportionally over the time interval for which she was monitored. To estimate the risk of recurrence over time, we used the Kaplan-Meyer method.

The present work was submitted to and approved by the research ethics committee of IFF/Fiocruz.

RESULTS

Two hundred and sixty-nine patients met the inclusion criteria, distributed according to Table 1. There were no significant differences concerning age during treatment or at the end of the follow-up, although the HIV-negative patients had been monitored for a significantly longer time.

Table 1
Characteristics of patients included in the cohort (from IFF/Fiocruz, 1996-2010) and diagnoses resulting from specimens obtained from large-loop excision of the transformation zone (LLETZ) for cervical intraepithelial neoplasia (CIN)

This study also observed that there were significant differences in the percentages of CIN III (higher in HIV-negative women) and ectocervical margin involvement in the specimens resulting from LLETZ (higher in HIV+). This was not observed for the other margins (endocervical and stromal) (Table 1).

Among the 60 HIV+ women, 6 presented recurrent disease during the follow-up. But among the 209 HIV-negative women, 7 showed a new precursor lesion. These figures were used to calculate the incidence density, which showed that the relative risk was 4.21 (95% CI = 1.42 to 12.43). The overall incidence of recurrence was 7.43 per 1,000 women per year (Table 2).

Table 2
Cumulative incidence and incidence density of cervical intraepithelial neoplasia (CIN) II/III after large-loop excision of the transformation zone (LLETZ) (IFF/Fiocruz, 1996-2010)

To estimate the risk of recurrence over time, we used the Kaplan-Meyer method (Figure 1). It could be seen that HIV+ women presented a significantly higher risk of CIN II/III recurrence after LLETZ (log-rank test: P = 0.0111). Because of the small number of outcomes, it was not possible to identify a period over which detection would be most likely. Moreover, it was not possible to perform analysis on subgroups of HIV+ women according to whether they were using potent antiretroviral therapy, since almost all the women were using it, or according to CD4+ T lymphocyte levels, since this information was only available for a small percentage of the women.

Figure 1.
Kaplan-Meyer curve showing the probability of recurrence over the years of follow-up among women undergoing large-loop excision of the transformation zone (LLETZ) (IFF/Fiocruz, 1996-2010) to treat CIN II or III (IFF/Fiocruz, 1996-2010).

In an attempt to identify other possible confounding factors, we tested the associations between grade of treated disease, some margin involvement, age at the time of treatment, age at the end of the follow-up and length of follow-up until detection of recurrent disease. Only the length of follow-up was statistically associated with recurrence, but this was an inverse relationship (Table 3).

Table 3
Possible factors related to recurrence after large-loop excision of the transformation zone (LLETZ) (IFF/Fiocruz, 1996-2010) to treat cervical intraepithelial neoplasia (CIN)

In another analysis, we sought to identify factors related to residual disease. Thus, we searched for an association between incompletely treated disease (some margin involvement) and persistent disease over the first two years. No such association could be demonstrated (Table 4).

Table 4
Analysis of margin involvement in persistent disease over first two years after large-loop excision of the transformation zone (LLETZ) (IFF/Fiocruz, 1996-2010)

DISCUSSION

The main finding of our study is that the risk of recurrence of cervical cancer precursor lesions was 4.21 times higher among HIV+ patients. This risk was at least 42% higher than among HIV-negative women, possibly reaching up to 12 times more (95% CI = 1.42 to 12.43).

The HIV-negative patients were monitored for a significantly longer time. However, there were no significant differences concerning age during the treatment or at the end of the follow-up.

Regarding the remaining possible confounding factors, we did not find any statistically significant differences relating to the grade of CIN treated, margin involvement, age at the time of treatment or age at the end of the follow-up. Paraskevaidis et al.1414. Paraskevaidis E, Kalantaridou SN, Paschopoulos M, et al. Factors affecting outcome after incomplete excision of cervical intraepithelial neoplasia. Eur J Gynaecol Oncol. 2003;24(6):541-3. reviewed all cases of LLETZ between 1989 and 2000. They found that the only feature that reached statistical significance was age, which was greater in patients with residual disease.

There was a significant difference in the percentages of CIN III and ectocervical margin of involvement in the specimens resulting from LLETZ, and this was higher in HIV-negative patients. Although these factors are related to higher risk of recurrent disease,1515. Hulman G, Pickles CJ, Gie CA, et al. Frequency of cervical intraepithelial neoplasia following large loop excision of the transformation zone. J Clin Pathol. 1998;51(5):375-7.

16. Maluf PJ, Adad SJ, Murta EF. Outcome after conization for cervical intraepithelial neoplasia grade III: relation with surgical margins, extension to the crypts and mitoses. Tumori. 2004;90(5):473-7.

17. Ghaem-Maghami S, Sagi S, Majeed G, Soutter WP. Incomplete excision of cervical intraepithelial neoplasia and risk of treatment failure: a meta-analysis. Lancet Oncol. 2007;8(11):985-93.
- 1818. Oliveira CA, Russomano FB, Gomes Júnior SC, Corrêa Fde M. Risk of persistent high-grade squamous intraepithelial lesion after electrosurgical excisional treatment with positive margins: a meta-analysis. Sao Paulo Med J. 2012;130(2):119-25. it was not possible to correlate the presence of margin involvement with residual disease in our study.

In a nested case-control study, Lodi et al. found that HIV infection and glandular involvement were independently associated with CIN recurrence.1919. 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(1):191-7. However, this histopathological characteristic was not taken into consideration in our study.

In our study, only the length of the follow-up was statistically associated with recurrence. Nevertheless, this was an inverse relationship, which contradicts the hypothesis that this factor contributes towards the risk of recurrent disease. This can be explained by the higher risk of lesion persistence observed in HIV-infected patients, especially those with low levels of CD4+ cells detected in the early years of follow-up.33. Pantanowitz L. Treatment failure and recurrence of cervical intraepithelial neoplasia in HIV-infected women. Womens Health (Lond Engl). 2010;6(6):781-3. According to Tacla et al.,2020. Tacla M, Freire JOO, Tubaki ME. Colposcopia. In: Martins NV, Ribalta JCL, editors. Patologia do trato genital inferior. São Paulo: Editora Roca; 2005. p. 405-12. patients with low levels of CD4+ T lymphocytes present higher risk of developing CIN, probably due to greater intracellular viral replication. However, we were unable to perform this analysis because no information on CD4+ lymphocyte levels was available from most of the patients.

CONCLUSION

The HIV-positive women in our cohort presented a risk of CIN II/III recurrence that was at least 42% higher than among the HIV-negative women. The overall incidence of recurrence was 7.43 per 1,000 women per year, and reached 20.3 per 1,000 women per year if HIV patients alone were considered. Thus, these patients should form part of a more rigorous and more extensive screening and follow-up protocol for identification and appropriate treatment of cervical cancer precursor lesions.

REFERENCES

  • 1
    Palella FJ Jr, Delaney KM, Moorman AC, et al. Declining morbidity and mortality among patients with advanced immunodeficiency virus infection, HIV Outpatient Study Investigators. N Engl J Med. 1998;338(13):853-60.
  • 2
    Marins JRP, Jamal LF, Chen S, et al. Sobrevivência atual dos pacientes com aids no Brasil. Evidência dos resultados de um esforço nacional. Boletim Epidemiológico - AIDS. 2002;XV(1):49-59. Available from: http://bvsms.saude.gov.br/bvs/periodicos/bol_marco_2002.pdf. Accessed in 2013 (Mar 4).
    » Available from: http://bvsms.saude.gov.br/bvs/periodicos/bol_marco_2002.pdf
  • 3
    Pantanowitz L. Treatment failure and recurrence of cervical intraepithelial neoplasia in HIV-infected women. Womens Health (Lond Engl). 2010;6(6):781-3.
  • 4
    Instituto Nacional do Câncer José Alencar Gomes da Silva. Coordenação Geral de Ações Estratégicas. Coordenação de Prevenção e Vigilância. Estimativa 2012: incidência de câncer no Brasil. Rio de Janeiro: INCA, 2011. Available from: http://www1.inca.gov.br/estimativa/2012/estimativa20122111.pdf. Accessed in 2013 (Mar 4).
    » Available from: http://www1.inca.gov.br/estimativa/2012/estimativa20122111.pdf
  • 5
    O desafio feminino do câncer. Rede Câncer. 2009;9(capa). Available from: http://www2.inca.gov.br/wps/wcm/connect/2dec21004eb69218854797f11fae00ee/20_capa.pdf?MOD=AJPERES. Accessed in 2012 (Apr 4).
    » Available from: http://www2.inca.gov.br/wps/wcm/connect/2dec21004eb69218854797f11fae00ee/20_capa.pdf?MOD=AJPERES
  • 6
    Russomano F, Reis A, Camargo MJ, Grinsztejn B, Tristão MA. Recurrence of cervical intraepithelial neoplasia grades 2 or 3 in HIV-infected women treated by large loop excision of the transformation zone (LLETZ). Sao Paulo Med J. 2008;126(1):17-22.
  • 7
    Lima MI, Tafuri A, Araújo AC, de Miranda Lima L, Melo VH. Cervical intraepithelial neoplasia recurrence after conization in HIV-positive and HIV-negative women. Int J Gynaecol Obstet. 2009;104(2):100-4.
  • 8
    Maluf PJ, Michelin MA, Etchebehere RM, Adad SJ, Murta EF. T lymphocytes (CD3) may participate in the recurrence of cervical intraepithelial neoplasia grade III. Arch Gynecol Obstet. 2008;278(6):525-30.
  • 9
    World Health Organization. International Agency for Research on Cancer. IARC. Monographs on the Evaluation of Carcinogenic Risks to Humans. Volume 90. Human Papillomaviruses. Lyon: World Health Organization. International Agency for Research on Cancer; 2007. Available from: http://monographs.iarc.fr/ENG/Monographs/vol90/mono90.pdf. Accessed in 2013 (Mar 4).
    » Available from: http://monographs.iarc.fr/ENG/Monographs/vol90/mono90.pdf
  • 10
    Prendiville W. LLETZ: theoretical rationale, practical aspects, clinical experience, optimizing the technique. In: Prendiville W, Ritter J, Tatti SA, Twiggs LB, editors. Colposcopy: management options. London: Saunders; 2003. p. 75-89.
  • 11
    Instituto Nacional de Câncer (Brasil). Coordenação Geral de Ações Estratégicas. Divisão de Apoio à Rede de Atenção Oncológica. Diretrizes brasileiras para o rastreamento do câncer do colo do útero. Rio de Janeiro: INCA; 2011. Available from: http://www1.inca.gov.br/inca/Arquivos/Diretrizes_rastreamento_cancer_colo_utero.pdf. Accessed in 2013 (Mar 4).
    » Available from: http://www1.inca.gov.br/inca/Arquivos/Diretrizes_rastreamento_cancer_colo_utero.pdf
  • 12
    Boonlikit S, Junghuttakarnsatit P, Asavapiriyanont S. Treatment failure following large loop excision of the transformation zone for the treatment of cervical intraepithelial neoplasia at Rajavithi Hospital. J Med Assoc Thai. 2008;91(1):31-6.
  • 13
    Laupacis A, Wells G, Richardson WS, Tugwell P. Users' guides to the medical literature. V. How to use an article about prognosis. Evidence-Based Medicine Working Group. JAMA. 1994;272(3):234-7.
  • 14
    Paraskevaidis E, Kalantaridou SN, Paschopoulos M, et al. Factors affecting outcome after incomplete excision of cervical intraepithelial neoplasia. Eur J Gynaecol Oncol. 2003;24(6):541-3.
  • 15
    Hulman G, Pickles CJ, Gie CA, et al. Frequency of cervical intraepithelial neoplasia following large loop excision of the transformation zone. J Clin Pathol. 1998;51(5):375-7.
  • 16
    Maluf PJ, Adad SJ, Murta EF. Outcome after conization for cervical intraepithelial neoplasia grade III: relation with surgical margins, extension to the crypts and mitoses. Tumori. 2004;90(5):473-7.
  • 17
    Ghaem-Maghami S, Sagi S, Majeed G, Soutter WP. Incomplete excision of cervical intraepithelial neoplasia and risk of treatment failure: a meta-analysis. Lancet Oncol. 2007;8(11):985-93.
  • 18
    Oliveira CA, Russomano FB, Gomes Júnior SC, Corrêa Fde M. Risk of persistent high-grade squamous intraepithelial lesion after electrosurgical excisional treatment with positive margins: a meta-analysis. Sao Paulo Med J. 2012;130(2):119-25.
  • 19
    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(1):191-7.
  • 20
    Tacla M, Freire JOO, Tubaki ME. Colposcopia. In: Martins NV, Ribalta JCL, editors. Patologia do trato genital inferior. São Paulo: Editora Roca; 2005. p. 405-12.
  • Erratum

    In the article “Recurrence of cervical intraepithelial neoplasia in human immunodeficiency virus-infected women treated by means of electrosurgical excision of the transformation zone (LLETZ) in Rio de Janeiro, Brazil”, published in the São Paulo Medical Journal, volume 131, issue number 6, 2013, the correct name of the fourth author is Beatriz Grinsztejn and not Beatriz Gilda Jegerhorn Grinstejn. The article should be cited thus: Russomano F, Paz BR, Camargo MJ, Grinsztejn B, Friedman RK, Tristao MAP, Oliveira CA. Recurrence of cervical intraepithelial neoplasia in human immunodeficiency virus-infected women treated by means of electrosurgical excision of the transformation zone (LLETZ) in Rio de Janeiro, Brazil. Sao Paulo Med J. 2013; 131(6):405-10. PubMed PMID: 24346780. DOI: 10.1590/1516-3180.2013.1316578.

Publication Dates

  • Publication in this collection
    2013

History

  • Received
    15 Aug 2012
  • Reviewed
    18 Mar 2013
  • Accepted
    09 Apr 2013
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