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2020, Número 09

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Ginecol Obstet Mex 2020; 88 (09)


Importancia de los márgenes quirúrgicos afectados en la conización uterina cervical

María-Ortiz JS, Álvarez-Silvares E, Bermúdez-González M, García LS, Pato MM, Couso CB
Texto completo Cómo citar este artículo Artículos similares

Idioma: Español
Referencias bibliográficas: 76
Paginas: 586-597
Archivo PDF: 266.22 Kb.


PALABRAS CLAVE

Neoplasia intraepitelial cervical, márgenes quirúrgicos, virus del papiloma humano, conización, anticonceptivos orales, uso de condón, vacuna contra VPH, infección por VPH.

RESUMEN

Objetivo: Determinar la asociación entre los márgenes afectados con la persistenciarecurrencia de neoplasia intraepitelial cervical, persistencia del virus del papiloma humano y las reintervenciones.
Materiales y Métodos: Estudio de casos y controles anidado en una cohorte retrospectiva del Complexo Hospitalario Universitario de Ourense (enero 2010-octubre 2017). Criterio de inclusión: mujeres con al menos una revisión postintervención. Criterios de exclusión: mujeres sin evidencia de displasia de alto grado en la pieza de conización y a las que no se dio seguimiento. Variables de estudio: edad, tabaquismo, preservativo, anticonceptivos orales, vacunación contra VPH, persistencia-recurrencia de NIC y de VPH y reintervención. Se realizaron pruebas paramétricas y no paramétricas entre las variables.
Resultados: La cohorte se integró con 248 mujeres, de éstas 81 (32.6%) tuvieron afectación de los márgenes quirúrgicos en la conización. La inmunosupresión, el tabaquismo y la anticoncepción oral fueron las asociaciones más frecuentes en los márgenes afectados. El uso de preservativo y la vacunación contra VPH fueron significativamente más frecuentes en los márgenes libres. Los márgenes afectados reportaron mayor persistencia de VPH (50 vs 23.9%; OR 3.17 (1.90-5.26), p ‹ 0.001), enfermedad persistente-recurrente (47.2 vs 22.5%; OR 3.07 (1.84-5.12), p ‹ 0.001) y reintervenciones (40.2 vs 15.4%; OR 3.679 (2.094-6.463), p ‹ 0.028). El margen más afectado fue, en orden descendente, endocervical (55.6%), exocervical (25%) y ambos (19.4%).
Conclusiones: El margen afectado confiere un riesgo importante en la evolución de la infección por VPH y la recurrencia de la enfermedad.


REFERENCIAS (EN ESTE ARTÍCULO)

  1. Howlader N, et al. SEER Cancer Statistics Review, 1975- 2016 [Internet]. Maryland, United States: National Cancer Institute. https://seer.cancer.gov/csr/1975_2016/

  2. Massad LS, et al. 2012 updated consensus guidelines for the management of abnormal cervical cancer screening tests and cancer precursors. Obstet Gynecol. 2013; 121 (4): 829-46. doi: 10.1097/AOG.0b013e31829b61d6

  3. Ramos MC, et al. High-grade cervical intraepithelial neoplasia, human papillomavirus and factors connected with recurrence following surgical treatment. Clin Exp Obstet Gynecol. 2008; 35 (4): 242-47. https://193.62.193.83/*

  4. Chang DY, et al. Prediction of residual neoplasia based on histopathology and margin status of conization specimens. Gynecol Oncol. 1996; 63 (1): 53-56. doi: 10.1006/ gyno.1996.0277

  5. Ørbo A, et al. Resection margins in conization as prognostic marker for relapse in high-grade dysplasia of the uterine cervix in northern Norway: a retrospective long-term follow-up material. Gynecol Oncol. 2004; 93 (2): 479-83. doi: 10.1016/j.ygyno.2004.03.010

  6. Khalid S, et al. The thickness and volume of LLETZ specimens can predict the relative risk of pregnancyrelated morbidity. BJOG. 2012; 119 (6): 685-91. doi: 10.1111/j.1471-0528.2011.03252.x

  7. Kyrgiou M, et al. Obstetric outcomes after conservative treatment for intraepithelial or early invasive cervical lesions: systematic review and meta-analysis. Lancet. 2006; 367 (9509): 489-98. doi: 10.1016/S0140- 6736(06)68181-6

  8. Danhof NA, et al. The risk of preterm birth of treated versus untreated cervical intraepithelial neoplasia (CIN): a systematic review and meta-analysis. Eur J Obstet Gynecol Reprod Biol. 2015; 188: 24-33. doi: 10.1016/j. ejogrb.2015.02.033

  9. Sadler L, et al. Treatment for cervical intraepithelial neoplasia and risk of preterm delivery. JAMA. 2004; 291 (17): 2100-06. doi: 10.1001/jama.291.17.2100

  10. Reich O, et al. Cervical intraepithelial neoplasia III: longterm outcome after cold-knife conization with clear margins. Obstet Gynecol. 2001; 97 (3): 428-30. doi: 10.1016/ s0029-7844(00)01174-1

  11. Lapaquette TK, et al. Management of patients with positive margins after cervical conization. Obstet Gynecol. 1993; 82 (3): 440-43.

  12. Ramchandani SM, et al. Predicting persistent/recurrent disease in the cervix after excisional biopsy. MedGenMed. 2007; 9 (2): 24. https://www.ncbi.nlm.nih.gov/pmc/articles/ PMC1994835/

  13. Young JL, et al. Cervical adenocarcinoma in situ: the predictive value of conization margin status. Am J Obstet Gynecol. 2007; 197 (2): e1-7. doi: 10.1016/j.ajog.2007.04.035

  14. Lubrano A, et al. Follow-up after LLETZ: a study of 682 cases of CIN 2-CIN 3 in a single institution. Eur J Obstet Gynecol Reprod Biol. 2012; 161 (1): 71-74. doi: 10.1016/j. ejogrb.2011.11.023

  15. Treacy A, et al. Can a more detailed evaluation of excision margins refine cytologic follow-up of women post-LLETZ for high-grade dysplasia? Int J Gynecol Pathol. 2010; 29 (5): 479-82. doi: 10.1097/PGP.0b013e3181dd4f76

  16. Cho HY, et al. Endocervical margin involvement as an important risk factor for abnormal cytology after LLETZ. Int J Gynecol Pathol. 2012; 31 (4): 377-81. doi: 10.1097/ PGP.0b013e31823ef970

  17. Serati M, et al. Risk factors for cervical intraepithelial neoplasia recurrence after conization: a 10-year study. Eur J Obstet Gynecol Reprod Biol. 2012; 165 (1): 86-90. doi: 10.1016/j.ejogrb.2012.06.026

  18. Ghaem-Maghami S, et al. Incomplete excision of cervical precancer as a predictor of treatment failure: a systematic review and meta-analysis. Lancet Oncol. 2017; 18(12): 1665-79. doi: 10.1016/S1470-2045(07)70283-8

  19. Colposcopy and Programme Management. Guidelines for the NHS Cervical Screening Programme [Internet]. UK: Public Health England. http://www.cancerscreening. nhs.uk

  20. Milojkovic M. Residual and recurrent lesions after conization for cervical intraepithelial neoplasia grade 3. Int J Gynaecol Obstet. 2002; 76 (1): 49-53. doi: 10.1016/s0020- 7292(01)00523-9

  21. Malapati R, et al. Factors influencing persistence or recurrence of cervical intraepithelial neoplasia after loop electrosurgical excision procedure. J Low Genit Tract Dis. 2011; 15 (3): 177-79. doi: 10.1097/LGT.0b013e3181fee61d

  22. Baloglu A, et al. Residual and recurrent disease rates following LEEP treatment in high-grade cervical intraepithelial lesions. Arch Gynecol Obstet. 2010; 282 (1): 69-73. doi: 10.1007/s00404-009-1298-3

  23. Kliemann LM, et al. Minimal cold knife conization height for high-grade cervical squamous intraepithelial lesion treatment. Eur J Obstet Gynecol Reprod Biol. 2012; 165 (2): 342-46. doi:10.1016/j.ejogrb.2012.08.016

  24. Narducci F, et al. Positive margins after conization and risk of persistent lesion. Gynecol Oncol. 2000; 76 (3): 311-14. doi: 10.1006/gyno.1999.5697

  25. Jakus S, et al. Margin status and excision of cervical intraepithelial neoplasia: a review. Obstet Gynecol Surv. 2000; 55 (8): 520-27. doi: 10.1097/00006254-200008000-00025

  26. Aluloski I, et al. Factors That Influence Surgical Margin State in Patients Undergoing Cold Knife Conization - A Single Center Experience. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017; 38 (3): 113-20. doi: 10.2478/ prilozi-2018-0012

  27. Acladious NN, et al. Persistent human papillomavirus infection and smoking increase risk of failure of treatment of cervical intraepithelial neoplasia (CIN). Int J Cancer. 2002; 98 (3): 435-39. doi: 10.1002/ijc.10080

  28. Sarian LO, et al. Factors associated with HPV persistence after treatment for high-grade cervical intra-epithelial neoplasia with large loop excision of the transformation zone (LLETZ). J Clin Virol. 2004; 31 (4): 270-74. doi: 10.1016/j. jcv.2004.05.012

  29. Johnson N, et al. Predicting residual disease after excision of cervical dysplasia. BJOG. 2003; 110 (10): 952-55. https:// obgyn.onlinelibrary.wiley.com/doi/epdf/10.1111/j.1471- 0528.2003.99034.x

  30. Costa S, et al. Factors predicting human papillomavirus clearance in cervical intraepithelial neoplasia lesions treated by conization. Gynecol Oncol. 2003; 90 (2): 358-65. doi: 10.1016/s0090-8258(03)00268-3

  31. Alonso I, et al. Pre- and post-conization high-risk HPV testing predicts residual/recurrent disease in patients treated for CIN 2-3. Gynecol Oncol. 2006; 103 (2): 631-36. doi: 10.1016/j.ygyno.2006.04.016

  32. Fogle RH, et al. Predictors of cervical dysplasia after the loop electrosurgical excision procedure in an inner-city population. J Reprod Med. 2004; 49 (6): 481-86.

  33. Moore BC, et al. Predictive factors from cold knife conization for residual cervical intraepithelial neoplasia in subsequent hysterectomy. Am J Obstet Gynecol. 1995; 173 (2): 361-68. doi: 10.1016/0002-9378(95)90253-8

  34. Papoutsis D, et al. Appropriate cone dimensions to achieve negative excision margins after large loop excision of transformation zone in the uterine cervix for cervical intraepithelial neoplasia. Gynecol Obstet Invest. 2013; 75 (3): 163-68. doi: 10.1159/000345864

  35. Dou Y, et al. Triage for management of cervical high-grade squamous intraepithelial lesion patients with positive margin by conization: a retrospective analysis. Front Med. 2017; 11 (2): 223-28. doi: 10.1007/ s11684-017-0517-8.

  36. Zhu M, et al. Factors that influence persistence or recurrence of high-grade squamous intraepithelial lesion with positive margins after the loop electrosurgical excision procedure: a retrospective study. BMC Cancer. 2015; 15: 744. doi: 10.1186/s12885-015-1748-1

  37. Chen Y, et al. Factors associated with positive margins in patients with cervical intraepithelial neoplasia grade 3 and postconization management. Int J Gynaecol Obstet. 2009; 107 (2): 107-10. doi: 10.1016/j.ijgo.2009.05.027

  38. Quéreux C, et al. Pathologie du col et immunodépression [Cervical pathology and immunodepression]. Contracept Fertil Sex. 1994; 22 (12): 771-76.

  39. Wieland U, et al. Human papillomavirus and immunosuppression. Curr Probl Dermatol. 2014; 45: 154-65. doi: 10.1159/000357907.

  40. Roensbo MT, et al. Cervical HPV prevalence and genotype distribution in immunosuppressed Danish women. Acta Obstet Gynecol Scand. 2018; 97 (2): 142-150. doi: 10.1111/aogs.13261.

  41. Kum-Nji P, et al. Tobacco smoke exposure as a risk factor for human papillomavirus infections in women 18-26 years old in the United States. PLoS One. 2019; 14 (10): e0223532. doi: 10.1371/journal.pone.0223532.

  42. Winer RL, et al. Prevalence and risk factors for oncogenic human papillomavirus infections in high-risk mid-adult women. Sex Transm Dis. 2012; 39 (11): 848-56. doi: 10.1097/ OLQ.0b013e3182641f1c

  43. Castle PE, et al. A prospective study of high-grade cervical neoplasia risk among human papillomavirus-infected women. J Natl Cancer Inst. 2002; 94 (18): 1406-14. doi: 10.1093/jnci/94.18.1406

  44. Markowitz LE, et al. Seroprevalence of human papillomavirus types 6, 11, 16, and 18 in the United States: National Health and Nutrition Examination Survey 2003-2004. J Infect Dis. 2009; 200 (7): 1059-67. doi:10.1086/604729

  45. Kreimer AR, et al. Gender differences in sexual biomarkers and behaviors associated with human papillomavirus-16, -18, and -33 seroprevalence. Sex Transm Dis. 2004; 31 (4): 247-56. doi: 10.1097/01.olq.0000118425.49522.2c

  46. Kelsey KT, et al. Human papillomavirus serology and tobacco smoking in a community control group. BMC Infect Dis. 2015; 15: 8. doi: 10.1186/s12879-014-0737-3

  47. Luhn P, et al. The role of co-factors in the progression from human papillomavirus infection to cervical cancer. Gynecol Oncol. 2013; 128 (2): 265-70. doi: 10.1016/j. ygyno.2012.11.003

  48. Bertram CC. Evidence for practice: oral contraception and risk of cervical cancer. J Am Acad Nurse Pract. 2004; 16 (10): 455-61. doi: 10.1111/j.1745-7599.2004.tb00424.x

  49. Appleby P, et al. Cervical cancer and hormonal contraceptives: collaborative reanalysis of individual data for 16,573 women with cervical cancer and 35,509 women without cervical cancer from 24 epidemiological studies. Lancet. 2007; 370 (9599): 1609-21. doi: 10.1016/S0140- 6736(07)61684-5

  50. Hogewoning CJ, et al. Condom use promotes regression of cervical intraepithelial neoplasia and clearance of human papillomavirus: a randomized clinical trial. Int J Cancer. 2003; 107 (5): 811-16. doi: 10.1002/ijc.11474

  51. Bleeker MC, et al. Condom use promotes regression of human papillomavirus-associated penile lesions in male sexual partners of women with cervical intraepithelial neoplasia. Int J Cancer. 2003; 107 (5): 804-10. doi: 10.1002/ ijc.11473

  52. Wheeler CM, et al. Efficacy, safety, and immunogenicity of the human papillomavirus 16/18 AS04-adjuvanted vaccine in women older than 25 years: 7-year follow-up of the phase 3, double-blind, randomised controlled VIVIANE study. Lancet Infect Dis. 2016; 16 (10): 1154-68. doi: 10.1016/ S1473-3099(16)30120-7

  53. Skinner SR, et al. Efficacy, safety, and immunogenicity of the human papillomavirus 16/18 AS04-adjuvanted vaccine in women older than 25 years: 4-year interim follow-up of the phase 3, double-blind, randomised controlled VIVIANE study. Lancet. 2014; 384 (9961): 2213-27. doi: 10.1016/ S0140-6736(14)60920-X

  54. Castle PE, Schmeler KM. HPV vaccination: for women of all ages? Lancet. 2014; 384 (9961): 2178-80. doi: 10.1016/ S0140-6736(14)61230-7

  55. Kang WD, et al. Is vaccination with quadrivalent HPV vaccine after loop electrosurgical excision procedure effective in preventing recurrence in patients with high-grade cervical intraepithelial neoplasia (CIN2-3)? Gynecol Oncol. 2013; 130 (2): 264-68. doi: 10.1016/j.ygyno.2013.04.050

  56. Nam K, et al. Factors associated with HPV persistence after conization in patients with negative margins. J Gynecol Oncol. 2009; 20 (2): 91-95. doi: 10.3802/jgo.2009.20.2.91

  57. Tasci T, et al. Is there any predictor for residual disease after cervical conization with positive surgical margins for HSIL or microinvasive cervical cancer? J Low Genit Tract Dis. 2015; 19 (2): 115-18. doi: 10.1097/LGT.0000000000000079

  58. Chambo Filho A, et al. Positive endocervical margins at conization: repeat conization or colposcopic follow-up? A retrospective study. J Clin Med Res. 2015; 7 (7): 540-44. doi: 10.14740/jocmr2171w

  59. Dos Santos Melli PP, et al. Multivariate analysis of risk factors for the persistence of high-grade squamous intraepithelial lesions following loop electrosurgical excision procedure. Int J Gynaecol Obstet. 2016; 133 (2): 234-37. doi: 10.1016/j.ijgo.2015.09.020

  60. Oliveira CA, et al. 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. doi: 10.1590/s1516- 31802012000200009

  61. Andrade CE, et al. Prognostic scores after surgical treatment for cervical intraepithelial neoplasia: a proposed model and possible implications for post-operative followup. Acta Obstet Gynecol Scand. 2014; 93 (9): 941-48. doi: 10.1111/aogs.12446

  62. Sangkarat S, et al. Long-term outcomes of a loop electrosurgical excision procedure for cervical intraepithelial neoplasia in a high incidence country. Asian Pac J Cancer Prev. 2014; 15 (2): 1035-39. doi: 10.7314/apjcp.2014.15.2.1035

  63. Wu J, et al. Analysis of Residual/Recurrent Disease and Its Risk Factors after Loop Electrosurgical Excision Procedure for High-Grade Cervical Intraepithelial Neoplasia. Gynecol Obstet Invest. 2016; 81 (4): 296-301. doi: 10.1159/000437423

  64. Arbyn M, et al. Incomplete excision of cervical precancer as a predictor of treatment failure: a systematic review and meta-analysis. Lancet Oncol. 2017; 18 (12): 1665-79. doi: 10.1016/S1470-2045(17)30700-3

  65. Kietpeerakool C, et al. Cervical intraepithelial neoplasia II-III with endocervical cone margin involvement after cervical loop conization: is there any predictor for residual disease? J Obstet Gynaecol Res. 2007; 33 (5): 660-64. doi: 10.1111/j.1447-0756.2007.00628.x

  66. Fu Y, et al. Residual disease and risk factors in patients with high-grade cervical intraepithelial neoplasia and positive margins after initial conization. Ther Clin Risk Manag. 2015; 11: 851-56. doi: 10.2147/TCRM.S81802

  67. Verguts J, et al. Prediction of recurrence after treatment for high-grade cervical intraepithelial neoplasia: the role of human papillomavirus testing and age at conization. BJOG. 2006; 113 (11): 1303-7. doi: 10.1111/j.1471- 0528.2006.01063.x

  68. Prato B, et al. Correlation of recurrence rates and times with posttreatment human papillomavirus status in patients treated with loop electrosurgical excision procedure conization for cervical squamous intraepithelial lesions. Int J Gynecol Cancer. 2008; 18 (1): 90-94. doi: 10.1111/j.1525-1438.2007.00965.x

  69. Kim WY, et al. Conservative management of stage IA1 squamous cell carcinoma of the cervix with positive resection margins after conization. Int J Gynaecol Obstet. 2010; 109 (2): 110-12. doi: 10.1016/j.ijgo.2009.11.017

  70. Chen L, et al. Risk Factor Analysis of Persistent High-Grade Squamous Intraepithelial Lesion After Loop Electrosurgical Excision Procedure Conization. J Low Genit Tract Dis. 2019; 23 (1): 24-27. doi: 10.1097/LGT.0000000000000444

  71. Houfflin Debarge V, et al. Value of human papillomavirus testing after conization by loop electrosurgical excision for high-grade squamous intraepithelial lesions. Gynecol Oncol. 2003; 90 (3): 587-92. doi: 10.1016/s0090- 8258(03)00372-x

  72. Bae JH, et al. Persistence of human papillomavirus as a predictor for treatment failure after loop electrosurgical excision procedure. Int J Gynecol Cancer. 2007; 17 (6): 1271-77. doi: 10.1111/j.1525-1438.2007.00945.x

  73. Venturoli S, et al. Correlation of high-risk human papillomavirus genotypes persistence and risk of residual or recurrent cervical disease after surgical treatment. J Med Virol. 2008; 80 (8): 1434-40. doi: 10.1002/jmv.21198

  74. Ayhan A, et al. Risk factors for residual disease after cervical conization in patients with cervical intraepithelial neoplasia grades 2 and 3 and positive surgical margins. Eur J Obstet Gynecol Reprod Biol. 2016; 201: 1-6. doi: 10.1016/j.ejogrb. 2016.03.021

  75. Diaz ES, et al. Predictors of residual carcinoma or carcinoma- in-situ at hysterectomy following cervical conization with positive margins. Gynecol Oncol. 2014; 132 (1): 76-80. doi: 10.1016/j.ygyno.2013.11.019

  76. Kjellberg L, et al. Smoking, diet, pregnancy and oral contraceptive use as risk factors for cervical intra-epithelial neoplasia in relation to human papillomavirus infection. Br J Cancer. 2000; 82 (7): 1332-38. doi: 10.1054/ bjoc.1999.1100




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