What is the follow-up for Cervical Intraepithelial Neoplasia (CIN) grade 1, mild cervical dysplasia?

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Last updated: April 21, 2025View editorial policy

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From the Guidelines

The follow-up for CIN-1 (mild cervical dysplasia) typically involves repeat HPV testing and/or Pap smear in 12 months rather than immediate treatment. For most patients, CIN-1 will resolve spontaneously without intervention as the immune system clears the underlying HPV infection 1. If follow-up testing remains abnormal after 12 months, colposcopy may be repeated. If CIN-1 persists for 2 years or progresses to higher-grade lesions, treatment options like loop electrosurgical excision procedure (LEEP), cryotherapy, or laser therapy may be considered.

  • Key considerations in managing CIN-1 include:
    • The high likelihood of spontaneous regression
    • The risks of unnecessary procedures that could affect future pregnancy outcomes
    • The importance of regular follow-up to monitor for potential progression to higher-grade lesions
  • Patient factors to consider during the observation period include:
    • Avoidance of tobacco use, as smoking impairs immune function and increases risk of persistence or progression
    • Regular follow-up, as approximately 10% of CIN-1 cases may progress to higher-grade lesions if left unmonitored
  • The decision to treat persistent CIN-1 should be based on patient and provider preferences, with consideration of the potential benefits and risks of treatment 1.
  • A diagnostic excisional procedure is recommended if the colposcopic examination is unsatisfactory, the endocervical sampling contains CIN, or the patient has been previously treated 1.

From the Research

Follow-up of CIN-1 Mild Cervical Dysplasia

  • The follow-up of CIN-1 mild cervical dysplasia typically involves a strict follow-up with colposcopy and treatment in case of persistence or progression of the abnormalities 2.
  • The risk of cancer is extremely low, and a conization is not necessary in an asymptomatic woman with a LSIL/ASC-US pap smear in case of CIN-1, even if the squamocolumnar junction is not entirely visualized 2.
  • The rate of progression of a CIN-1 to a CIN-3 or more severe lesion is less than 9% in the two years following the initial diagnosis 2.
  • A CIN-1 is associated with a risk of evolution to a CIN-2 or more severe lesion that is not markedly more important than the risk associated with a LSIL/ASC-US pap smear while the colposcopy is normal or the biopsy is negative 2.

Management Strategies

  • The management of CIN-1 involves a follow-up with cytology and/or HPV testing at 12 months, and a repeat control is necessary at 18 months if the results are positive or persisting ASC-US/LSIL 2.
  • A single negative cotest approximately 1 year after colposcopy predicts a lower subsequent 5-year risk of CIN-2+ than 2 sequential negative HPV tests or 2 sequential negative Pap results 3.
  • Two negative posttreatment tests of each kind confer slightly lower 5-year CIN-2+ risk than one, and the 5-year CIN-2+ risk after 2 negative cotests approaches the risk after a negative Pap test during routine screening 4.

Natural History of CIN-1

  • The natural history of CIN-1 shows that a low rate of progression, suggesting it may be reasonable to prolong the screening interval in women with CIN-1 5.
  • At 6 months, 49% of patients with CIN-1 regress to normal, 45% have persistent low-grade, and 7% progress to high-grade lesions 5.
  • At 12 months, of those with negative pathology at 6 months, 80% remain negative, 16% demonstrate low-grade, and 4% progress to high-grade lesions 5.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

[Management of CIN1].

Journal de gynecologie, obstetrique et biologie de la reproduction, 2008

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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