Tips for Best Practice on Role of Ablative Therapy in the United States
Post date: November 15, 2024
Reviewed by: Joanne Sheu, MD, MPH
Excision vs. Ablation
Cervical intraepithelial neoplasia (CIN) can be treated with surgical excision or ablation methods. Loop electrosurgical excision procedure (LEEP), the most commonly used excision treatment in high-resource settings, involves surgical removal of the squamocolumnar junction (SCJ) using a wire loop with a high-frequency electric current. Ablative therapies include cryotherapy, thermal ablation and carbon dioxide (CO2) laser ablation. Cryotherapy uses freezing and thawing to cause tissue necrosis, thermal ablation uses heat to cause tissue inflammation and necrosis, and CO2 laser ablation removes tissue by vaporization. Ablative methods are not common in settings where there are LEEP resources and providers trained to perform excision. One disadvantage of ablation is that, unlike excision, it does not yield a pathology specimen for confirmatory diagnosis. Limited studies comparing cryotherapy to LEEP have shown that they have similar recurrence and complication rates, but there are no randomized trials that compare LEEP performance to thermal ablation.
Thermal Ablation
Thermal ablation recently received endorsement by the World Health Organization (WHO) for treatment of CIN 2/3. WHO guidelines are expected to mostly impact low-resource settings where excision is not feasible or accessible. The procedure does not require general anesthetic and the majority of women report mild or moderate discomfort. Several hand-held thermal ablation devices have been introduced into the U.S. market. These instruments are lightweight, portable, work on electricity or a battery, and do not require complex training. These new devices could be used by non-OB/GYN physicians and providers not trained to perform LEEP, increasing the availability of cervical precancer treatment in hard-to-reach or underserved populations.
ASCCP Guidelines Regarding Ablation
ASCCP guidelines state that ablative treatment for CIN 2/3 is acceptable but that excisional treatment is preferred. Excisional treatment is recommended for adenocarcinoma in situ (AIS). The WHO guidelines recommend LEEP over cryotherapy in settings where LEEP is available and accessible. Where LEEP is available, ablation is unacceptable for a lesion that extends into the canal and for a lesion that covers more than 75% of the surface area of the ectocervix or extends beyond the tip of the device being used. Additional situations for which cryotherapy is not recommended are listed in Table 1. Laser ablation, unlike the other ablative techniques, may be appropriate when performed by highly experienced providers in the treatment of large cervical lesions or when the lesion extends to the vagina.
Table 1. Additional situations for which cryotherapy is not recommended (adapted from the ASCCP guidelines, p. 118).
Squamocolumnar junction or the upper limit of any lesion is not fully visualized |
Endocervical canal sample is diagnosed as CIN 2+ or CIN that cannot be graded |
After previous treatment for CIN 2+ |
In the setting of inadequate biopsies of the cervix to confirm histologic diagnosis |
If cancer is suspected |
References:
WHO Guidelines for the Use of Thermal Ablation for Cervical Pre-Cancer Lesions, Geneva: World Health Organization, 2019. Available at https://apps.who.int/iris/handle/10665/329299
Perkins RB, Guido RS, Castle PE, Chelmow D, Einstein MH, Garcia F, et al. 2019 ASCCP Risk-Based Management Consensus Guidelines for Abnormal Cervical Cancer Screening Tests and Cancer Precursors. J. Low Genit Tract Disease 24(2): 102–131.
WHO Guidelines: Use of Cryotherapy for Cervical Intraepithelial Neoplasia, Geneva: World Health Organization, 2011. Available at https://www.ncbi.nlm.nih.gov/books/NBK138476/
Pinder LF, Parham GP, Basu P, Muwonge R, Lucas E, Nyambe N, Sauvaget C, Mwanahamuntu MH, Sankaranarayanan R, Prendiville W. Thermal ablation versus cryotherapy or loop excision to treat women positive for cervical precancer on visual inspection with acetic acid test: pilot phase of a randomized controlled trial. Lancet Oncol. 2020 Jan;21(1):175-184.
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