0036-3634 0036-3634 S0036-36342003000900007 France 00 00 2003 00 00 2003 45 340 344

ARTICLE ARTÍCULOS

 

The 2001 Bethesda System

 

El Sistema Bethesda 2001

 

 

Christine Bergeron, MD

Laboratoire Pasteur Cerba, Cergy Pontoise, Cedex9, France

 

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ABSTRACT

The Bethesda system is a system of terminology for reporting the results of cervical cytology. It was developed in 1988, and is now widely used in the United States. This system was updated in April 2001. The most important modifications are the following: a) elimination of the category "satisfactory but limited by", b) the reintegration of benign modifications in the normal category, c) "atypical squamous cells of undetermined significance" is now named "atypical squamous cells" and subdivided into "atypical squamous cells of undetermined significance" and "cannot exclude high grade squamous intraepithelial lesion"; and d) endocervical adenocarcinoma in situ which is now a separate entity. Low grade squamous intraepithelial lesions and high grade squamous intraepithelial cells remain unchanged. Recommendations have been proposed concerning automated review and ancillary testing. This paper is available too at: http://www.insp.mx/salud/index.html

Key words: Bethesda System; cytology screening; cervical cancer; human papillomavirus

RESUMEN

El Sistema Bethesda es un sistema de terminología para informar los resultados de citología cervical. Se inició en 1988 y en la actualidad se usa en todos los Estados Unidos de América. Este sistema se actualizó en abril de 2001. Las modificaciones más importantes son las siguientes: a) eliminación de la categoría "satisfactorio pero limitado por", b) se reintegraron las modificaciones benignas en la categoría normal, c) la categoría "células escamosas atípicas de significado indeterminado" ahora se denomina "células escamosas atípicas", y se subdivide en "células escamosas atípicas de significado indeterminado" y "no se puede excluir una lesión escamosa de alto grado", y d) adenocarcinoma endocervical in situ, que ahora es una entidad separada. Las lesiones escamosas intraepiteliales de bajo y alto grado quedan sin cambios. Se proponen recomendaciones relacionadas con el uso de la revisión automatizada y la utilización de pruebas auxiliares. Este artículo también está disponible en: http://www.insp.mx/salud/index.html

Palabras clave: Sistema Bethesda; citología; detección oportuna de cáncer; cáncer cervical; virus de papiloma humano

 

 

The Bethesda system was first proposed in 19881 as a response model for the interpretation of cervical cell cytology. The aim was to unify the terminology and thereby improve patient management. Following several test years, the system was evaluated in 1991 during a second workshop.2 More than 90% of laboratories currently use this response system in the United States.3 The aim of the Bethesda conference which was convened from 30 April to 2 May, 2001, was to re-evaluate the terminology used since 1991, and if necessary propose new modifications.4 Six to ten experts discussed each of the following topics: quality of sampling, benign alterations, endometrial cells, among other topics. A discussion website was used for six months to receive comments regarding recommendations. Each of these groups included a cytopathologist, a cytotechnician, and a clinician among other international experts. The conference convened more than 400 representatives including cytologists, cytotechnicians, pathologists, general physicians, public health physicians and epidemiologists. The conference was organized by the National Cancer Institute (NCI) and sponsored by 44 cytology associations. More than 20 countries were represented.

]]> The recommendations have been presented in the form of a literature review, expert opinions, and commentaries sent through the website over the six months before and after the April 2001 conference.4

I. Specimen adequacy

Sampling quality was one of the most innovative proposals made in 1988. Three categories were proposed: satisfactory, satisfactory but limited due to unsatisfactory sampling, and unsatisfactory. The second category was used for smears not containing endocervical or metaplastic cells, which are the proof of sampling the transformation area, or partial inflammatory smears. This category was eliminated since clinicians felt obliged to redo the smears. It is now suggested that along with the evaluation of smears, note should be made regarding the presence of less than 10 endocervical cells, inflammation clouding evaluation of more than 75% of the smear, and that the clinician must make the decision whether or not to redo a new smear.

If the smear is considered inadequate, the reason must be noted. Between 8 000 and 12 000 squamous cells must be present in a conventional smear, and 5 000 cells for a liquid smear. Other reasons for not being able to interpret smears were identical to those presented in 1991. Smears without appropriate patient identification, or those which arrive broken must be considered unsatisfactory. Table I summarizes the Bethesda 2001 system.

 

 

II. General categorization

This is an optional category which allows for statistical analysis of principal categories: absence of suspected malignant cells, epithelial abnormalities, and others (see below).

]]> III. Interpretation/Results

A) Negative for intraepithelial lesion or malignancy

The category "absence of intraepithelial squamous lesion or suspected malignant cell" regroups the categories "normal and benign alterations". The term infection is replaced by microorganisms and the final list has been slightly modified (Table I). Alterations due to inflammation, irradiation, or the presence of an intrauterine contraceptive device (IUD) are classified within normal smears.

B) Epithelial squamous cell abnormalities

Atypical squamous cells (ASC)

Following numerous discussions, based on the practicality of maintaining or not an invalid category, it has been decided to keep this category which is associated with approximately 10% of severe intraepithelial neoplasm from biopsies.5,6 On the other hand, the subdivisions of this category have been modified (Table I). The general term for this category is no longer "atypical cells of undetermined significance" (ASC-US). It is replaced by the term "atypical squamous cells". The term "atypical squamous cell of undetermined significance" (ASC-US) will be used for abnormalities suggesting a low grade intraepithelial squamous lesion which has not been confirmed, or for non-specific atypical cells. Not more than 3% of the smears should have this designation.5 Atypical findings of undetermined significance associated with inflammation come out of this group and should now be included among normal smears. The term "atypical cellular findings not permitting exclusion of a high grade intraepithelial squamous lesion" (ASC-H) is proposed for those unconfirmed, although suspected cases of high grade intraepithelial squamous lesion. This term should apply to 5-10% of atypical squamous cell alterations and are often associated with a high grade intraepithelial squamous lesion confirmed through biopsy taken by colposcopy.7-9

Squamous intraepithelial lesion

The Bethesda 2001 system has the same two categories as proposed in 1988 which are "low grade intraepithelial squamous lesion" and "high grade intraepithelial squamous lesion" (Table I). Both categories are associated with oncogenic virus or high risk, although they have different natural history. Low grade intraepithelial squamous lesions regress spontaneously and evolve slowly to a high grade intraepithelial squamous lesion. High grade intraepithelial lesions are associated with persistent viral infection and with high grade intraepithelial neoplasias detected from biopsy and which can progress to an invasive lesion.

C) Epithelial glandular cells abnormalities

Atypical glandular cells (AG-C )

]]> The term "atypical endocervical, endometrial or glandular cells" replaces the term "atypical glandular cells of undetermined significance" (AGUS) (Table I). The nature of glandular, endocervical or endometrial cells should be noted; this will permit a more appropriate diagnostic approach, cervical biopsy, and examination of the endocervix to identify endocervical lesion, or endometrial biopsy to identify an endometrial lesion.10

Endocervical adenocarcinoma in situ (AIS)

"In situ adenocarcinoma" is a new category which corresponds to specific morphological abnormalities, some have already been using this term for several years. These abnormalities join others which are based on morphological changes from invasive adenocarcinomas of endocervical origin. This category allows for a more aggressive diagnostic approach such as a diagnosis "conization", if the initial diagnostic findings are negative.

Adenocarcinoma

The category "atypical glandular or endocervical cells suggesting neoplasia" is badly defined on morphological grounds.11-13 It should permit early identification of intraepithelial glandular lesions even though it requires prospective studies for confirmation. The category for invasive adenocarcinomas remains identical.

D) Other

Cervical cytology is not a good diagnostic assay for endometrial cancer. Morphologically benign endometrial cells were not mentioned in the 1988 Bethesda system, except referring to menopausal women. The category "other" is now proposed to classify smears without morphological abnormalities but which have apparently benign endometrial cells, in women over 40 years. The presence of these cells indicates an increased risk for endometrial cancer, and therefore an endometrial biopsy is recommended.14,15 Benign glandular cells found after hysterectomy should be noted as "absence of malignant-like cells".

IV Automated review

The automated system for reading slides should be mentioned in the report and the printout from the machine attached. If the slide was checked by microscopy, this should also be mentioned apart in the report.

V Ancillary testing

]]> It is considered useful to propose recommendations for additional tests which may be complementary to cytology. Suggestions for human papillomavirus DNA (HPV) detection is a primary example of an additional test which can be complementary to cytology.

These recommendations were discussed during a meeting of the North American Society for Colposcopy and Cervical Pathology (ASCCP) between 6-9 Sept. 2001, prior to their acceptance as definitive.16

A) Description of methods

Several methods can be used to detect HPV-DNA. Some of these are type specific, and others use a cocktail of probes which allow detection of oncogenic vs non-oncogenic cell types. Each method has a specificity and sensitivity which depends on the threshold of detection. Detection of low risk or non oncogenic HPV is not essential in the majority of cases.

The report must record the method used and the type of oncogenic HPV tested. If the method uses a cocktail of probes, the result must be described as positive or negative.

B) Clinical indication for management of abnormal smear

Published data suggest that testing for oncogenic DNA of HPV can be useful for a patient with cytological diagnosis of "atypical squamous cells of undetermined significance".6,16,17 Virology has a higher sensitivity than cytological follow-up to detect the presence of high grade cervical intraepithelial neoplasia (CIN) in this context. On the other hand, virology assay specificity is not as good as cytology. Specificity is the probability that a woman with no intraepithelial neoplasia has a negative viral test. If the prevalence of high grade CIN is 5% in these patients, the benefit of early detection of a small number of precancerous lesions should be evaluated in light of the cost of unnecessary colposcopy for many patients.18 Cost-efficacy studies are required in each country to consider the cost of colposcopy, access to these facilities, cost of monolayer cytology, and cost of virology assays. These types of studies will allow us to evaluate whether virology should be considered for a better case management as compared to cytological follow-up for patients with a cytological diagnosis of "atypical cells of undetermined significance".

According to published data, identification of DNA from a human HPV oncogene is not useful for the majority of patients who have a cytological diagnosis of either low or high grade intraepithelial squamous lesion.17,19 However, detection may be useful in certain cases such as for a patient who has persistently negative cytology and negative biopsy for intraepithelial squamous lesion.

There are little data to support the need for identification of an HPV oncogene in patients with cytological diagnosis of "atypical glandular cells".20

Other recommendations for identification of an HPV oncogene are being evaluated, although published data are insufficient to propose recommendations. These recommendations would be:

C) Example of reporting

It is recommended that cytological and virology results should be combined. If the two tests are not conducted in the same laboratory, it is recommended that they refer to each other.

Results can be reported according to several models: