The microscopic phenotype of cervical intraepithelial neoplasia (CIN) reflects a fine balance between factors that promote or reduce CIN development. A shortcoming of the current grading system is its reliance on static morphology and microscopic haematoxylin–eosin features of the epithelium alone. In reality, CIN is a dynamic process, and the epithelium may exhibit differing results over time. Functional biomarkers p16, Ki-67, p53, retinoblastoma protein cytokeratin (CK)14 and CK13, help in the assessment of an individual CIN’s lesion’s potential for progression and regression. The aggregate information provided by these biomarkers exceeds the value of the classic grading system. Consequently, many more CINs that will either regress or progress can be accurately identified. These findings agree with known molecular interactions between HPV and the host. For accurate interpretation of a CIN, it is essential that these biomarkers be determined quantitatively and separately in the superficial, middle and deep layers of the epithelium. Such geography-specific epithelial evaluations of quantitative biomarkers emphasise the dynamic nature of a particular CIN lesion, thereby changing the art of static morphology grading into dynamic interpretation of the diseased tissue, with a strong prognostic effect.
- CIN, cervical intraepithelial neoplasia
- CK, cytokeratin
- HLA, human leucocyte antigen
- HPV, human papillomavirus
- hrHPV, high-risk human papillomavirus
- HSIL, high-grade squamous intraepithelial lesion
- pRb, retinoblastoma protein
- SI, Stratification Index
- SIL, squamous intraepithelial lesion
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- CIN, cervical intraepithelial neoplasia
- CK, cytokeratin
- HLA, human leucocyte antigen
- HPV, human papillomavirus
- hrHPV, high-risk human papillomavirus
- HSIL, high-grade squamous intraepithelial lesion
- pRb, retinoblastoma protein
- SI, Stratification Index
- SIL, squamous intraepithelial lesion
The microscopic phenotype of cervical intraepithelial neoplasia (CIN, also referred to as squamous intraepithelial lesion (SIL)) reflects a fine balance between factors that promote or accelerate the development of progressively more advanced disease and factors that reduce or decelerate its progression. Critical ingredients are genotypes of the human papillomavirus (HPV) and the patient’s immune resistance. The severity of CIN or SIL is expressed by its microscopic grade, which is a standard part of the surgical pathology report, and greatly influences treatment of the patient (fig 1). This is understandable in view of the regression, persistence and progression figures of different CIN grades1 (table 1).
A shortcoming of the grading by microscopic pathology is that it assesses exclusively epithelial features and usually only those visible with the standard haematoxylin–eosin staining, thereby not taking into account other possibly valuable information. Another serious disadvantage is that the three distinct grades used in CIN (or two in SIL) can easily give a faulty static impression of a solidified sculpture, as if CIN or SIL were a static event, whereas in reality a CIN lesion is a dynamic process (a balance) that can progress and persist but also regress. Compounding the above are the well-known issues of intraobserver and interobserver reproducibility, which, for grading of CIN, is far from perfect.2–9 It is also difficult to distinguish CIN reliably from non-neoplastic lesions, resulting in either overtreatment or undertreatment.10,11 These points emphasise the need for adjuvant methods to interpret the actual morphological impression of a CIN lesion in dynamic terms rather than in static morphological grades. Such adjunctive methods are also important for better distinction of CIN from non-neoplastic lesions and to predict accurately the risk for progression of low-grade and regression of high-grade CIN lesions. Even small improvements in prognostic accuracy will enormously reduce the number of patients erroneously or unnecessarily treated, as shown for CIN2 (table 2). Figure 2 shows the prognostic accuracy of CIN grade as opposed to the ideal prognosticator of a CIN lesion.
Inasmuch as CIN causes progressive dysfunction in the proliferation and differentiation of cervical epithelial cells, many studies have focused on evaluating the merits of features related to proliferation and differentiation.12–20 Without doubt, p16 and Ki-67 are the most widely available, robust, stable and strong predictive biomarkers currently available for handling CIN lesions. (The antibody MIB-1 is often used in paraffin wax sections to assess Ki-67 expression. In this article, for consistency, we use only the term Ki-67, even if it relates to MIB-1). Others, such as the retinoblastoma protein (pRb), p53, CK13 and CK14, add substantial insight.21–25 This paper summarises current knowledge and gives practical guidelines for using these most important biomarkers in daily surgical pathology practice.
CIN AND HPV
Persistent infection with oncogenic HPV (high-risk HPV or hrHPV) is necessary for cervical precursors to evolve into invasive carcinoma.26–37 Many believe that CIN does not exist without HPV and that earlier publications on HPV-negative CINs are flawed by insensitive methods or materials. The viral load may be a predictor of the development of a CIN lesion, although this has been doubted.38–42 Large, worldwide vaccination programmes are in progress with promising results, clearly indicating the important role of the host’s local immune response to HPV infection.43 HPV is clearly highly infectious, as in infected women it can be found not only in the cervix but also in the vagina, vulva, perianal region, urethra and even tampons.44 HPV is often also found in women without overt signs of infection.35 HPV enters only the parabasal cells of the cervical epithelium, not the superficial cells (in which the nuclear material for all intents and purposes is already largely dead), so infection requires small transepithelial microtraumas reaching to the basal cells of the cervical epithelium.
HPV infection often results in nothing more than a slightly increased proliferation of the epithelium. In fact, most (about 80%) of these women show no remarkable microscopic abnormalities of the epithelium or no more than a minimal glycogen loss from the epithelium, slightly enlarged nuclei, or sometimes parakeratosis or hyperkeratosis,45 but about 20% of those infected with hrHPV develop a real CIN lesion (fig 3).46–55 Clearance of the virus is followed by regression of cervical lesions. An altered transcriptional regulation of the viral oncogenes E6 and E7, especially in the oncogenic types, results in a topographic shift of E6 or E7 expression from the differentiated layers to the proliferating parabasal cell layers. When overexpressed in proliferating cells, E6 and E7 interfere with the cell cycle control regulated by p53 and pRb, respectively.56 These morphologically abnormal cells migrate towards the surface (just as normal cells do), but without normal maturation. The degree of abnormal maturation is expressed by the changes referred to as the poorly glycogenated epithelium or even CIN.45 The dysplastic cells are estimated to arrive at the surface in one to several weeks and then desquamate, so a full-blown CIN3 may develop in up to a few weeks (fig 3B), although many CINs regress spontaneously, either slowly or after a prolonged period (fig 3C,D).
Morphologically, a wide range of non-neoplastic changes is associated with HPV infection. Features that characterise neoplastic change include decreased upward maturation and proliferation (mitoses above the level of the parabasal cells), variation in size, shape and polarity, and coarse chromatin of nuclei at all levels of the epithelium. In all cases of intraepithelial neoplasia, abnormal changes are visible throughout all layers of the epithelium, including the surface. However, when the bulk of the most abnormal changes are confined to the lower one third of the epithelium, the lesion is designated as CIN1. Similarly, CIN2 occurs when the most abnormal changes extend into the middle third. In CIN3, the changes are uniform and throughout the epithelium.
HPV AND MOLECULAR MECHANISMS LEADING TO CIN
Over the past years, several reviews have described the molecular biological mechanisms of HPV in detail.56–58 For the working surgical pathologists, we will give a summary here, as far as the mechanisms are relevant.
HPV is a double-stranded circular (episomal) DNA virus whose genome can be divided into three regions: the upstream regulatory region, the early region and the late region. The upstream regulatory region is important in regulating viral replication and transcription of downstream sequences in the early region. The early region encodes predominantly viral proteins (E1–E8) that are important in viral replication. The late region encodes viral structural proteins (L1, L2) that are important in the formation of the capsid (a structural protein envelope that encapsulates each virion). Much research has been conducted over the past years on the functions of E1–E8, L1 and L2. E6 and E7 are the principal transforming proteins of HPV.59 The expression of these proteins in hrHPVs such as subtypes HPV16 and HPV18 (but not of those having low oncogenic risk such as HPV6 and HPV11) causes cells to become completely transformed,60 principally by inactivating the host’s p53 and pRb, respectively. After getting access to the basal cell compartment of the cervical epithelium through microwounds, HPV infects these epithelial stem cells, and initially is a phenotypically latent passenger in the form of an episome (a DNA ring) in the cytoplasm of these basal layer cells. A few of the infected stem cells give rise to daughter cells capable of replicating the viral genome and synthesising capsid proteins in the terminally differentiated cell layers above the basal cell layer. The viral replicating cells display typical cytopathic changes, including, most prominently, koilocytosis or koilocytotic atypia—that is, the squamous cells with vacuolated appearance—as well as some minor changes in the nuclear morphology. Finally, mature viral particles are released along with the squamous debris that is exfoliated at the surface of the epithelium.
The transition from normal to dysplasia or invasive carcinoma is triggered by uncontrolled expression of E6 or E7 in proliferating basal and parabasal epithelial cells.61 This phenomenon distinguishes the process of cell transformation from productive viral infection and may be due to integration of the viral DNA in the host cell genome, which is observed in most invasive cancers and in a subset of high-grade lesions.62 The integration of HPV DNA into the host’s chromosomes is a critical event in HPV-related oncogenesis, although little information is currently available on the effect of integration on the host genome. Conversely, viral integration may be the result of a genetically unstable environment in parabasal cells caused by p53 inactivation, the guardian of the human genome.56 Molecular studies have shown that HPV integration results in disruption of the open-reading frames for E1 or E2 of the HPV genome, leading to increased expression of E6 and E7 in particular, favouring a growth advantage and neoplastic transformation.63–65 Both E6 and E7 proteins can bind to multiple cellular targets.66 Figure 4 shows a simplified scheme of the interactions that are thought to be most relevant for their transforming functions. A detailed discussion is beyond the scope of this article; useful information can be found at www.hpvtoday.com. E6 binds to the tumour suppressor gene product p53, which prevents cells from undergoing p53-mediated apoptosis and p53-independent activation of telomerase. E7 binds to the retinoblastoma tumour suppressor gene product pRb, resulting in hyperproliferation and inducing abnormal centrosome duplication independent of inactivation of pRb and its family members.67,68
VIRAL AND HOST FACTORS IN HPV PERSISTENCE AND PROGRESSION
Viral and host factors play interdependent parts that foster the regression persistence and progression of HPV infections. Viral factors include viral variants, viral load and viral integration. Host factors include the host immune response and susceptibility genes.69
Several studies have now documented an association between HPV16 variants and the development of cervical cancer, with non-European variants being associated with excess risk for cervical cancer.70 The limited data available for HPV types other than HPV16 suggest that non-European variants of HPV18 and HPV58 are also associated with increased risk for cervical cancer.71,72 Cross-sectional epidemiological studies showed an association between increasing HPV viral load and the risk for cervical cancer.37–42 However, the longitudinal data evaluating the pattern of viral load over time and the subsequent risk for progression of HPV infection to cervical neoplasms (CIN2 and CIN3) and cancer are insufficient to support this association.73,74 Although HPV is usually in the episomal form in cervical lesions, viral integration has generally been reported to be associated with oncogenesis. Unfortunately, the currently widely available tests determining HPV do not distinguish between episomal and integrated HPV. The frequency of HPV integration increases with the degree of disease severity, thus potentially correlating with progression to cervical cancer.62 Other viral events are epigenetic events in the HPV genome—that is, those events that alter gene expression (eg, phenotype) without a change in the DNA sequence (eg, genotype). Examples are hypermethylation or hypomethylation of viral oncogenes and the potential implications for suppression or activation, respectively, of viral oncogenic expression.
A positive association exists between the detection of HPV antibodies (humoral immunity) and the risk for cervical neoplasia.75–77 Although these antibodies may effectively prevent infection, they seem to be unimportant effectors in causing regression in established HPV infections and related cervical lesions.78 In contrast to antibodies, T cell responses (cellular immunity) to HPV are likely to be an important effector mechanism for clearing established infections.79,80 Thus, adequate T cell responses generated after infection may help to protect against the progression of infection and against early lesions. Natural polymorphisms or genetic variations (genetic susceptibility) between people in immune-related genes may also help to explain differences in the regulation of immune function. For example, human leucocyte antigen (HLA) DRB1*1301 seems to have a protective role in the pathogenesis of cervical cancer.70 However, this individual allele association is not likely to be explained by underlying haplotypes.81 Studies focusing on inherited susceptibility showed that having a sister or a mother with cervical cancer increases a woman’s risk for cervical cancer twofold and that heredity may explain some of the variation in risk for cervical cancer.82,83 But the question is whether it is the presence of inherited susceptibility or the sharing of promiscuous sexual behaviour among family members that may cause cervical cancer. Shared familial environment was not found to be a major effect among mother–daughter relationships.83
KI-67 CELL CLUSTERS AND P16 DISTINGUISH CIN FROM REACTIVE LESIONS
The development and behaviour of CIN is correlated with proliferation, an observation known for many decades. Ki-67 is one of the most widespread biomarkers correlated with proliferation; one of the simplest applications therefore is to use Ki-67 expression as a marker for CIN. In sections embedded in paraffin wax, the MIB-1 equivalent of Ki-67 is widely used, as its immunohistochemical staining pattern is stable, robust and gives rich contrast. Evaluation of Ki-67-positive cell clusters in the epithelium is a strong diagnostic adjunct in distinguishing CIN from normal or benign reactive cervical squamoepithelial lesions.18,25 However, to prevent overdiagnosis, Ki-67-positive, tangentially cut parabasal cells, inflammatory cells and immature metaplasia must be carefully excluded.
The cyclin-dependent kinase inhibitor-2A p16 is also useful in distinguishing CIN from reactive lesions.84 As p16 expression is regulated by a pRb-dependent negative feedback loop, continuous inactivation of pRb by hrHPV E7 results in increased p16 levels. Hence, increased p16 levels may reflect HPV-induced dysplasia with deregulated E7 expression.85 Information about the presence of HPV has no additional diagnostic value, as many non-CIN epithelia can be HPV positive. Marked overexpression of p16—that is, diffuse and strong immunostaining—is seen in all cervical cancers and pre-neoplastic lesions with infection by high-risk and intermediate-risk HPVs of subtypes HPV16, HPV18, HPV31, HPV33, HPV52 and HPV58 and weak or focal staining in lesions infected by HPV6 or HPV11.21 Others have confirmed the strong correlation between the presence of HPV DNA and p16 staining.23 At low magnification, p16 staining facilitates finding a dysplastic area, especially if the epithelium is heavily infested with leucocytes, as occurs often in CIN lesions.86 In addition, overexpression of p16 can be used to identify individual dyskaryotic cells in ThinPrep smears.87 Caution must be exercised, as occasionally inflammatory cells themselves may exhibit p16 reactivity in clearly non-dysplastic lesions.24 However, during routine prospective evaluation of p16 over 12 months in a large gynaecopathology practice, no false-positive p16 lesions have occurred (unpublished results), showing that false-positive p16 is a very rare phenomenon and probably has a negligible role. The combination of Ki-67 and p16 is useful to ascertain whether a suspicious yet uncertain cell group is indeed CIN and not atrophic epithelium (fig 5).
KI-67 AND CIN GRADE
Immunoquantitation of Ki-67 is an important diagnostic adjunct for the grading of CIN.19,20,88 Figure 6 shows the quantitative image analysis method. The combination of the Stratification Index (SI, which indicates, how high Ki-67-positive nuclei are located in the epithelium; the higher the SI, the higher the CIN grade) and the number of Ki-67-positive nuclei per 100 µm basal membrane (the more Ki-67-positive nuclei, the higher the grade) is the best discriminating set of features that distinguishes the three CIN grades at the same time (fig 7). Some CIN1 cases that were initially “misclassified” with these two quantitative Ki-67 features showed a higher CIN grade on deeper levels from re-cut of the paraffin wax blocks, whereas the other CIN1 cases that were correctly classified with Ki-67 quantitation remained so in the deeper cuts. In a subsequent prospective evaluation of 121 routine CIN cases (test set), six independent pathologists, some of whom were general pathologists, achieved exact agreement in 78% of cases when they compared CIN grades with histology by staining with haematoxylin–eosin and quantitative Ki-67. When the two reviewers were experts in gynaecological pathology, the agreement jumped to 97%, and the sensitivity, specificity and positive and negative predictive values were very high, further indicating the supportive role of Ki-67 in general surgical pathology practice. Immunoquantitative parameters for Ki-67 are also correlated with the presence of hrHPV in CIN lesions (fig 8).20
BIOMARKERS AND BIOLOGICAL AGGRESSION OF EARLY CIN LESIONS
Pathologists often regard koilocytosis as an additional sign of CIN aggression (ie, is more likely to progress). In reality, the finding or absence of koilocytosis is of no value, and in fact may be misleading. Koilocytosis is the microscopic image of the productive phase of the HPV life cycle. In this state, the viral particles needed to form the koilocyte replicate and accumulate in the superficial differentiating layers of the epithelium, not in the basal proliferating part, which is the critical region for the developing dysplasia.59,61 The presence of koilocytosis is irrespective of HPV type. In a series where patients were evaluated only if the biopsy result was normal, atypical or CIN1, 35% of the patients with koilocytosis did not have HPV infection, 25% of patients with prominent koilocytes had a low-risk HPV type and 40% had an hrHPV type.89 For a cell to show the presence of a well-developed koilocyte, the cell should contain a considerably high viral load; thus, the absence of koilocytosis implies nothing about the presence of oncogenic organisms. In corroboration, progression-or-not analysis of original early CIN lesions showed that patients with koilocytosis had a considerably lower likelihood of progression than those without koilocytosis. Thus, CIN lesions with koilocytosis are productive viral infections, but are generally overdiagnosed when classified as high-grade CIN. Instead, most should be grouped with low-grade CIN1 at best. A further complicating evaluation of koilocytosis is that the presence of the features among observers is poorly reproducible.16
Prognostic value of Ki-67 and other biomarkers in early CIN lesions
Ki-67 features in small histological punch (marker) biopsy specimens predict progression to CIN3 in early CIN lesions more strongly than subjective CIN grade (both for routine and experts’ review CIN grades).12,17 The prognostically strongest Ki-67 features were the Ki-67 SI (fig 6) and the percentage of the Ki-67-positive nuclei located in the middle third layer of the epithelium (MIDTHIRD; fig 9). The strongest prognostic thresholds of these features (SI = 0.57 and MIDTHIRD = 30%) were detected in the first study we conducted by multivariate regression analysis (Cox model). These features and thresholds are highly reproducible. High reproducibility is important but perhaps not enough to be used in another laboratory, as interlaboratory differences in tissue processing and staining of the sections undoubtedly occur and may perhaps influence the Ki-67 features. The prognostic Ki-67 test was therefore once more validated in two new patient sets from another country (Norway), first on historical archive material and then prospectively. Prospective validation is usually the most difficult phase when implementing a new laboratory test, as minor variations will occur despite the measurement and interpretation protocol being well defined. Although differences in the processing and staining procedures undoubtedly existed between the Dutch and Norwegian laboratories, the findings in the two Norwegian validation studies confirmed that the quantitative Ki-67 test in CIN lesions was strongly predictive for CIN3 in the follow-up (fig 9), whereas the routine CIN grade was not.12,14
The critical value of Ki-67 SI = 0.57 needs some further explanation. In the normal epithelium, proliferation occurs in the parabasal cells. In high-grade CIN, proliferation is abnormally high and is also found in the middle and superficial layers. As Ki-67 SI = 0.57 and MIDTHIRD = 30%, the critical prognostic values, are in agreement with the idea of “upward proliferation” in high-grade squamous intraepithelial lesion (HSIL), higher localisation of Ki-67-positive cells leads to an increase in Ki-67 SI. Importantly, independent validation studies confirmed that these threshold values were essential to predict progression, making them strong and reliable prognostic factors.
The prognostic value of the various cell cycle regulatory proteins and markers of squamous cell differentiation have been compared in various studies. Some found telomerase to be important in cytological material, but others had negative results90,91 and in one study on punch biopsy, telomerase was not a prognostic marker in early CIN.15 This is understandable as telomerase activity reflects a rather late step in the sequence from CIN3 to squamous cell carcinoma, explaining why it was not prognostic for early CIN progression.84 The results for pRb, p53, cyclins A, E and D, p16, p21, p27, telomerase, involucrin, CK13 and CK14 are not always in agreement with each other. However, this may be partly due to technical shortcomings, as an important biomarker function should also assess the dynamics of the cervical epithelium. Epithelial cells are born in the parabasal layer and then mature and migrate to the surface (where they are desquamated); therefore, an average assessment of biomarkers throughout the entire epithelial thickness may blur important dynamic information. All biomarker features were thus separately analysed in the basal, deeper and upper half of the epithelium with quantitative image analysis techniques to get the best reproducibility. Multivariate analysis showed that the combination of high Ki-67 SI and reduced expression of pRb in the deeper half of the squamous epithelium predicted progression of CIN lesions (fig 10). Moreover, addition of reduced CK13 and CK14 expression identified a subgroup that had an even greater risk of progression, but this additional prognostic value of CK14 and CK13 was only in the prognostically high-risk subgroup with high Ki-67 and low pRb. Other studies found that loss of involucrin and CK13 expression occurred only in the high-grade lesions and was therefore related to lesion grade. Loss of CK14 expression also occurred considerably more often in high-grade than in low-grade lesions.92 Quantitation of combined Ki-67, pRb, CK13 and CK14 in early CIN lesions gives accurate information about their progression risk.15 These results are summarised in the prognostic decision scheme shown in fig 11.
On the basis of the above findings, a model for the development of an early CIN lesion has been developed (fig 12). Central to this hypothesis is that hrHPV E7, when expressed during HPV infection, impairs pRb. pRb normally acts to reduce growth. When impaired by E7, the growth-reducing effect of pRb diminishes as shown by increased and upward proliferation (as a result, the Ki-67 SI increases and finally exceeds a critical level of 0.57). When hrHPV is cleared by the host, the CIN lesion heals. The first sign (before disappearance of morphological haematonylin–eosin CIN features) is increased pRb levels in the deep layers of the epithelium. Shortly after that, proliferation reduces, and the subsequent upward spread of proliferating cells is also reduced, as manifested by lowering Ki-67 reactivity. Naturally, p53 is also impaired (by E6), but the prognostic role of pRb is much stronger and overshadows the importance of p53 in predicting early CIN progression. However, in HSIL lesions, p53 has more value in identifying CIN3 lesions that will regress.
PREDICTION OF BEHAVIOUR OF CIN2 AND CIN3 (HSIL) WITH BIOMARKER PATTERNS
Biomarker patterns are also prognostic in HSIL, which has important implications. When left untreated, many patients continue to show persistent disease (as shown by follow-up biopsies in cases of HSIL or CIN2 and CIN3). Consequently, many doctors now ablate all HSILs; nonetheless, without treatment 15–45% will naturally regress (ie, no HSIL detected on follow-up).1 The average age of patients with HSIL is around 29 years, whereas patients with (micro)invasive cancer are on average 9–10 years older. Complicating the decision of whether to treat HSIL is the reality that excision, with either cold-knife cone or diathermic loop method, is a considerable medical procedure, with potentially serious complications, most commonly cervical insufficiency. As many patients treated for HSIL will at some later time become pregnant, cervical insufficiency becomes a major concern and commonly leads to immature birth,93 demanding preventive cervical cerclage under general anaesthesia at 16–20 weeks’ gestation. Obviously, today’s clinical goal is to prevent unnecessary treatment by cone or loop electrosurgical excision procedure. The remedy, naturally, is to identify those HSILs that would regress spontaneously.
To identify factors related to histologically proven persistence or regression, small histological colposcopically directed (punch) biopsy specimens were analysed for HPV genotypes and different immunoquantitative proliferation, cell cycle regulation and differentiation markers.94 Special attention was paid to p53 and pRb in biopsy specimens as potential markers for hrHPV E6 and E7 function.95 All cases had a biopsy interval of at least 100 days between the marker and first follow-up biopsy. This interval is important to mitigate the effects of the initial punch biopsy procedure, which causes considerable damage to the cervix and, consequently, a local inflammatory and repair response. Healing is generally complete after 3 months. Within this interval, there is a serious risk of overdiagnosing dysplastic remnant lesions because of the superimposed reactive changes in the epithelium. To minimise this risk, we and others excluded biopsy specimens taken shortly after the initial biopsy, and included only those with an interval of at least 100 days between the marker and follow-up biopsy.94,96 On the basis of the microscopic findings in the diagnoses by follow-up cone or loop electrosurgical excision procedure, each initial marker CIN lesion was classified as regressive or persistent.97 All lesions had hrHPV infection and were diffusely positive for p16: 63% were positive for HPV16 or HPV16 mixed with other hrHPV genotypes and 37% had other hrHPV types. The rate of spontaneous histological regression was 43%. Others have found similar rates of spontaneous regression.96,98,99,100 The initial marker (punch) biopsy specimens of the persistent HSILs had considerably lower levels of pRb and p53 in the deep half of the epithelium than those having non-persistent (regressive) HSILs. The degrees of positivity of p16, Ki-67, cyclin D1 reactivity, lesion extent in the punch (marker) biopsy specimen and patient age were all unrelated to persistence or regression, as found later in the follow-up cone biopsies. HPV16-positive HSIL had a lower regression percentage of pRb and p53 than those with other HPV types (fig 13), and we found a (not significant) trend for HPV16-containing lesions to persist more often than non-HPV16 lesions (in agreement with others94). However, the percentages of pRb–positive and p53-positive nuclei in the deep half of the epithelium of a histological punch cervical biopsy specimen were much stronger predictors of CIN3 regression than HPV genotype (fig 14).
In a prospective observational cohort study on prognostic variables associated with clinical behaviour, 100 women with HPV-infected HSIL were followed up from about 4 months before the entire lesion was resected.96 Of them, 28% had spontaneous histological regression (CIN1 or less at resection). In the study, lesions in women with only HPV16 infection were less likely to regress than those in women with infection of HPV16 mixed with other HPV types, compared with lesions in women with infection of HPV types other than HPV16 (p = 0.049). In the cohort with only HPV16 infection, the presence or absence of the HLA*A201 allele had no effect on outcome, in contrast with patients having other HPV types in which persistence of the lesions was associated with the presence of the HLA*A201 allele. These results suggest that interactions among HPV type and HLA type as expressed by regression rates support a role for HLA-restricted HPV-specific immune responses in determining disease outcome.
It seems that the interaction (balance) between a patient’s immune response and HPV factors results in a prognostically important epithelial cell reaction, measured by epithelial levels of pRb and p53. Future studies comparing the different markers will help to clarify the intriguing correlations among these biomarkers, hrHPV subtype, the host immune response and HLA allele interaction.
WHY ARE THE DEEP EPITHELIAL LAYER BIOMARKERS ESPECIALLY PROGNOSTIC IN CIN?
We must realise that the microscopic image of a cervical epithelium is a snapshot (a photograph) of a dynamic process (a film) that normally would consist of many images taken over time (fig 15). The question of why measurement of biomarkers in the deep epithelium is especially predictive of CIN behaviour pulls together the different dynamic biological aspects already discussed earlier in this article.
The cervical epithelium is a dynamic tissue of socially and orderly moving cells with tightly balanced and controlled proliferation and differentiation. The HPV infection disturbs this process. Through oncoproteins E6 and E7, HPV immobilises or degrades and thereby reduces the amount of pRb and p53 available for normal function. This results in basal cells that do not enter into the normal maturation process, resulting after a short time in high (abnormal) proliferation of the cells of the superficial layers (mitoses or Ki-67-positive cells and abnormal chromatin patterns) and altered differentiation markers. Once the virus infection clears, p53 and pRb function in the deep layers restarts. This is so far the earliest sign of cure and normalisation of cell metabolism. Hereafter (perhaps after some weeks), proliferation and hence the number of Ki-67-positive cells falls, initially in the deep layer. These normal cells (now with mostly Ki-67-negative nuclei) will move up, mature and reach the epithelial surface in several weeks. Some time after the pRb and p53 have normalised, signs of abnormal proliferation and differentiation in the superficial layers (diagnostic for CIN3) will also disappear, and the condition becomes normal. Thus, the assessment of levels of p53 and pRb in the deep layer predicts the future events that will take place in the superficial epithelium, some weeks after the biopsy was carried out. The clearance and cure process expressed by the biomarkers is not always such that the CIN lesion just slowly disappears. The CIN3 lesion may regress to CIN2, hang there for some time, increase back to CIN3, and only then slide down to CIN1, totally regress or even persist. Quantifying biomarkers therefore can change the pathologist’s role from reporting static morphology to the much more exciting possibility of dynamically interpreting and forecasting future events that will take place in the tissue. In this context, it is of utmost importance that biomarkers are analysed in certain specific geographical areas of the epithelium. An average measurement taken randomly in the epithelium, not considering the basal, deep and superficial layers, ignores the dynamic nature of the cervical epithelium, obscuring important prognostic information. The familiarity of pathologists with the biology and dynamics of tissues allows them to extract the biologically relevant information correctly. When this important facet of tissue—that is, geographical location—is not considered, important information is lost.
HANDLING AND INTERPRETING BIOMARKER PATTERNS IN CIN LESIONS
On the basis of the discussion earlier, we now recommend the following routine when handling a cervical punch biopsy specimen in the surgical pathology laboratory, especially when an early CIN lesion is contemplated:
Analyse the diagnostic section stained with haematoxylin–eosin, for routine evaluation.
Scan a serial section, stained for p16, to identify diffusely reactive squamous areas. These are nearly always dysplastic (false-positive p16 reactivity is rare and easily recognised).
Evaluate the next serial section with Ki-67. Ki-67-positive cell clusters further support a diagnosis of CIN.
Carry out quantitative Ki-67 image analysis for objective grading support and indication of progression risk in case of CIN1 and CIN2. If the Ki-67 SI90>0.57 or the percentage of Ki-67-positive nuclei in the middle third layer of the epithelium exceeds 30%, the likelihood of progression to CIN3 in the follow-up is high (about 30%).
In the subsequent section, analyse the percentage of pRb-positive nuclei in the lower half of the epithelium.
Interpret the results as follows. If the combination of Ki-67 SI90>0.57 occurs together with pRb<40%, progression risk in early CIN to CIN3 is high (about 50%). The progression risk in the remaining patients is almost zero. Moreover, in the subgroup at high risk according to Ki-67 and pRb, a combination of CK13-positive cells<80% and CK14-positive cells<50% identifies patients with an excessively high progression risk. In other patients (with Ki-67 SI90<0.57 or pRb>40%), the cytokeratins are not informative (fig 11).
The results for HSIL (CIN2 and CIN3) are promising; they also are in agreement with current molecular biological knowledge but have not been validated to the same degree as for low-grade CIN. The following therefore should be used with care.
Evaluate the percentage of pRb-positive and p53-positive nuclei in the deep half of the epithelium. If either the percentage of pRb-positive nuclei >40% or that of p53-positive nuclei >15%, the likelihood of regression is high. All other HSIL lesions will probably persist or even progress.
Biomarker-mediated dynamic clinical behaviour prediction of CIN has been adequately validated. Routine biomarker applications can considerably change the manner in which afflicted women are followed up and treated. Definitive treatment in patients at high risk will be instituted earlier, whereas women whose biomarkers suggest that the process may resolve of its own accord will not receive treatment or will be treated only at a later time. Other important aspects of a dynamic CIN lesion—for example, the local immunoresponse factors—are relevant variables that may in the future affect prognosis and treatment. It is not yet certain whether the host’s essential immune reactions can be adequately extracted from the usual paraffin-wax-embedded tissue alone, and independent validation studies are required. Moreover, other immunological and protein parameters must also be evaluated. Such proteomic analyses may go well beyond the analysis of classic formaldehyde-fixed biopsy specimens.101
We thank Mrs Susan Allen-de Jong for critically reading the text.
Published Online First 19 May 2006
Competing interests: None.
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