Labial salivary gland (LSG) biopsy is used in the classification of primary Sjögren's syndrome (PSS) and in patient stratification in clinical trials. It may also function as a biomarker. The acquisition of tissue and histological interpretation is variable and needs to be standardised for use in clinical trials. A modified European League Against Rheumatism consensus guideline development strategy was used. The steering committee of the ad hoc working group identified key outstanding points of variability in LSG acquisition and analysis. A 2-day workshop was held to develop consensus where possible and identify points where further discussion/data was needed. These points were reviewed by a subgroup of experts on PSS histopathology and then circulated via an online survey to 50 stakeholder experts consisting of rheumatologists, histopathologists and oral medicine specialists, to assess level of agreement (0–10 scale) and comments. Criteria for agreement were a mean score ≥6/10 and 75% of respondents scoring ≥6/10. Thirty-nine (78%) experts responded and 16 points met criteria for agreement. These points are focused on tissue requirements, identification of the characteristic focal lymphocytic sialadenitis, calculation of the focus score, identification of germinal centres, assessment of the area of leucocyte infiltration, reporting standards and use of prestudy samples for clinical trials. We provide standardised consensus guidance for the use of labial salivary gland histopathology in the classification of PSS and in clinical trials and identify areas where further research is required to achieve evidence-based consensus.
- Sjøgren's Syndrome
- Outcomes research
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Labial salivary gland (LSG) biopsy is widely used in the diagnosis of primary Sjögren's syndrome (PSS) and plays an integral role in the established American-European Consensus Group classification criteria1 and the proposed American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) criteria.2 Evidence suggests that it has the potential to stratify patients,3–6 and may have potential as a biomarker in clinical trials.7
The most characteristic feature of PSS on biopsy with a sensitivity and specificity of >80%8 is focal lymphocytic sialadenitis (FLS), which describes the presence of dense aggregates (foci) of ≥50 mononuclear cells (mostly lymphocytes), in a periductal or perivascular localisation.9 A modification based on focus score (FS) calculation was proposed in 1974,10 and further work established FS ≥1 (ie, ≥1 focus per 4 mm2) for use in classification criteria.8 ,11–14 The Sjögren's International Clinical Collaborative Alliance (SICCA) have published a widely used protocol for sample preparation and the assessment of FS in suspected Sjögren's syndrome .14 ,15 Nevertheless, the initial determination of FLS, prior to calculation of a FS, is still a cause of variability of practice in the SS community.7 We previously discussed additional areas of variability including the acquisition and processing of the salivary gland tissue and the histological interpretation of the local infiltrate.7 ,16–18 The SICCA protocol specifies that foci in FLS occur adjacent to normal appearing acini, but features of non-specific chronic sialadenitis (NSCS) such as atrophy and duct dilation are common in the population and so may coexist with PSS. NSCS may also be associated with infiltration of lymphocytes and even aggregation, thus raising issues for interpretation and FS calculation.7 ,16 The SICCA protocol provides no additional guidance beyond FS calculation on the reporting of size of foci, their degree of organisation, germinal centres (GCs) and lymphoepithelial lesions (LESA), the latter being characterised by lymphocytic infiltration of ducts and basal cell hyperplasia resulting in a multilayered epithelium, and which may also have prognostic significance.19
The goal of this study was to develop a process of standardisation in order to confirm areas of consensus and highlight areas of uncertainty, with a view to stimulating further research and evidence-based recommendations. A few centres use parotid gland biopsies6 but we have focused this work on LSG tissue, as this remains the most commonly employed in clinical practice.20 In this study, we do not address the biopsy procedure itself but focus on the processing of the tissue and measurement of PSS-related inflammation. The target users include histopathologists, rheumatologists, oral medicine and oral and maxillofacial surgeons and ophthalmologists, as well as pharmaceutical companies planning clinical trials in PSS.
The standard operating procedures produced by EULAR on guidelines development in rheumatic and musculoskeletal disorders broadly formed the basis of the process followed.21
A literature review was carried out by the steering committee members of the ad hoc working group. This has been published and identified points of outstanding uncertainty for discussion.7 These comprised the agenda items for the workshop.
A 2-day workshop was held in February 2014 in Birmingham, UK.
The first day focused on histopathology in the diagnosis of PSS. Presentations addressed the rationale for biopsy, histological features and scoring systems, challenges and variability in application of the SICCA protocol, GCs and LESA, and methods for measuring change in biopsies in clinical trials as a prelude for day 2. There were 23 clinical expert attendees with a background in rheumatology, histopathology or oral medicine. The relevant issues were interactively discussed to establish a draft framework of points to consider in the areas of (1) glandular tissue requirements, (2) criteria defining FLS and FS and (3) assessment of GCs and LESAs.
A larger number of attendees were present on the second day (n=39), representing an increased number of specialists with an interest in PSS clinical trials and including a clinical trials statistician, a health psychologist and three patient partners. Presentations summarised issues around the scoring of biopsies, additional pathological features that may be relevant to clinical trials and the natural history and reliability of histopathological changes. Breakout groups and roundtable discussion were used to propose points relevant to clinical trials in the areas of (1) calculation of focus size, (2) additional parameters that could be measured, (3) reporting standards and (4) timing of biopsy and requirement for a placebo group. In a parallel session facilitated by a health psychologist, the patient partners discussed the acceptability of LSG biopsies as a clinical trials outcome measure. A concluding discussion addressed the agenda for future work.
The provisional points gathered at the workshop were substituted for a traditional first round of a Delphi process.22 These were reviewed and edited for clarity and completeness by a subgroup of six experts. A subsequent eDelphi round was conducted with 50 experts (comprising the original workshop attendees together with additional experts). These were asked to rate 20 points on a 0–10 scale, where 0 indicated no agreement and 10 complete agreement, and to provide explanation when there was disagreement. Points were divided into those of general application, and those most relevant to a clinical trials setting. Explanatory text and selected references accompanied the points.
A total of 39 experts (78%) responded to the eDelphi exercise, of which 22 identified their principal specialty as rheumatology/internal medicine (54%), 11 as oral medicine (30%) and 6 (16%) as histopathology. Nine rheumatologists (41%) and four (36%) oral medicine specialists described their experience of actually reviewing LSG histopathology as moderate, 8 (36%) and 2 (18%) as extensive. No discrepancy in responses was noted between specialty groups. Following the eDelphi exercise, a total of 16 points (table 1) met the criteria for agreement. These are listed in table 1, together with the strength of recommendations, and expert scores. The spread of scores is illustrated in figure 1. These points are discussed below. Points not meeting criteria for agreement are listed in online supplementary table S1.
Glandular tissue requirements
Given the scattered nature of foci, it is important that there is sufficient material available to allow a robust and reliable analysis. In point 1 (table 1), we propose obtaining a minimum of four LSGs, unless these are small (<2 mm), in which case six glands should be obtained if feasible. Three respondents argued for the use of fewer glands (two to three), and two for a greater number (five to seven).
A minimum glandular surface area to be examined of 8 mm2 was proposed to facilitate agreement. This minimum should comprise good quality glandular tissue. In the case of an inconclusive biopsy, for example, uncertainty over FLS, borderline FS for diagnosis or insufficient surface area, then two additional cutting levels could be employed (point 3). Glandular surface area from a single cutting level of multiple glands may also be optimised by aligning glands during preparation of the paraffin blocks (point 4).
Assessment of FLS and FS
The presence of FLS should be determined prior to FS calculation (point 5) (figure 2).14 Foci may be confluent and foci of any size may include plasma cells, although there was some divergence of expert opinion regarding the extent of plasma cell infiltration that is compatible with FLS. FLS cannot be attributed when the histological appearance of the glands is dominated by features associated with NSCS, such as acinar atrophy, duct dilation and fibrosis, with no evidence of any foci being adjacent to normal parenchyma. Conversely, given the prevalence of NSCS, some foci in PSS may be expected to be adjacent to atrophic features. Expert recommendation is that the extent of the atrophic features should be graded and reported to aid the referring clinician in their interpretation (point 6).
In order to calculate the FS, the total number of foci in the specimen is divided by the glandular surface area, and multiplied by 4, to give the number of foci per 4 mm2 (figure 2) Above a FS of 10, foci are typically confluent, and a ‘ceiling’ score of 12 may be applied. Glandular area can be measured with a calibrated eyepiece grid,15 but measurement-validated microscope-associated software may also be employed (figure 2B). An important decision is whether to include apparent foci in areas of atrophy, duct dilation and fibrosis, and whether to include the background area in the glandular surface area denominator. Different approaches include excluding infiltrate in compact fibrosis but including that around abnormal acini and ducts, excluding all foci and abnormal areas from the numerator and denominator, or including all. This decision will have an impact on the calculated FS.16 There was agreement that FS calculation should include the whole of the glandular surface area in the denominator, including abnormal areas, to avoid introduction of bias (point 7; figure 2B). This includes areas of fibrosis, which cannot reliably be removed from the glandular surface area denominator, although their inclusion may have the potential to reduce the FS, meaning that some patients with a FS ≥1 may become <1 at a late stage of disease (figure 2C).24 There was also agreement that in the case of PSS clinical trials at least, the least biased approach and the one likely to have the greatest reproducibility, would be to assume all foci are PSS-related and to be included in the FS (point 10). In the case of repeated biopsies, the patients themselves serve as an internal control. Arguably, this could also be applied to clinical diagnosis, once the presence of FLS has been determined.
Calculation of focus area
There was support for using the area of mononuclear cell infiltration in addition to the FS as a biomarker in clinical trials (point 9). Data can be presented as percentage of total area infiltrated and mean focus size. This could be achieved with digital analysis of H&E or CD45 immunostaining.
Ectopic GCs and LESAs
There was strong agreement that the presence of GCs should be reported in routine practice (point 8). However, some respondents commented on the need for a clear definition of these structures. H&E is considered sufficient to allow accurate detection of a fully formed GC by a histopathologist, although additional staining can be used such as B-cell lymphoma 6 (BCL-6) and CD21.
In the context of clinical trials, we have suggested additional staining with CD21, a marker of follicular dendritic cells (FDCs) and CD3 and CD20 to better define the presence of GCs (point 11) (figure 3). While CD21 long isoform staining by itself does not indicate the presence of a GC, the presence of a FDC network together with B-cell and T-cell segregation would be expected in all,25 and this combined approach would avoid the recently highlighted risk of overestimating GCs if relying on CD21 alone.26 ,27
Staining for CD3 and CD20 will also allow calculation of the B/T cell ratio in foci (point 11). While this alone would be insufficient to indicate the degree of segregation, it can be readily measured with digital recognition software.
Additional parameters for clinical trials
Although some workshop participants were strong advocates of measuring the proportion of IgA and IgG plasma cells, this did not receive sufficient support (mean 6.6; 65% ≥6). Some evidence suggests that the IgA:IgG plasma cell ratio may have diagnostic utility, based on the assumption that IgA plasma cells are normal within the gland (producing secretory IgA) with the role of IgG plasma cells being unclear,28–31 but arising as a consequence of chronic inflammation.32 However, more background work is required to understand its diagnostic utility and biomarker potential.
Glandular epithelial cell human leukocyte antigen class II expression appears directly related to local T-cell activation and interferon-γ production, and might therefore function as a biomarker.33 ,34 However, again there was insufficient support for measuring this routinely (mean 6.3; 65% ≥6).
Reporting standards for clinical trials
We recommend that clinical trials using the FS have two observers who report their interobserver variability (point 12) and who score samples blind to subject and chronological order (point 13). Ideally, high-resolution image morphometry of each sample should be stored to facilitate future comparative studies (point 14).
Timing of biopsy and placebo groups in clinical trials
It was agreed that pre-existing diagnostic biopsies could be substituted for baseline biopsies, provided that sufficient material of acceptable quality was available (point 15). Remarkably, little data exist on the natural history of histopathological changes in PSS.7 Therefore, the 1-year cut-off proposed is arbitrary. An optimal period for rebiopsy has not been determined and may depend on the agent studied (point 16). A 6-month timeframe seems reasonable with 3 months being a minimum.
Despite this apparent stability, little is known about variation in scores with repeat sampling, and so it was proposed to retain placebo groups even when histology was the primary outcome, until further experience with heterogeneity of sampling was available. Overall, there was strong support for this, with scores close to the defined agreement (mean 6.8 and 74% rating ≥6). However, a number of responses were strongly negative. Ethical concerns were raised about performing repeat biopsies on patients treated with placebo. Furthermore, it was argued that even in the absence of a placebo group, an improvement in biopsy scores in a small early phase study would still provide a positive go/no-go decision and justify further work.
Patient perspective on biopsies in clinical trials
Our patient partners felt that two biopsies over a 12-week period would be acceptable, although the rationale and objectives should be clearly explained and feedback of the results would be valued. The ability to use pre-existing samples where available was considered important.
Agenda for future work
Development of a web-based reference slide set.
Establish variability of assessments over short time frames using placebo arms of clinical trials. Using these data determine a minimum number of subjects and minimum detectable difference.
Establish optimal glandular surface area requirements/number of LSGs.
Multicentre study of interobserver variability
Further comparative work between parotid and LSG biopsies.
Agreement on immunohistochemistry staining protocols, particularly regarding identification of GCs.
Future application of these assessments in ‘positive’ clinical trials is required to establish discriminant validity.
Revision of this guidance will be undertaken when significant new data are available from the above studies.
Further work on the natural history of FLS in PSS and the potential biomarker role of IgA, IgG and IgM plasma cells would be desirable.
Importantly, the patient perspective will be further studied and morbidity data collected.
Standardising histopathological assessment in PSS is an important objective for routine diagnosis and for clinical trials, to ensure homogeneity of study populations, and improve reliability of assessments and comparability between studies. Extensive work on this topic has been performed by the members of the SICCA group.14
Despite so many years of use, however, there remains considerable lack of data regarding the natural history of the histopathological changes associated with PSS, the test reliability or repeatability and interobserver variability.7 Therefore, the principal weakness of our report is its dependence on expert opinion. While this might be a barrier to implementation, we hope that the points in this report might facilitate communication between histopathologists and physicians caring for patients. Furthermore, in the process we have identified a number of areas where the evidence base is weak and hope that this will stimulate further research.
It seems probable that, given the scattered nature of foci, the reliability of the test would improve in line with increasing surface area examined, particularly with a lower FS and with fewer ducts in the sample. However, an optimum surface area which balances FS reliability with practicality has yet to be determined. We have recommended obtaining four glands, although the minimum of 8 mm2 surface area may often be achieved with two to three glands. However, some glands may be atrophic or damaged and the material obtained should be sufficient to overcome these limitations and achieve a valid result. The surface area examined should be reported to aid the clinician in their interpretation and for transparency in clinical trial reports. A single study has demonstrated an increase in cutting levels to be useful for categorising patients with borderline FS,35 although, arguably, increasing the number of glands should be prioritised over the number of cutting levels. If multiple cutting levels are employed in a clinical trial setting, this should be protocolised, with scoring based on cumulative number of foci and glandular area across all slides, to avoid introduction of bias by selecting the ‘best’ slide. This latter consideration is less relevant for routine diagnosis, where an interpretation may be made based on the clearest level diagnostically, or a cumulative FS in case of insufficient surface area. We have suggested that additional cutting levels are done at 200 µm intervals, as this has been used in the referenced study, although further work would be required to define optimal intervals.
We have sought to clarify the issues we identified with the determination of FLS and FS calculation. For clinical trials we have also recommended a focus area calculation. One study found this correlated better with clinical and autoantibody parameters than the FS.36 Measurement of infiltrated area avoids difficulties in determining whether to count partially confluent foci as one or two, and remove the arbitrary ‘ceiling’ score in case of more widespread confluence. Furthermore, it is not unreasonable to expect that where foci are large, a significant reduction in area may occur following therapy despite the number of foci not being reduced, therefore, affording greater sensitivity.6 Foci are three-dimensional structures, and so the area of an individual focus will vary depending on the level at which it is sectioned. This issue could be minimised by either (i) ensuring sufficient glandular surface area is examined and (ii) taking more than one cutting level to avoid bias in the analysis.
There was a strong desire for further guidance on identification of GCs. Progressive organisation of foci into lymphoid-like structures is likely to have pathological consequences and function may occur without the fully formed appearance on H&E that can be seen in secondary lymphoid organs. In secondary lymphoid organs, areas of lighter staining often characterised by a rounded appearance are easily distinguished within the denser follicular area. Within these, a light and dark zone segregation is often also visible. The dark zone is the area of centroblast proliferation and the light zone is inhabited by centrocytes, T follicular helper cells and FDCs (whose large dendritic-like cytoplasm is responsible for the lighter staining with H&E). In LSGs, the detection of such structures is more challenging than in lymph nodes and GCs are often only appreciable with H&E as areas of lighter staining within the follicular area without the classical dark/light zone segregation. The varying prevalence (18%–59%)37 reported may reflect this difficulty and the consequent threshold for identification, alongside the differences in cohorts. This is important to clarify given the discordant data on the prognostic value of GCs for later lymphoma development.3 ,4 ,38 For the purpose of trials we have suggested additional immunostaining to study the organisation of foci. Other markers could be proposed, such as BCL-6 for GC detection,26 and may be appropriate depending on the study and agent proposed. Activation-induced cytidine deaminase (AID) is expressed if the GCs are functional but accurate staining for this is technically challenging.39
We have focused primarily on LSG tissue. The presence of LESA is more commonly observed in parotid tissue than in LSGs,40 with lymphoma development also occurring more often in the former. While this might be a consideration for the site of biopsy, the majority of centres still rely on LSGs due to the ease, familiarity and acceptance of this approach.
Extensive work on measurement of radiographic progression in rheumatoid arthritis (RA) has shown that inclusion of >1 reader reduces measurement error, and may allow smaller group sizes. Two readers is a good balance between accuracy and feasibility, and reader training is essential.41 We have extrapolated this to FS assessment in PSS. There has also been debate in the RA literature about whether sequential radiographs from the same patient should be scored together, and whether this should be done with knowledge of the chronological order.41 ,42 As different glands are being sampled with LSG biopsy, this latter consideration is less relevant.
Further evaluation of alternative biomarkers to biopsy should be encouraged, including imaging modalities, salivary proteomics and peripheral blood immunophenotyping.43–47 Imaging would not provide biological proof of mechanism however, or mechanistic understanding in the context of a failed study.
In summary, we have provided a series of recommendations relating to the use of salivary gland histopathology in the diagnosis of PSS and in clinical trials, as a step towards the important objective of standardisation.
We thank our other patient partners Claire Pritchard and Margaret Pritchard for their contribution to this work.
Handling editor Tore K Kvien
Collaborators Appendix: Additional Participants of the Histopathology Workshop Group: Rui PP de Albuquerque, Department of Oral Medicine, Birmingham Dental Hospital and School of Dentistry, University of Birmingham, UK. Rigel Allen, Oral Medicine, University of Manchester, Manchester, UK. Elisa Astorri, Centre for Experimental Medicine and Rheumatology, Queen Mary University of London, London, UK. Chiara Baldini, Rheumatology Unit, University of Pisa, Pisa, Italy. Rajdeep Bhabra, patient partner. Pilar Brito-Zerón, Department of Autoimmune Diseases, University of Barcelona, Barcelona, Spain. Preetha Chengot, Department of Histopathology, St. James's University Hospital, Leeds, UK. Stefano Fedele, UCL Eastman Dental Institute London, University College London and National Institute for Health Research UCLH Biomedical Research Centre, London, UK. Aike A Kruize, Department of Rheumatology and Clinical Immunology, University Medical Centre Utrecht, Utrecht, The Netherlands. Roald Omdal, Clinical Immunology Unit, Stavanger University Hospital, Stavanger, Norway. Kingsley Osayi, Department of Pathology, Basildon and Thurrock University Hospital, Basildon, UK. Stephen Porter, UCL Eastman Dental Institute London, University College London, London, UK. John Potts, Department of Oral Medicine, School of Dentistry, University of Cardiff, Cardiff, UK. Ana Poveda-Gallego, Department of Oral Medicine, Dental Hospital, Birmingham, UK. Elizabeth Price, Great Western Hospitals NHS Foundation Trust, Swindon, UK. Roberta Priori, Rheumatology Unit, Sapienza University of Rome, Rome Italy. Manuel Ramos-Casals, Department of Autoimmune Diseases, University of Barcelona, Barcelona, Spain. Soledad Retamozo, Department of Autoimmune Diseases, University of Barcelona, Barcelona, Spain. Krishna Suchak, Department of Pathology, Institute of Dentistry, Queen Mary University of London, London, UK. Nurhan Sutcliffe, Department of Rheumatology, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK. Zahra Syed, Department of Oral Medicine, Leeds Dental Institute, Leeds, UK. Anwar R Tappuni, Institute of Dentistry, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK. Elke Theander, Department of Rheumatology, Skåne University Hospital, Lund University, Malmö, Sweden. Marie Wahren-Herlenius, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden. Asterios Triantafyllou, Oral and Maxillofacial Pathology, School of Dentistry, University of Liverpool, Liverpool, UK. Arjan Vissink, Department of Oral and Maxillofacial Surgery, University of Groningen, Groningen, The Netherlands. Salvatore de Vita, Department of Medical and Biological Sciences, Azienda Ospedaliero-Universitaria “S. Maria della Misericordia”, Udine, Italy. Christina Yap, Cancer Research UK Clinical Trials Unit, University of Birmingham, Birmingham, UK.
Contributors All authors have contributed to the development of the recommendations and the Delphi process, and have contributed to and approved the final manuscript.
Funding The workshop was funded by the Translational Research Partnership in Joint and related Inflammatory Disease, established by the National Institute for Health Research Office for Clinical Research Infrastructure to facilitate early phase translational research and clinical trials, on a collaborative basis between industry, academia and the National Health Service in the UK. FB has a senior fellowship from Arthritis Research UK (21236). The Arthritis Research UK Rheumatoid Arthritis Pathogenesis Centre of Excellence was part-funded by Arthritis Research UK (20298); this Centre is a collaboration between the Universities of Glasgow, Newcastle and Birmingham. The funders did not influence the content of these recommendations.
Competing interests SJB has received honoraria/consultancy fees in the field of Sjögren's syndrome in 2015–2016 for AstraZeneca, Celgene, Glenmark, Eli Lilly, Novartis, Ono and UCB Pharmaceuticals. Roche provided rituximab for the TRACTISS study. BAF has received honoraria/consultancy fees from Novartis, Roche and Medimmune. FB has received honoraria/consultancy fees from Roche, GlaxoSmithKline, Glenmark and Medimmune, and research funding from UCB. Other authors have declared no competing interests.
Provenance and peer review Not commissioned; externally peer reviewed.
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