Abstract
Objective
To investigate risk factors for non‐Hodgkin's lymphoma (NHL) and analyse NHL subtypes and characteristics in patients with systemic lupus erythematosus (SLE).
Methods
A national SLE cohort identified through SLE discharge diagnoses in the Swedish hospital discharge register during 1964 to 1995 (n = 6438) was linked to the national cancer register. A nested case control study on SLE patients who developed NHL during this observation period was performed with SLE patients without malignancy as controls. Medical records from cases and controls were reviewed. Tissue specimens on which the lymphoma diagnosis was based were retrieved and reclassified according to the WHO classification. NHLs of the subtype diffuse large B cell lymphoma (DLBCL) were subject to additional immunohistochemical staining using antibodies against bcl‐6, CD10 and IRF‐4 for further subclassification into germinal centre (GC) or non‐GC subtypes.
Results
16 patients with SLE had NHL, and the DLBCL subtype dominated (10 cases). The 5‐year overall survival and mean age at NHL diagnosis were comparable with NHL in the general population—50% and 61 years, respectively. Cyclophosphamide or azathioprine use did not elevate lymphoma risk, but the risk was elevated if haematological or sicca symptoms, or pulmonary involvement was present in the SLE disease. Two patients had DLBCL‐GC subtype and an excellent prognosis.
Conclusions
NHL in this national SLE cohort was predominated by the aggressive DLBCL subtype. The prognosis of NHL was comparable with that of the general lymphoma population. There were no indications of treatment‐induced lymphomas. Molecular subtyping could be a helpful tool to predict prognosis also in SLE patients with DLBCL.
Evidence of an increased risk to develop haematological malignancy, and especially non‐Hodgkin's lymphoma (NHL) in autoimmune diseases, has been gathered since the 1970s. First studies of Sjögren's syndrome,1 then rheumatoid arthritis (RA)2 and now in the last decade studies from uni‐/multicentre SLE cohorts3,4,5,6,7,8 and national SLE cohorts9,10 have consistently shown a markedly increased risk of NHLs. As for NHL subtype, knowledge is more limited. RA and SLE share several disease manifestations like arthritis and “extra‐articular manifestations” such as serositis, sicca symptoms and interstitial inflammatory lung disease. In RA, a pronounced over‐representation of diffuse large B cell lymphoma (DLBCL) has been reported from a large population‐based cohort.11 This lymphoma subtype was also the most frequent in an international multicentre study with lupus patients.12 In Sjögren's syndrome, approximately 85% are MALT lymphomas,13 although a recent study from a mono‐centre primary Sjögren's syndrome cohort—with patients fulfilling the American–European Consensus Group criteria14—showed a predominance of DLBCL.15
The pathophysiological mechanisms for the enhanced risk of developing NHL in patients with chronic inflammatory diseases are still not fully understood. Similarities of a variety of immunological disturbances that characterise both rheumatic conditions and lymphomas have been suggested as a linkage between these disorders as well as a possible potentiation of immunosuppressive drugs or certain viral infections, especially Epstein–Barr virus (EBV).5,16
Recently, advances in molecular characterisation have enabled more detailed subclassification of lymphomas based on the molecular expression of the tumour cells. For DLBCL, two prognostic groups have been identified among DLBCL in the general lymphoma population depending on the resemblance of gene expression profile with normal germinal centre (GC) or activated B cells by using global gene expression profiling17,18 and immunophenotyping of tumour cells.19,20 The GC DLBC lymphomas had a significantly better survival than those with non‐GC subtype.17,18,19,20 No such subtyping has been reported in SLE patients.
In a previous register study of a population‐based national Swedish SLE cohort, a threefold increased risk of lymphoma was found.10 This nested case‐control study focuses on those SLE patients that developed NHL. Information on clinical manifestations and pharmacological (cytotoxic) treatment of the SLE disease was retrieved from patient records. The lymphomas were re‐examined and reclassified, and DLBCLs were further divided into GC or non‐GC subtypes by immunohistochemistry. The presence of EBV in the lymphomas was also analysed.
Patients and methods
Selection of patients and collection of clinical data
From the Swedish Hospital Discharge Register, we identified all patients discharged from hospitals in Sweden with a diagnosis of SLE (ICD‐7: 456,20; ICD‐8: 734,10; ICD‐9: 710A), as either a primary or a secondary diagnosis, during 1964–1995. We excluded all patients younger than 20 years at the first discharge and those who had ever been discharged with a diagnostic code of RA, psoriatic arthritis or ankylosing spondylitis. Exclusions were also made if the patient had a discharge diagnosis of cancer before or at the first discharge.
By linking the Swedish Cancer Register with the Swedish Hospital Discharge Register, we identified 42 cases of non‐Hodgkin's lymphoma (NHL) (ICD‐7, ICD‐8: 200, 202) among 6438 patients with SLE.
To identify risk factors of developing NHL in a SLE population, a nested case control study was performed. For each case where SLE as well as NHL diagnoses were confirmed, five controls from the SLE cohort were selected. The controls were matched for gender and were required to have an observation period free from cancer as long as or longer than the matched NHL–SLE case. The follow‐up time for survival of the lymphoma cases was extended to June 2005.
From the Swedish Hospital Discharge Register, the medical records from the hospital admissions of each patient were retrieved. Every case and all but 8 control patients (10%) could be evaluated from the medical records that were obtained. The included patients had been treated in 43 different hospitals throughout Sweden. The clinical data were reviewed and evaluated with respect to whether the patients fulfilled the 1997 American College of Rheumatology (ACR) revised criteria for the classification of SLE.21 Patients not fulfilling these criteria as well as patients with incorrect diagnosis registrations were excluded. Data retrieved from the medical records also included treatment, medical events and comorbidities.
Statistics
Calculations of relative risks, with 95% confidence intervals, for each clinical/serological feature against the lymphoma outcome were performed using Statistical Packages for the Social Sciences (SPSS).
Analysis of lymphoma tissues
From the medical records, we identified code numbers of the tissue specimens on which the lymphoma diagnosis was based. The original slides and paraffin blocks were collected from 10 Swedish pathology departments. The original slides were reviewed to confirm the diagnosis of lymphoma, additional tissue sections were cut, and appropriate routine immunostainings were performed. One experienced haematopathologist (CS) blinded to all clinical data classified the lymphomas according to the recently described WHO classification.13 Additional immunohistochemical characterisation was performed on those lymphomas diagnosed as DLBCL. Occurrence of EBV was examined by in situ hybridisation (ISH).
Subtyping of lymphoma by immunohistochemistry
A Ventana XT module (Ventana medical systems, Tucson, AZ) was used for the immunohistochemical staining procedure. Briefly, paraffin‐embedded sections (4 μm thick) were deparaffinised, and all sections except for kappa and lambda antigen stainings were subjected to heat‐induced antigen retrieval programmes. Primary antibodies directed against bcl‐2, bcl‐6, CD3, CD5, CD8, CD20, CD45, CD79a, CD138, Cyklin D1, Ki‐67, kappa, lambda, TDT (Dakocytomation, Glostrup, Denmark), CD4 (Novacastra laboratories Newcastle upon Tyne, UK), CD10, CD23 (Ventana) and CD30 (Beckman Coulter, Brea CA) antigens were incubated for 30 min. An amplification kit (Ventana) was used to enhance staining for CD4, CD30, bcl‐6 and cyklin D1, and the Iview DAB detection kit (Ventana) was used for stainings. Sections were counterstained with haematoxylin, with the blueing reagent kit (Ventana).
Immunostaining for CD7 (DakoCytomation), perforin, granzyme B, CD56 (Novacastra) and IRF‐4 (Santa Cruz biotechnology, Santa Cruz, CA) antigens were performed manually. Following deparaffinisation of sections, heat‐induced antigen retrieval was used for each antibody. Primary antibodies, secondary rabbit antimouse or rabbit antigoat (for IRF‐4 antibody detection) antibodies and ABC complex were added sequentially for 30 min (DakoCytomation). Immunoreactivity was visualised with 3,3‐diaminobenzidine and counterstained with Mayer's haematoxylin. All incubations were performed in room temperature. Staining results were estimated by conventional microscopy of coded slides (CS). To subclassify the DLBCLs into GC and non‐GC subtypes, the same method (stainings with CD10, bcl‐6, IRF‐4) and cutoff values as described previously19,20 were used. A staining result was considered positive if 30% or more of the tumour cells were stained.
In situ hybridisation for Epstein–Barr virus related RNA
ISH for Epstein–Barr virus related RNA (EBER) was performed on paraffin‐embedded sections (4 μm thick) in Ventana XT module according to the manufacturer's instructions (Ventana). The study was approved by the local ethics committee at the Karolinska Institute.
Results
Of the original 42 patients with NHL, 2 were excluded because of incorrect diagnosis code (tuberculosis and non‐specific synovitis). Twenty‐three were excluded for not fulfilling the ACR criteria for SLE. Seventeen patients fulfilled the ACR criteria for SLE, and their lymphoid tissues were subject to analysis and reclassification. One patient was excluded, since the lymphoma diagnosis could not be confirmed from the tissues that were available. The remaining 16—out of 40 (40%)—cases with SLE and NHL were included in the study. From the 80 SLE control patients, 22 had to be omitted because of an incorrect diagnosis code or because the medical records could not be found. From the remaining 58, the same proportion of SLE patients fulfilling ACR criteria as in the SLE‐NHL cases remained after examination of medical records, 26 (45%).
Cases (with NHL and SLE) and controls were all women. The age at onset of SLE and at NHL diagnosis and the overall survival time from date of lymphoma diagnosis are presented in table 1. The mean age at onset of SLE for the control patients was 44 (10–70).
Table 1 Clinical data, overall survival, lymphoma type and results of in situ hybridisation for EBV in lymphomas of the 16 reviewed female cases with SLE and NHL.
| No. | Age at SLE onset | Age at NHL diagnosis | Surviving years | Living/death age | Lymphoma type according to WHO classification | EBV‐pos lymphoma |
|---|---|---|---|---|---|---|
| 1 | 19 | 32 | >11 | Yes | DLBCL | No |
| 2 | 22 | 33 | >22 | Yes | DLBCL | Yes |
| 3 | 43 | 56 | >11 | Yes | DLBCL | No |
| 4 | 54 | 56 | <1 | No/56 | DLBCL | No |
| 5 | 54 | 63 | >14 | Yes | DLBCL | No |
| 6 | 50 | 66 | >14 | Yes | DLBCL | No |
| 7 | 39 | 67 | <1 | No/67 | DLBCL | No |
| 8 | 69 | 73 | <1 | No/73 | DLBCL | No |
| 9 | 69 | 74 | >11 | No/85 | DLBCL | No |
| 10 | 53 | 82 | >2 | No/84 | DLBCL | No |
| 11 | 37 | 48 | <1 | No/48 | Peripheral T cell lymphoma | No |
| 12 | 44 | 65 | <1 | No/65 | Unspec high‐grade B cell lymphoma | No |
| 13 | 15 | 43 | <1 | No/43 | Unspec high‐grade B cell lymphoma | Not analysed |
| 14 | 61 | 69 | >10 | No/79 | Follicular lymphoma | No |
| 15 | 67 | 68 | >7 | No/75 | Lymphoplasmacytic lymphoma | No |
| 16 | 66 | 74 | <1 | No/74 | Lymphoplasmacytic lymphoma | Yes |
| Mean 48 | Mean 61 |
DLBCL, diffuse large B cell lymphoma.
The lymphoma subtype according to the WHO classification is listed in table 1.
There was a striking predominance of DLBCL, recorded in 10 out of 16 cases (62%). The remaining cases were diagnosed as lymphoplasmacytic lymphoma (n = 2), unspecified high‐grade B cell lymphoma (n = 2), follicular lymphoma (n = 1) and unspecified peripheral T cell lymphoma (n = 1). EBV was detected in 2 of 15 investigated cases (n = 13%).
Clinical and immunological characteristics are listed in tables 2 and 3.
Table 2 Medical treatment and clinical characteristics of the SLE cases with NHL and the controls and the relative risk of lymphoma.
| SLE patients with NHL n = 16 (%) | SLE patients: controls n = 26 (%) | RR (95% CI) | |
|---|---|---|---|
| Oral glucocorticosteroids | 16 (100) | 26 (100) | |
| Cytotoxic agents | 7 (43) | 10 (38) | 1.1 (0.5, 2,5) |
| Azathioprine | 5 (31) | 9 (35) | 0.9 (0.4, 2.1) |
| Cyclophosphamide | 2 (12) | 3 (12) | 1.1 (0.3, 3.3) |
| Malar rash | 3 (19) | 7 (27) | 0.7 (0.3, 2.1) |
| Discoid rash | 1 (6) | 4 (15) | 0.5 (0.1, 3.0) |
| Photosensitivity | 6 (38) | 7 (27) | 1.3 (0.6, 2.9) |
| Oral ulcers | 3 (19) | 1 (4) | 2.2 (1.1, 4.5) |
| Sicca symptoms and/or salivary‐gland swellings | 5 (31) | 1 (4) | 2.7 (1.5, 5.0) |
| Arthritis | 13 (81) | 21 (81) | 1.0 (0.4, 2.7) |
| Pleuritis | 12 (75) | 18 (69) | 1.2 (0.5, 3.0) |
| Recurrent pneumonias and/or pulmonary infiltrates | 7 (43) | 3 (12) | 2.5 (1.3, 4.9) |
| Pericarditis | 6 (38) | 4 (15) | 1.9 (0.9, 3.9) |
| Glomerulonephritis | 2 (12) | 6 (23) | 0.6 (0.2, 2.2) |
| Epilepsia, psychosis, CNS vasculitis | – (0) | 5 (19) | |
| Leucopenia | 13 (81) | 17 (65) | 1.7 (0.6, 5.0) |
| Thrombocytopenia | 5 (31) | 10 (38) | 0.8 (0.4, 1.9) |
| Autoimmune haemolytic anaemia | 4 (25) | – (0) | 3.2 (2.0, 5.0) |
| ANA | 14 (88) | 24 (92) | 0.7 (0.3, 2.1) |
| DNA | 4 (25) | 16 (62) | 0.4 (0.1, 1.0) |
| SS‐A and/or SS‐B | 4 (25) | 2 (8) | 2.0 (1.0, 4.1) |
| Elevated IgG | 9 (56) | 12 (46) | 1.3 (0.6, 2.8) |
| Coombs test positive | 3 (19) | 1 (4) | 2.2 (1.1, 4.5) |
| Complement disorder | 4 (25) | 7 (27) | 0.9 (0.4, 2.3) |
| False positive Wasserman reaction and/or anticardiolipin antibodies | 4 (25) | 2 (8) | 2.0 (1.0, 4.2) |
ANA, antinuclear antibodies; DNA, antibodies to native DNA; SS‐A, antibodies to Ro antigens; SS‐B, antibodies to La antigens.
Table 3 Clinical and immunological features and lymphoma treatment in patients with SLE and NHL.
| Patient no. | Clinical features of SLE | Laboratorial and immunological features | Clinical presence of lymphoma/Ann Arbor staging at lymphoma diagnosis | Lymphoma treatment | Cause of death |
|---|---|---|---|---|---|
| In parentheses: time interval between first haematological symptom—NHL diagnosis (years) | |||||
| 1 | Arthritis, malar rash, photosensitivity, salivary gland swellings, xerostomia, pulmonary infiltrates, recurrent pneumonias | ANA | B‐symptoms, cervical lymph nodes/IV | Prednimustin | – |
| SS‐A, SS‐B | |||||
| IgG 31 g/l | |||||
| IgM 5.7 g/l | |||||
| 2 | Arthritis, photosensitivity, oral ulcers, pleuritis, leucopenia (4), sicca symptoms | ANA | Nausea, eating problems/IV | Surgery | – |
| SS‐A, SS‐B | 8 CHOP‐M | ||||
| IgG 39 g/l | 5 VePAC | ||||
| IgA 10 g/l | Radiotherapy | ||||
| 3 | Arthritis, pleuritis, pericarditis, pulm infiltrates, leucopenia (13) | ANA | Eye irritation, unilateral exoftalmus/III.1 | Surgery | – |
| DNA | Prednimustin | ||||
| IgG 20 g/l | |||||
| Coombs test + | |||||
| Compl do (C4) | |||||
| 4 | Arthritis, pleuritis, thrombocytopenia (1½), glomerulonephritis | ANA neg | Cervical, axillar lymph nodes, Fever/III.1 | 9 CHVP | Lymphoma |
| SS‐A, SS‐B | |||||
| Compl do (C4) | |||||
| Subnormal IgG | |||||
| 5 | Perimyocardits, pleuritis, leucopenia (10) | ANA | Inch‐sized protuberance in chest wall/II | 4 CHOP | – |
| DNA | Radiotherapy | ||||
| 6 | Arthritis, malar rash, discoid rash, photosensitivity, KCS, leucopenia (15) | ANA | Pathological femur fracture when walking/IV | Radiotherapy | – |
| DNA | Relapse 1 year later: 8 CNOP | ||||
| (False positive) WR | |||||
| IgG 30 g/l | |||||
| 7 | Arthritis, photosensitivity, malar rash, pleuritis, leucopenia, thrombocytopenia, haemolytic anaemia (21) | ANA | Fatigue | Death short after lymphoma diagnosis | Lymphoma |
| “Hypergamma” | Pancytopenia/IV | ||||
| 8 | Arthritis, pleuritis, pulmonary infiltrates, anaemia, leucopenia, severe immunological thrombocytopenia (4) | ANA | Swelling, pain left cheek/II | CHOP | Lymphoma (after second CHOP) |
| Coombs test+ | |||||
| Anticardiolipin antibodies | |||||
| IgG 21 g/l | |||||
| 9 | Arthritis, pleuritis, pleuropneumonia, leucopenia, autoimmune haemolytic anaemia (8) | ANA | Severe abdominal pain/II | Surgery | Info |
| (False positive) WR | Missing | ||||
| Compl do (C4) | |||||
| Coombs test+ | |||||
| IgA 4,9 g/l | |||||
| 10 | Arthritis, recurrent pneumonias, pulmonary infiltrates, leucopenia (9) | ANA | Lymphadenopatia, fever/III | Klorambucil+Prednisolone | Respiratory insufficiency, cor pulmonale |
| IgG 20 g/l | |||||
| Serume M protein | |||||
| 11 | Arthritis, photosensitivity, oral ulcers, recid serositis | ANA | Unilateral pelvis dilatation, B‐symptoms/IV | Vincristine, cerubidin, cyclophosphamide, methotrexate, cytarabine started | Ad mortem 1 month after chemotherapy start; septic shock |
| DNA | |||||
| IgG 16 g/l | |||||
| 12 | Arthritis, sicca symptoms, pleuritis, leucopenia, (4) thrombocytopenia (ITP), pulmonary infiltrates | ANA | B‐symptoms/IV | 8 CHOP + | …Ad mortem in clinical picture of septic chock |
| Sm, RNP | Etoposide start but… | ||||
| SS‐A | |||||
| IgG 40 g/l | |||||
| IgM 7 g/l | |||||
| IgA deficiency | |||||
| 13 | Glomerulonephritis, leucopenia, thrombocytopenia (>16), oral ulcers, pericarditis | ANA | B‐symptoms, lymph nodes/III.2 | 8 CHOP | Ad mortem |
| Candida sepsis | |||||
| 14 | Photosensitivity, pleuropericarditis, KCS, leucopenia (8) | ANA | Impaired nose breathing, swelling/I | Radiotherapy | Info |
| (False positive) WR | Relapse: radiotherapy | Missing | |||
| IgA 4,5 g/l | |||||
| 15 | Arthritis, pleuritis, haemolytic anaemia, leucopenia (16) | ANA | Fever, fatigue/IV | Chlorambucil | Septicaemia (pseudomonas) |
| IgM 24 g/l | |||||
| Compl do (C4) | |||||
| 16 | Arthritis, pericarditis, pleuropneumonia, pulmonary infiltrates, leucopenia (8) | LE‐cells | Fever/IV | – | Lymphoma diagnosis at autopsy |
| IgG 23 g/l |
ANA, antinuclear antibodies; DNA, antibodies to native DNA; SS‐A, antibodies to Ro‐antigens; SS‐B, antibodies to La‐antigens; RNP, antibodies to U1RNP antibodies; Sm, antibodies to Sm antigens; LE‐cells, pos LE cell phenomenon; WR, Wasserman reaction; Compl do (C4), Complement disorder with low C4; Ig, etc, highest measure of an elevated immunoglobulin; KCS, keratoconjunctivitis sicca; CHOP, Cyclophosphamide, Doxorubicin, Vincristine, Prednisolone. CHVP, Vinblastine instead of vincristine; VePAC, Etoposide, Prednisolone, Cytarabine, Lomustine.
Fourteen (88%) patients with SLE and NHL had signs of haematological aberration (leuco‐/thrombocytopenia and or haemolytic anaemia). The time interval between the first onset of a haematological manifestation and the lymphoma diagnosis is shown in table 3. In all but one, this time span was more than 4 years, mostly considerably longer.
Besides frequent haematological aberrations, the NHL cases significantly more often than controls had sicca symptoms and/or salivary gland swellings as well as diffuse, non‐infectious pulmonary infiltrates (table 2) that preceded lymphoma by several years. The last two associations are statistically significant but have to be interpreted with caution, since the absolute numbers are low.
In contrast, a severe prompt treatment demanding organ manifestation like glomerulonephritis was found more frequently, albeit not significantly, among the SLE controls. Immunological tests revealed an almost obligatory presence of antinuclear antibodies and/or LE cells without any difference between the NHL–SLE cases and the SLE controls, 88 and 92%, respectively.
All patients, cases as well as controls, had been treated for their SLE with oral glucocorticoids. In addition, 7 patients among the lymphoma cases had been treated with cytotoxic agents (44%), 5 with azathioprine and 2 with cyclophosphamide (table 3). Among the SLE controls, 10 out of 26 (38%) patients had been treated with cytotoxic agents.
Ever use of azathioprine (RR 0.9; 0.5 to 2.5) and cyclophosphamide (RR 1.1; 0.3 to 3.3) did not increase the risk of NHL. Symptoms that raised suspicion of a malignant process/lymphoma and Ann Arbor staging at lymphoma diagnosis are also listed in table 3, together with treatment for the lymphomas and the causes of death in the SLE cases. Fever, fatigue and often all B‐symptoms, as well as changes in lymph‐node swellings and other protuberances led to most of the lymphoma diagnosis. Two patients died before lymphoma treatment was started. All other patients were treated according to medical practice at the time of lymphoma diagnosis, including use of alcylating drugs, combination chemotherapy, radiation and/or surgery. The lymphoma itself or treatment‐induced sepsis was in most cases the apprehended cause of death.
Survival data had a bimodal pattern. Seven of the SLE–NHL cases (44%) did not survive their first year after lymphoma diagnosis. On the other hand, the 5‐year survival was good, 50%, and the 10‐year survival only slightly less, 43% for all SLE patients with NHL. Two of the 10 DLBCL cases could be classified as a GC type owing to positive stainings for CD 10 or bcl‐6 as well as negative staining for IR‐4 (Table 4). These two patients were still alive 14 and 22 years, respectively, after lymphoma diagnosis.
Table 4 Immunohistochemical expression and overall survival in SLE patients with DLBCL.
| Patient no. | CD 10 (%) | bcl‐6 (%) | IRF‐4 (%) | bcl‐2 (%) | Survival (years) |
|---|---|---|---|---|---|
| 1 | 0 | 0 | 100 | 17 | >11 |
| 2 | 100 | 6 | 0 | 0 | >22 |
| 3 | 8 | 0 | 17 | 41 | >11 |
| 4 | 0 | 0 | 0 | 0 | <1 |
| 5 | 0 | 42 | 18 | 0 | >14 |
| 6 | 0 | 0 | 95 | 0 | >14 |
| 7 | 0 | 35 | 40 | 0 | <1 |
| 8 | 0 | 0 | 0 | 0 | <1 |
| 9 | 0 | 0 | 80 | 0 | >11 |
| 10 | 0 | 0 | 15 | 63 | 2 |
GC subtypes are shown in bold. %, percentage of tumour cells with positive antibody staining.
Discussion
The striking predominance of one specific lymphoma subtype, DLBCL, among patients with SLE confirms the previously published data from Bernatsky et al in their multisite international SLE cohort from 23 rheumatological centres.12 In the general population in western countries, DLBCL constitutes 30–40% of adult NHL,13 and in our national SLE cohort, the proportion was 62%. The presence of certain clinical SLE phenotypes including haematological manifestations, sicca symptoms/salivary gland swellings as well as pulmonary infiltrates and/or recurrent pneumonias was associated with increased risk to develop lymphoma, whereas treatment with the traditional antirheumatic, cytotoxic drugs azathioprine and cyclophosphamide was not. The prognosis in this nested case control study, a 50% 5‐year overall survival after NHL diagnosis, is fairly good and comparable with the general lymphoma population—in striking contrast to previous observations in SLE patients.12
Treatment decisions for lymphoma are based on clinical staging. The Ann Arbor staging for lymphoma divides the tumour at diagnosis into nodal, extra nodal or disseminated disease.22 In NHL, staging has more often been based on clinical than pathological findings. An often‐used prognostic tool is the International Prognostic Index (IPI).23 To further improve prognostication, molecular expression analysis of NHL tissue has been developed. Thus, by molecular classification using cDNA micro‐array analysis, DLBCL can be divided into prognostically significant subgroups with GC, activated B cell‐like (ABC) or type 3 expression profiles where the GC group has a significantly better survival.19,20 Several studies have used the immunohistochemical expression of, among others, CD 10, bcl‐6, IRF‐4 and bcl‐2 to classify cases of DLBCL into GC or non‐GC groups.24,25,26,27 Positive staining for CD 10 as well as positive staining for bcl‐6 (and IRF‐4 negative) is considered indicative of superior survival in lymphoma in the general population, while the prognostic value of bcl‐2 staining is still controversial.19 By subtyping SLE patients with DLBCL into GC and non‐GC subtype, we found a small proportion of patients with a better prognosis, the GC subtype, which in the general population of lymphoma patients is associated with good prognosis. Although anecdotal, this observation could indicate that this classification could also be relevant in patients with SLE who develop NHL.
Our knowledge of the aetiology and the pathogenesis of lymphoma development in rheumatic diseases is still limited. In RA, patients with the highest burden of inflammatory activity have the highest risk of lymphoma, and antirheumatic pharmacological treatment including cytotoxic agents does not seem to be a major risk factor for RA‐associated lymphomas.28,29 Similar studies have not yet been conducted in SLE patients. Each of the published studies on SLE and lymphomas contains very few lymphoma cases, and information on clinical characteristics including medical treatment is often missing.3,4,7,9,10 Our nested case‐control study is to our knowledge the largest study where clinical and laboratory findings as well as information on medical treatment are reported. From this retrospective, medical records‐based study, it is hazardous to try to draw definite conclusions on clinical characteristics of SLE patients that confer a risk of developing NHL. Although our study population is small, we could still determine certain clinical features that were more frequent in the SLE patients that developed NHL. The indication of significantly more frequent involvement of mucosal membrane, salivary glands and lung parenchyma in those who developed lymphoma could imply that, in an immune‐deficient individual like an SLE patient, an impaired barrier for exogenous agents, as for instance certain viruses, and recurrent infections are of importance for lymphoma transformation. We also recorded more frequently occurring haematological manifestations, both autoimmune haemolytic anaemia and leucopenia as well as hyperglobulinemia, in the cases that developed lymphoma, indicating that activation of the immune system was a risk factor of developing lymphoma
The role of EBV in the aetiology and pathogenesis of SLE has not yet been fully investigated. There are observations that EBV may act as a trigger in the development of SLE in some cases.30 In our study, EBV was detected by ISH in the lymphoma tissue of 2 of 15 patients. Even if there are few cases, and EBV infections could not explain the elevated risk of developing NHL in SLE, a connection cannot be ruled out in these 2 individual cases.
The study period covered 1965–1995, an era when manifestations of an inflammatory systemic disease like SLE in Sweden meant hospitalising, perhaps with the exception of SLE patients with a predominating skin rash, reflected by the relatively few patients with cutaneous manifestations in our cohort. One strength of our study was that we included SLE patients from a variety of medical specialty departments, with only 8 of 16 patients with SLE and lymphoma ever seeing a rheumatologist. We therefore believe that our patients are unselected, and the data generalizable to the Swedish SLE population. The median age at onset of our SLE cases was 48 years, which is similar to other SLE cohorts from the same time period.31
A limitation of our study is the high dropout rate. This could be explained by rigorous exclusion procedures (strictly ACR classification criteria), resulting in missing cases, however, both among SLE‐NHL cases and SLE controls. Thus, the dropouts would not affect the estimation of risk factors in established SLE cases. Validation of the diagnoses in the Swedish Hospital Discharge Register has been made in several studies with a correct ICD‐code at the 4‐digit level in 86% of all main discharge diagnoses.32 There is, however, no previous report on the validity of the SLE diagnosis. Our experience from this study, and similar ones, is that the SLE diagnosis in the Swedish Hospital Discharge Register, defined as fulfilling the 1997 ACR criteria, is less specific. This may not be surprising, as the ACR criteria are classification criteria and were not developed to be diagnostic criteria for clinical practise.
The differential diagnosis of SLE versus primary Sjögren's syndrome is sometimes difficult, and the possibility of an overlap syndrome must be kept in mind. This difficulty in differentiating among the systemic autoimmune diseases has recently been discussed.33 We have no reason to believe that patients with Sjögren's syndrome have been misclassified as SLE in our study, though the SLE diagnosis in our 16 lymphoma cases was well founded (table 3). On the other hand, there are several patients with a clinical and laboratory profile consistent with Sjögren's syndrome as well. Thus, some of our patients presented signs of autoimmune inflammatory disease with a possible overlap of SLE and Sjögren's syndrome; those were among the SLE patients with the highest risk of developing lymphoma in our cohort.
In conclusion, the most common subtype of lymphoma in SLE patients is DLBCL. Certain clinical features seem to confer risk factors to develop lymphoma, including haematological manifestations, Sjögren‐like disease and pulmonary involvement
The use of immunosuppressive drugs was not substantial in our cohort of SLE cases with lymphoma arguing against treatment‐induced lymphoma. Immunohistochemical analysis for subtyping of DLBCLs to predict prognosis seems to be applicable also for patients with SLE and lymphoma but needs confirming on a larger scale. Clinicians caring for SLE patients should keep the lymphoma risk in mind and regularly check for lymphadenopathy.
Acknowledgements
We want to thank associate professor Ronald van Vollenhoven for linguistic advice, Hans G Eriksson for statistical analyses and Eva Baecklund for comments on the manuscript. This study was supported by The Swedish Cancer Society and by a Stipend from the Sörmland County Council.
Abbreviations
DLBCL - diffuse large B cell lymphoma
EBV - Epstein–Barr virus
NHL - non‐Hodgkin's lymphoma
RA - rheumatoid arthritis
SLE - systemic lupus erythematosus
Footnotes
Competing interests: None.
References
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