International Journal of Nephrology
Volume 2017 (2017), Article ID 8409829, 7 pages
https://doi.org/10.1155/2017/8409829

Research Article

Malignancy in Membranous Nephropathy: Evaluation of Incidence

Basil Alnasrallah,¹ John F. Collins,¹ and L. Jonathan Zwi²

¹Department of Nephrology, Auckland City Hospital, 2 Park Drive, Grafton, Auckland 1023, New Zealand
²Department of Pathology, Auckland City Hospital, 2 Park Drive, Grafton, Auckland 1023, New Zealand

Correspondence should be addressed to Basil Alnasrallah; polbeas@yahoo.com

Received 28 February 2017; Revised 15 May 2017; Accepted 7 June 2017; Published 16 July 2017

Academic Editor: Anil K. Agarwal

Copyright © 2017 Basil Alnasrallah et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. Membranous nephropathy (MN) can be associated with malignancy. However, the relative risk for malignancy remains unclear. It has been reported that higher numbers of inflammatory cells seen in the glomeruli at biopsy correlate with the occurrence of malignancy in patients with MN and might be used to direct screening. Methods. We examined the occurrence of malignancy in 201 MN patients in Auckland, New Zealand. We also examined the pathology of renal biopsies from 17 MN patients with malignancies and compared the number of inflammatory cells per glomerulus with matched control patients with MN but no malignancy. Results. 40 malignancies were identified in 37 patients, 28 of which occurred after the MN diagnosis. The standardized incidence ratio (SIR) was 2.1 (95% CI, 1.3–2.85) which was similar between patients ≥ 60 years and those <60 years. The median number of inflammatory cells per glomerulus did not differ between MN patients with and without malignancy at 1.86 (IQR, 1.17–2.7) and 2.07 (IQR, 1.17–3.65), respectively (p value 0.56). Conclusions. The relative risk of malignancy in MN patients was similar across different age groups. The number of inflammatory cells per glomerulus did not differentiate between MN patients with and without malignancies.

1. Introduction

Membranous nephropathy (MN) is a pathologic term that defines a specific glomerular lesion characterized by thickened glomerular capillary walls due to subepithelial deposition or in situ formation of immune-complex deposits [1]. The formation of these immune deposits leads to injury and impairment of glomerular basement membrane [2].

MN remains one of the most frequent glomerular diseases that cause nephrotic syndrome, accounting for around a third of renal biopsies in nondiabetic adults [3, 4]. About 75% of MN cases are idiopathic with no identifiable immunological stimulus and the remaining cases are secondary to a wide variety of primary causes, including neoplasia, infections, autoimmunity, and drugs [5, 6].

The link between MN and malignancy has been reported as early as 1966 by Lee et al. [7] and this association was confirmed later in a number of observational studies. However, the actual risk of malignancy has been shown to be quite variable between different studies, ranging from 2- to 10-fold increase relative to a matched population [8–11]. The malignancies most frequently associated with MN are solid tumors, including lung, gastrointestinal, and prostate carcinomas [9, 10, 12, 13].

This association has led to recommendations for regular screening for malignancy in MN patients around the time of diagnosis, especially when no obvious primary cause is identified [14]. The risk of malignancy in the following years is even less clear. In a population based analysis, the increased risk of malignancy associated with glomerulonephritis diminished after the first year of diagnosis and was not seen beyond 5 years [11].

A more recent study reported a significantly high annual risk of malignancy in patients with MN, which persisted up to 15 years after the diagnosis of MN [9]. This finding could impact on clinical practice and patients’ outcomes, as more rigorous screening for malignancy during follow-up might be warranted. Identifying risk factors for malignancy can assist targeting at risk patients for future screening. However, only older age has been consistently found to be associated with malignancy risk [8–10]. Histological findings such as strong immunofluorescence staining with anti-immunoglobulin (Ig) G1 and G2 antibodies have been linked to malignancy-associated membranous nephropathy whereas IgG4 deposits were found predominantly in the idiopathic form of the disease [15, 16]. However, both of these findings have been challenged [17] and a recent review did not find a reliable immunoglobulin glomerular deposition pattern to differentiate between the two groups [18]. The high number of inflammatory cells infiltrating the glomeruli has been previously reported to be strongly associated with malignancy in MN patients compared to those without malignancy [10]. To our knowledge this has not been further validated or challenged. However, if true it could be a useful additional guide for clinicians to target their screening without the need for further staining.

We undertook a retrospective study of 201 MN patients to try to clarify the incidence of malignancies in patients with MN in Auckland, New Zealand, at the time of diagnosis and during follow-up and to examine the associated factors.

2. Materials and Methods

Ethical approval was obtained through the Northern B Health and Disability Ethics Committee of the Ministry of Health in New Zealand. Ethics approval number is 15/NTB/196.

2.1. Identification of Patients

Patients were identified from the renal biopsy records of the Department of Pathology in Auckland City Hospital. All adult patients (≥18 years old) in whom the diagnosis of MN was made on renal biopsy between January 2003 and December 2013 were included. Baseline data at the time of renal biopsy were collected which included the following: age, sex, eGFR (4-variable Modification of Diet in Renal Disease Study equation), serum albumin level by BCG dye-binding method, degree of haematuria (as per urine , no haematuria if <10, microscopic haematuria if between 10 and 100, and gross haematuria if >100), and proteinuria (g/day) or protein/creatinine ratio (mgs/mmol).

2.2. Definition of Observation Period

The observation period of patients was defined as the time between kidney biopsy and December 31, 2015; death; or loss to follow-up.

2.3. Data for Kidney Biopsies

The pathology slides of renal biopsies in MN patients with malignancy diagnosed around the time of MN (from 1 year before to 5 years after renal biopsy) were reviewed, excluding patients with nonmalignant primary causes of MN. A group of idiopathic MN patients without malignancy were matched in age and gender at a rate of 2 : 1 to the cases and reviewed. All the renal biopsies were examined by a renal pathologist (LJZ) who was blinded to the clinical and laboratory data of the patients. The diagnosis of MN was confirmed histologically and the number of inflammatory cells per glomerulus was reported.

2.4. Identification of Malignancy in Patients with MN

We linked the patients’ records using the New Zealand National Health Index number with the New Zealand Cancer Registry (NZCR), which is a register established in 1948 of all primary malignant diseases diagnosed in New Zealand, excluding squamous and basal cell skin cancers. In addition, the clinical records of all patients were systematically reviewed by a Renal Fellow (BA) to confirm the presence or absence of malignancy. All malignancies diagnosed from 1998 (5 years before the first renal biopsy) to December 2015 (end of observation period) were recorded.

At the time of conducting the study, NZCR had full data of malignancies to the end of 2013. For the years 2014 and 2015, malignancies were recorded based only on systematic review of the clinical records.

32 malignancies were reported on NZCR between 1998 and 2013 in 29 patients and confirmed on clinical records (6 malignancies in 3 patients, 2 each). In addition, on review of clinical records for the same period, 2 malignancies in 2 patients were identified and had not been reported by NZCR.

For the years 2014 and 2015, 6 more malignancies in 6 patients were identified on clinical records and therefore we report on 40 malignancies in 37 patients.

2.5. Statistical Analyses

Standardized incidence ratios (SIRs) were calculated as ratios between observed and expected numbers for site-specific malignancies and all malignancies. For the SIR for all malignancies and their subanalyses, the individual annual expected rate for a matched population in gender and in 5-year age groups was added for every year of follow-up using the rate of that particular year as a reference.

For example, for a 64-year-old male who is followed up for 10 years from 2004, the expected national malignancy rate of the year 2004 for males aged 60 to 65 years was used for the first year, for the second year, the national rate of the year 2005 of the same group was used, and, for the third year, the 2006 rate for males aged 65 to 70 years was used and so on. This was to provide the best representation of the expected malignancy risk and to minimize underestimation of the expected risk of malignancy, as malignancy risk increases with age.

Independent-samples -test was used with continuous variables and chi-square test was used with categorical variables. Median and interquartile ranges (IQR) are reported by the weighted average method.

3. Results

The clinical records of 201 MN patients were reviewed, MN was classified by the treating nephrologist to be idiopathic in 158 patients (78.6%), and this was made after excluding primary causes of MN. Investigations for malignancy, immunological disorders, and hepatitis B and C were universal in this cohort. However, the details of some of the tests were not available to us for many of the patients. Testing for phospholipase A2 receptor (PLA2R) antibodies was not available in New Zealand at the period of patients’ diagnoses (2003–2013) and therefore was not done in any of the patients. The diagnosis of secondary MN was made in 43 patients (21.4%). MN was classified as related to malignancy in 4 patients (2%) and to nonmalignant primary causes in 39 patients (19.4%) (30 patients, systemic lupus erythematosus; 5 patients, hepatitis B; 2 patients, graft-versus-host disease, 1 patient; visceral leishmaniasis, 1 patient; connective tissue disease-NOS). It should be emphasized that there is no clear definition for malignancy related MN in the literature; few criteria have been proposed to confirm a truly causal relationship between the two [12, 13].

The overall follow-up period from the date of biopsy was 1384 patient-years. Baseline characteristics at the time of renal biopsy are shown in Table 1.

Table 1: Cohort characteristics at time of MN diagnosis.

Age (years)
56 (41–65)

Male
117 (58.2%)

Follow-up (months)
88 (45–117)

Serum albumin g/L
29 (23–35)

Proteinuria g/d
5 (2.6–9.55)

eGFR ml/min
70 (43.2–97.5)

Haematuria
84, no haematuria (43.3%)

51, microscopic haematuria (26.3%)

59, gross haematuria (30.4%)

Results are expressed as median (interquartile range) or as percentage.

3.1. Malignancies

40 malignancies were identified in 37 patients (6 malignancies in 3 patients, 2 each) with a prevalence of 18.4%. Of the patients with nonmalignant primary causes of MN, only one had a malignancy during the observation period.

12 out of the 40 malignancies (30%) had been diagnosed before the diagnosis of MN in 10 patients (2 malignancies in each of 2 patients). The median time from diagnosis of these malignancies to renal biopsy was 65 months (IQR, 8.75–76.25). 28 malignancies were diagnosed after MN diagnosis in 27 patients, 4 of these were in malignancy related MN and were diagnosed within 6 months after renal biopsies. The median time from the diagnosis of MN to the diagnosis of malignancy was 40 months (IQR, 14–67.5). When the 4 cases of malignancy related MN were excluded, the median time to the diagnosis of malignancy was 44 months (IQR, 29–73.25). A de novo malignancy after MN was not diagnosed in any of the patients with malignancy prior to MN.

3.2. Risk Factors

Only age was a significant risk factor for malignancy as in Table 2.

Table 2: Clinical and laboratory data at time of kidney biopsy in patients with and without malignancy.

Without malignancy
With malignancy
value

Age (years)
53 (38.5–63.5)
65.5 (58.5–72)
<0.001

Proteinuria (g/d)
5 (2.7–8.85)
6.7 (2.05–10)
NS

Albumin (g/L)
30 (23–36)
26.5 (21.25–35)
NS

eGFR (ml/min)
70 (43–97)
65 (43.4–99.5)
NS

Haematuria

    (i) Nil
68 (43%)
16 (44.4%)
NS

    (ii) Microscopic
41 (26%)
10 (27.8%)

    (iii) Gross

49 (31%)
10 (27.8%)

Results are expressed as median (interquartile range) or as percentage; NS: value > 0.05.

3.3. Immunosuppressive Therapy

The use of immunosuppressive therapy (cyclophosphamide and/or calcineurin inhibitors and/or mycophenolate and/or azathioprine) for more than 3 months was not different between MN patients who did and did not develop malignancy at 42.9% (9 patients) and 42.7% (50 patients), respectively. However, when only looking at the use of cyclophosphamide, more patients had 3 months or more of therapy in the malignancy group at 20.5% (8 patients) compared to 13.8% (13 patients), respectively, p value < 0.001. The mean cumulative dose to cyclophosphamide was 19.8 grams (SD +/− 12.2), with no significant difference between the 2 groups.

3.4. During Follow-Up

After excluding patients with malignancy prior to MN diagnosis, the follow-up period was 1284 person years from the date of renal biopsy. The Standardized Incidence Ratio (SIR) for cancer was significantly raised at 2.1 (95% CI, 1.3–2.85), it was 1.925 (95% CI, 1.06–2.79) in males and 2.51 (95% CI, 0.87–4.15) in females. When the cases of malignancy related MN were excluded, the SIR remained significantly elevated at 1.78 (95% CI, 1.06–2.49) in the follow-up period.

Interestingly, the SIRs for patients who are ≥60 years and those <60 years were similar at 2.08 (95% CI, 1.16–2.99) and 2.06 (95% CI, 0.63–3.49), respectively. This is despite a higher risk of malignancies in the older group and subsequently a significantly lower malignancy-free survival rate (), as seen in Figure 1.

Figure 1: Malignancy-free survival in patients ≥ 60 years of age and those <60 years.

When broken down by time from biopsy to 0–5 years and >5 years, the SIR was significantly high for the first 5 years at 2.3 (95% CI, 1.29–3.4) and lost statistical significance after that at 1.7 (95% CI, 0.58–2.77).

3.5. Symptoms

For the 27 patients who were found to have malignancy after the MN diagnosis, the symptomatic status prior to the diagnostic test for malignancy was known in 26 of the 28 malignancies (92.9%). 24 of 26 malignancies (92.3%) were symptomatic prior to investigations. The list of symptoms is shown in Table 3.

Table 3: Types of malignancy and symptoms in new malignancies after MN.

localization of tumour
Histology
Age
Sex
Months after renal biopsy
Symptoms before malignancy diagnosis (Y: yes/N: no)

Rectal C20
Adenocarcinoma
66
m
1
Y, rectal bleeding

Pancreatic C259
Adenocarcinoma
65
f
1
Y, abdominal pain

Lung NSCLC C349
Not done
75
f
4
Y, dyspnea

Lung NSCLC C343
SCC
57
f
6
N

Cervical D069
CIN III
34
f
7
Y, vaginal bleeding

Colon C187
Adenocarcinoma
82
m
12
Y, symptomatic anaemia

Lung NSCLC C341
SCC
68
m
14
Y, haemoptysis

Prostate C61
Adenocarcinoma
62
m
17
Unknown

Left upper back C435
Metastatic melanoma
72
m
18
Y, skin lump

Lung NSCLC C341
SCC
74
m
27
Y, dry cough and dyspnea

Lung NSCLC C340
Adenocarcinoma
80
m
36
Y, chronic cough

Colon C19
Adenocarcinoma
74
m
37
Y, obstructive bowel symptoms

Lung NSCLC C343
Not done
74
m
37
Y, weight loss

Intestine C179
Neuroendocrine
72
f
41
Y, breast nodule

Unknown
Metastatic melanoma
79
f
41
Y, Dyspnea

Prostate C61
Adenocarcinoma
64
m
45
Y, Urinary voiding symptoms

Prostate C61
Adenocarcinoma
58
m
46
unknown

Intestinal C494
Liposarcoma
54
m
47
Y, Bloody diarrhoea

Unknown primary C269
metastatic adenocarcinoma
51
m
48
Y, Lower groin pain

Prostate C61
Adenocarcinoma
51
m
61
Y, Urinary voiding symptoms

Prostate C61
Adenocarcinoma
68
m
66
Y, Urinary voiding symptoms

Bile duct C240
Adenocarcinoma
64
f
69
Y, Jaundice

CLL C9110
CLL
55
f
76
Y, Cervical lymphadenopathy

Lung NSCLC C341
Adenocarcinoma
64
m
76
Y, Chest wall pain

Colon C182
Adenocarcinoma
61
m
101
Y, Change of bowel habit

Kidney C64
Clear cell carcinoma
55
f
108
N

Lung NSCLC C349
Adenocarcinoma
60
m
117
Y, Dry cough and dyspnea

Prostate C61
Adenocarcinoma
61
m
143
Y, Macroscopic haematuria

3.6. SIR for Types of Malignancies

The SIR for lung malignancy was significantly increased at 8.9 (95% CI, 2.73–15). All of these happened in patients with a history of heavy smoking. The median time from MN diagnosis to the diagnosis of lung malignancy was 35 months (IQR. 14.5–61.5). The SIRs for colorectal and prostate malignancies in males were also high but not statistically significant at 4 (95% CI, 0.08–7.92) and 2.51 (95% CI, 0.5–4.5), respectively.

3.7. Review of Renal Biopsy Tissue

There were 20 patients with malignancy diagnosed between 1 year before and 5 years after MN diagnosis on renal biopsy. Two of these patients had the malignancy diagnosed prior to the biopsy and 18 had the malignancy diagnosed after. We attempted to obtain the pathology slides of these patients and compare them with matched controls with no malignancy at a ratio of 1 : 2.

17 biopsies from patients with malignancies were reviewed (3 could not be retrieved). All of these patients had 10 or more glomeruli on the biopsy with a median interval between the biopsy and the malignancy of 18 months (IQR, 4.5–41). 37 biopsies from patients with no malignancies were reviewed (3 could not be retrieved). The median numbers of glomeruli per biopsy in patients with and without malignancies were similar at 15 (IQR, 13–25.5) and 15 (IQR, 9–23), respectively. The median number of inflammatory cells per glomerulus was not different between the 2 groups at 1.86 (IQR, 1.17–2.7) in patients with malignancy and 2.07 (IQR, 1.17–3.65) in those without, value 0.56, as in Figure 2.

Figure 2: The median number of inflammatory cells per glomerulus in patients with and without malignancies.

The number of glomeruli analyzed on different levels was 917 (311 in the malignancy group and 606 in the control group).

A univariate analysis on Pearson test showed no correlation between the number of inflammatory cells per glomerulus and the period between cancer diagnosis and renal biopsy, p value 0.44. The median number of inflammatory cells per glomerulus was not different in the 6 patients with malignancies within 12 months of renal biopsy compared to the remaining 11 patients with malignancies at 1.01 (IQR, 0.87–1.95) and 2 (IQR 1.8–3), respectively, p value 0.3. No correlation between the total number of inflammatory cells in the biopsy or the inflammatory cells per glomerulus has been identified with any of the clinical variables (age, proteinuria, haematuria, eGFR, or serum albumin).

4. Discussion

This study provides strong evidence for a twofold increased risk of malignancy in MN patients in the follow-up years when compared to a matched population. The SIR of 2.1 is similar to that reported by Bjørneklett et al. at 2.25 who had a median follow-up of 6.2 years [9]. The minor disparity might be related to the different methods used. In the present study, the expected risk was calculated taking into account the annual change of risk, which minimized overestimation of the SIR.

MN patients are regularly screened for malignancy around the time of their diagnosis, and given the known association there might be a lower threshold for future screening compared to general population, which raises the possibility of detection bias. Lefaucheur et al. attempted to address this by identifying those patients with symptomatic malignancies and found that 11 patients (52%) were symptomatic, and the SIRs were raised at 7.1 (95% CI: 3.4–13) in males and 4.4 (95% CI: 0.5–16) in females [10]. However, this was a subsidiary analysis of a group with a very high risk at the start (10-fold). During the follow-up after MN diagnosis in our study of 88 months, the number of symptomatic malignancies before diagnostic testing was high at 24 (92.3%). This might relate to the long follow-up as MN patients usually have screening for malignancy around the time of MN diagnosis, especially if no primary cause is found [1], but not routinely investigated during follow-up unless indicated or symptomatic. Therefore, the detected malignancies in our study are likely to be representative of the actual risk in these patients and not of better surveillance.

The data on long-term risk of malignancy in MN patients remains limited. In the present study, the risk of new malignancies decreased and lost significance beyond 5 years after the diagnosis of MN. After excluding patients with previous malignancies we had 1284 patient-years, which makes this study the largest of its kind.

Older age (≥60 years) has again been shown to be a strong risk factor for malignancy in MN patients; however, the SIRs were almost identical between old and younger patients. This should be emphasized to patients and clinicians when describing the malignancy risk in MN patients.

In the patients receiving cyclophosphamide for more than 3 months in our study, there was a higher rate of malignancy in the follow-up years. van den Brand et al. reported a significant increase in malignancy risk in MN patients receiving cyclophosphamide from 0.3% to 1% [19]. Cyclophosphamide has been linked historically to bladder malignancy [20] and haematological malignancies [21] especially when the mean cumulative dose is >36 g. However, none of the 44 MN patients who had cyclophosphamide in this study developed either. This might be partly explained by the fact that the mean cumulative dose in our cohort was not particularly high at 19.6 g, which falls within the current recommendations for managing idiopathic MN [14].

Lung malignancy has been reported to be the commonest malignancy in MN patients at 26% [8]. In our study the SIR was high at 8.9 and this was within the range of previously reported rates, 3.33 (95% CI: 0.91–8.52) [3] and 31.9 (95% CI: 12.8–65.7) [10]. All lung malignancies in our cohort were in heavy smokers. We thus support the recommendation that a Computed Tomography of the chest be undertaken for smokers with MN as proposed by Pani et al. [22]. However its value has not been prospectively examined.

Efforts have been made to identify histological markers in renal biopsies of MN patients which predict malignancy. Earlier papers suggested that different IgG subclass pattern of deposition could be helpful. Ohtani et al. reported a significantly more intense IgG1 and IgG2 deposition in malignancy-associated MN compared with idiopathic MN [15]. Later on, Qu et al. found no significant difference in IgG1 deposition and a small but significantly more intense IgG2 deposition in malignancy related MN compared to idiopathic MN [16]. Qu et al. also found that the IgG4 deposition was significantly different between the 2 groups, being absent in 88% of malignancy related MN compared to 14% of idiopathic MN. More recently, Lönnbro-Widgren et al. showed no difference between idiopathic MN and malignancy related MN in IgG1 or IgG2 deposition and reported a difference only in the IgG4 deposition between the two at 65% and 31%, respectively [17]. Murtas and Ghiggeri reported on a recent review that there was no reliable deposition pattern to differentiate between the two entities [18].

In their paper, Lefaucheur et al. reported that MN patients with malignancies had a significantly higher number of inflammatory cells in the glomeruli compared with matched idiopathic MN patients. The number of inflammatory cells was on average more than double that of the matched controls, and 8 inflammatory cells was the best cut-off value to distinguish between the 2 groups, with a specificity of 75% and a sensitivity of 92% (). This has not been further examined.

In the present study, there was no relation of the number of inflammatory cells in the glomeruli to the malignancy status or to the interval between the renal biopsy and the malignancy diagnosis. We had 3 patients in our cohort with 8 inflammatory cells or more per glomerulus on their renal biopsies and none of these patients had malignancy.

The exact mechanism underlying the association between MN and malignancy remains a matter of debate. Nevertheless, few mechanisms have been proposed [23, 24]. Antibodies may be generated against an antigen on the malignant tissues similar to an endogenous podocyte antigen, thereby leading to in situ glomerular immune-complex formation. Alternatively, shed tumor antigens may form circulating immune complexes that become trapped in the capillary wall. These complexes may initially form in a subendothelial location where the immune clearance is limited [25], dissociate, and reform in a subepithelial position. Another possibility is an extrinsic process such as an oncogenic virus or an altered immune function that causes both malignancy and MN.

A major argument against a causal association between malignancy and MN stems from the fact that they are both more common in older individuals which might merely represent two coincidental disease processes [24]. However, in our study we demonstrated clearly that this association persists across the age groups.

5. Conclusion

The relative risk for malignancy after the diagnosis of MN is more than twice that of a matched population and is similar across age groups. This increased risk is only found in the first 5 years of follow-up. The increased risk does not appear to relate to better surveillance, as it remains significantly high even for patients only with malignancy-specific symptoms prior to investigations. The risk of lung malignancy is particularly high at almost 9-fold. The number of inflammatory cells per glomerulus was not a helpful tool to differentiate between MN patients with and without malignancy.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

This work was supported by the Renal Department in Auckland City Hospital, Auckland, New Zealand.

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