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Abstract Number: 1607

Tumor-Related Autoantibodies and Cancers in SLE: A Case-Control Study from a Single Centre

Sasha Bernatsky1, Ann E. Clarke2, Joyce Rauch3, Christian Pineau4, Evelyne Vinet5 and Marvin J. Fritzler6, 1Divisions of Rheumatology and Clinical Epidemiology, Research Institute of the McGill University Health Centre, Montreal, QC, Canada, 2Division of Rheumatology, University of Calgary, Calgary, AB, Canada, 3Division of Rheumatology, Research Institute of the McGill University Health Centre, Montreal, QC, Canada, 4Rheumatology, McGill University Health Center, Montreal, QC, Canada, 5Divisions of Rheymatology and Clinical Epidemiology, McGill University Health Centre, Montreal, QC, Canada, 6Medicine, University of Calgary, Calgary, AB, Canada

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: autoantibodies, cancer and systemic lupus erythematosus (SLE)

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Session Information

Date: Monday, November 6, 2017

Title: Systemic Lupus Erythematosus – Clinical Aspects and Treatment Poster II: Damage and Comorbidities

Session Type: ACR Poster Session B

Session Time: 9:00AM-11:00AM

Background/Purpose: Patients with systemic lupus (SLE) have altered cancer profiles compared to the general population, with a higher risk of some cancers (e.g. lymphoma) and apparently a lower risk of others (e.g. breast).  Tumor-associated antibodies to centromere proteins and other antigens have been reported in many types of cancers (including lymphoma and breast) and may serve as diagnostic or prognostic indicators. Our purpose was to compare the prevalence of an array of tumor-associated antibodies in SLE patients with and without cancer.

Methods: We performed a case-control study nested within a large cohort of SLE patients followed at a clinic in Montreal, Canada. These patients have been consecutively enrolled and followed yearly with sera stored at each visit. Cancer events were ascertained by linkage with the Quebec tumor registry. In this analysis, we performed a cross-sectional analysis of antibodies in 23 SLE patients who developed a new cancer after SLE cohort entry, and compared them to 23 SLE cancer-free controls, frequency matched for sex, race/ethnicity and time since cohort entry. We assessed antibodies that in the literature had previously been suggested as associated with cancer in rheumatic disease and/or general populations. These included, but were not limited to, antibodies against anti-centromere protein (CENP), proliferating cell nuclear antigen (PCNA), Scl-70, and RNA polymerase III.

Results: Of the cancers in the 23 SLE patients, 11 were lymphoma, 8 were breast, two were endometrial, and 1 each were colon and kidney.  The average age at cancer diagnosis was 52.3 years (standard deviation, SD 13.1) and the median SLE duration at cancer diagnosis was 14 years. The vast majority (91.3%) of the SLE patients with cancer were white and all but two of the SLE cancer cases were women.

For all antibodies examined, there were trends for higher levels in SLE cancer cases as a group, versus cancer-free SLE controls. Certain antibodies were found more often in specific cancer types, such as anti-RNA Pol III antibodies in breast cancer, and anti-CENPF1, anti-CENPF-4, and anti-centromere antibodies in lymphoma.   

TABLE AND FIGURE SHOW MEDIAN LEVELS OF ANTIBODIES IN EACH GROUP

 

CENPF1 (n=18)

CENPF4 (n=19)

PCNA (n=21)

RNPC3

(n=20)

Scl-70

Centromere

Th/To-Rpp38

RNA Pol III

Th/To-Rpp25

PM/Scl

BIC-D2

breast

56.5

111.5

33.5

87.5

69

41.5

50.25

170.5

25

84.25

30

lymphoma

63

145

39

46

85

85

59

132.5

21

77

26

all

63

117

39

71

70

45

53.5

138

25

82

27

controls

54

104

28

63

41

29

29

84

20

76

22

Conclusion : In the SLE patients with cancer, the levels of certain tumor-related antibodies tended to be higher than the levels in SLE patients who were cancer-free. This may suggest potential roles for these as cancer markers, but further research is needed.


Disclosure: S. Bernatsky, None; A. E. Clarke, UCB, 2; J. Rauch, None; C. Pineau, None; E. Vinet, None; M. J. Fritzler, Inova Diagnostics, Inc., 5.

To cite this abstract in AMA style:

Bernatsky S, Clarke AE, Rauch J, Pineau C, Vinet E, Fritzler MJ. Tumor-Related Autoantibodies and Cancers in SLE: A Case-Control Study from a Single Centre [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/tumor-related-autoantibodies-and-cancers-in-sle-a-case-control-study-from-a-single-centre/. Accessed .
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