Malignant neoplasms in autoimmune rheumatic diseases - Examination of the risk of developing a malignancy among five different rheumatic diseased in one institution
Ar. Villa et al., Malignant neoplasms in autoimmune rheumatic diseases - Examination of the risk of developing a malignancy among five different rheumatic diseased in one institution, JCR-J CLIN, 6(4), 2000, pp. 176-183
Relationships between autoimmune rheumatic diseases nad malignant neoplasms
have been discussed, but there is no study of the different rheumatic dise
ases examining the risk of developing cancer. Our study has examined probab
ilities for developing malignancy among patients with connective tissue dis
eases seen in single institution. Patients with autoimmune rheumatic diseas
e and malignancy were compared with patients with the same autoimmune rheum
atic diseases without malignancy. All case identified through record-linkag
e from 1964 to 1996 were selected. Four controls per case were randomly sel
ected from a pool of 3228 patients. The rheumatic disease considered were r
heumatoid arthritis (RA), systemic lupus erythematosus (SLE), primary Sjogr
en's syndrome (pSS), dermatomyositis-polymyositis (DM-PM), and systemic scl
erosis (Scl). The statistical analysis was conducted by conditional logisti
c regression, testing rheumatic disease as main effect. We identified 72 ca
ses and 288 controls. Fifty-three of the cases had solid tumors, and 19 had
lymphoproliferative neoplasms. The risk of developing a malignancy was con
siderably higher in DM-PM than in SLE (odds ratio [OR] = 17.5, 95% confiden
ce interval [CI] 4.1-75.7), in pSS than in SLE (OR = 5.7, 95% CI2.2-`5.1),
and in Scl than in SLE (OR = 5.4, 95% CI 1.6-18.0). These risks persisted a
fter controlling for rheumatic disease duration, the time the disease was a
ctive, and anti-rheumatic treatment. RA had an OR of 1.8 (95% CI 0.9-3.4) w
ith respect to SLE.
This is the first study which describes the magnitude of risks among rheuma
tic diseases associated with the probability of developing a malignant neop
lasm whether lymphoproliferative or solid. The risks in this series depend
on the primary rheumatic disease, with DM-PM, pSS, and Scl all having great
er risk than SLE.