Predicting factors of malignancy in dermatomyositis and polymyositis: a case-control study

被引:147
|
作者
Chen, YJ
Wu, CY
Shen, JL
机构
[1] Taichung Vet Gen Hosp, Dept Dermatol, Taichung, Taiwan
[2] Taichung Vet Gen Hosp, Dept Internal Med, Taichung, Taiwan
[3] China Med Coll, Taichung, Taiwan
关键词
dermatomyositis; malignancy; polymyositis; predictive factor;
D O I
10.1046/j.1365-2133.2001.04140.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background An association between dermatomyositis (DM)/polymyositis (PM) and malignancies has been widely reported in the literature. The validity of extensive evaluation for malignancies in those patients has also been questioned for decades. Only limited papers regarding the signs of malignancy and the prognostic factors in DM/PM have been reported. Objectives To define the potential risk factors of concomitant neoplastic diseases in patients diagnosed as having DM/PM. Methods From 1 April 1983 to 30 June 1999, 147 patients were diagnosed as having probable or definite DM/PM at the Veterans General Hospital, Taichung, Taiwan. We excluded four patients who had preceding neoplastic diseases diagnosed before DM/PM, then retrospectively reviewed the data of the remaining 143 patients and subgrouped the cases as four main types: primary idiopathic DM, primary idiopathic PM, juvenile DM/PM and amyopathic DM (ADM). We next performed univariate analysis using logistic regression to evaluate the possible predictive factors for malignancies, such as mean age at onset, gender, manifestations at onset, association with other connective tissue diseases, initial skin presentations, complications and laboratory data. Then we chose the significant factors for multivariate analysis by logistic regression, to determine the independent risk factors of malignancies in DM/PM patients. Results Among the 143 patients, DM was the most common type (64%), followed by ADM (14%), juvenile DM/PM (13%) and PM (10%). The mean age at onset overall was 42.4 years. Other connective tissue diseases were present in 22% of all patients, especially PM (50%) and juvenile DM/PM patients (28%). Internal malignancies were present in 13% of patients, and most were associated with DM, Nasopharyngeal carcinomas (NPCs) were the most common tumours. Patients with primary idiopathic DM, with an older age at onset, higher serum creatine phosphokinase levels and male gender, had more chance of developing concomitant malignancies. Those associated with complications, especially interstitial lung diseases, had a lower risk of associated neoplasia. In multivariate analysis, an older age at onset (odds ratio 9.10) and male gender (odds ratio 4.06) were associated with greater risk of developing malignancies. Conclusions The two independent predictive factors for malignancy (P < 0.05) in patients with DM/PM were an older age at onset (> 45 years) and male gender. The primary idiopathic DM group was shown to have higher risk of developing internal malignancies, especially NPC. However, this was not identified as an independent predictive factor for concomitant neoplastic diseases in multivariate analysis. In addition, patients who had the complication of interstitial lung disease had a significantly lower frequency of malignancies (P < 0.001).
引用
收藏
页码:825 / 831
页数:7
相关论文
共 50 条
  • [1] Features of polymyositis and dermatomyositis in the elderly:: A case-control study
    Pautas, E
    Chérin, P
    Piette, JC
    Pelletier, S
    Wechsler, B
    Cabane, J
    Herson, S
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2000, 18 (02) : 241 - 244
  • [2] Hospitalization mortality and associated risk factors in patients with polymyositis and dermatomyositis: A retrospective case-control study
    Wu, Chanyuan
    Wang, Qian
    He, Linrong
    Yang, Enhao
    Zeng, Xiaofeng
    PLOS ONE, 2018, 13 (02):
  • [3] HOSPITALISATION MORTALITY AND ASSOCIATED RISK FACTORS IN PATIENTS WITH POLYMYOSITIS AND DERMATOMYOSITIS: A RETROSPECTIVE CASE-CONTROL STUDY
    Wu, C.
    Wang, Q.
    He, L.
    Yang, E.
    Zeng, X.
    ANNALS OF THE RHEUMATIC DISEASES, 2018, 77 : 749 - 749
  • [4] MALIGNANCY IN POLYMYOSITIS/DERMATOMYOSITIS
    CALLEN, JP
    CLINICS IN DERMATOLOGY, 1988, 6 (02) : 55 - 63
  • [5] POLYMYOSITIS/DERMATOMYOSITIS AND MALIGNANCY
    LAKHANPAL, S
    BUNCH, TW
    ILSTRUP, DM
    MELTON, LJ
    CLINICAL RESEARCH, 1985, 33 (04): : A920 - A920
  • [6] Polymyositis/dermatomyositis and Malignancy Risk: A Metaanalysis Study
    Yang, Zaixing
    Lin, Feng
    Qin, Baodong
    Liang, Yan
    Zhong, Renqian
    JOURNAL OF RHEUMATOLOGY, 2015, 42 (02) : 282 - 291
  • [7] Subclinical Cardiac Dysfunction in Polymyositis and Dermatomyositis: A Speckle-tracking Case-control Study
    Guerra, Federico
    Gelardi, Chiara
    Capucci, Alessandro
    Gabrielli, Armando
    Danieli, Maria Giovanna
    JOURNAL OF RHEUMATOLOGY, 2017, 44 (06) : 815 - 821
  • [8] THE RELATIONSHIP OF DERMATOMYOSITIS POLYMYOSITIS TO MALIGNANCY
    CALLEN, JP
    JOURNAL OF RHEUMATOLOGY, 1991, 18 (11) : 1645 - 1646
  • [9] CHILDHOOD POLYMYOSITIS - CASE-CONTROL STUDY
    KOCH, MJ
    BRODY, JA
    GILLESPIE, MM
    AMERICAN JOURNAL OF EPIDEMIOLOGY, 1976, 104 (06) : 627 - 631
  • [10] Predicting factors of interstitial lung disease in dermatomyositis and polymyositis
    Chen, Yi-Ju
    Wu, Chun-Ying
    Shen, Jui-Lung
    ACTA DERMATO-VENEREOLOGICA, 2007, 87 (01) : 33 - 38