Increased incidence of cancer in the follow-up of obstetric antiphospholipid syndrome within the NOH-APS cohort
Jean-Christophe Gris,
Éve Mousty,
Sylvie Bouvier,
Sylvie Ripart,
Éva Cochery-Nouvellon,
Pascale Fabbro-Peray,
Jonathan Broner,
Vincent Letouzey,
Antonia Pérez-Martin
Affiliations
Jean-Christophe Gris
Department of Hematology, University Hospital of Nîmes, Nîmes, France;Faculty of Pharmaceutical and Biological Sciences, University of Montpellier, Montpellier, France;UPRES EA2992 “Caractéristiques Féminines des Dysfonctions des Interfaces Vasculaires”, University of Montpellier, Montpellier, France;I.M. Sechenov First Moscow State Medical University, Moscow, Russian Federation
Éve Mousty
Department of Gynecology and Obstetrics, University Hospital of Nîmes, Nîmes, France
Sylvie Bouvier
Department of Hematology, University Hospital of Nîmes, Nîmes, France;Faculty of Pharmaceutical and Biological Sciences, University of Montpellier, Montpellier, France;UPRES EA2992 “Caractéristiques Féminines des Dysfonctions des Interfaces Vasculaires”, University of Montpellier, Montpellier, France
Sylvie Ripart
Department of Gynecology and Obstetrics, University Hospital of Nîmes, Nîmes, France
Éva Cochery-Nouvellon
Department of Hematology, University Hospital of Nîmes, Nîmes, France;UPRES EA2992 “Caractéristiques Féminines des Dysfonctions des Interfaces Vasculaires”, University of Montpellier, Montpellier, France
Pascale Fabbro-Peray
Department of Biostatistics, Epidemiology, Public Health, Innovation and Methodology, University Hospital of Nîmes, Nîmes, France
Jonathan Broner
Department of Internal Medicine, University Hospital of Nîmes, Nîmes, France
Vincent Letouzey
Department of Gynecology and Obstetrics, University Hospital of Nîmes, Nîmes, France
Antonia Pérez-Martin
UPRES EA2992 “Caractéristiques Féminines des Dysfonctions des Interfaces Vasculaires”, University of Montpellier, Montpellier, France;Department of Vascular Medicine, University Hospital of Nîmes, Nîmes, France
Malignancies can be associated with positive antiphospholipid antibodies but the incidence of cancer among women with the purely obstetric form of antiphospholipid syndrome (APS) is currently unknown. Our aim was to investigate the comparative incidence of cancers in women with a history of obstetric APS within a referral university hospital-based cohort (NOH-APS cohort). We performed a 17-year observational study of 1,592 non-thrombotic women with three consecutive spontaneous abortions before the 10th week of gestation or one fetal death at or beyond the 10th week of gestation. We compared the incidence of cancer diagnosis during follow-up among the cohort of women positive for antiphospholipid antibodies (n=517), the cohort of women carrying the F5 rs6025 or F2 rs1799963 polymorphism (n=279) and a cohort of women with negative thrombophilia screening results (n=796). The annualized rate of cancer was 0.300% (0.20%-0.44%) for women with obstetric APS and their cancer risk was substantially higher than that of women with negative thrombophilia screening [adjusted hazard ratio (aHR) 2.483; 95% confidence interval (CI) 1.27-4.85]. The computed standardized incidence ratio for women with obstetric APS was 2.89; 95% CI: 1.89-4.23. Among antiphospholipid antibodies, lupus anticoagulant was associated with incident cancers (aHR 2.608; 95% CI: 1.091-6.236). Our cohort study shows that the risk of cancer is substantially higher in women with a history of obstetric APS than in the general population, and in women with a similar initial clinical history but negative for antiphospholipid antibodies.