TY - JOUR
T1 - Pregnancy outcomes after exposure to tocilizumab
T2 - A retrospective analysis of 61 patients in Japan
AU - Nakajima, Ken
AU - Watanabe, Omi
AU - Mochizuki, Mayumi
AU - Nakasone, Ayako
AU - Ishizuka, Nobuhiko
AU - Murashima, Atsuko
N1 - Publisher Copyright:
© 2016 Japan College of Rheumatology.
PY - 2016/9/2
Y1 - 2016/9/2
N2 - Objectives: To assess the effects of tocilizumab on pregnancy outcomes in Japanese patients with rheumatic disease. Methods: Data from Chugai’s tocilizumab safety database (April 2005 to October 2014) were retrospectively analyzed to identify pregnancy outcomes in patients exposed to tocilizumab. Results: Data were available for 61 pregnancies exposed to tocilizumab, and outcomes were reported for 50 of those pregnancies. In 36 births, no congenital anomalies were identified; however, six neonatal abnormalities were reported: five cases of low birth weight (<2500 g) and one case of neonatal asphyxia. Of 36 births, tocilizumab was resumed during lactation in two patients, with no subsequent adverse events reported in newborns. The spontaneous abortion rate was 18.0% (9 of 50 pregnancies), which is comparable to the rate in the general population. The five terminated pregnancies included one case of caudal regression syndrome. Conclusions: The present retrospective study of 61 pregnancies exposed to tocilizumab at conception indicated no increased rates of spontaneous abortion or congenital abnormalities in patients with rheumatic disease. However, further study is necessary to confirm the benefit-risk profile of tocilizumab treatment during pregnancy.
AB - Objectives: To assess the effects of tocilizumab on pregnancy outcomes in Japanese patients with rheumatic disease. Methods: Data from Chugai’s tocilizumab safety database (April 2005 to October 2014) were retrospectively analyzed to identify pregnancy outcomes in patients exposed to tocilizumab. Results: Data were available for 61 pregnancies exposed to tocilizumab, and outcomes were reported for 50 of those pregnancies. In 36 births, no congenital anomalies were identified; however, six neonatal abnormalities were reported: five cases of low birth weight (<2500 g) and one case of neonatal asphyxia. Of 36 births, tocilizumab was resumed during lactation in two patients, with no subsequent adverse events reported in newborns. The spontaneous abortion rate was 18.0% (9 of 50 pregnancies), which is comparable to the rate in the general population. The five terminated pregnancies included one case of caudal regression syndrome. Conclusions: The present retrospective study of 61 pregnancies exposed to tocilizumab at conception indicated no increased rates of spontaneous abortion or congenital abnormalities in patients with rheumatic disease. However, further study is necessary to confirm the benefit-risk profile of tocilizumab treatment during pregnancy.
KW - Abortions
KW - Pregnancy outcome
KW - Rheumatoid arthritis
KW - Tocilizumab
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U2 - 10.3109/14397595.2016.1147405
DO - 10.3109/14397595.2016.1147405
M3 - Article
C2 - 26873562
AN - SCOPUS:84961204382
SN - 1439-7595
VL - 26
SP - 667
EP - 671
JO - Japanese Journal of Rheumatology
JF - Japanese Journal of Rheumatology
IS - 5
ER -