Background: Eculizumab, a humanized monoclonal antibody against complement protein C5 that inhibits terminal complement activation, has been shown to prevent complications of paroxysmal nocturnal hemoglobinuria (PNH) and improve quality of life and overall survival, but data on the use of eculizumab in women during pregnancy are scarce.
Methods: We designed a questionnaire to solicit data on pregnancies in women with PNH and sent it to the members of the International PNH Interest Group and to the physicians participating in the International PNH Registry. We assessed the safety and efficacy of eculizumab in pregnant patients with PNH by examining the birth and developmental records of the children born and adverse events in the mothers.
Results: Of the 94 questionnaires that were sent out, 75 were returned, representing a response rate of 80%. Data on 75 pregnancies in 61 women with PNH were evaluated. There were no maternal deaths and three fetal deaths (4%). Six miscarriages (8%) occurred during the first trimester. Requirements for transfusion of red cells increased during pregnancy, from a mean of 0.14 units per month in the 6 months before pregnancy to 0.92 units per month during pregnancy. Platelet transfusions were given in 16 pregnancies. In 54% of pregnancies that progressed past the first trimester, the dose or the frequency of use of eculizumab had to be increased. Low-molecular-weight heparin was used in 88% of the pregnancies. Ten hemorrhagic events and 2 thrombotic events were documented; both thrombotic events occurred during the postpartum period. A total of 22 births (29%) were premature. Twenty cord-blood samples were examined for the presence of eculizumab; the drug was detected in 7 of the samples. A total of 25 babies were breast-fed, and in 10 of these cases, breast milk was examined for the presence of eculizumab; the drug was not detected in any of the 10 breast-milk samples.
Conclusions: Eculizumab provided benefit for women with PNH during pregnancy, as evidenced by a high rate of fetal survival and a low rate of maternal complications. (ClinicalTrials.gov number, NCT01374360.).
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http://dx.doi.org/10.1056/NEJMoa1502950 | DOI Listing |
Ann Hematol
November 2024
Department of Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Vienna, Austria.
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare hematological disorder characterized by the absence of complement regulatory proteins on the surface of erythrocytes, leading to intravascular hemolysis and thrombosis. Managing PNH during pregnancy poses significant challenges due to increased risks of morbidity and mortality. This case report describes the detailed obstetric course of a 44-year-old woman with PNH and additional hereditary protein C deficiency who had previously experienced multiple thrombotic events and adverse pregnancy outcomes (two early miscarriages and one stillbirth at 25 weeks gestation [WG]), treated with eculizumab (terminal C5 inhibitor) and optimal anticoagulation management.
View Article and Find Full Text PDFZhonghua Xue Ye Xue Za Zhi
September 2024
Huashan Hospital Affiliated to Fudan University, Shanghai 200040, China.
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare disease, and a standardized treatment and follow-up management strategy for pregnant women with this disease are crucial for ensuring the safety of both the mothers and their newborns. This study includes a case of pregnant women with PNH. In accordance with the guidelines, the patient was successfully delivered after treatment with eculizumab.
View Article and Find Full Text PDFEur Heart J Case Rep
October 2024
Department of Cardiovascular Medicine, Saiseikai Shiga Hospital, 2-4-1 Ohashi, Ritto, Shiga 520-3046, Japan.
Radiol Case Rep
November 2024
Department of Medical Genetics, Hospital de Santa Maria, Unidade Local de Saúde Santa Maria, Av. Professor Egas Moniz, Lisboa 1649-035, Portugal.
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