Belimumab use during pregnancy: a summary of birth defects and pregnancy loss from belimumab clinical trials, a pregnancy registry and postmarketing reports

被引:17
作者
Petri, Michelle [1 ]
Landy, Helain [2 ,3 ]
Clowse, Megan E. B. [4 ]
Gemzoe, Kim [5 ]
Khamashta, Munther [6 ]
Kurtinecz, Milena [7 ]
Levy, Roger A. [8 ]
Liu, Andrew [9 ]
Marino, Rebecca [10 ]
Meizlik, Paige [11 ]
Pimenta, Jeanne M. [12 ]
Sumner, Kelsey [13 ,14 ]
Tilson, Hugh [14 ]
Connolly, Mary Beth [15 ]
Wurst, Keele [16 ]
Harris, Julia [17 ]
Quasny, Holly [18 ]
Juliao, Patricia [19 ]
Roth, David A. [11 ]
机构
[1] Johns Hopkins Univ, Sch Med, Rheumatol, Baltimore, MD USA
[2] Georgetown Univ, Med Ctr, Maternal & Fetal Med, Northwest Washington, Washington, DC 20007 USA
[3] MedStar Georgetown Univ Hosp, Dept Obstet & Gynecol, Northwest Washington, Washington, DC USA
[4] Duke Univ, Sch Med, Dept Med, Durham, NC 27706 USA
[5] GSK, Value Evidence & Outcomes, Stevenage, Herts, England
[6] GSK, Med Affairs, Dubai, U Arab Emirates
[7] GSK, Biostat, Collegeville, PA USA
[8] GSK, Global Med Affairs, Specialty Care, Collegeville, PA USA
[9] GSK, Global Clin Safety & Pharmacovigilance, Brentford, England
[10] GSK, US Case Management Grp, Res Triangle Pk, NC USA
[11] GSK, Immunoinflammat, Collegeville, PA USA
[12] GSK, Epidemiol, Uxbridge, Middx, England
[13] GSK, Value Evidence Outcomes Epidemiol, Res Triangle Pk, NC USA
[14] Univ N Carolina, Dept Epidemiol, Gillings Sch Global Publ Hlth, Chapel Hill, NC 27515 USA
[15] GSK, Safety & Med Governance, Res Triangle Pk, NC USA
[16] GSK, Epidemiol, Res Triangle Pk, NC USA
[17] GSK, Immunol Biostat, Brentford, England
[18] GSK, Clin Sci, Res Triangle Pk, NC USA
[19] GSK, Vaccines, Collegeville, PA USA
关键词
Biological Therapy; Lupus Erythematosus; Systemic; Autoimmune Diseases; SYSTEMIC-LUPUS-ERYTHEMATOSUS; CONGENITAL HEART-BLOCK; MONOCLONAL-ANTIBODY; ANTIRHEUMATIC DRUGS; PHASE-III; OUTCOMES; POPULATION; MANAGEMENT; SAFETY; MALFORMATIONS;
D O I
10.1136/ard-2022-222505
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective Describe available data on birth defects and pregnancy loss in women with systemic lupus erythematosus (SLE) exposed to belimumab. Methods Data collected from belimumab clinical trials, the Belimumab Pregnancy Registry (BPR), and postmarketing/spontaneous reports up to 8 March 2020 were described. Belimumab exposure timing, concomitant medications and potential confounding factors were summarised descriptively. Results Among 319 pregnancies with known outcomes (excluding elective terminations), 223 ended in live births from which birth defects were identified in 4/72 (5.6%) in belimumab-exposed pregnancies and 0/9 placebo-exposed pregnancies across 18 clinical trials, 10/46 (21.7%) belimumab-exposed pregnancies in the BPR prospective cohort (enrolled prior to pregnancy outcome) and 0/4 belimumab-exposed pregnancies in the BPR retrospective cohort (enrolled after pregnancy outcome), and 1/92 (1.1%) in belimumab-exposed pregnancies from postmarketing/spontaneous reports. There was no consistent pattern of birth defects across datasets. Out of pregnancies with known outcomes (excluding elective terminations), pregnancy loss occurred in 31.8% (35/110) of belimumab-exposed women and 43.8% (7/16) of placebo-exposed women in clinical trials; 4.2% (2/48) of women in the BPR prospective cohort and 50% (4/8) in the BPR retrospective cohort; and 31.4% (43/137) of belimumab-exposed women from postmarketing/spontaneous reports. All belimumab-exposed women in clinical trials and the BPR received concomitant medications and had confounding factors and/or missing data. Conclusions Observations reported here add to limited data published on pregnancy outcomes following belimumab exposure. Low numbers of exposed pregnancies, presence of confounding factors/other biases, and incomplete information preclude informed recommendations regarding risk of birth defects and pregnancy loss with belimumab use.
引用
收藏
页码:217 / 225
页数:9
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