Pharmacovigilance pregnancy data in a large population of patients with chronic inflammatory disease exposed to certolizumab pegol

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Pharmacovigilance pregnancy data in a large population of patients with chronic inflammatory disease exposed to certolizumab pegol. / Clowse, Megan; Fischer-Betz, Rebecca; Nelson-Piercy, Catherine; Scheuerle, Angela E; Stephan, Brigitte; Dubinsky, Marla; Kumke, Thomas; Kasliwal, Rachna; Lauwerys, Bernard; Förger, Frauke.

In: THER ADV MUSCULOSKEL, Vol. 14, 1759720X221087650, 2022.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Clowse, M, Fischer-Betz, R, Nelson-Piercy, C, Scheuerle, AE, Stephan, B, Dubinsky, M, Kumke, T, Kasliwal, R, Lauwerys, B & Förger, F 2022, 'Pharmacovigilance pregnancy data in a large population of patients with chronic inflammatory disease exposed to certolizumab pegol', THER ADV MUSCULOSKEL, vol. 14, 1759720X221087650. https://doi.org/10.1177/1759720X221087650

APA

Clowse, M., Fischer-Betz, R., Nelson-Piercy, C., Scheuerle, A. E., Stephan, B., Dubinsky, M., Kumke, T., Kasliwal, R., Lauwerys, B., & Förger, F. (2022). Pharmacovigilance pregnancy data in a large population of patients with chronic inflammatory disease exposed to certolizumab pegol. THER ADV MUSCULOSKEL, 14, [1759720X221087650]. https://doi.org/10.1177/1759720X221087650

Vancouver

Bibtex

@article{ae7a0381be944dc69b25bfbd318d358d,
title = "Pharmacovigilance pregnancy data in a large population of patients with chronic inflammatory disease exposed to certolizumab pegol",
abstract = "INTRODUCTION: Chronic inflammatory diseases (CIDs), including rheumatic diseases and other inflammatory conditions, often affect women of reproductive age. Tumor necrosis factor inhibitors (TNFi) are widely used to treat CID, but there is limited information on outcomes of TNFi-exposed pregnancies. We evaluated pregnancy outcomes from 1392 prospectively reported pregnancies exposed to certolizumab pegol (CZP), a PEGylated, Fc-free TNFi with no to minimal placental transfer.METHODS: CZP-exposed pregnancies in patients with CID from the UCB Pharmacovigilance global safety database were reviewed from the start of CZP clinical development (July 2001) to 1 November 2020. To limit bias, the analysis focused on prospectively reported cases with known pregnancy outcomes.RESULTS: In total, 1392 prospective pregnancies with maternal CZP exposure and known pregnancy outcomes (n = 1425) were reported; 1021 had at least first-trimester CZP exposure. Live birth was reported in 1259/1425 (88.4%) of all prospective outcomes. There were 150/1425 (10.5%) pregnancy losses before 20 weeks (miscarriage/induced abortion), 11/1425 (0.8%) stillbirths, and 5/1392 (0.4%) ectopic pregnancies. Congenital malformations were present in 30/1259 (2.4%) live-born infants, of which 26 (2.1%) were considered major according to the Metropolitan Atlanta Congenital Defects Program criteria. There was no pattern of congenital malformations.DISCUSSION AND CONCLUSION: No signal for adverse pregnancy outcomes or congenital malformations was observed in CZP-exposed pregnancies. Although the limitations of data collected through this methodology (including underreporting, missing information, and absence of a comparator group) should be considered, these data provide reassurance for women with CID who require CZP treatment during pregnancy, and their treating physicians.",
author = "Megan Clowse and Rebecca Fischer-Betz and Catherine Nelson-Piercy and Scheuerle, {Angela E} and Brigitte Stephan and Marla Dubinsky and Thomas Kumke and Rachna Kasliwal and Bernard Lauwerys and Frauke F{\"o}rger",
note = "{\textcopyright} The Author(s), 2022.",
year = "2022",
doi = "10.1177/1759720X221087650",
language = "English",
volume = "14",
journal = "THER ADV MUSCULOSKEL",
issn = "1759-720X",
publisher = "SAGE Publications",

}

RIS

TY - JOUR

T1 - Pharmacovigilance pregnancy data in a large population of patients with chronic inflammatory disease exposed to certolizumab pegol

AU - Clowse, Megan

AU - Fischer-Betz, Rebecca

AU - Nelson-Piercy, Catherine

AU - Scheuerle, Angela E

AU - Stephan, Brigitte

AU - Dubinsky, Marla

AU - Kumke, Thomas

AU - Kasliwal, Rachna

AU - Lauwerys, Bernard

AU - Förger, Frauke

N1 - © The Author(s), 2022.

PY - 2022

Y1 - 2022

N2 - INTRODUCTION: Chronic inflammatory diseases (CIDs), including rheumatic diseases and other inflammatory conditions, often affect women of reproductive age. Tumor necrosis factor inhibitors (TNFi) are widely used to treat CID, but there is limited information on outcomes of TNFi-exposed pregnancies. We evaluated pregnancy outcomes from 1392 prospectively reported pregnancies exposed to certolizumab pegol (CZP), a PEGylated, Fc-free TNFi with no to minimal placental transfer.METHODS: CZP-exposed pregnancies in patients with CID from the UCB Pharmacovigilance global safety database were reviewed from the start of CZP clinical development (July 2001) to 1 November 2020. To limit bias, the analysis focused on prospectively reported cases with known pregnancy outcomes.RESULTS: In total, 1392 prospective pregnancies with maternal CZP exposure and known pregnancy outcomes (n = 1425) were reported; 1021 had at least first-trimester CZP exposure. Live birth was reported in 1259/1425 (88.4%) of all prospective outcomes. There were 150/1425 (10.5%) pregnancy losses before 20 weeks (miscarriage/induced abortion), 11/1425 (0.8%) stillbirths, and 5/1392 (0.4%) ectopic pregnancies. Congenital malformations were present in 30/1259 (2.4%) live-born infants, of which 26 (2.1%) were considered major according to the Metropolitan Atlanta Congenital Defects Program criteria. There was no pattern of congenital malformations.DISCUSSION AND CONCLUSION: No signal for adverse pregnancy outcomes or congenital malformations was observed in CZP-exposed pregnancies. Although the limitations of data collected through this methodology (including underreporting, missing information, and absence of a comparator group) should be considered, these data provide reassurance for women with CID who require CZP treatment during pregnancy, and their treating physicians.

AB - INTRODUCTION: Chronic inflammatory diseases (CIDs), including rheumatic diseases and other inflammatory conditions, often affect women of reproductive age. Tumor necrosis factor inhibitors (TNFi) are widely used to treat CID, but there is limited information on outcomes of TNFi-exposed pregnancies. We evaluated pregnancy outcomes from 1392 prospectively reported pregnancies exposed to certolizumab pegol (CZP), a PEGylated, Fc-free TNFi with no to minimal placental transfer.METHODS: CZP-exposed pregnancies in patients with CID from the UCB Pharmacovigilance global safety database were reviewed from the start of CZP clinical development (July 2001) to 1 November 2020. To limit bias, the analysis focused on prospectively reported cases with known pregnancy outcomes.RESULTS: In total, 1392 prospective pregnancies with maternal CZP exposure and known pregnancy outcomes (n = 1425) were reported; 1021 had at least first-trimester CZP exposure. Live birth was reported in 1259/1425 (88.4%) of all prospective outcomes. There were 150/1425 (10.5%) pregnancy losses before 20 weeks (miscarriage/induced abortion), 11/1425 (0.8%) stillbirths, and 5/1392 (0.4%) ectopic pregnancies. Congenital malformations were present in 30/1259 (2.4%) live-born infants, of which 26 (2.1%) were considered major according to the Metropolitan Atlanta Congenital Defects Program criteria. There was no pattern of congenital malformations.DISCUSSION AND CONCLUSION: No signal for adverse pregnancy outcomes or congenital malformations was observed in CZP-exposed pregnancies. Although the limitations of data collected through this methodology (including underreporting, missing information, and absence of a comparator group) should be considered, these data provide reassurance for women with CID who require CZP treatment during pregnancy, and their treating physicians.

U2 - 10.1177/1759720X221087650

DO - 10.1177/1759720X221087650

M3 - SCORING: Journal article

C2 - 35464812

VL - 14

JO - THER ADV MUSCULOSKEL

JF - THER ADV MUSCULOSKEL

SN - 1759-720X

M1 - 1759720X221087650

ER -