Anti-CD20 monoclonal antibody therapy in postpartum women with neurological conditions.


Journal

Annals of clinical and translational neurology
ISSN: 2328-9503
Titre abrégé: Ann Clin Transl Neurol
Pays: United States
ID NLM: 101623278

Informations de publication

Date de publication:
11 2023
Historique:
revised: 08 08 2023
received: 17 07 2023
accepted: 09 08 2023
medline: 16 11 2023
pubmed: 7 9 2023
entrez: 7 9 2023
Statut: ppublish

Résumé

Postpartum, patients with multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD) have increased risk for disease activity. Anti-CD20 IgG1 monoclonal antibodies (mAb) are increasingly used as disease-modifying therapies (DMTs). Patients may wish to both breastfeed and resume DMT postpartum. This study aimed to determine the transfer of anti-CD20 IgG1 mAbs, ocrelizumab, and rituximab (OCR/RTX), into mature breastmilk and describe maternal and infant outcomes. Fifty-seven cis-women receiving OCR/RTX after 59 pregnancies and their infants were enrolled and followed up to 12M postpartum or 90 days post-infusion. Breastmilk was collected pre-infusion and serially up to 90 days and assayed for mAb concentration. Medical records and patients' questionnaire responses were obtained to assess neurologic, breastfeeding, and infant development outcomes. The median average concentration of mAb in breastmilk was low (OCR: 0.08 μg/mL, range 0.05-0.4; RTX: 0.03 μg/mL, range 0.005-0.3). Concentration peaked 1-7 days post-infusion in most (77%) and was nearly undetectable after 90 days. Median average relative infant dose was <1% (OCR: 0.1%, range 0.07-0.7; RTX: 0.04%, range 0.005-0.3). Forty-three participants continued to breastfeed post-infusion. At 8-12 months, the proportion of infants' growth between the 3rd and 97th World Health Organization percentiles did not differ for breastfed (36/40) and non-breastfed (14/16, p > 0.05) infants; neither did the proportion with normal development (breastfed: 37/41, non-breastfed: 11/13; p > 0.05). After postpartum infusion, two mothers experienced a clinical relapse. These confirm minimal transfer of mAb into breastmilk. Anti-CD20 mAb therapy stabilizes MS activity before conception to the postpartum period, and postpartum treatments appears to be safe and well-tolerated for both mother and infant.

Identifiants

pubmed: 37675826
doi: 10.1002/acn3.51893
pmc: PMC10647007
doi:

Substances chimiques

Antibodies, Monoclonal 0
Rituximab 4F4X42SYQ6
Antineoplastic Agents 0
Immunoglobulin G 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2053-2064

Informations de copyright

© 2023 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

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Auteurs

Annika Anderson (A)

UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.

William Rowles (W)

UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.

Shane Poole (S)

UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.

Ayushi Balan (A)

UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.

Carolyn Bevan (C)

Department of Neurology, Northwestern University, Chicago, Illinois, USA.

Rachel Brandstadter (R)

Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Andrea I Ciplea (AI)

Department of Neurology, Ruhr University Bochum, Bochum, Germany.

Joanna Cooper (J)

Sutter East Bay Medical Group, Lafayette, California, USA.

Michelle Fabian (M)

Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Thomas W Hale (TW)

Texas Tech University Health Sciences Center, Amarillo, Texas, USA.

Dina Jacobs (D)

Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Mihir Kakara (M)

Department of Neurology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Kristen M Krysko (KM)

Division of Neurology, Department of Medicine, St Michael's Hospital, University of Toronto, Toronto, ON, Canada.
Li Ka Shing Knowledge Institute, University of Toronto, Toronto, ON, Canada.

Erin E Longbrake (EE)

Department of Neurology, Yale University, New Haven, Connecticut, USA.

Jacqueline Marcus (J)

Department of Neurology, Kaiser Permanente San Francisco, San Francisco, California, USA.

Pavle Repovic (P)

Department of Neurology, Swedish Medical Center, Seattle, Washington, USA.

Claire S Riley (CS)

Department of Neurology, Columbia University Irving Medical Center, New York, New York, USA.

Andrew R Romeo (AR)

Department of Neurology, University of Michigan, Ann Arbor, Michigan, USA.

Alice Rutatangwa (A)

UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.

Timothy West (T)

Rocky Mountain MS Center, Salt Lake City, Utah, USA.

Kerstin Hellwig (K)

Department of Neurology, Ruhr University Bochum, Bochum, Germany.

Sara C LaHue (SC)

UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.
Buck Institute for Research on Aging, Novato, California, USA.

Riley Bove (R)

UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.

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Classifications MeSH