Immunoglobulin Depletion and Recovery Following Blinatumomab in Infants With KMT2A‐Rearranged ALL

Adding blinatumomab to standard chemotherapy for infants with KMT2A-rearranged acute B-cell lymphoblastic leukemia (KMT2A-r B-ALL) improves outcomes. Although blinatumomab impairs immunoglobulin G (lgG) production, increasing infection susceptibility, IgG recovery remains poorly understood. Thirty infants received Interfant-06 protocol chemotherapy with one course of blinatumomab added post-induction. We screened 169 IgG levels post-blinatumomab and IVIg supplementation timepoints. An increase in IgG was subsequently noted until maintenance, where practically all available values returned to normal (>4 g/L). Blinatumomab leads to an IgG reduction, with near-complete recovery occurring before end of treatment. Future trials should monitor immunoglobulin recovery post-blinatumomab to guide infection-preventing strategies. Trial Registration: EudraCT no: 2016-004674-17.

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Publication Details

Journal
Pediatric Blood & Cancer
Published
2026-07-24
DOI
https://doi.org/10.1002/1545-5017.70547
Primary Topic
Acute Lymphoblastic Leukemia research
Type
article
Field-Weighted Citation Impact
0.00

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article

Immunoglobulin Depletion and Recovery Following Blinatumomab in Infants With KMT2A‐Rearranged ALL

Rishi S. Kotecha, Peggy E. Scholte-van Houtem, Inge M. van der Sluis, Alina Ferster et al.
Pediatric Blood & Cancer
Acute Lymphoblastic Leukemia research
article

Immunoglobulin Depletion and Recovery Following Blinatumomab in Infants With KMT2A‐Rearranged ALL

Rishi S. Kotecha, Peggy E. Scholte-van Houtem, Inge M. van der Sluis, Alina Ferster, Franco Locatelli, Jan Starý, Miguel Vieira Martins, Karsten Nysom, Paola De Lorenzo, M Schrappe, Maria G. Valsecchi, A Attarbaschi, Gabriele Escherich, Rob Pieters, Benoit Brethon
article en

Abstract

Adding blinatumomab to standard chemotherapy for infants with KMT2A-rearranged acute B-cell lymphoblastic leukemia (KMT2A-r B-ALL) improves outcomes. Although blinatumomab impairs immunoglobulin G (lgG) production, increasing infection susceptibility, IgG recovery remains poorly understood. Thirty infants received Interfant-06 protocol chemotherapy with one course of blinatumomab added post-induction. We screened 169 IgG levels post-blinatumomab and IVIg supplementation timepoints. An increase in IgG was subsequently noted until maintenance, where practically all available values returned to normal (>4 g/L). Blinatumomab leads to an IgG reduction, with near-complete recovery occurring before end of treatment. Future trials should monitor immunoglobulin recovery post-blinatumomab to guide infection-preventing strategies. Trial Registration: EudraCT no: 2016-004674-17.

Pediatric Blood & Cancer
Universität Hamburg (DE), Curtin University (AU), Charles University (CZ), Princess Margaret Hospital for Children (AU), Copenhagen University Hospital (DK), Rigshospitalet (DK), Assistance Publique – Hôpitaux de Paris (FR), University Hospital in Motol (CZ), Childhood Leukemia Foundation (US), Queen Fabiola Children's University Hospital (BE), University Medical Center Hamburg-Eppendorf (DE), Azienda Ospedaliera San Gerardo (IT), University Hospital Schleswig-Holstein (DE), Bambino Gesù Children's Hospital (IT), St Anna Children's Hospital (AT), Hôpital Robert-Debré (FR), Princess Máxima Center (NL), ANZCHOG (AU), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Leukemia and Lymphoma Society (US), University of Milano-Bicocca (IT), University of Lübeck (DE)
Amgen
Good health and well-being
Openalex Percentile: Top 7%
Acute Lymphoblastic Leukemia research
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