Pediatric patients with acute lymphoblastic leukemia treated with blinatumomab in a real-world setting: Results from the NEUF study.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
04 2022
Historique:
revised: 19 12 2021
received: 11 08 2021
accepted: 20 12 2021
pubmed: 20 1 2022
medline: 6 5 2022
entrez: 19 1 2022
Statut: ppublish

Résumé

Prior to regulatory approval of blinatumomab in pediatric patients with relapsed/refractory Philadelphia chromosome-negative B-cell precursor acute lymphoblastic leukemia (R/R Ph- BCP-ALL), blinatumomab was made available via an expanded access program (EAP). This retrospective observational study included patients receiving blinatumomab in the EAP between January 1, 2014 and June 30, 2017 who were followed until death, entry into a clinical trial, end of follow-up, or end of the study period (December 31, 2017), whichever occurred first. Among 113 children enrolled, 72 were diagnosed with R/R Ph- BCP-ALL and 41 were minimal residual disease positive (MRD+, either Ph- or Ph+). In the R/R group, 38 (53%) patients achieved hematological response within two cycles. Of these, 19 (50%) proceeded to hematopoietic stem cell transplantation (HSCT) without bridging myelosuppressive therapy. Of 36 patients in the R/R group evaluable for MRD, 30 (83%) had an MRD response. In the R/R group, median relapse-free survival was 5.4 months and median overall survival (OS) was 8.2 months. Of 36 patients in the MRD+ group who were evaluable for MRD after two cycles, 27 (75%) had an MRD response. Overall, 24 (59%) of the MRD+ patients proceeded to HSCT without other bridging therapy. Median disease-free survival was 13.6 months; median OS was not reached. In this real-world pediatric cohort, blinatumomab was effective within two cycles. Over half of patients with R/R Ph- BCP-ALL achieved hematological response and most achieved MRD response in the MRD+ group, confirming the efficacy of blinatumomab in pediatric trials.

Sections du résumé

BACKGROUND
Prior to regulatory approval of blinatumomab in pediatric patients with relapsed/refractory Philadelphia chromosome-negative B-cell precursor acute lymphoblastic leukemia (R/R Ph- BCP-ALL), blinatumomab was made available via an expanded access program (EAP).
PROCEDURE
This retrospective observational study included patients receiving blinatumomab in the EAP between January 1, 2014 and June 30, 2017 who were followed until death, entry into a clinical trial, end of follow-up, or end of the study period (December 31, 2017), whichever occurred first.
RESULTS
Among 113 children enrolled, 72 were diagnosed with R/R Ph- BCP-ALL and 41 were minimal residual disease positive (MRD+, either Ph- or Ph+). In the R/R group, 38 (53%) patients achieved hematological response within two cycles. Of these, 19 (50%) proceeded to hematopoietic stem cell transplantation (HSCT) without bridging myelosuppressive therapy. Of 36 patients in the R/R group evaluable for MRD, 30 (83%) had an MRD response. In the R/R group, median relapse-free survival was 5.4 months and median overall survival (OS) was 8.2 months. Of 36 patients in the MRD+ group who were evaluable for MRD after two cycles, 27 (75%) had an MRD response. Overall, 24 (59%) of the MRD+ patients proceeded to HSCT without other bridging therapy. Median disease-free survival was 13.6 months; median OS was not reached.
CONCLUSIONS
In this real-world pediatric cohort, blinatumomab was effective within two cycles. Over half of patients with R/R Ph- BCP-ALL achieved hematological response and most achieved MRD response in the MRD+ group, confirming the efficacy of blinatumomab in pediatric trials.

Identifiants

pubmed: 35044079
doi: 10.1002/pbc.29562
doi:

Substances chimiques

Antibodies, Bispecific 0
blinatumomab 4FR53SIF3A

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e29562

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2022 The Authors. Pediatric Blood & Cancer published by Wiley Periodicals LLC.

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Auteurs

Franco Locatelli (F)

Department of Pediatric Hematology and Oncology, IRCCS, Ospedale Pediatrico Bambino Gesù, Rome, Italy.
Sapienza, University of Rome, Rome, Italy.

Alexey Maschan (A)

Oncology and Immunology, Dmitri Rogachev National Research Centre for Pediatric Hematology, Moscow, Russian Federation.

Nicolas Boissel (N)

Division of Hematology, EA3518 Saint-Louis Institute for Research, Saint-Louis Hospital, Paris, France.

Luisa Strocchio (L)

Department of Pediatric Hematology and Oncology, IRCCS, Ospedale Pediatrico Bambino Gesù, Rome, Italy.

Naufil Alam (N)

Center for Observational Research, Amgen Ltd, Uxbridge, UK.

Isabella Pezzani (I)

Amgen (Europe) GmbH, Rotkreuz, Switzerland.

Alessandra Brescianini (A)

Amgen (Europe) GmbH, Rotkreuz, Switzerland.

Georg Kreuzbauer (G)

Amgen (Europe) GmbH, Rotkreuz, Switzerland.

Andre Baruchel (A)

Hôpital Universitaire Robert Debré, Paris, France.
Université de Paris, Paris, France.

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