Blinatumomab consolidation and maintenance therapy in adults with relapsed/refractory B-precursor acute lymphoblastic leukemia.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
14 04 2020
Historique:
received: 04 09 2019
accepted: 11 03 2020
entrez: 15 4 2020
pubmed: 15 4 2020
medline: 15 5 2021
Statut: ppublish

Résumé

In a phase 3 clinical study of heavily pretreated adults with relapsed/refractory (R/R) acute lymphoblastic leukemia (ALL), overall survival (OS) following blinatumomab, a BiTE (bispecific T-cell engager) immunooncology therapy, was significantly improved vs chemotherapy following induction (cycles 1 to 2). Here we report the efficacy and safety of those who received additional cycles of blinatumomab. Blinatumomab was administered as a continuous IV infusion for 4 weeks in a 6-week cycle. Patients who achieved a bone marrow response (≤5% blasts) or complete remission (full, partial, or incomplete hematological recovery) during induction could receive additional cycles of blinatumomab. OS and relapse-free survival (RFS) for consolidation (cycles 3 to 5) vs no consolidation, and maintenance (cycles ≥6) vs no maintenance were analyzed using Simon-Makuch and Mantel-Byar odds ratios. Of 267 patients who received blinatumomab induction, 86 (32%) entered consolidation and 36 (13%) entered maintenance. Evidence of longer OS was demonstrated among the maintenance group compared with no-maintenance (median OS [95% confidence interval, CI]: not reached for maintenance vs 15.5 months for no maintenance). Median RFS (months; 95% CI) was numerically longer among maintenance group (14.5; 7.1 to 21.9) compared with no-maintenance (9.8; 8.5 to 11.1). A lower incidence of adverse events was seen during maintenance (72.2%) compared with induction (97.2%) and consolidation (86.1%). Adults with R/R ALL who achieved remission following blinatumomab induction had longer survival on continuation therapy than those who discontinued blinatumomab early, supporting the use of blinatumomab as long-term therapy. No new safety signals were reported. This trial was registered at www.clinicaltrials.gov as #NCT02013167.

Identifiants

pubmed: 32289160
pii: S2473-9529(20)31413-0
doi: 10.1182/bloodadvances.2019000874
pmc: PMC7160264
doi:

Substances chimiques

Antibodies, Bispecific 0
Antineoplastic Agents 0
blinatumomab 4FR53SIF3A

Banques de données

ClinicalTrials.gov
['NCT02013167']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1518-1525

Informations de copyright

© 2020 by The American Society of Hematology.

Références

N Engl J Med. 2017 Mar 2;376(9):836-847
pubmed: 28249141
Drug Saf. 2019 May;42(5):587-601
pubmed: 30565020
Haematologica. 2016 Dec;101(12):1524-1533
pubmed: 27587380
Curr Hematol Malig Rep. 2018 Aug;13(4):289-299
pubmed: 30078158
Stat Med. 1984 Jan-Mar;3(1):35-44
pubmed: 6729287
Lancet Oncol. 2015 Jan;16(1):57-66
pubmed: 25524800
Patient Relat Outcome Meas. 2018 Oct 02;9:329-337
pubmed: 30323696
Blood Adv. 2018 Jul 10;2(13):1522-1531
pubmed: 29954814

Auteurs

Alessandro Rambaldi (A)

Università Statale di Milano, Milan and Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.

Francoise Huguet (F)

Institut Universitaire du Cancer, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.

Pavel Zak (P)

Fakultni Nemocnice Hradec Králové, Hradec Králové, Czech Republic.

Paul Cannell (P)

Fiona Stanley Hospital, Perth, Australia.

Qui Tran (Q)

Amgen Inc, Thousand Oaks, CA; and.

Janet Franklin (J)

Amgen Inc, Thousand Oaks, CA; and.

Max S Topp (MS)

Medizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, Würzburg, Germany.

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Classifications MeSH