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Real-world outcomes of adult B-cell acute lymphocytic leukemia patients treated with blinatumomab.

Authors :
Badar T
Szabo A
Advani A
Wadleigh M
Arslan S
Khan MA
Aldoss I
Siebenaller C
Schultz E
Hefazi M
Shallis RM
Yurkiewicz I
Podoltsev N
Patel AA
Curran E
Balasubramanian S
Yang J
Mattison RJ
Burkart M
Dinner S
Liedtke M
Litzow MR
Atallah E
Source :
Blood advances [Blood Adv] 2020 May 26; Vol. 4 (10), pp. 2308-2316.
Publication Year :
2020

Abstract

The availability and use of blinatumomab symbolizes a paradigm shift in the management of B-cell acute lymphoblastic leukemia (ALL). We conducted a retrospective multicenter cohort analysis of 239 ALL patients (227 relapsed refractory [RR], n = 227; minimal residual disease [MRD], n = 12) who received blinatumomab outside of clinical trials to evaluate safety and efficacy in the "real-world" setting. The median age of patients at blinatumomab initiation was 48 years (range, 18-85). Sixty-one (26%) patients had ≥3 prior therapies and 46 (19%) had allogeneic hematopoietic cell transplantation before blinatumomab. The response rate (complete remission/complete remission with incomplete count recovery) in patients with RR disease was 65% (47% MRD-). Among 12 patients who received blinatumomab for MRD, 9 (75%) patients achieved MRD negativity. In patients with RR disease, median relapse-free survival and overall survival (OS) after blinatumomab was 32 months and 12.7 months, respectively. Among patients who received blinatumomab for MRD, median relapse-free survival was not reached (54% MRD- at 2 years) and OS was 34.7 months. Grade ≥3 cytokine release syndrome, neurotoxicity, and hepatotoxicity were observed in 3%, 7%, and 10% of patients, respectively. Among patients who achieved complete remission/complete remission with incomplete count recovery, consolidation therapy with allogeneic hematopoietic cell transplantation retained favorable prognostic significance for OS (hazard ratio, 0.54; 95% confidence interval, 0.30-0.97; P = .04). In this largest "real-world" experience published to date, blinatumomab demonstrated responses comparable to those reported in clinical trials. The optimal sequencing of newer therapies in ALL requires further study.<br /> (© 2020 by The American Society of Hematology.)

Details

Language :
English
ISSN :
2473-9537
Volume :
4
Issue :
10
Database :
MEDLINE
Journal :
Blood advances
Publication Type :
Academic Journal
Accession number :
32453836
Full Text :
https://doi.org/10.1182/bloodadvances.2019001381