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Open AccessJournal ArticleDOI

Blinatumomab in Pediatric Acute Lymphoblastic Leukemia-From Salvage to First Line Therapy (A Systematic Review).

Manon Queudeville, +1 more
- 08 Jun 2021 - 
- Vol. 10, Iss: 12, pp 2544
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TLDR
In this article, a systematic review discusses all published results for blinatumomab in children as well as all ongoing clinical trials in R/R-ALL and concludes that the use of BLINATOMAB is beneficial for patients with a high risk of severe chemotherapy-associated toxicities.
Abstract
Acute lymphoblastic leukemia is by far the most common malignancy in children, and new immunotherapeutic approaches will clearly change the way we treat our patients in future years. Blinatumomab is a bispecific T-cell-engaging antibody indicated for the treatment of relapsed/refractory acute lymphoblastic leukemia (R/R-ALL). The use of blinatumomab in R/R ALL has shown promising effects, especially as a bridging tool to hematopoietic stem cell transplantation. For heavily pretreated patients, the response to one or two cycles of blinatumomab ranges from 34% to 66%. Two randomized controlled trials have very recently demonstrated an improved reduction in minimal residual disease as well as an increased survival for patients treated with blinatumomab compared to standard consolidation treatment in first relapse. Current trials using blinatumomab frontline for high-risk patients or as a consolidation treatment post-transplant will show whether efficacy is even higher in less heavily pretreated patients. Due to the distinct pattern of adverse events compared to high-dose conventional chemotherapy, blinatumomab could play an important role for patients with a risk for severe chemotherapy-associated toxicities. This systematic review discusses all published results for blinatumomab in children as well as all ongoing clinical trials.

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Journal ArticleDOI

Blinatumomab Prior to CAR-T Cell Therapy—A Treatment Option Worth Consideration for High Disease Burden

TL;DR: In this paper , a single-center experience in seven children with chemorefractory B-cell precursor acute lymphoblastic leukemia (r/r BCP-ALL) treated with blinatumomab before CAR-T cell therapy either to reduce disease burden before apheresis (six patients) or as a bridging therapy (two patients).
Journal ArticleDOI

Need for pneumococcal revaccination after blinatumomab therapy: A case report

TL;DR: In this article , a 27-month-old male with B-cell acute lymphoblastic leukemia (ALL) in first remission who received blinatumomab, subsequently developed recurrent Streptococcus pneumoniae bacteremias during maintenance, and was found to have diminished vaccine titer levels.
Journal ArticleDOI

Acute Lymphoblastic Leukemia Immunotherapy Treatment: Now, Next, and Beyond

TL;DR: A review of new treatment paradigms being used in the relapsed/refractory setting as well as current trials through which these new therapies might be introduced to the frontline setting is provided in this article .
Journal ArticleDOI

Immunotherapy for Pediatric Acute Lymphoblastic Leukemia: Recent Advances and Future Perspectives

TL;DR: This review will thoroughly discuss the emerging immunotherapeutics for the treatment of pediatric ALL, as well as side-effects and new development.
References
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Journal ArticleDOI

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement

TL;DR: Moher et al. as mentioned in this paper introduce PRISMA, an update of the QUOROM guidelines for reporting systematic reviews and meta-analyses, which is used in this paper.
Journal ArticleDOI

Immunophenotyping of blood lymphocytes in childhood: Reference values for lymphocyte subpopulations

TL;DR: It is strongly recommended that immunophenotyping of blood lymphocytes for the diagnosis of hematologic and immunologic disorders be based on the absolute rather than on the relative size of lymphocyte subpopulations.
Journal ArticleDOI

Serial killing of tumor cells by cytotoxic T cells redirected with a CD19-/CD3-bispecific single-chain antibody construct

TL;DR: This is the first study showing that a bispecific antibody can sustain multiple rounds of target cell lysis by T cells, and it is suggested that the rate of serial killing was mostly determined by T‐cell movement and target cell scanning and lysis.
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