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Blinatumomab versus Chemotherapy for Advanced Acute Lymphoblastic Leukemia

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TLDR
Treatment with blinatumomab resulted in significantly longer overall survival than chemotherapy among adult patients with relapsed or refractory B‐cell precursor ALL, and remission rates within 12 weeks after treatment initiation were significantly higher.
Abstract
BackgroundBlinatumomab, a bispecific monoclonal antibody construct that enables CD3-positive T cells to recognize and eliminate CD19-positive acute lymphoblastic leukemia (ALL) blasts, was approved for use in patients with relapsed or refractory B-cell precursor ALL on the basis of single-group trials that showed efficacy and manageable toxic effects. MethodsIn this multi-institutional phase 3 trial, we randomly assigned adults with heavily pretreated B-cell precursor ALL, in a 2:1 ratio, to receive either blinatumomab or standard-of-care chemotherapy. The primary end point was overall survival. ResultsOf the 405 patients who were randomly assigned to receive blinatumomab (271 patients) or chemotherapy (134 patients), 376 patients received at least one dose. Overall survival was significantly longer in the blinatumomab group than in the chemotherapy group. The median overall survival was 7.7 months in the blinatumomab group and 4.0 months in the chemotherapy group (hazard ratio for death with blinatumomab...

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Immunotherapy in leukaemia

TL;DR: In this paper , the authors summarized the basic approaches to immunotherapy for leukaemia and focus on the research progress made in immunotherapy development for AML and ALL, and summarized novel immunotherapy strategies for treating lymphocytic leukemia and clinical trial results.
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Monoclonal antibodies in frontline acute lymphoblastic leukemia.

TL;DR: The role of monoclonal antibodies and how the incorporation of these agents has revolutionized and changed the treatment management of ALL in the frontline setting are reviewed.
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CLEC12A: A Promise Target for Cancer Therapy

TL;DR: The complexity of the human bone marrow, with context to haematological malignancies, is more difficult to elucidate with the present strategies compared to the niche of solid tumors as mentioned in this paper .
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Immunotherapy in Pediatric Acute Lymphoblastic Leukemia

TL;DR: Treatment for patients with B-ALL remains a therapeutic challenge despite successes due to multi-agent chemotherapy regiments, CNS prophylaxis and better risk stratification.
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Case Report: Blinatumomab therapy for the treatment of B-cell acute lymphoblastic leukemia patients with central nervous system infiltration

TL;DR: In this article , the authors used bispecific antibody for the treatment of B-cell acute lymphoblastic leukemia (B-ALL) with central nervous system (CNS) involvement.
References
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Journal ArticleDOI

Chimeric antigen receptor T cells for sustained remissions in leukemia.

TL;DR: Chimeric antigen receptor-modified T-cell therapy against CD19 was effective in treating relapsed and refractory ALL and was associated with a high remission rate, even among patients for whom stem-cell transplantation had failed, and durable remissions up to 24 months were observed.
Journal ArticleDOI

A multiple testing procedure for clinical trials.

TL;DR: The overall size of the procedure is shown to be controlled with virtually the same accuracy as the single sample chi-square test based on N(m1 + m2) observations and the power is found to bevirtually the same.
Journal ArticleDOI

Discrete sequential boundaries for clinical trials

K. K. Gordon Lan, +1 more
- 01 Dec 1983 - 
TL;DR: In this article, the authors proposed a more flexible method to construct discrete sequential boundaries based on the choice of a function, a*(t), which characterizes the rate at which the error level ac is spent.
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