Treatment of pediatric acute lymphoblastic leukemia

A technology for acute lymphocytes and leukemia, applied in chemical instruments and methods, anti-receptor/cell surface antigen/cell surface determinant immunoglobulin, immunoglobulin, etc., can solve the problem of overall curative effect decline, tolerance reduction, Increased morbidity and other problems, to achieve the effect of eliminating the risk of recurrence and effective anti-leukemia effect

Active Publication Date: 2011-10-05
AMGEN RES (MUNICH) GMBH
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  • Abstract
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Problems solved by technology

Problems in the management of relapsed ALL are the resistance of leukemia cells, and the reduced tolerance of patients to second rounds of therapy after first-line intensive therapy, leading to lower remission rates, higher incidence of subsequent relapses, and overall Decreased curative effect
Although recently introduced chemotherapeutic agents for refractory leukemia are available (Jeha, Semin Hematol. 46 (2009), 76-88), patients who relapse after HSCT often have chemotherapy-refractory disease and these patients are resistant to chemotherapy-related disease. very sensitive to toxicity

Method used

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  • Treatment of pediatric acute lymphoblastic leukemia
  • Treatment of pediatric acute lymphoblastic leukemia
  • Treatment of pediatric acute lymphoblastic leukemia

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Embodiment

[0162] 1. CD19xCD3 bispecific single chain antibody

[0163] WO 99 / 54440 describes the production, expression and cytotoxic activity of a CD19xCD3 bispecific single chain antibody. The corresponding amino acid and nucleic acid sequences of the CD19xCD3 bispecific single chain antibody are shown in SED ID NO.1 and 2, respectively. The VH and VL regions of the CD3-binding domain of the CD19xCD3 bispecific single-chain antibody are shown in SED ID NO.7-10, respectively, while the VH and VL regions of the CD19-binding domain of the CD19xCD3 bispecific Shown in SED ID NO.3-6.

[0164] 2. Lymphocyte phenotype analysis and chimerism analysis

[0165] Before, during, and after treatment with the CD19xCD3 bispecific single-chain antibody, blood was collected from patients using collection tubes containing EDTA for lymphocyte phenotype analysis and chimerism analysis. The absolute number of lymphocytes in the blood sample was determined by performing differential blood analysis (diff...

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Abstract

The present invention relates to a method for the treatment, amelioration or elimination of pediatric acute lymphoblastic leukemia (ALL), the method comprising the administration of a pharmaceutical composition comprising a CD19xCD3 bispecific single chain antibody construct to a pediatric ALL patient in the need thereof.

Description

technical field [0001] The present invention relates to a method for treating, improving or eliminating childhood acute lymphoblastic leukemia (ALL), the method comprising administering a pharmaceutical composition comprising a CD19xCD3 bispecific single chain antibody construct to a pediatric ALL patient in need thereof. Background technique [0002] With current treatment of childhood ALL, the event-free survival rate is about 75%. So, relapses are still frequent. Problems in the management of relapsed ALL are the resistance of leukemia cells, and the reduced tolerance of patients to second rounds of therapy after first-line intensive therapy, leading to lower remission rates, higher incidence of subsequent relapses, and overall Efficacy decreased. Intensive combination chemotherapy is thus currently necessary to induce a second complete remission. Depending on various prognostic factors, remission may be maintained with chemotherapy and brain irradiation alone or with ...

Claims

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Application Information

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IPC IPC(8): C07K16/28C07K16/46
CPCC07K16/2803C07K16/2809C07K16/468C07K16/3061C07K2317/56A61K2039/505A61P35/00A61P35/02A61K39/395
Inventor 格哈德·祖格迈尔
Owner AMGEN RES (MUNICH) GMBH
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