TREATMENT OF PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA
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 CD19×CD3 bispecific single chain antibody construct to a pediatric ALL patient in the need thereof.
1 . 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.
2 . The method of claim 1 , wherein said pediatric acute lymphoblastic leukemia (ALL) is pediatric B-lineage acute lymphoblastic leukemia (ALL), preferably pediatric B-precursor acute lymphoblastic leukemia ALL, more preferably pediatric pro-B ALL, pre-B ALL or common ALL (cALL).
3 . The method of claim 1 , wherein said acute lymphoblastic leukemia (ALL) is refractory and/or relapsed ALL.
4 . The method of claim 3 , wherein said acute lymphoblastic leukemia (ALL) is relapsed ALL, preferably ALL relapsed within three years of diagnosis.
5 . The method of claim 1 , wherein the method is for the treatment, amelioration or elimination of minimal residual disease (MRD) in a pediatric ALL patient.
6 . The method of claim 5 , wherein said pediatric ALL patient is MRD-positive in complete hematological remission.
7 . The method of claim 5 , wherein said method converts MRD positive ALL into an MRD negative status.
8 . The method of claim 5 , wherein MRD is measured with quantitative detection of at least one of the cytogenetic abnormalities or rearrangements selected from the group consisting of:
t(12;21)[TEL-AML1];
t(1;19;)[E2A-PBX];
t(4;11)[AF4-MLL];
t(9;22)[BCR-ABL];
hyperdiploidy or trisomies of chromosomes 4, 10, and 17;
hypodiploidy;
rearrangements of immunoglobulin genes; and
T-cell receptor (TCR) rearrangements.
9 . The method of claim 8 , wherein said pediatric ALL patient shows a signal for the cytogenetic abnormalities above detection limit and/or at least one marker by rearrangement with a sensitivity of ≦10 −4 .
10 . The method of claim 1 , wherein the corresponding variable heavy chain regions (VH) and the corresponding variable light chain regions (VL) regions in said CD19xCD3 bispecific single chain antibody construct are arranged, from N-terminus to C-terminus, in the order, VL(CD19)-VH(CD19)-VH(CD3)-VL(CD3).
11 . The method of claim 10 , wherein said CD19xCD3 bispecific single chain antibody construct comprises an amino acid sequence as set forth in SEQ ID NO. 1, or an amino acid sequence at least 90%, preferably 95% identical to SEQ ID NO. 1.
12 . The method of claim 1 , wherein the pharmaceutical composition comprising a CD19xCD3 bispecific single chain antibody construct is to be administered by continuous infusion for at least four weeks followed by a 2-week treatment-free interval.
13 . The method of claim 12 , wherein said administration is to be repeated at least two, three, four, five, six, seven, eight, nine of ten times, after determination of a MRD negative status.
14 . The method of claim 12 , wherein the method is prior to allogeneic stem cell transplantation (HSCT) to convert the MRD positive ALL into an MRD negative status.
15 . The method of claim 12 , wherein the method is after allogeneic hematopoietic stem cell transplantation (HSCT).
16 . The method of claim 15 , wherein a CD19xCD3 bispecific single chain antibody construct induces a graft-versus-leukemia (GvL) effect.
17 . The method of claim 1 , wherein the CD19xCD3 bispecific single chain antibody construct is to be administered in a daily dose of 10 μg to 100 μg per square meter patient body surface area.
18 . The method of claim 17 , wherein the CD19xCD3 bispecific single chain antibody construct is to be administered in a daily dose of 15 μg to 30 μg per square meter patient body surface area.
19 . The method of claim 1 , wherein said method is for a pediatric ALL patient with high risk of relapse according to the COGAALL03B1 classification of acute lymphoblastic leukemia.
20 . The method of claim 1 , wherein said patient is non-eligible for allogeneic stem cell transplantation.
21 . A CD19xCD3 bispecific single chain antibody construct for the treatment, amelioration or elimination of pediatric acute lymphoblastic leukemia (ALL).