Protein phosphatase 2a inhibitors for treating myelodysplastic syndromes

Patent metadata

Field	Value
Publication number	US-2017340628-A1
Application number	US-201515328235-A
Country	US
Kind code	A1
Filing date	Jul 23, 2015
Priority date	Jul 24, 2014
Publication date	Nov 30, 2017
Grant date	—

Abstract

Disclosed are methods for treating a myelodysplastic syndrome (MDS) in a subject that involves administering to the subject a therapeutically effective amount of a protein phosphatase 2A (PP2A) inhibitor.

First claim

1 . A method for treating myelodysplastic syndrome (MDS) in a subject afflicted therewith, comprising administering to the subject a therapeutically effective amount of a protein phosphatase 2A (PP2A) inhibitor.

2 . The method of claim 1 , wherein the MDS in the subject is del(5q) MDS.

3 . The method of claim 1 , wherein the MDS in the subject is non-del(5q) MDS or unclassified myelodysplastic syndrome (MDS-U).

4 . The method of claim 3 , wherein the MDS is characterized by refractory anemia (RA), refractory neutropenia (RN), refractory thrombocytopenia (RT), refractory anemia (RA) with ringed sideroblasts (RARS), refractory cytopenia with multilineage dysplasia (RCMD), refractory cytopenia with multilineage dysplasia and ringed sideroblasts (RCMD-RS), refractory anemia (RA) with excess blasts-1 (RAEB-1), refractory anemia (RA) with excess blasts-2 (RAEB-2) or refractory anemia (RA) with excess Blasts in Transformation (RAEB-t), or a combination thereof.

5 .- 12 . (canceled)

13 . The method of claim 1 , wherein the MDS has become resistant to a current therapy, wherein the current therapy comprises treatment with lenalidomide, azacitidine or decitabine.

14 .- 17 . (canceled)

18 . The method of claim 1 , further comprising administering to the subject a therapeutically effective amount of lenalidomide (LEN) or dexamethasone.

19 . (canceled)

20 . (canceled)

21 . The method of claim 13 , wherein the PP2A inhibitor reduces or reverses the resistance of the MDS to the lenalidomide, or re-sensitizes the MDS to the lenalidomide.

22 . (canceled)

23 . (canceled)

24 . A method for treating a myelodysplastic syndrome (MDS) in a subject, comprising administering to the subject an effective amount of
(a) a first composition comprising lenalidomide, or a pharmaceutically acceptable salt thereof; and (b) a second composition comprising a protein phosphatase 2A (PP2A) inhibitor.

25 . The method of claim 1 , wherein the treating comprises reducing the number of blasts in the bone marrow or peripheral blood of the subject, or reducing the number of myeloblasts in the bone marrow or peripheral blood of the subject, or reducing the number of sideroblasts or ringed sideroblasts in the bone marrow or peripheral blood of the subject, or increasing the concentration of normal red blood cells, normal white blood cells and/or platelets in the subject, or increasing the concentration of hemoglobin in the subject.

26 .- 29 . (canceled)

30 . The method of claim 1 , wherein the MDS in the subject is low risk MDS based on the IPSS system, intermediate-1 risk MDS based on the IPSS system, intermediate-2 risk MDS based on the IPSS system or high risk MDS based on the IPSS system.

31 .- 34 . (canceled)

35 . The method of claim 1 , wherein the PP2A inhibitor is a compound having the structure:

wherein
bond α is present or absent;
R 1 and R 2 together are ═O;
R 3 is OH, O − , OR 9 , O(CH 2 ) 1-6 R 9 , SH, S − , or SR 9 ,
wherein R 9 is H, alkyl, alkenyl, alkynyl or aryl;

R 4 is

where X is O, S, NR 10 , N + HR 10 or N + R 10 R 10 ,
where each R 10 is independently H, alkyl, alkenyl, alkynyl, aryl,

—CH 2 CN, —CH 2 CO 2 R 11 , or CH 2 COR 11 ,
wherein each R 11 is independently H, alkyl, alkenyl or alkynyl;
R 5 and R 6 taken together are ═O;
R 7 and R 8 are each H,

or a salt, zwitterion, or ester thereof.

36 . (canceled)

37 . (canceled)

38 . The method of claim 35 , wherein bond α in the compound is absent.

39 .- 48 . (canceled)

49 . The method of claim 35 , wherein the compound has the structure

wherein
bond α is present or absent;
R 9 is present or absent and when present is H, alkyl, alkenyl, alkynyl or phenyl; and
X is O, NR 10 , NH + R 10 or N + R 10 R 10 ,
where each R 10 is independently H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl,

—CH 2 CN, —CH 2 CO 2 R 12 , or —CH 2 COR 12 ,
where R 12 is H or alkyl,

or a salt, zwitterion or ester thereof.

50 . The method of claim 35 , wherein the compound has the structure

wherein
bond α is present or absent;
X is O or NR 10 ,
where each R 10 is independently H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl,

—CH 2 CN, —CH 2 CO 2 R 12 , or —CH 2 COR 12 ,
where R 12 is H or alkyl,

or a salt, zwitterion or ester thereof, or has the structure

wherein
bond α is present or absent;
X is O or NH + R 10 ,
where R 10 is H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl,

—CH 2 CN, —CH 2 CO 2 R 12 , or —CH 2 COR 12 ,
where R 12 is H or alkyl,

or a salt, zwitterion or ester thereof.

51 . (canceled)

52 . The method of claim 35 , wherein the compound has the structure

or a salt or ester thereof.

53 . The method of claim 35 , wherein the compound has the structure

or a salt or ester thereof.

54 . The method of claim 35 , wherein the compound is contained in a pharmaceutical composition comprising monosodium glutamate.

55 . The method of claim 52 , wherein the compound is contained in a pharmaceutical composition comprising monosodium glutamate.

56 . The method of 54 , wherein the treating comprising inducing apoptosis of abnormal bone marrow cells, inducing apoptosis of at least 50% of abnormal bone marrow cells or inducing G1 cell arrest in at least 30% of abnormal bone marrow cells.

57 . The method of claim 55 , wherein the treating comprises inducing apoptosis of abnormal bone marrow cells, inducing apoptosis of at least 50% of abnormal bone marrow cells or inducing G1 cell arrest in at least 30% of abnormal bone marrow cells.

58 . (canceled)

Assignees

• H Lee Moffitt Cancer Ct & Res
• Lixte Biotechnology Inc

Inventors

• List Alan F
• Sallman David A
• Kovach John S

Classifications

• A61P7/06

  Antianaemics · CPC title

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P7/00

  Drugs for disorders of the blood or the extracellular fluid · CPC title

• A61P7/04

  Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents · CPC title

• A61P35/00

  Antineoplastic agents · CPC title