IP Library Granted Patent US 10,980,804
Granted Patent B2
US 10,980,804 · App. 14/761,518 · Granted Apr 20, 2021

Methods of treating cholangiocarcinoma

Inventors: Siraj Mahamed Ali (Cambridge, MA); Matthew J. Hawryluk (Watertown, MA); Jie He (Newton, MA); Doron Lipson (Chestnut Hill, MA); Vincent A. Miller (West Orange, NJ); Jeffrey S. Ross (Lebanon Springs, NY); Philip James Stephens (Lexington, MA)
Assignee: FOUNDATION MEDICINE, INC.
A61K31/5025A61K31/404A61K31/435A61K31/4412A61K31/4439A61K31/47A61K31/496A61K31/498A61K31/506A61K31/517A61K31/519A61K31/53A61K31/5383A61K31/553A61K45/06C07K14/705C07K14/71C07K16/40C12N9/12C12N15/1137C12Q1/6883C12Q1/6886C12Y207/10001G01N33/573C07K2319/00C12N2310/11C12N2310/12C12N2310/14C12Q2600/156C12Q2600/158G01N2333/912G01N2500/04
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Quick Facts
Patent No.
US 10,980,804
App. No.
14/761,518
Granted
Apr 20, 2021
Kind
B2
Abstract

Methods and compositions for treating cholangiocarcinoma.

Claims (23)

1. A method of treating a subject having a cholangiocarcinoma, comprising:

acquiring knowledge of the presence of a fusion polypeptide or a fusion nucleic acid molecule encoding the fusion polypeptide in a sample from said subject, wherein the fusion polypeptide comprises an FGFR2-BICC1 fusion polypeptide encoded by a nucleic acid molecule comprising a fusion junction of exon 16 of SEQ ID NO: 1 and exon 18 of SEQ ID NO: 7; and

administering to the subject an effective amount of a kinase inhibitor chosen from: ACTB1003; ARRY-470; ARRY-786; AV369b; AZ-23; AZD-2171 (Cediranib); AZD-4547; BGJ398; BIBF1120; Brivanib; Brivanib Alaninate; Danusertib; Dovitinib; Dovitinib Dilactic Acid; ENMD-2076; JNJ 42756493; K252a; Lenvatinib; Lestaurtinib; Loxo-101; LY2874455; Masitinib; MK-2461; Oxindole-3; Pazopanib; PD173074; PD-173955; PHA-848125; Ponatinib; TSU-68; Tyrphostin AG 1296; R1530; R406; Regorafenib; RXDX-101; RXDX-102; Volasertib, or a combination thereof,

thereby treating the cholangiocarcinoma in the subject.

2. The method of claim 1 , wherein the kinase inhibitor is administered responsive to the determination of the presence of the fusion nucleic acid molecule or the fusion polypeptide in a sample from said subject.

3. The method of claim 2 , wherein the determination of the presence of the fusion nucleic acid molecule or the fusion polypeptide comprises sequencing.

4. The method of claim 1 , wherein the subject is undergoing or has undergone treatment with a different therapeutic agent or therapeutic modality.

5. The method of claim 4 , wherein responsive to the determination of the presence of the fusion nucleic acid molecule or the fusion polypeptide, the method further comprises discontinuing the different therapeutic agent or therapeutic modality.

6. The method of claim 4 , wherein the different therapeutic agent or therapeutic modality is a chemotherapy or a surgical procedure.

7. The method of claim 1 , wherein the FGFR2-BICC1 fusion polypeptide is encoded by a nucleic acid molecule comprising exons 1-16 of SEQ ID NO: 1 and exons 18-21 of SEQ ID NO: 7.

8. The method of claim 1 , wherein the FGFR2-BICC1 fusion polypeptide comprises an FGFR2 receptor tyrosine kinase domain or a functional fragment thereof.

9. The method of claim 1 , wherein the cholangiocarcinoma comprises one or more mutated cells that originate in the bile duct.

10. The method of claim 1 , wherein the cholangiocarcinoma is an intrahepatic carcinoma or an extrahepatic carcinoma.

11. A method of treating a subject having a cholangiocarcinoma, comprising:

detecting the presence of a fusion polypeptide or a fusion nucleic acid molecule encoding the fusion polypeptide in a sample from said subject, wherein the fusion polypeptide comprises an FGFR2-BICC1 fusion polypeptide encoded by a nucleic acid molecule comprising a fusion junction of exon 16 of SEQ ID NO: 1 and exon 18 of SEQ ID NO: 7; and

administering to the subject an effective amount of a kinase inhibitor chosen from: ACTB1003; ARRY-470; ARRY-786; AV369b; AZ-23; AZD-2171 (Cediranib); AZD-4547; BGJ398; BIBF1120; Brivanib; Brivanib Alaninate; Danusertib; Dovitinib; Dovitinib Dilactic Acid; ENMD-2076; JNJ 42756493; K252a; Lenvatinib; Lestaurtinib; Loxo-101; LY2874455; Masitinib; MK-2461; Oxindole-3; Pazopanib; PD173074; PD-173955; PHA-848125; Ponatinib; TSU-68; Tyrphostin AG 1296; R1530; R406; Regorafenib; RXDX-101; RXDX-102; Volasertib, or a combination thereof;

thereby treating the cholangiocarcinoma in the subject.

12. The method of claim 1 , wherein the sample is a nucleic acid sample.

13. The method of claim 1 , wherein the sample is a blood, serum, or plasma sample.

14. The method of claim 1 , wherein the sample comprises a tumor biopsy or a circulating tumor cell or nucleic acid.

15. The method of claim 11 , wherein the sample is a nucleic acid sample.

16. The method of claim 11 , wherein the sample is a blood, serum, or plasma sample.

17. The method of claim 11 , wherein the sample comprises a tumor biopsy or a circulating tumor cell or nucleic acid.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Jun 30, 2021
From: ROCHE FINANCE LTD
To: FOUNDATION MEDICINE, INC.
Reel/Frame 056715/0711 →
PATENT SECURITY AGREEMENT Recorded Sep 27, 2016
From: FOUNDATION MEDICINE, INC.
To: ROCHE FINANCE LTD
Reel/Frame 040165/0615 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2015
From: ALI, SIRAJ MAHAMED; HAWRYLUK, MATTHEW J.; HE, JIE; LIPSON, DORON; MILLER, VINCENT A.; ROSS, JEFFREY S.; STEPHENS, PHILIP JAMES
To: FOUNDATION MEDICINE, INC.
Reel/Frame 037314/0471 →
Cited By (4)
US 12,274,699 US 12,378,302 US 12,522,873 US 12,649,952