HRP20141158T1 - Postupak za dijagnosticiranje raka koji izražava skraä†enu varijantu her2-receptora - Google Patents

Postupak za dijagnosticiranje raka koji izražava skraä†enu varijantu her2-receptora Download PDF

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HRP20141158T1
HRP20141158T1 HRP20141158AT HRP20141158T HRP20141158T1 HR P20141158 T1 HRP20141158 T1 HR P20141158T1 HR P20141158A T HRP20141158A T HR P20141158AT HR P20141158 T HRP20141158 T HR P20141158T HR P20141158 T1 HRP20141158 T1 HR P20141158T1
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cancer
antibody
her2
receptor
seq
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Joaquín ARRIBAS LÓPEZ
Kim Pedersen
Pier-Davide Angellini
Palau Josep Lluis Parra
Sirle Laos
Torres José Baselga
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Fundació Privada Institut De Recerca Hospital, Universitari Vall Hebron
Fundació Privada Institució Catalana De Recerca I Estudis Avançants
Fundació Privada Institut D'investigació Oncològica De Vall-Hebron
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Claims (25)

1. Protutijelo ili njegov fragment, naznačen/o time, da ono prepoznaje epitop od HER2-receptora u skraćenom obliku, koji je određen sa SEQ ID NO:1, gdje je navedeni epitop određen sa sekvencom uključenom u SEQ ID NO:2, pri čemu je protutijelo ili njegov fragment sposobno/sposoban razlikovati protein sa SEQ ID NO:1 od HER2-receptora.
2. Protutijelo ili njegov fragment prema zahtjevu 1, naznačen/o time, da navedeni epitop je onaj koji je uključen u SEQ ID NO:3.
3. Protutijelo ili njegov fragment prema jednom ili više od prethodnih zahtjeva, naznačen/o time, da protutijelo ili njegov fragment je sposobno/sposoban razlikovati protein sa SEQ ID NO:1 od skraćenog oblika 648-CTF/p95 od HER2-receptora.
4. Protutijelo ili njegov fragment prema zahtjevu 2 ili 3, naznačen/o time, da se razlika može vizualizirati pomoću jedne ili više od sljedećih metoda: imunofluorescencija, citometrijski protok, imunohistokemija u staničnim kulturama i imunohistokemija u uzorcima od pacijenata.
5. Protutijelo ili njegov fragment prema jednom ili više od prethodnih zahtjeva, naznačen/o time, da je to poliklonalno protutijelo.
6. Protutijelo ili njegov fragment prema jednom ili više od zahtjeva 1 do 4, naznačen/o time, da je to monoklonalno protutijelo ili njegov fragment.
7. Protutijelo ili njegov fragment prema zahtjevu 6, naznačen/o time, da se proizvodi pomoću stanične linije hibridoma, deponirane kod “Deutschland Sammlung von Mikroorganismen und Zellen - DSMZ” s pristupnim brojem DSM ACC2904, ili pomoću stanične linije hibridoma, deponirane kod “Deutschland Sammlung von Mikroorganismen und Zellen - DSMZ” s pristupnim brojem DSM ACC2980.
8. Protutijelo ili njegov fragment prema jednom ili više od prethodnih zahtjeva, naznačen/o time, da je taj fragment odabran iz skupine koju čine F(ab), F(ab’) i Fv.
9. Hibridom, naznačen time, da on proizvodi monoklonalno protutijelo prema zahtjevu 6 ili 7.
10. Peptid koji se sastoji od SEQ ID NO:3 ili SEQ ID NO:4, naznačen time, da je opcijski konjugiran s imunogenom i upotrebljava se u postupku proizvodnje protutijela prema jednom ili više zahtjeva 1 ili 2, dok taj postupak uključuje imunizaciju sa spomenutim peptidom.
11. Postupak dobivanja monoklonalnog protutijela, naznačen time, da se stanična linija hibridoma uzgaja u prikladnom mediju za kultiviranje i zatim se monoklonalno protutijelo obnavlja iz toga medija.
12. Postupak dijagnosticiranja raka, naznačen time, da obuhvaća otkrivanje prisutnosti HER2-receptora skraćenog oblika, koji sadrži aminokiselinsku sekvencu SEQ ID NO:1, u uzorku od pacijenta, pri čemu se to pronalaženje izvodi pomoću načina neovisno izabranog iz skupine koju čine: (i) otkrivanje preko diferencijalne migracije HER2-receptora skraćenog oblika, koji se sastoji od SEQ ID NO:1, u odnosu prema cjelovitom obliku navedenog HER2-receptora; i (ii) otkrivanje pomoću vezivanja s jednim ili više protutijela koja su definirana u jednom ili više od zahtjeva 1 do 11.
13. Postupak prema zahtjevu 12, naznačen time, da je to prognostički postupak koji omogućava prognoziranje povećanja rasta tumora i/ili metastaza.
14. Uporaba protutijela ili njegovog fragmenta prema bilo kojem od zahtjeva 1 do 8, naznačena time, da je za dijagnosticiranje i određivanje prognoze u izoliranim uzorcima raka u kojima se izražava HER2-receptor.
15. Sredstvo za dijagnosticiranje i određivanje prognoze u izoliranim uzorcima raka tipa koji izražava HER2-receptor ili njegove skraćene varijante, naznačeno time, da obuhvaća najmanje jedno protutijelo ili njegov fragment prema bilo kojem od zahtjeva 1 do 8.
16. Sredstvo za dijagnosticiranje prema zahtjevu 15, naznačeno time, da je protutijelo ili njegov fragment smješteno/smješten na čvrstom osloncu.
17. Garnitura za dijagnosticiranje i određivanje prognoze u izoliranim uzorcima raka tipa koji izražava HER2-receptor ili njegove skraćene varijante, naznačena time, da obuhvaća protutijelo ili njegov fragment prema bilo kojem od zahtjeva 1 do 8, za otkrivanje prisutnosti HER2-receptora skraćenog oblika, koji sadrži SEQ OD NO:1, u uzorku.
18. Garnitura za dijagnosticiranje i određivanje prognoze prema zahtjevu 17, naznačena time, da način otkrivanja obuhvaća najmanje jedno sredstvo prema zahtjevima 15 ili 16.
19. Garnitura za dijagnosticiranje i određivanje prognoze prema zahtjevu 17, naznačena time, da se način pronalaženja sastoji od otkrivanja pomoću diferencijalne migracije, HER2 receptora skraćenog oblika sa SEQ ID NO:1, u odnosu prema cjelovitom obliku spomenutog HER2-receptora.
20. Protutijelo ili njegov fragment prema jednom ili više od zahtjeva 1 do 9, naznačen/o time, da se upotrebljava za terapeutske svrhe.
21. Protutijelo ili njegov fragment prema zahtjevu 20, naznačen/o time, da se upotrebljava za liječenje ili prevenciju raka kod kojega se izražava barem HER2-receptor skraćenog oblika, koji sadrži SEQ ID NO:1.
22. Protutijelo ili njegov fragment prema zahtjevu 21, naznačen/o time, da se upotrebljava za liječenje ili prevenciju raka dojke kod sisavaca, uključujući i ljude.
23. Protutijelo ili njegov fragment prema zahtjevu 21, naznačen/o time, da se upotrebljava za liječenje ili prevenciju raka odabranog iz skupine koju čine: rak pluća, rak gušterače, rak debelog crijava, rak želuca, rak prostate, rak glave i vrata, rak kože, rak bubrega, rak testisa, rak štitnjače, rak mokraćnog mjehura, rak maternice, rak vulve, endometrijski rak, rak jajnika, rak jednjaka, rak usta, rak žlijezda slinovnica, rak grkljana, peritonealni rak, rak područja nosa i grla, rak Falopijeve tube, Wilmsovi tumori, kao što su limfomi, Ewingov sarkom, sinovijalni sarkom, meduloblastomi, trofoblastični tumori, gliomi, glioblastomi, kolangiokarcinomi, kolesteatomi, kondrosarkomi, ependimomi, neurilemomi, neoromi, rabdomiosarkomi.
24. Uporaba protutijela ili njegovog fragmenta prema jednom ili više od zahtjeva 1 do 8, naznačena time, da je za proizvodnju lijeka za liječenje raka u kojem se izražava barem skraćeni oblik HER2-receptora koji sadrži SEQ ID NO:1.
25. Farmaceutski sastav za liječenje raka u kojem se izražava barem skraćeni oblik HER2-receptora koji sadrži SEQ ID NO:1, naznačen time, da obuhvaća protutijelo ili njegov fragment prema bilo kojem od zahtjeva 1 do 8, i najmanje jedno farmaceutski prihvatljivo pomoćno sredstvo i/ili nosač.
HRP20141158AT 2008-06-02 2014-11-27 Postupak za dijagnosticiranje raka koji izražava skraä†enu varijantu her2-receptora HRP20141158T1 (hr)

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ES200801652A ES2342646B1 (es) 2008-06-02 2008-06-02 Metodo de diagnostico de canceres que expresan el receptor her-2 o sus variantes truncadas.
PCT/EP2009/056976 WO2010000565A1 (en) 2008-06-02 2009-06-05 Method for diagnosing cancers expressing the her2 receptor or its truncated variants
EP09772265.6A EP2293819B1 (en) 2008-06-02 2009-06-05 Method for diagnosing cancers expressing a truncated her2 receptor variant

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US (1) US8389227B2 (hr)
EP (1) EP2293819B1 (hr)
JP (2) JP5753079B2 (hr)
KR (2) KR101785117B1 (hr)
CN (1) CN102202692B (hr)
AU (2) AU2009265921B2 (hr)
BR (1) BRPI0914969A2 (hr)
CA (1) CA2727365A1 (hr)
CY (1) CY1115798T1 (hr)
DK (1) DK2293819T3 (hr)
EA (1) EA025218B1 (hr)
ES (2) ES2342646B1 (hr)
HK (1) HK1157658A1 (hr)
HR (1) HRP20141158T1 (hr)
IL (1) IL209769A (hr)
MX (1) MX2010013419A (hr)
PL (1) PL2293819T3 (hr)
PT (1) PT2293819E (hr)
SI (1) SI2293819T1 (hr)
WO (1) WO2010000565A1 (hr)
ZA (1) ZA201009010B (hr)

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