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Crizotinib in ALK-Rearranged Inflammatory Myofibroblastic Tumor
Oleh:
Butrynski, James E.
;
D'Adamo, David R.
;
Hornick, Jason L.
;
Cin, Paola Dal
Jenis:
Article from Journal - ilmiah internasional
Dalam koleksi:
The New England Journal of Medicine (keterangan: ada di Proquest) vol. 363 no. 18 (Oct. 2010)
,
page 1727-1733.
Topik:
Inflammatory Myofibroblastic Tumor
;
IMT
Ketersediaan
Perpustakaan FK
Nomor Panggil:
N08.K.2010.01
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Inflammatory myofibroblastic tumor (IMT) is a distinctive mesenchymal neoplasm characterized by a spindle-cell proliferation with an inflammatory infiltrate. Approximately half of IMTs carry rearrangements of the anaplastic lymphoma kinase (ALK) locus on chromosome 2p23, causing aberrant ALK expression. We report a sustained partial response to the ALK inhibitor crizotinib (PF-02341066, Pfizer) in a patient with ALK-translocated IMT, as compared with no observed activity in another patient without the ALK translocation. These results support the dependence of ALK-rearranged tumors on ALK-mediated signaling and suggest a therapeutic strategy for genomically identified patients with the aggressive form of this soft-tissue tumor.
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