Dramatic bone remodeling following larotrectinib administration for bone metastasis in a patient with TRK fusion congenital mesoblastic nephroma

被引:28
|
作者
Halalsheh, Hadeel [1 ]
McCarville, Mary Beth [2 ]
Neel, Michael [3 ]
Reynolds, Mark [4 ]
Cox, Michael C. [4 ]
Pappo, Alberto S. [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Oncol, 262 Danny Thomas Pl, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Diagnost Imaging, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Surg, 332 N Lauderdale St, Memphis, TN 38105 USA
[4] Loxo Oncol Inc, San Francisco, CA USA
关键词
bone metastasis; ETV6-NTRK; larotrectinib; mesoplastic nephroma; TRK inhibitor; ETV6-NTRK3 GENE FUSION; INFANTILE FIBROSARCOMA; RECURRENT; INFANCY;
D O I
10.1002/pbc.27271
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mesoblastic nephroma is the most frequent renal tumor in newborns and young infants, and the cellular type is characterized by an ETV6-NTRK fusion, which constitutively activates the tropomyosin-related kinase (TRK) signaling pathway. Larotrectinib is a highly selective TRK inhibitor with activity in adult and pediatric patients who have TRK fusions. We present a rare case of a patient with mesoblastic nephroma metastatic to bone who had a dramatic response to larotrectinib.
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页数:3
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