Dramatic bone remodeling following larotrectinib administration for bone metastasis in a patient with TRK fusion congenital mesoblastic nephroma
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 i...
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| Veröffentlicht in: | Pediatric blood & cancer Jg. 65; H. 10; S. e27271 - n/a |
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01.10.2018
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| Abstract | 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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| AbstractList | 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.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. 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. |
| Author | Reynolds, Mark Cox, Michael C. Neel, Michael Pappo, Alberto S. Halalsheh, Hadeel McCarville, Mary Beth |
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29893456$$D View this record in MEDLINE/PubMed |
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| Cites_doi | 10.1542/peds.40.2.272 10.1200/JCO.1984.2.8.956 10.1016/S0002-9440(10)65732-X 10.1002/pbc.21389 10.1002/cncr.21836 10.1038/ng0298-184 10.1002/pbc.26925 10.4081/oncol.2017.321 10.1038/modpathol.2017.127 10.1002/1097-0142(19931015)72:8<2499::AID-CNCR2820720831>3.0.CO;2-# 10.1002/pbc.26433 10.1056/NEJMoa1714448 10.1007/s00383-017-4149-5 10.1002/pbc.26437 |
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| SubjectTerms | bone metastasis Bone remodeling ETV6–NTRK Hematology Infants larotrectinib mesoplastic nephroma Metastases Neonates Oncology Pediatrics Signal transduction TRK inhibitor Tropomyosin |
| Title | Dramatic bone remodeling following larotrectinib administration for bone metastasis in a patient with TRK fusion congenital mesoblastic nephroma |
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