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
Hauptverfasser: Halalsheh, Hadeel, McCarville, Mary Beth, Neel, Michael, Reynolds, Mark, Cox, Michael C., Pappo, Alberto S.
Format: Journal Article
Sprache:Englisch
Veröffentlicht: United States Wiley Subscription Services, Inc 01.10.2018
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ISSN:1545-5009, 1545-5017, 1545-5017
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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.
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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  surname: Halalsheh
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  givenname: Mary Beth
  surname: McCarville
  fullname: McCarville, Mary Beth
  organization: St. Jude Children's Research Hospital
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  givenname: Michael
  surname: Neel
  fullname: Neel, Michael
  organization: St. Jude Children's Research Hospital
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  givenname: Mark
  surname: Reynolds
  fullname: Reynolds, Mark
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  fullname: Cox, Michael C.
  organization: Loxo Oncology Inc
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  givenname: Alberto S.
  surname: Pappo
  fullname: Pappo, Alberto S.
  email: alberto.pappo@stjude.org
  organization: St. Jude Children's Research Hospital
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Issue 10
Keywords mesoplastic nephroma
larotrectinib
bone metastasis
ETV6-NTRK
TRK inhibitor
Language English
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2018 The Authors. Pediatric Blood & Cancer Published by Wiley Periodicals, Inc.
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Snippet 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...
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...
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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
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fpbc.27271
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