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Relationship between PDGFR expression and the response to pazopanib in intimal sarcoma of the pulmonary artery: A case report
Author(s) -
Satoshi Sai,
Yoshinori Imamura,
Naomi Kiyota,
Naoe Jimbo,
Masanori Toyoda,
Yohei Funakoshi,
Naoko Chayahara,
Yasuko Hyogo,
Kei Takenaka,
Hirotaka Suto,
Hironobu Minami
Publication year - 2020
Publication title -
molecular and clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.442
H-Index - 7
eISSN - 2049-9469
pISSN - 2049-9450
DOI - 10.3892/mco.2020.2168
Subject(s) - pazopanib , platelet derived growth factor receptor , tyrosine kinase inhibitor , cancer research , soft tissue sarcoma , sarcoma , tyrosine kinase , oncogene , medicine , growth factor receptor , cancer , vascular endothelial growth factor , receptor tyrosine kinase , oncology , biology , growth factor , receptor , pathology , cell cycle , vegf receptors , sunitinib
Intimal sarcoma of the pulmonary artery (PAIS) is a rare disease with a poor prognosis. Pazopanib, which has been indicated in metastatic non-adipocytic soft-tissue sarcomas and is expected to be active in PAIS, is a multi-kinase inhibitor that targets the tyrosine kinase activity of vascular endothelial growth factor receptor (VEGFR), platelet-derived growth factor receptor (PDGFR) and stem cell factor receptor. The present study reports findings related to two cases of PAIS with PDGF and VEGF expression following treatment with pazopanib. A case with a moderate to strong expression of PDGFR-α and -β presented a long-term stable disease when treated with pazopanib (progression-free survival, 5.8 months). In a second case with a weak expression of PDGFR-α and -β, the disease progressed rapidly on pazopanib (progression-free survival, 1.1 months). VEGFR-2 was not expressed in the tumors of both cases. The level of PDGFR expression in the tumor tissue may therefore be predictive of pazopanib efficacy.

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