Fleur Weeber1, Marco J Koudijs2, Marlous Hoogstraat3, Nicolle J M Besselink4, Stef VAN Lieshout5, Isaac J Nijman6, Edwin Cuppen6, G Johan Offerhaus7, Emile E Voest8. 1. Department of Molecular Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands f.weeber@nki.nl. 2. Department of Medical Genetics, University Medical Center Utrecht, Utrecht, the Netherlands. 3. Department of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, the Netherlands. 4. Department of Medical Oncology, University Medical Center Utrecht, Utrecht, the Netherlands. 5. Department of Pathology, VU Medical Center, Amsterdam, the Netherlands. 6. Hubrecht Institute, Utrecht, The Netherlands Department of Human Genetics, University Medical Center Utrecht, Utrecht, the Netherlands. 7. Department of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands. 8. Department of Molecular Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Abstract
BACKGROUND/AIM: Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal neoplasms. The exact genetic alterations underlying the pathophysiology of PEComas are largely unknown, although it has been shown that activation of the Mammalian target of rapamycin (mTOR) signaling pathway plays a pivotal role. Herein we describe the successful treatment of a patient with metastatic PEComa with the mTOR inhibitor everolimus and a comprehensive analysis to identify mechanisms for response. MATERIALS AND METHODS: Immunohistochemistry, array comparative genomic hybridization (aCGH) and genetic analyses were performed. RESULTS: Immunohistochemistry confirmed constitutive activation of mTOR. aCGH revealed a hyperdiploid karyotype affecting large regions of the genome. Next-generation sequencing did not reveal any tumor-specific mutations in mTOR-related genes. CONCLUSION: Our results show the complexity of determining causal genetic alterations that can predict responsiveness to mTOR inhibition, even for a tumor with a complete remission to this specific treatment. Copyright
BACKGROUND/AIM: Perivascular epithelioid cell tumors (PEComas) are rare mesenchymal neoplasms. The exact genetic alterations underlying the pathophysiology of PEComas are largely unknown, although it has been shown that activation of the Mammalian target of rapamycin (mTOR) signaling pathway plays a pivotal role. Herein we describe the successful treatment of a patient with metastatic PEComa with the mTOR inhibitor everolimus and a comprehensive analysis to identify mechanisms for response. MATERIALS AND METHODS: Immunohistochemistry, array comparative genomic hybridization (aCGH) and genetic analyses were performed. RESULTS: Immunohistochemistry confirmed constitutive activation of mTOR. aCGH revealed a hyperdiploid karyotype affecting large regions of the genome. Next-generation sequencing did not reveal any tumor-specific mutations in mTOR-related genes. CONCLUSION: Our results show the complexity of determining causal genetic alterations that can predict responsiveness to mTOR inhibition, even for a tumor with a complete remission to this specific treatment. Copyright
Authors: Andrew J Wagner; Vinod Ravi; Richard F Riedel; Kristen Ganjoo; Brian A Van Tine; Rashmi Chugh; Lee Cranmer; Erlinda M Gordon; Jason L Hornick; Heng Du; Berta Grigorian; Anita N Schmid; Shihe Hou; Katherine Harris; David J Kwiatkowski; Neil P Desai; Mark A Dickson Journal: J Clin Oncol Date: 2021-10-12 Impact factor: 50.717