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The Impact of TSC-1 and -2 Mutations on Response to Therapy in Malignant PEComa: A Multicenter Retrospective Analysis.
Liu, Lawrence; Dehner, Carina; Grandhi, Nikhil; Lyu, Yang; Borcherding, Dana C; Chrisinger, John S A; Zhang, Xiao; Luo, Jingqin; Tao, Yu; Parkes, Amanda; Bui, Nam Q; Davis, Elizabeth J; Milhem, Mohammed M; Monga, Varun; Weiss, Mia; Tine, Brian Van; Hirbe, Angela C.
Afiliação
  • Liu L; City of Hope Comprehensive Cancer Center, Duarte, CA 91010, USA.
  • Dehner C; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Grandhi N; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Lyu Y; Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Borcherding DC; Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Chrisinger JSA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Zhang X; Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Luo J; Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Tao Y; Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Parkes A; Carbone Cancer Center, University of Wisconsin, Madison, WI 53706, USA.
  • Bui NQ; Stanford Cancer Institute, Stanford University, Palo Alto, CA 94305, USA.
  • Davis EJ; Ingram Cancer Center, Vanderbilt University, Nashville, TN 37232, USA.
  • Milhem MM; Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA 52722, USA.
  • Monga V; Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA 52722, USA.
  • Weiss M; Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Tine BV; Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Hirbe AC; Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
Genes (Basel) ; 13(11)2022 10 24.
Article em En | MEDLINE | ID: mdl-36360169
ABSTRACT

BACKGROUND:

Perivascular epithelioid cell neoplasms (PEComas) are a diverse family of mesenchymal tumors with myomelanocytic differentiation that disproportionately affect women and can be associated with tuberous sclerosis (TS). Although mTOR inhibition is widely used as first-line treatment, it is unclear what genomic alterations exist in these tumors and how they influence the response to therapy.

METHODS:

This was a multicenter study conducted at five sites within the US. The data were collected from 1 January 2004 to 31 January 2021. We conducted a retrospective analysis to identify PEComa patients with next-generation sequencing (NGS) data and compared outcomes based on mutations.

RESULTS:

No significant differences in survival were identified between TSC-1 and TSC-2 mutated PEComa or TSC-1/-2 versus other mutations. No significant difference was seen in progression-free survival (PFS) after first-line therapy between mTOR inhibition versus other systemic therapies.

CONCLUSIONS:

We were unable to detect differences in survival based on genomic alterations or PFS between mTOR inhibition versus other systemic therapies. Future studies should seek to identify other drivers of TSC-1/-2 silencing that could predict response to mTOR inhibition.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias de Células Epitelioides Perivasculares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias de Células Epitelioides Perivasculares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article