Literature DB >> 30069763

Everolimus.

Jens Hasskarl1.   

Abstract

Everolimus (RAD001) is an oral protein kinase inhibitor of the mTOR (mammalian target of rapamycin) serine/threonine kinase signal transduction pathway. The mTOR pathway regulates cell growth, proliferation and survival, and is frequently deregulated in cancer.The EMA has approved Everolimus as Afinitor® for the treatment of hormone receptor-positive, HER2/neu-negative advanced breast cancer, in combination with exemestane, in postmenopausal women without symptomatic visceral disease after recurrence or progression following a nonsteroidal aromatase inhibitor, for the treatment of unresectable or metastatic, well- or moderately differentiated neuroendocrine tumors of pancreatic origin in adults with progressive disease, and for the treatment of unresectable or metastatic, well-differentiated (Grade 1 or Grade 2) nonfunctional neuroendocrine tumors of gastrointestinal or lung origin in adults with progressive disease, and for the treatment of patients with advanced renal cell carcinoma, whose disease has progressed on or after treatment with VEGF-targeted therapy And as Votubia® for the treatment of adult patients with renal angiomyolipoma associated with tuberous sclerosis complex (TSC), who are at risk of complications (based on factors such as tumor size or presence of aneurysm, or presence of multiple or bilateral tumors) but who do not require immediate surgery, and for the treatment of patients with subependymal giant cell astrocytoma (SEGA) associated with TSC who require therapeutic intervention but are not amenable to surgery, and as an add-on treatment in patients from 2 years of age with seizures related to TSC that have not responded to other treatments ( https://www.novartis.com/news/media-releases/novartis-drug-votubiar-receives-eu-approval-treat-refractory-partial-onset ). The FDA has approved Everolimus as Afinitor® for the treatment of postmenopausal women with advanced hormone receptor-positive, HER2-negative breast cancer in combination with exemestane, after the failure of treatment with letrozole or anastrozole, for the treatment of adult patients with progressive neuroendocrine tumors of pancreatic origin (PNET) with unresectable, locally advanced or metastatic disease, for the treatment of adult patients with advanced RCC after failure of treatment with sunitinib or sorafenib, for the treatment of adult patients with renal angiomyolipoma and tuberous sclerosis complex (TSC), not requiring immediate surgery. for the treatment of adult and pediatric patients, 3 years of age or older, with SEGA associated with TSC who require therapeutic intervention but are not candidates for curative surgical resection. Everolimus shows promising clinical activity in additional indications. Multiple Phase II and Phase III trials of everolimus alone or in combination and will help to further elucidate the role of mTOR in oncology. For a review on everolimus as immunosuppressant, please consult other sources.

Entities:  

Keywords:  Cancer; Everolimus; NET; RAD001; TSC; mTOR

Mesh:

Substances:

Year:  2018        PMID: 30069763     DOI: 10.1007/978-3-319-91442-8_8

Source DB:  PubMed          Journal:  Recent Results Cancer Res        ISSN: 0080-0015


  21 in total

1.  DRD2 Agonist Cabergoline Abolished the Escape Mechanism Induced by mTOR Inhibitor Everolimus in Tumoral Pituitary Cells.

Authors:  Federica Mangili; Emanuela Esposito; Donatella Treppiedi; Rosa Catalano; Giusy Marra; Genesio Di Muro; Anna Maria Barbieri; Marco Locatelli; Andrea G Lania; Alessandra Mangone; Anna Spada; Maura Arosio; Erika Peverelli; Giovanna Mantovani
Journal:  Front Endocrinol (Lausanne)       Date:  2022-06-03       Impact factor: 6.055

2.  In Vitro Interactions of Antifungal Agents and Everolimus Against Aspergillus Species.

Authors:  Huiping Jiang; Jianqun Xiong; Lihua Tan; Ping Jin; Yi Sun; Lianjuan Yang; Jingwen Tan
Journal:  Front Cell Infect Microbiol       Date:  2022-07-05       Impact factor: 6.073

Review 3.  Recent Progress and Challenges for Drug-Resistant Tuberculosis Treatment.

Authors:  Filia Stephanie; Mutiara Saragih; Usman Sumo Friend Tambunan
Journal:  Pharmaceutics       Date:  2021-04-21       Impact factor: 6.321

Review 4.  Development of antifibrotic therapy for stricturing Crohn's disease: lessons from randomized trials in other fibrotic diseases.

Authors:  Si-Nan Lin; Ren Mao; Chenchen Qian; Dominik Bettenworth; Jie Wang; Jiannan Li; David H Bruining; Vipul Jairath; Brian G Feagan; Min-Hu Chen; Florian Rieder
Journal:  Physiol Rev       Date:  2021-09-27       Impact factor: 37.312

Review 5.  Biological Actions of the Hsp90-binding Immunophilins FKBP51 and FKBP52

Authors:  Nadia R Zgajnar; Sonia A De Leo; Cecilia M Lotufo; Alejandra G Erlejman; Graciela Piwien-Pilipuk; Mario D Galigniana
Journal:  Biomolecules       Date:  2019-02-01

Review 6.  The role of EMT-related lncRNA in the process of triple-negative breast cancer metastasis.

Authors:  Haomeng Zhang; Jiao Wang; Yulong Yin; Qingjie Meng; Yonggang Lyu
Journal:  Biosci Rep       Date:  2021-02-26       Impact factor: 3.840

Review 7.  Evolution of Cancer Pharmacological Treatments at the Turn of the Third Millennium.

Authors:  Luca Falzone; Salvatore Salomone; Massimo Libra
Journal:  Front Pharmacol       Date:  2018-11-13       Impact factor: 5.810

Review 8.  Targeting PI3K/Akt/mTOR in AML: Rationale and Clinical Evidence.

Authors:  Salihanur Darici; Hazem Alkhaldi; Gillian Horne; Heather G Jørgensen; Sandra Marmiroli; Xu Huang
Journal:  J Clin Med       Date:  2020-09-11       Impact factor: 4.241

Review 9.  Calorie Restriction for Cancer Prevention and Therapy: Mechanisms, Expectations, and Efficacy.

Authors:  Chiara Vidoni; Alessandra Ferraresi; Andrea Esposito; Chinmay Maheshwari; Danny N Dhanasekaran; Vincenzo Mollace; Ciro Isidoro
Journal:  J Cancer Prev       Date:  2021-12-30

10.  Inhibition of the mechanistic target of rapamycin induces cell survival via MAPK in tuberous sclerosis complex.

Authors:  Yiyang Lu; Erik Y Zhang; Jie Liu; Jane J Yu
Journal:  Orphanet J Rare Dis       Date:  2020-08-17       Impact factor: 4.303

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