Literature DB >> 22994502

Everolimus in the treatment of hormone receptor-positive breast cancer.

Mariana Chavez-MacGregor1, Ana Maria Gonzalez-Angulo.   

Abstract

INTRODUCTION: The phosphoinositide triphosphate kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) is a central regulatory pathway involved in cell proliferation, growth, differentiation, metabolism and survival. Deregulation of this pathway is well described in breast cancer and is associated to the development of endocrine resistance among hormone receptor (HR)-positive tumors. Everolimus , an mTOR-inhibitor has clinical activity against breast cancer and has shown to restore sensitivity to endocrine therapy. AREAS COVERED: We review the clinical data and the results of the recently published clinical trials evaluating the use of everolimus in HR-positive breast cancer patients in combination with endocrine therapy. We discuss the data regarding efficacy but also describe in detail the side effect profile of this drug. EXPERT OPINION: Everolimus represents a new therapeutic alternative for the treatment of HR-positive metastatic breast cancer. Everolimus is in general a well-tolerated drug, however, stomatitis, fatigue and hematological abnormalities are common. It is still unclear if there are specific subgroups of patients that receive greater benefit from everolimus and whether there is a relationship between the presence of PIK3CA mutations and efficacy. The results of biomarker studies will hopefully provide information that will help us determine which patients are most likely to benefit from this treatment.

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Year:  2012        PMID: 22994502     DOI: 10.1517/13543784.2012.726218

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  8 in total

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Review 2.  Triple-negative breast cancer: bridging the gap from cancer genomics to predictive biomarkers.

Authors:  S Lindsey Davis; S Gail Eckhardt; John J Tentler; Jennifer R Diamond
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3.  Acute myeloid leukemia: potential for new therapeutic approaches targeting mRNA translation pathways.

Authors:  Jessica K Altman; Leonidas C Platanias
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4.  Prevalence of PIK3CA mutations and the SNP rs17849079 in Arab breast cancer patients.

Authors:  Bedri Karakas; Dilek Colak; Namik Kaya; Hazem Ghebeh; Abeer Al-Qasem; Fawziah Hendrayani; Mohamed Toulimat; Taher Al-Tweigeri; Ben Ho Park; Abdelilah Aboussekhra
Journal:  Cancer Biol Ther       Date:  2013-08-12       Impact factor: 4.742

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Authors:  Amancio Carnero; Carmen Blanco-Aparicio; Hiroshi Kondoh; Matilde E Lleonart; Juan Fernando Martinez-Leal; Chiara Mondello; A Ivana Scovassi; William H Bisson; Amedeo Amedei; Rabindra Roy; Jordan Woodrick; Annamaria Colacci; Monica Vaccari; Jayadev Raju; Fahd Al-Mulla; Rabeah Al-Temaimi; Hosni K Salem; Lorenzo Memeo; Stefano Forte; Neetu Singh; Roslida A Hamid; Elizabeth P Ryan; Dustin G Brown; John Pierce Wise; Sandra S Wise; Hemad Yasaei
Journal:  Carcinogenesis       Date:  2015-06       Impact factor: 4.944

6.  Signaling mechanisms that suppress the cytostatic actions of rapamycin.

Authors:  Stephan C Jahn; Mary E Law; Patrick E Corsino; Bradley J Davis; Jeffrey K Harrison; Brian K Law
Journal:  PLoS One       Date:  2014-06-13       Impact factor: 3.240

Review 7.  Understanding genomics and the immune environment of penile cancer to improve therapy.

Authors:  Ahmet Murat Aydin; Jad Chahoud; Jacob J Adashek; Mounsif Azizi; Anthony Magliocco; Jeffrey S Ross; Andrea Necchi; Philippe E Spiess
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Review 8.  Oral mucosal injury caused by mammalian target of rapamycin inhibitors: emerging perspectives on pathobiology and impact on clinical practice.

Authors:  Douglas E Peterson; Joyce A O'Shaughnessy; Hope S Rugo; Sharon Elad; Mark M Schubert; Chi T Viet; Cynthia Campbell-Baird; Jan Hronek; Virginia Seery; Josephine Divers; John Glaspy; Brian L Schmidt; Timothy F Meiller
Journal:  Cancer Med       Date:  2016-06-23       Impact factor: 4.452

  8 in total

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