Literature DB >> 20681032

A phase 2 study of the oral mammalian target of rapamycin inhibitor, everolimus, in patients with recurrent endometrial carcinoma.

Brian M Slomovitz1, Karen H Lu, Taren Johnston, Robert L Coleman, Mark Munsell, Russell R Broaddus, Cheryl Walker, Lois M Ramondetta, Thomas W Burke, David M Gershenson, Judith Wolf.   

Abstract

BACKGROUND: Dysregulation of phosphatase and tensin homolog (PTEN) and the gene that encodes the p110α catalytic subunit of phosphatidylinositol-3-kinase (PI3K), PIK3CA, are the most common mutations in endometrial carcinoma (EC). Loss of PTEN or activation of PIK3CA results in constitutive activation of AKT, which leads to up-regulation of mammalian target of rapamycin (mTOR). Everolimus is an oral rapamycin analog that acts by selectively inhibiting mTOR.
METHODS: A single-institution, open-labeled, phase 2 study of everolimus in patients with measurable recurrent EC who had failed at least 1 and no more than 2 prior chemotherapeutic regimens was performed. Everolimus was administered at a dose of 10 mg orally daily for 28-day cycles. Patients were treated until disease progression or toxicity. The primary endpoint was clinical benefit response (CBR), defined as a confirmed complete or partial response or prolonged stable disease (SD) (≥8 weeks). Inclusion was limited to patients with endometrioid histology.
RESULTS: A total of 35 patients were enrolled (median age, 58 years; range, 38-81 years). A total of 81 cycles were administered. Twelve of 28 (43%) evaluable patients had not developed disease progression at the time of the first objective evaluation (8 weeks). All these patients had SD (median, 4.5 cycles; range, 2-10 cycles). Six of the 28 (21%) patients had a confirmed CBR at 20 weeks of therapy. Patients with CBR discontinued treatment because of toxicity (6 patients), disease progression (5 patients), and noncompliance (1 patient). Seven patients were unevaluable after receiving ≤1 cycle because of toxicity (5 patients) or noncompliance (2 patients). The most common drug-related toxicities were fatigue, anemia, pain, lymphopenia, and nausea.
CONCLUSIONS: Everolimus demonstrated encouraging single-agent CBR in pretreated patients with recurrent endometrioid EC. Future studies will evaluate this agent in combination with hormonal and/or cytotoxic therapy.
Copyright © 2010 American Cancer Society.

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Year:  2010        PMID: 20681032      PMCID: PMC5120730          DOI: 10.1002/cncr.25515

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  10 in total

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Authors:  Mary-Ann Bjornsti; Peter J Houghton
Journal:  Nat Rev Cancer       Date:  2004-05       Impact factor: 60.716

2.  Regulation of G1 progression by the PTEN tumor suppressor protein is linked to inhibition of the phosphatidylinositol 3-kinase/Akt pathway.

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3.  PIK3CA and PTEN mutations in uterine endometrioid carcinoma and complex atypical hyperplasia.

Authors:  Monica Prasad Hayes; Hong Wang; Rosanny Espinal-Witter; Wayne Douglas; Garron J Solomon; Suzanne J Baker; Lora Hedrick Ellenson
Journal:  Clin Cancer Res       Date:  2006-10-15       Impact factor: 12.531

4.  Correlation between loss of PTEN expression and Akt phosphorylation in endometrial carcinoma.

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Journal:  Clin Cancer Res       Date:  2001-04       Impact factor: 12.531

5.  An inhibitor of mTOR reduces neoplasia and normalizes p70/S6 kinase activity in Pten+/- mice.

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Journal:  Proc Natl Acad Sci U S A       Date:  2001-08-14       Impact factor: 11.205

6.  Rapamycin inhibits telomerase activity by decreasing the hTERT mRNA level in endometrial cancer cells.

Authors:  Chunxiao Zhou; Paola A Gehrig; Young E Whang; John F Boggess
Journal:  Mol Cancer Ther       Date:  2003-08       Impact factor: 6.261

7.  Phase II randomized study of neoadjuvant everolimus plus letrozole compared with placebo plus letrozole in patients with estrogen receptor-positive breast cancer.

Authors:  José Baselga; Vladimir Semiglazov; Peter van Dam; Alexey Manikhas; Meritxell Bellet; José Mayordomo; Mario Campone; Ernst Kubista; Richard Greil; Giulia Bianchi; Jutta Steinseifer; Betty Molloy; Erika Tokaji; Humphrey Gardner; Penny Phillips; Michael Stumm; Heidi A Lane; J Michael Dixon; Walter Jonat; Hope S Rugo
Journal:  J Clin Oncol       Date:  2009-04-20       Impact factor: 44.544

8.  Loss of PTEN expression followed by Akt phosphorylation is a poor prognostic factor for patients with endometrial cancer.

Authors:  N Terakawa; Y Kanamori; S Yoshida
Journal:  Endocr Relat Cancer       Date:  2003-06       Impact factor: 5.678

9.  Significance of PTEN alterations in endometrial carcinoma: a population-based study of mutations, promoter methylation and PTEN protein expression.

Authors:  Helga B Salvesen; Ingunn Stefansson; Ellen I Kretzschmar; Paula Gruber; Nicola D MacDonald; Andy Ryan; Ian J Jacobs; Lars A Akslen; Soma Das
Journal:  Int J Oncol       Date:  2004-12       Impact factor: 5.650

10.  Reduced progression of endometrial hyperplasia with oral mTOR inhibition in the Pten heterozygote murine model.

Authors:  Michael R Milam; Joseph Celestino; Weiguo Wu; Russell R Broaddus; Kathleen M Schmeler; Brian M Slomovitz; Pamela T Soliman; David M Gershenson; Hong Wang; Lora H Ellenson; Karen H Lu
Journal:  Am J Obstet Gynecol       Date:  2007-03       Impact factor: 8.661

  10 in total
  79 in total

1.  The search continues: looking for predictive biomarkers for response to mammalian target of rapamycin inhibition in endometrial cancer.

Authors:  Larissa A Meyer; Brian M Slomovitz; Bojana Djordjevic; Shannon N Westin; David A Iglesias; Mark F Munsell; Yunyun Jiang; Rosemarie Schmandt; Russell R Broaddus; Robert L Coleman; John M Galbincea; Karen H Lu
Journal:  Int J Gynecol Cancer       Date:  2014-05       Impact factor: 3.437

2.  Loss of p27 Associated with Risk for Endometrial Carcinoma Arising in the Setting of Obesity.

Authors:  A S McCampbell; M L Mittelstadt; R Dere; S Kim; L Zhou; B Djordjevic; P T Soliman; Q Zhang; C Wei; S D Hursting; K H Lu; R R Broaddus; C L Walker
Journal:  Curr Mol Med       Date:  2016       Impact factor: 2.222

3.  Temsirolimus with or without megestrol acetate and tamoxifen for endometrial cancer: a gynecologic oncology group study.

Authors:  Gini F Fleming; Virginia L Filiaci; Brandon Marzullo; Richard J Zaino; Susan A Davidson; Michael Pearl; Vicky Makker; James J Burke; Susan L Zweizig; Linda Van Le; Parviz Hanjani; Gordon Downey; Joan L Walker; Henry D Reyes; Kimberly K Leslie
Journal:  Gynecol Oncol       Date:  2014-01-20       Impact factor: 5.482

Review 4.  Differentiating mTOR inhibitors in renal cell carcinoma.

Authors:  Sumanta K Pal; David I Quinn
Journal:  Cancer Treat Rev       Date:  2013-02-21       Impact factor: 12.111

Review 5.  New Targeted Agents in Endometrial Cancer: Are We Really Making Progress?

Authors:  Victor Rodriguez-Freixinos; Katherine Karakasis; Amit M Oza
Journal:  Curr Oncol Rep       Date:  2016-04       Impact factor: 5.075

6.  A genetic mouse model of invasive endometrial cancer driven by concurrent loss of Pten and Lkb1 Is highly responsive to mTOR inhibition.

Authors:  Hailing Cheng; Pixu Liu; Fan Zhang; Erbo Xu; Lynn Symonds; Carolynn E Ohlson; Roderick T Bronson; Sauveur-Michel Maira; Emmanuelle Di Tomaso; Jane Li; Andrea P Myers; Lewis C Cantley; Gordon B Mills; Jean J Zhao
Journal:  Cancer Res       Date:  2013-12-09       Impact factor: 12.701

7.  Nuclear receptor 4A1 (NR4A1) antagonists induce ROS-dependent inhibition of mTOR signaling in endometrial cancer.

Authors:  Kumaravel Mohankumar; Xi Li; Subhashree Sridharan; Keshav Karki; Stephen Safe
Journal:  Gynecol Oncol       Date:  2019-04-30       Impact factor: 5.482

8.  mTOR and its downstream pathway are activated in the dorsal root ganglion and spinal cord after peripheral inflammation, but not after nerve injury.

Authors:  Lingli Liang; Bo Tao; Longchang Fan; Myron Yaster; Yi Zhang; Yuan-Xiang Tao
Journal:  Brain Res       Date:  2013-04-11       Impact factor: 3.252

9.  Antitumor effects and molecular mechanisms of ponatinib on endometrial cancer cells harboring activating FGFR2 mutations.

Authors:  Do-Hee Kim; Yeonui Kwak; Nam Doo Kim; Taebo Sim
Journal:  Cancer Biol Ther       Date:  2016       Impact factor: 4.742

Review 10.  Targeting tumorigenesis: development and use of mTOR inhibitors in cancer therapy.

Authors:  Ruirong Yuan; Andrea Kay; William J Berg; David Lebwohl
Journal:  J Hematol Oncol       Date:  2009-10-27       Impact factor: 17.388

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