Literature DB >> 19228743

A phase I trial to determine the safety, tolerability, and maximum tolerated dose of deforolimus in patients with advanced malignancies.

Christine M Hartford1, Apurva A Desai, Linda Janisch, Theodore Karrison, Victor M Rivera, Lori Berk, John W Loewy, Hedy Kindler, Walter M Stadler, Heather L Knowles, Camille Bedrosian, Mark J Ratain.   

Abstract

PURPOSE: This was a phase I trial to determine the maximum tolerated dose and toxicity of deforolimus (AP23573, MK-8669), an inhibitor of mammalian target of rapamycin (mTOR). The pharmacokinetics, pharmacodynamics, and antineoplastic effects were also studied. EXPERIMENTAL
DESIGN: Deforolimus was administered intravenously over 30 min every 7 days according to a flat dosing schedule. Dose was escalated according to an accelerated titration design. Patients remained on study until disease progression as long as they tolerated the drug without significant toxicities.
RESULTS: Forty-six patients were enrolled on the study. Common side effects included fatigue, anorexia, and mucositis. The maximum tolerated dose was 75 mg and mucositis was the dose-limiting toxicity. Similar to other mTOR inhibitors, deforolimus exhibited nonlinear pharmacokinetics and a prolonged half-life. Among 34 patients evaluable for response, 1 patient had a partial response, 21 patients had stable disease, and 12 had progressed. Percent change in tumor size was significantly associated with AUC (P=0.015). A significant association was also detected for maximum change in cholesterol within the first two cycles of therapy and change in tumor size (r=-0.38; P=0.029).
CONCLUSIONS: Deforolimus was well tolerated on the schedule tested in this trial with toxicity and pharmacokinetic profiles that were similar to that of other mTOR inhibitors. Additional phase II studies are needed to determine if deforolimus is superior to other mTOR inhibitors in terms of efficacy. The change in serum cholesterol as a potential biomarker of activity should be studied further.

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Year:  2009        PMID: 19228743      PMCID: PMC3147153          DOI: 10.1158/1078-0432.CCR-08-2076

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  21 in total

1.  A phase 2 clinical trial of deforolimus (AP23573, MK-8669), a novel mammalian target of rapamycin inhibitor, in patients with relapsed or refractory hematologic malignancies.

Authors:  David A Rizzieri; Eric Feldman; John F Dipersio; Nashat Gabrail; Wendy Stock; Roger Strair; Victor M Rivera; Maher Albitar; Camille L Bedrosian; Francis J Giles
Journal:  Clin Cancer Res       Date:  2008-05-01       Impact factor: 12.531

2.  Rapamycin inhibits primary and metastatic tumor growth by antiangiogenesis: involvement of vascular endothelial growth factor.

Authors:  Markus Guba; Philipp von Breitenbuch; Markus Steinbauer; Gudrun Koehl; Stefanie Flegel; Matthias Hornung; Christiane J Bruns; Carl Zuelke; Stefan Farkas; Matthias Anthuber; Karl-Walter Jauch; Edward K Geissler
Journal:  Nat Med       Date:  2002-02       Impact factor: 53.440

3.  Rapamycin (AY-22,989), a new antifungal antibiotic. II. Fermentation, isolation and characterization.

Authors:  S N Sehgal; H Baker; C Vézina
Journal:  J Antibiot (Tokyo)       Date:  1975-10       Impact factor: 2.649

4.  Randomized discontinuation design: application to cytostatic antineoplastic agents.

Authors:  Gary L Rosner; Walter Stadler; Mark J Ratain
Journal:  J Clin Oncol       Date:  2002-11-15       Impact factor: 44.544

5.  Enhanced sensitivity of PTEN-deficient tumors to inhibition of FRAP/mTOR.

Authors:  M S Neshat; I K Mellinghoff; C Tran; B Stiles; G Thomas; R Petersen; P Frost; J J Gibbons; H Wu; C L Sawyers
Journal:  Proc Natl Acad Sci U S A       Date:  2001-08-14       Impact factor: 11.205

6.  Accelerated titration designs for phase I clinical trials in oncology.

Authors:  R Simon; B Freidlin; L Rubinstein; S G Arbuck; J Collins; M C Christian
Journal:  J Natl Cancer Inst       Date:  1997-08-06       Impact factor: 13.506

7.  Rapamycin causes poorly reversible inhibition of mTOR and induces p53-independent apoptosis in human rhabdomyosarcoma cells.

Authors:  H Hosoi; M B Dilling; T Shikata; L N Liu; L Shu; R A Ashmun; G S Germain; R T Abraham; P J Houghton
Journal:  Cancer Res       Date:  1999-02-15       Impact factor: 12.701

8.  Safety and pharmacokinetics of escalated doses of weekly intravenous infusion of CCI-779, a novel mTOR inhibitor, in patients with cancer.

Authors:  Eric Raymond; Jérôme Alexandre; Sandrine Faivre; Karina Vera; Eric Materman; Joseph Boni; Cathie Leister; Joan Korth-Bradley; Axel Hanauske; Jean-Pierre Armand
Journal:  J Clin Oncol       Date:  2004-05-10       Impact factor: 44.544

9.  Randomized phase II study of multiple dose levels of CCI-779, a novel mammalian target of rapamycin kinase inhibitor, in patients with advanced refractory renal cell carcinoma.

Authors:  Michael B Atkins; Manuel Hidalgo; Walter M Stadler; Theodore F Logan; Janice P Dutcher; Gary R Hudes; Young Park; Song-Heng Liou; Bonnie Marshall; Joseph P Boni; Gary Dukart; Matthew L Sherman
Journal:  J Clin Oncol       Date:  2004-03-01       Impact factor: 44.544

10.  Rapamycin-induced G1 arrest in cycling B-CLL cells is associated with reduced expression of cyclin D3, cyclin E, cyclin A, and survivin.

Authors:  Thomas Decker; Susanne Hipp; Ingo Ringshausen; Christian Bogner; Madlene Oelsner; Folker Schneller; Christian Peschel
Journal:  Blood       Date:  2002-08-29       Impact factor: 22.113

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  32 in total

1.  Management of metabolic effects associated with anticancer agents targeting the PI3K-Akt-mTOR pathway.

Authors:  Naifa L Busaidy; Azeez Farooki; Afshin Dowlati; John P Perentesis; Janet E Dancey; Laurence A Doyle; Joanna M Brell; Lillian L Siu
Journal:  J Clin Oncol       Date:  2012-07-09       Impact factor: 44.544

Review 2.  mTOR inhibitors and its role in the treatment of head and neck squamous cell carcinoma.

Authors:  Shaun A Nguyen; David Walker; M Boyd Gillespie; J Silvio Gutkind; Terry A Day
Journal:  Curr Treat Options Oncol       Date:  2012-03

Review 3.  Common toxicities of mammalian target of rapamycin inhibitors.

Authors:  Scott A Soefje; Anand Karnad; Andrew J Brenner
Journal:  Target Oncol       Date:  2011-04-16       Impact factor: 4.493

4.  Dual targeting of the Akt/mTOR signaling pathway inhibits castration-resistant prostate cancer in a genetically engineered mouse model.

Authors:  Nicolas Floc'h; Carolyn Waugh Kinkade; Takashi Kobayashi; Alvaro Aytes; Celine Lefebvre; Antonina Mitrofanova; Robert D Cardiff; Andrea Califano; Michael M Shen; Cory Abate-Shen
Journal:  Cancer Res       Date:  2012-07-19       Impact factor: 12.701

Review 5.  Updates of mTOR inhibitors.

Authors:  Hongyu Zhou; Yan Luo; Shile Huang
Journal:  Anticancer Agents Med Chem       Date:  2010-09       Impact factor: 2.505

Review 6.  Treatment of HER2-positive breast cancer: current status and future perspectives.

Authors:  Carlos L Arteaga; Mark X Sliwkowski; C Kent Osborne; Edith A Perez; Fabio Puglisi; Luca Gianni
Journal:  Nat Rev Clin Oncol       Date:  2011-11-29       Impact factor: 66.675

Review 7.  mTOR signaling and drug development in cancer.

Authors:  Janet Dancey
Journal:  Nat Rev Clin Oncol       Date:  2010-03-16       Impact factor: 66.675

Review 8.  Medulloblastoma development: tumor biology informs treatment decisions.

Authors:  Vidya Gopalakrishnan; Rong-Hua Tao; Tara Dobson; William Brugmann; Soumen Khatua
Journal:  CNS Oncol       Date:  2015

9.  Multimodality therapy for metastatic sarcomas confined to the lung.

Authors:  Russell P Gollard; J Francis Turner
Journal:  Oncol Lett       Date:  2012-07-24       Impact factor: 2.967

10.  Combined targeting of mTOR and AKT is an effective strategy for basal-like breast cancer in patient-derived xenograft models.

Authors:  Siguang Xu; Shunqiang Li; Zhanfang Guo; Jingqin Luo; Matthew J Ellis; Cynthia X Ma
Journal:  Mol Cancer Ther       Date:  2013-05-20       Impact factor: 6.261

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