Literature DB >> 18038218

Phase II study of ispinesib in recurrent or metastatic squamous cell carcinoma of the head and neck.

Patricia A Tang1, Lillian L Siu, Eric X Chen, Sebastien J Hotte, Stephen Chia, James K Schwarz, Gregory R Pond, Caitlin Johnson, A Dimitrios Colevas, Timothy W Synold, Lakshmi S Vasist, Eric Winquist.   

Abstract

Ispinesib (SB-715992) inhibits the mitotic kinesin spindle protein (KSP), a novel target for anticancer therapy. A phase II study was conducted to examine the efficacy of ispinesib in recurrent or metastatic head and neck squamous cell carcinoma (RMHNSC). Patients with up to one prior line of chemotherapy for RMHNSC were treated with ispinesib 18 mg/m2 IV over 1 hour every 21 days. Twenty-one patients were enrolled onto this study with a target stage I sample size of 19. Of 20 evaluable patients, no objective responses were seen and stable disease > 2 cycles was observed in five patients (25%). The median time to progression was 1.4 (95% CI 1.3-2.3) months, median survival was 3.5 (95% CI 2.8-7.8) months, and 1 year overall survival was 20% (95% CI 8.3-48.1%). The most frequent attributable grades III-V adverse events were neutropenia (60% of patients) and leukopenia (55%). The pharmacokinetic profile was consistent with results from phase I studies. Archival tissues (n = 14) demonstrated low to moderate KSP expression by immunohistochemistry. In addition, no pharmacodynamic changes were observed in peripheral blood mononuclear cells. We detected no antitumor activity of ispinesib in RMHNSC on this dosing schedule.

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Year:  2007        PMID: 18038218     DOI: 10.1007/s10637-007-9098-8

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  12 in total

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Journal:  Cancer       Date:  1986-01-01       Impact factor: 6.860

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Authors:  C Jacobs; G Lyman; E Velez-García; K S Sridhar; W Knight; H Hochster; L T Goodnough; J E Mortimer; L H Einhorn; L Schacter
Journal:  J Clin Oncol       Date:  1992-02       Impact factor: 44.544

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Authors:  H M Kantarjian; S Padmanabhan; W Stock; M S Tallman; G A Curt; J Li; A Osmukhina; K Wu; D Huszar; G Borthukar; S Faderl; G Garcia-Manero; T Kadia; K Sankhala; O Odenike; J K Altman; M Minden
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Review 2.  New combination therapies with cell-cycle agents.

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Review 5.  Kinesin-5: cross-bridging mechanism to targeted clinical therapy.

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6.  Synthesis and characterization of tritylthioethanamine derivatives with potent KSP inhibitory activity.

Authors:  Delany Rodriguez; Chinnasamy Ramesh; Lauren H Henson; Lori Wilmeth; Bj K Bryant; Samuel Kadavakollu; Rebecca Hirsch; Johnelle Montoya; Porsha R Howell; Jon M George; David Alexander; Dennis L Johnson; Jeffrey B Arterburn; Charles B Shuster
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7.  Phase II study to assess the efficacy, safety and tolerability of the mitotic spindle kinesin inhibitor AZD4877 in patients with recurrent advanced urothelial cancer.

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8.  Eg5 inhibitor, a novel potent targeted therapy, induces cell apoptosis in renal cell carcinoma.

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Journal:  Tumour Biol       Date:  2014-05-07

Review 9.  Beyond taxanes: a review of novel agents that target mitotic tubulin and microtubules, kinases, and kinesins.

Authors:  Michael R Harrison; Kyle D Holen; Glenn Liu
Journal:  Clin Adv Hematol Oncol       Date:  2009-01

10.  The expression of Eg5 predicts a poor outcome for patients with renal cell carcinoma.

Authors:  Dingqi Sun; Jiaju Lu; Kejia Ding; Dongbin Bi; Zhihong Niu; Qingwei Cao; Jie Zhang; Sentai Ding
Journal:  Med Oncol       Date:  2013-02-01       Impact factor: 3.064

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